<i>Paliurus ramosissimus </i>(Lour.) Poir. extract and preparation methods and uses thereof

Abstract

The invention belongs to the field of medicine, involving new uses of Paliurus ramosissimus (Lour.) Poir. and its extract, in particular the use of Paliurus ramosissimus (Lour.) Poir. and its extract in preparation of drugs with anti-fibrotic, anti-fungal, and anti-tumor activities, for the treatment of oral and digestive tract inflammation or (and) ulcer-related diseases, or with bi-directional immunomodulatory effects.

Claims

1. A method for treating a tumor in a subject, said method comprising administering to the subject in need thereof a composition comprising Paliurus ramosissimus, wherein the Paliurus ramosissimus is a Paliurus ramosissimus fresh leaf ethanolic extract or a Paliurus ramosissimus whole plant ethanolic extract.

2. The method according to claim 1, wherein the composition comprising Paliurus ramosissimus is a pharmaceutical composition comprising a Paliurus ramosissimus fresh leaf ethanolic extract or a Paliurus ramosissimus whole plant ethanolic extract as the active ingredient, and further comprising a pharmaceutically acceptable carrier.

Description

DETAILED DESCRIPTION

(1) The following detailed description, in the form of embodiment, further describes the aforementioned content in the present invention in details, and it illustrates but does not limit the invention.

(2) The study on ingredients of Paliurus ramosissimus (Lour.) Poir. extract is as follows.

(3) Preparation of sample test solution: take 1 g of the extract sample, dissolve in 25 ml of anhydrous ethanol, and centrifuge. Take 2 ml of the supernatant, dilute 5-fold with ethanol to a final concentration of 0.008 g/ml.

(4) (1) Identification of Triterpenoids

(5) A. L-B Reaction

(6) Dissolve the sample in acetic anhydride, add a few drops of concentrated sulfuric acid-acetic anhydride (1:20), yellow.fwdarw.red.fwdarw.purple.fwdarw.blue color changes appear, and the color finally fades, indicating the presence of triterpenoids.

(7) B. Kahlenberg Reaction

(8) Spot the sample in chloroform or alcohol solution on filter paper, spray 20% antimony pentachloride in chloroform solution (or saturated antimony trichloride in chloroform solution), heat at 60-70° C. after drying, blue appears, indicating the presence of triterpenoids.

(9) C. R—H Reaction

(10) Spot sample test solution on filter paper, spray 25% trichloroacetic acid in ethanol solution, heat to 100° C., red appears and gradually becomes purple, indicating the presence of triterpenoids.

(11) D. Salkowki Reaction

(12) Dissolve the sample in chloroform, add concentrated sulfuric acid, the sulfuric acid layer appears red or blue, and the chloroform layer appears green fluorescence, indicating triterpenoids.

(13) E. Tschugaeff Reaction

(14) Dissolve the sample in glacial acetic acid, add a few drops of acetyl chloride and a few grains of zinc chloride crystal, mildly heat, it appears pale pink or purple, indicating the presence of triterpenoids.

(15) (2) Identification of Flavonoids

(16) A. Hydrochloric Acid—Magnesium Reduction Reaction (Chromogenic Reduction Reaction)

(17) Dissolve a small amount of sample in 1 ml of ethanol, and add a little magnesium powder and concentrated hydrochloric acid, shake for a while, and purple appears, indicating the presence of flavonoids.

(18) B. Aluminum Trichloride Reaction (Chromogenic Metal Ions Complexation)

(19) Apply the sample test solution on filter paper with a glass rod, blow to dryness, spray 1% aluminum chloride in ethanol solution, blow to dryness, place under a UV lamp and bright yellow appears, indicating the presence of flavonoids.

(20) C. Ferric Chloride Reaction (Chromogenic Metal Ions Complexation)

(21) Apply the sample test solution on filter paper with a glass rod, blow to dryness, observe the fluorescence under ultraviolet light, spray 3% ferric chloride in ethanol solution, blow to dryness, a dark blue fluorescent spot appears and turns into a brown fluorescent spot after being smoked by ammonia, indicating the presence of flavonoids.

(22) D. Chromogenic Reaction with Alkaline Reagent

(23) Apply the sample test solution on filter paper with a glass rod, dry, spray sodium hydroxide solution or exposure to ammonia vapors, observe under sunlight light, and ammonia vapor turns sample spot to bright yellow, indicating the presence of flavonoids.

(24) (3) Identification of Alkaloids

(25) A. Modified Bismuth Potassium Iodide (Dragendorff) Method

(26) {circle around (1)} Dissolve 0.85 g of bismuth nitrate in 10 ml of glacial acetic acid and 40 ml of water; {circle around (2)} Dissolve 8 g of potassium iodide in 20 ml of water. Mix the equal amount of {circle around (1)} {circle around (2)} test solutions, place in a brown bottle as the stock solution. Before use, mix 1 ml of the stock solution, 4 ml of glacial acetic acid and 12 ml of water. Add the sample test solution into the above reagent, the solution becomes reddish brown, and after adding distilled water and shaking, precipitate forms, indicating the presence of alkaloids.

(27) B. Iodine—Potassium Iodide (Wagner) Method

(28) Dissolve 1 g of iodine and 10 g of potassium iodide in 50 ml of water, add 2 ml of acetic acid, and add water to 100 ml. Take appropriate amount of the above reagent, add 1 ml of the sample test solution, and the solution becomes brown, indicating the presence of alkaloids.

(29) C. Silicotungstic Acid (Bertrand) Method

(30) Dissolve 5 g of silicotungstic acid in 100 ml of water, add a small amount of concentrated hydrochloric acid to adjust pH to approximately 2. Take appropriate amount of the above reagent, add 1 ml of the sample test solution, and the solution becomes brown, indicating the presence of alkaloids.

(31) (4) Identification of coumarins

(32) A. Iron-hydroxamate reaction

(33) {circle around (1)} a. Dissolve 20 g of hydroxylamine hydrochloride in 50 ml of water, dilute to 200 ml with ethanol, store in a cool place; b. dissolve 50 g of potassium hydroxide in a little water, add 500 ml of ethanol. {circle around (2)} Dissolve 10 g of ferric chloride (FeCl.sub.3. 6H.sub.2O) in 20 ml 36% hydrochloric acid solution, add 200 ml of ethyl ether, shake well, and store in a sealed container. When using, mix one portion of {circle around (1)} a. and 2 portions of {circle around (1)} b, filter the precipitate, and store the filtrate in a fridge. Apply the sample test solution on filter paper with a glass rod, spray a. b. mixture test solution, slightly dry, then spray test solution {circle around (2)}, and red color appears, indicating the presence of coumarins.

(34) B. Diazotization Reaction

(35) {circle around (1)} Dissolve 0.35 g of paranitroaniline in 5 ml of concentrated hydrochloric acid, add water to 50 ml; {circle around (2)} add 50 ml of water to 5 g of sodium nitrite. Take the same amount of {circle around (1)}, {circle around (2)} solutions, and mix in an ice-water bath for future use. Take a small amount of the sample, add diazonium reagent dropwise, and orange-red appears, indicating the presence of coumarins.

(36) These studies have identified that the main ingredients of Paliurus ramosissimus (Lour.) Poir. extract in the present invention include flavonoids, triterpenoids, alkaloids, coumarins, and glycosides and monomers of the above flavonoids, triterpenoids, alkaloids, coumarins, as well as polysaccharides and celluloses.

I. The Antitumor Activity of Paliurus ramosissimus (Lour.) Poir. Leaf Extract

(37) 1. Extraction from Paliurus ramosissimus (Lour.) Poir. Leaves

(38) (1) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. fresh leaves, add 8-10 times of 95% ethanol for 1-2 days (purpose: 1. to deactivate the activity of enzymes in fresh leaves, thus avoiding the destruction of active ingredients; 2. to increase fresh leaves hardness, thus facilitating the next crushing process), crush fresh leaves, then add 10 times of 95% ethanol (60-100% ethanol extraction), soak for three days to extract alcohol-soluble ingredients. Collect the extract liquid, recover ethanol at 30-40° C. under reduced pressure to no alcohol smell, and further freeze-dry the extract concentrated liquid to obtain Paliurus ramosissimus (Lour.) Poir. fresh leaf ethanol extract.

(39) (2) Dry the extraction residue, add 8 to 10 times of water, soak for three days to extract water-soluble ingredients, collect the extract liquid, and freeze-dry to obtain Paliurus ramosissimus (Lour.) Poir. fresh leaf aqueous extract.

(40) (3) Extract Paliurus ramosissimus (Lour.) Poir. dry products (natural drying at room temperature) as the method described above to obtain Paliurus ramosissimus (Lour.) Poir. dry product alcohol extract and water extract.

(41) (4) Soak Paliurus ramosissimus (Lour.) Poir. fresh leaves in ethanol, dry in a dark place to obtain dry leaves, and extract the obtained dry leaves after soaking in ethanol and dryness as the method described above to obtain alcohol extract and water extract.

(42) 2. Anti-Tumor Activity

(43) The study compares antitumor activity of Paliurus ramosissimus (Lour.) Poir. leaf extract. Take a variety of tumor cells in logarithmic growth phase (tumor cell lines used are the followings: cervical carcinoma cell line Hela; human hepatoma cell line SMMC-7721; human lung carcinoma cell line A549; human colon carcinoma cell line Caco-2; leukemia cell line K562; gastric carcinoma cell line MGC-803;), centrifuge at 2000 rpm for 5 min, adjust precipitate cell concentration of cell suspension to 1×10.sup.5 cells/ml with corresponding culture medium containing 10% fetal bovine serum, and seed cells in 96-well culture plates. To each well, add 200 μl of cell suspension, respectively add sterile extract solution of certain concentration to make the final concentration of extract in each well is 0.02, 0.1, 0.2, 0.4, 0.5, 0.8, 1.0, 2.0 mg/ml, mix well, place in 37° C., 5% CO.sub.2 incubator for 24 h, precipitate the culture, wash twice with PBS, to each well, add 20 μl of 5 mg/ml MTT phosphate buffer and 150 μl of culture medium, culture under the same conditions for 4 h, and then terminate the culture. Centrifuge at 2000 rpm for 5 min, then discard the culture medium in wells, to each well, add 150 μl of DMSO, shake for 10 min so that the formed formazan particles are fully dissolved, and determine absorbance with microplate reader. Select 570 nm as the measurement wavelength. Calculate IC50 of the extract to tumor cells. The results are shown in Table 1.

(44) TABLE-US-00001 TABLE 1 Inhibition effects of Paliurus ramosissimus (Lour.) Poir. extract on different tumor cells: Cell line Hela SMMC-7721 A549 Caco-2 MGC-803 Paliurus ramosissimus 0.0473 mg/ml 0.1957 mg/ml 0.0126 mg/ml 0.1174 mg/ml 0.2367 mg/ml (Lour.) Poir. Fresh leaf alcohol extract Paliurus ramosissimus — — — — — (Lour.) Poir. Fresh leaf water extract Paliurus ramosissimus — — — — — (Lour.) Poir. Dried leaf alcohol extract Paliurus ramosissimus — — — — — (Lour.) Poir. Dried leaf water extract Alcohol extract of 0.0442 mg/ml 0.2038 mg/ml 0.0175 mg/ml 0.1060 mg/ml 0.2512 mg/ml Paliurus ramosissimus (Lour.) Poir. Leaf soaked in ethanol and air dried Water extract of — — — — — Paliurus ramosissimus (Lour.) Poir. Leaf soaked in ethanol and air dried

(45) The results have showed that, Paliurus ramosissimus (Lour.) Poir. fresh leaf alcohol extract and alcohol extract of Paliurus ramosissimus (Lour.) Poir. leaf soaked in ethanol and air dried have good anti-tumor activity, while other extracts do not have anti-tumor activity. The reasons may be related to the solubility and stability of the active extract.

(46) 3. Determination of Ingredient Content in Paliurus ramosissimus (Lour.) Poir. Leaf Alcohol Extract

(47) (1) Determination of Triterpenoids Content

(48) Take three portions of approximately 0.1 g of the coarse powder of this product, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of alcohol extract contains 0.052±0.010 g of triterpenoids.

(49) (2) Determination of Flavonoids Content

(50) Take three portions of approximately 0.1 g (equivalent to 2 g raw material) of the coarse powder of this product, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of alcohol extract contains 0.325±0.043 g of flavonoids.

(51) (3) Determination of Alkaloids Content

(52) Take three portions of approximately 1 g of the coarse powder of this product, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of alcohol extract contains 0.028±0.007 g of alkaloids.

(53) (4) Determination of Coumarins Content

(54) It is determined that the coumarins content is 1% to 10%.

(55) 4. Studies on Antitumor Activity of Paliurus ramosissimus (Lour.) Poir. Leaf Alcohol Extract at Three Polar Parts

(56) Extract Paliurus ramosissimus (Lour.) Poir. leaf alcohol extract with petroleum ether, ethyl acetate and n-butanol in sequence, recover solvents and freeze dry to obtain extracts at three polar parts, and dissolve in isopropanol. Take a variety of tumor cells in logarithmic growth phase (tumor cell lines used are the followings: cervical carcinoma cell line Hela; human hepatoma cell line SMMC-7721; human lung carcinoma cell line A549; human colon carcinoma cell line Caco-2; leukemia cell line K562; gastric carcinoma cell line MGC-803;), centrifuge at 2000 rpm for 5 min, adjust precipitate cell concentration of cell suspension to 1×10.sup.5 cells/ml with corresponding culture medium containing 10% fetal bovine serum, and seed cells in 96-well culture plates. To each well, add 200 μl of cell suspension, respectively add sterile extract solution of certain concentration to make the final concentration of extract in each well is 0.002, 0.01, 0.02, 0.04, 0.05, 0.08, 0.1, 0.2 mg/ml, mix well, place in 37° C., 5% CO.sub.2 incubator for 24 h, precipitate the culture, wash twice with PBS, to each well, add 20 μl of 5 mg/ml MTT phosphate buffer and 150 μl of culture medium, culture under the same conditions for 4 h, and then terminate the culture. Centrifuge at 2000 rpm for 5 min, then discard the culture medium in wells, to each well, add 150 μl of DMSO, shake for 10 min so that the formed formazan particles are fully dissolved, and determine absorbance with microplate reader. Select 570 nm as the measurement wavelength. Calculate IC50 of the extract to tumor cells. The results are shown in Table 2. The results are that Paliurus ramosissimus (Lour.) Poir. leaf alcohol extract at petroleum ether part and ethyl acetate part have good anti-tumor activity, especially extract at ethyl acetate part has better activity, while IC50 of extract at n-butanol part cannot be calculated within the experiment concentration range. We further study the ethyl acetate part.

(57) TABLE-US-00002 TABLE 2 Inhibition effects of Paliurus ramosissimus (Lour.) Poir. extract at different polar part on tumor cells: Cell line Petroleum ether part Ethyl acetate part N-butanol part Hela 0.0492 mg/ml 0.0139 mg/ml — SMMC-7721 0.0993 mg/ml 0.0365 mg/ml — A549 0.0142 mg/ml 0.0075 mg/ml — Caco-2 0.0545 mg/ml 0.0778 mg/ml — MGC-803 0.0702 mg/ml 0.0305 mg/ml —

(58) 5. Studies on Effects of Ethyl Acetate Polar Part on Mice Bearing Ehrlich Ascites Tumor

(59) Inhibition of mice transplanted tumor S180:

(60) Take Kunming mice, subcutaneously inject 0.2 ml of S180 suspension (about 1×10.sup.6 tumor cells) in a routine way at the right anterior lobe. 24 hours after injection, mice are randomly grouped and numbered. There are 10 mice in the control groups, and 10 mice each in test groups of high dose, middle dose, and low dose. Mice in each group receive drugs via intragastric administration once a day for a total of 14 times. In positive control group, cyclophosphamide (85 mg/kg) is given daily, and the dose, frequency, time are identical with the test groups. 24 hours after the last administration, sacrifice the animals, weigh body weight, completely remove tumor lump, weigh, and calculate tumor inhibition rate, the results are shown in Table 3.

(61) TABLE-US-00003 TABLE 3 Effects of ethyl acetate polar part on mice bearing Ehrlich ascites tumor Ethyl acetate polar part (low Ethyl acetate polar Ethyl acetate polar Group Control group dose) part (middle dose) part (high dose) Tumor 38.45 ± 3.62% 13.85 ± 4.59% 40.76 ± 5.40% 76.13 ± 8.32%* inhibition rate *Compared with the control group, P < 0.05; the difference is statistically significant.

II. The Antitumor Activity of Paliurus ramosissimus (Lour.) Poir. Whole Plant Extract

Embodiment 1

(62) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add 95% ethanol of 8 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight, soak for 2 days, collect the extract liquid, recover ethanol at 50° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

Embodiment 2

(63) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. stems and leaves, add 95% ethanol of 10 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight for reflux extraction, collect the extract liquid, recover ethanol at 60° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. ethanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

Embodiment 3

(64) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add methanol of 10 times the weight, soak for one day, then crush, add methanol of 8 times the weight, soak for 2 days, collect the extract liquid, recover methanol at 40° C. under reduced pressure, and dry to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. methanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

Embodiment 4

(65) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 23 mg of triterpenoids.

(66) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 103 mg of flavonoids.

(67) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 21 g of alkaloids.

(68) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 10.2 mg of total coumarins.

Embodiment 5

(69) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 108 g of triterpenoids.

(70) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 497 mg of flavonoids.

(71) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 107 mg of alkaloids.

(72) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 186 mg of coumarins.

(73) 1. Studies on In Vitro Anti-Tumor Activity of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract

(74) Take a variety of tumor cells in logarithmic growth phase (tumor cell lines used are the followings: cervical carcinoma cell line Hela; human hepatoma cell line SMMC-7721; human lung carcinoma cell line A549; human colon carcinoma cell line Caco-2; leukemia cell line K562; gastric carcinoma cell line MGC-803;), centrifuge at 2000 rpm for 5 min, adjust precipitate cell concentration of cell suspension to 1×10.sup.5 cells/ml with corresponding culture medium containing 10% fetal bovine serum, and seed cells in 96-well culture plates. To each well, add 200 μl of cell suspension, respectively add sterile extract solution of certain concentration to make the final concentration of extract in each well is 0.02, 0.1, 0.2, 0.4, 0.5, 0.8, 1.0, 2.0 mg/ml, mix well, place in 37° C., 5% CO.sub.2 incubator for 24 h, precipitate the culture, wash twice with PBS, to each well, add 20 μl of 5 mg/ml MTT phosphate buffer and 150 μl of culture medium, culture under the same conditions for 4 h, and then terminate the culture. Centrifuge at 2000 rpm for 5 min, then discard the culture medium in wells, to each well, add 150 μl of DMSO, shake for 10 min so that the formed formazan particles are fully dissolved, and select 570 nm as the measurement wavelength, determine absorbance with microplate reader. Calculate IC50 of the Paliurus ramosissimus (Lour.) Poir. ethanol extract in embodiment 1 to tumor cells. The results are shown in Table 4. The results have showed that, Paliurus ramosissimus (Lour.) Poir whole plant extract has good anti-tumor effect.

(75) TABLE-US-00004 TABLE 4 The inhibition effects of Paliurus ramosissimus (Lour.) Poir. ethanol extract on different tumor cells Paliurus ramosissimus Cell line (Lour.) Poir. ethanol extract Hela 0.0216 mg/ml SMMC-7721 0.1452 mg/ml A549 0.0101 mg/ml Caco-2 0.0875 mg/ml MGC-803 0.1862 mg/ml

(76) 2. Studies on In Vitro Anti-Tumor Activity of 3 Paliurus ramosissimus (Lour.) Poir. Extracts in Embodiment 2

(77) Extract Paliurus ramosissimus (Lour.) Poir. ethanol extract in Embodiment 1 with petroleum ether, ethyl acetate and n-butanol in sequence, recover solvents and freeze dry to obtain Paliurus ramosissimus (Lour.) Poir. petroleum ether extract, ethyl acetate extract and n-butanol extract, and dissolve in isopropanol. Take a variety of tumor cells in logarithmic growth phase (tumor cell lines used are the followings: cervical carcinoma cell line Hela; human hepatoma cell line SMMC-7721; human lung carcinoma cell line A549; human colon carcinoma cell line Caco-2; leukemia cell line K562; gastric carcinoma cell line MGC-803;), centrifuge at 2000 rpm for 5 min, adjust precipitate cell concentration of cell suspension to 1×10.sup.5 cells/ml with corresponding culture medium containing 10% fetal bovine serum, and seed cells in 96-well culture plates. To each well, add 200 μl of cell suspension, respectively add sterile extract solution of certain concentration to make the final concentration of extract in each well is 0.002, 0.01, 0.02, 0.04, 0.05, 0.08, 0.1, 0.2 mg/ml, mix well, place in 37° C., 5% CO.sub.2 incubator for 24 h, precipitate the culture, wash twice with PBS, to each well, add 20 μl of 5 mg/ml MTT phosphate buffer and 150 μl of culture medium, culture under the same conditions for 4 h, and then terminate the culture. Centrifuge at 2000 rpm for 5 min, then discard the culture medium in wells, to each well, add 150 μl of DMSO, shake for 10 min so that the formed formazan particles are fully dissolved, and select 570 nm as the measurement wavelength, determine absorbance with microplate reader. Calculate IC50 of the extract to tumor cells. The results are shown in Table 5. The results are that Paliurus ramosissimus (Lour.) Poir. petroleum ether extract and ethyl acetate extract have good anti-tumor activity, especially extract at ethyl acetate part has better activity, while IC50 of n-butanol extract cannot be calculated within the experiment concentration range.

(78) TABLE-US-00005 TABLE 5 The inhibition effects of different Paliurus ramosissimus (Lour.) Poir. extracts on tumor cells Petroleum ether Cell line extract Ethyl acetate extract N-butanol extract Hela 0.0357 mg/ml 0.0102 mg/ml — SMMC-7721 0.1242 mg/ml 0.0357 mg/ml — A549 0.0156 mg/ml 0.0064 mg/ml — Caco-2 0.0915 mg/ml 0.0623 mg/ml — MGC-803 0.0812 mg/ml 0.0487 mg/ml — “—”: IC50 cannot be calculated within the experiment concentration range

(79) 3. Effects of Paliurus ramosissimus (Lour.) Poir. Ethanol, Methanol, Petroleum Ether and Ethyl Acetate Extracts on Mice Bearing S180

(80) Choose mice which are in good health conditions and received 5180 tumor injection 8 days ago, disinfect abdominal skin, draw ascites, mix with normal saline as ratio of 1:4 (ascites volume: normal saline volume) to make suspension. Take 82 male Kunming mice, weighing 18-20 g, randomly divide into 7 groups with stratification of body weight, namely model control group (0.5% mucilage tragacanth), positive control group (cyclophosphamide, CTX), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. In all groups, subcutaneously inject 0.2 ml of the aforementioned suspension at the right anterior lobe. 2 hours after injection, mice in control group and drug groups receive test substance or suspension via intragastric administration once a day for 14 consecutive days. In positive control group, CTX is administered intraperitoneally once every other day for a total of 7 times. 24 h after the last administration, sacrifice the mice by cervical dislocation, remove tumor lump, weigh, and calculate inhibition rate ((1−average tumor weight in the experimental group/average tumor weight in the model control group)*100%). The results are shown in Table 6.

(81) TABLE-US-00006 TABLE 6 Effect of Paliurus ramosissimus (Lour.) Poir. whole plant extract on mice bearing S180 (x ± s) Number Tumor of Tumor weight inhibition Group animals Dose (g) rate (%) Model control 11 — 1.20 ± 0.45 — Positive control (ctx) 9  40 mg/kg 0.35 ± 0.58** 70.8 Ethyl acetate extract 12 0.4 g/kg 1.14 ± 0.46 5.0 low-dose Ethyl acetate extract 12 1.6 g/kg 0.34 ± 0.43** 71.7 high-dose Methanol extract 12 4.8 g/kg 0.57 ± 0.45** 52.5 Petroleum ether extract 12 4.8 g/kg 0.39 ± 0.23** 67.5 Ethanol extract 12 4.8 g/kg 0.44 ± 0.29** 63.3 *Compared with the model control group, *P < 0.05, **P < 0.01

(82) Experimental results have showed that intraperitoneal administration of 1.6 g/kg of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract can significantly inhibit the growth of S180 in mice, and potency of 1.6 g/kg dose is similar to intraperitoneal administration of 40 mg/kg of cyclophosphamide every other day; 4.8 g/kg of ethanol, methanol, petroleum ether extracts can also effectively reduce tumor weight, and the tumor inhibition rate is over 50%, suggesting that the four extracts have good anti-tumor activity.

(83) 4. Effects of Paliurus ramosissimus (Lour.) Poir. Ethanol, Methanol, Petroleum Ether and Ethyl Acetate Extracts on Mice Bearing Ehrlich Ascites Tumor

(84) Choose mice which are in good health conditions and received Ehrlich ascites tumor injection 8 days ago, disinfect abdominal skin, draw ascites, mix with normal saline to 4×10.sup.6 ml for future use. Take 82 male Kunming mice, weighing 18-20 g, randomly divide into 7 groups with stratification of body weight, namely model control group (0.5% mucilage tragacanth), positive control group (cyclophosphamide, CTX), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. In all groups, subcutaneously inject 0.2 ml of the aforementioned suspension at the right anterior lobe. 2 hours after injection, mice in control group and drug groups receive test substance or suspension via intragastric administration once a day, administer continuously until the animal is dying. In positive control group, CTX is administered intraperitoneally once every other day for a total of 7 times. When the animal is dying, sacrifice it by cervical dislocation; the day of dying is calculated as survival time; after death, weigh, exhaust ascites, weigh again, and the difference is the weight of ascites. The results are shown in Table 7.

(85) TABLE-US-00007 TABLE 7 Effect of Paliurus ramosissimus (Lour.) Poir. whole plant extract on mice bearing Ehrlich ascites tumor (x ± s) Number Survival of time Weight Group Dose animals (Day) of ascites Model control — 12 16.3 ± 2.5 21.4 ± 1.8 Positive control (ctx)  40 mg/kg 12 17.2 ± 2.3 15.9 ± 1.5** Ethyl acetate extract 0.4 g/kg 12 19.9 ± 3.9* 17.3 ± 1.8** low-dose Ethyl acetate extract 1.6 g/kg 12 20.5 ± 2.7** 14.2 ± 2.0** high-dose Methanol extract 4.8 g/kg 12 19.0 ± 3.1* 16.9 ± 2.5** Petroleum ether extract 4.8 g/kg 12 19.6 ± 2.2** 15.5 ± 1.1** Ethanol extract 4.8 g/kg 12 20.1 ± 2.9** 17.2 ± 2.2** Compared with the model control group, *P < 0.05, **P < 0.01

(86) Experimental results have showed that intraperitoneal administration of 0.4 g/kg and above of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract can significantly inhibit the growth of Ehrlich ascites tumor in mice, and prolong animal survival time; the potency of 1.6 g/kg dose is similar to cyclophosphamide on inhibiting the amount of ascites, but the latter cannot prolong animal survival time, suggesting that certain unique advantages; 4.8 g/kg of ethanol, methanol, petroleum ether extracts can also effectively prolong survival time, inhibit ascites formation, suggesting that the four extracts have good anti-tumor activity.

(87) 5. Effects of Paliurus ramosissimus (Lour.) Poir. Ethyl Acetate Extract in Combination of Paclitaxel and Cinobufotalin on Mice Bearing S180

(88) Choose mice which are in good health conditions and received S180 tumor injection 8 days ago, disinfect abdominal skin, draw ascites, mix with normal saline as ratio of 1:4 (ascites volume:normal saline volume) to make suspension. Take 84 male Kunming mice, weighing 18-20 g, randomly divide into 7 groups with stratification of body weight, namely model control group (0.5% mucilage tragacanth), positive control group (cyclophosphamide, CTX), ethyl acetate extract group, paclitaxel group, cinobufotalin group, in combination with paclitaxel group, in combination with cinobufotalin group. In all groups, subcutaneously inject 0.2 ml of the aforementioned suspension at the right anterior lobe. 2 hours after injection, mice in control group and drug groups receive test substance or suspension via intragastric or intravenous administration once a day for 14 consecutive days. In positive control group, CTX is administered intraperitoneally once every other day for a total of 7 times. 24 h after the last administration, sacrifice the mice by cervical dislocation, remove tumor lump, weigh, and calculate inhibition rate ((1−average tumor weight in the experimental group/average tumor weight in the model control group)*100%). The results are shown in Table 8.

(89) TABLE-US-00008 TABLE 8 Effect of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract in combination of paclitaxel and cinobufotalin on mice bearing S180 (x ± s) Number Tumor of Tumor inhibition Group animals Dose weight (g) rate (%) Model control 11 — 1.30 ± 0.55 — Positive control 12 40 mg/kg 0.48 ± 0.41** 63.1 (CTX) Ethyl acetate 12 0.4 g/kg 1.04 ± 0.40 20.0 extract Paclitaxel 12 5 mg/kg 0.85 ± 0.38* 34.6 In combination 12 Ethyl acetate extract 0.4 g/kg + 0.52 ± 0.26**@ 60.0 with paclitaxel paclitaxel 5 mg/kg Cinobufotalin 12 1 ml/kg 0.73 ± 0.42* 43.8 In combination 12 Ethyl acetate extract 0.4 g/kg + 0.37 ± 0.18**# 71.5 with cinobufotalin 1 ml/kg cinobufotalin Compared with the model control group, *P < 0.05, **P < 0.01; Compared with the paclitaxel group, @P < 0.05; Compared with the cinobufotalin group, #P < 0.05;

(90) Experimental results have showed that intraperitoneal administration of 0.4 g/kg of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract does not have significant inhibition effect on the growth of S180 in mice, while 5 mg/kg of paclitaxel and 1 ml/kg of cinobufotalin show certain effects. However, the combination of the same dose of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract and 5 mg/kg of paclitaxel and 1 ml/kg of cinobufotalin can significantly improve the inhibition rate of paclitaxel, suggesting that the combination of Paliurus ramosissimus (Lour.) Poir. whole plant extract and other antitumor drugs can improve the efficacy of these drugs.

III. Antifibrotic Activity of Paliurus ramosissimus (Lour.) Poir. Extract

Embodiment 1

(91) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add 95% ethanol of 8 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight, soak for 2 days, collect the extract liquid, recover ethanol at 50° C. under reduced pressure until no ethanol smell to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

Embodiment 2

(92) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. stems and leaves, add 95% ethanol of 10 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight for reflux extraction, collect the extract liquid, recover ethanol at 60° C. under reduced pressure until no ethanol smell to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. ethanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

Embodiment 3

(93) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add methanol of 10 times the weight, soak for one day, then crush, add methanol of 8 times the weight, soak for 2 days, collect the extract liquid, recover methanol at 40° C. under reduced pressure, and dry to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. methanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

Embodiment 4

(94) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 23 g of triterpenoids.

(95) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 103 mg of flavonoids.

(96) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L-1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 21 g of alkaloids.

(97) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 10.2 mg of total coumarins.

Embodiment 5

(98) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 108 g of triterpenoids.

(99) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 497 mg of total flavonoids.

(100) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L-1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 107 mg of alkaloids.

(101) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract in Embodiment 2, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 186 mg of coumarins.

(102) 1. Effect on Liver Fibrosis in Rats

(103) Take 60 SD rats (200-240 g, male), randomly divide into blank control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (dexamethasone, 1 mg/kg), Paliurus ramosissimus (Lour.) Poir. extract (prepared according to Embodiment 1) low-dose group (0.4 g/kg), Paliurus ramosissimus (Lour.) Poir. extract middle-dose group (0.8 g/kg), and Paliurus ramosissimus (Lour.) Poir. extract high-dose group (1.6 g/kg) with stratification of body weight. Except the blank control group, rats in other groups receive subcutaneous injection of 1 ml/kg of 40% carbon tetrachloride in vegetable oil solution, 2 times a week for 3 consecutive months, while receiving high-fat diet and 5% ethanol aqueous solution. Test substance is given via intragastric administration once daily for 3 consecutive months. On the next day after drug administration, draw abdominal aortic blood, separate plasma, determine the levels of alanine aminotransferase (ALT), III procollagen (PC-III), hyaluronic acid (HA) and laminin (LH); the sacrifice the animals, and take the liver for pathological examination. Serum biochemical test results are shown in Table 9.

(104) TABLE-US-00009 TABLE 9 Effect of Paliurus ramosissimus (Lour.) Poir. extract on experimental hepatic fibrosis rat liver and blood biochemical indices (n = 10, x ± s) Group ALT (U/L) PC-III (μg/L) HA (μg/L) LN (μg/L) Normal control  43 ± 4**  9.5 ± 1.7** 131 ± 29** 12 ± 2** Model control 678 ± 123 32.2 ± 6.9 319 ± 71 86 ± 19 Positive Control 456 ± 98** 20.8 ± 3.1** 280 ± 54 62 ± 20* Paliurus ramosissimus (Lour.) 617 ± 107 30.5 ± 6.2 289 ± 62 80 ± 23 Poir. Extract (0.4 g/kg) Paliurus ramosissimus (Lour.) 412 ± 126** 25.1 ± 4.2* 263 ± 69 59 ± 17* Poir. extract (0.8 g/kg) Paliurus ramosissimus (Lour.) 335 ± 138** 18.5 ± 4.8** 217 ± 58** 41 ± 9** Poir. Extract (1.6 g/kg) Compared with the model control group, *P < 0.05, **P < 0.01

(105) The results have showed that, compared with the model group, 0.8 g/kg and 1.6 g/kg of Paliurus ramosissimus (Lour.) Poir. extract have a protective role in carbon tetrachloride-induced experimental fibrosis rat liver injury; particularly in higher dose, each index is improved significantly.

(106) Pathological examination has showed that liver cells of rats in the model group show obvious water degeneration, obvious liver necrosis and fatty degeneration, with obvious liver fibrosis manifestations; compared to the model group, in Paliurus ramosissimus (Lour.) Poir. extract high-dose group and middle-dose group, the degree of liver cell water degeneration and fatty degeneration is significantly lower, suggesting that it has good inhibitory effect on liver fibrosis.

(107) 2. Effect on Pulmonary Fibrosis in Rats

(108) Take 60 SD rats (200-240 g, male), randomly divide into sham operation control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (dexamethasone, 1 mg/kg), Paliurus ramosissimus (Lour.) Poir. extract (prepared according to Embodiment 1) low-dose group (0.4 g/kg), Paliurus ramosissimus (Lour.) Poir. extract middle-dose group (0.8 g/kg), and Paliurus ramosissimus (Lour.) Poir. extract high-dose group (1.6 g/kg) with stratification of body weight. All animals receive trachea separation under anesthesia by intraperitoneal injection of 10% chloral hydrate (350 mg/kg). Except the sham operation control group, rats in other groups receive injection of 5 mg/kg of bleomycin in 0.4 ml of normal saline solution, while rats in sham operation control group receive normal saline solution only. From the next day after surgery, test substance is given daily for 30 consecutive days. Sacrifice the animals by cervical dislocation, and take the lungs; some organs are homogenized for hydroxyproline content determination, and some are for pathological examination. The results of determined hydroxyproline content in lung tissue are shown in Table 10.

(109) TABLE-US-00010 TABLE 10 The change of hydroxyproline content in the lungs of rats in each group (n = 10, x ± s) Hydroxyproline content Group (mg/gpro) Sham operation control 10.3 ± 3.8** Model control 18.4 ± 5.0 Positive Control 13.6 ± 3.3* Paliurus ramosissimus 16.5 ± 4.7 (Lour.) Poir. Extract (0.4 g/kg) Paliurus ramosissimus 14.1 ± 6.2* (Lour.) Poir. Extract (0.8 g/kg) Paliurus ramosissimus 12.3 ± 3.7* (Lour.) Poir. Extract (1.6 g/kg) Compared with the model control group, *P < 0.05, **P < 0.01

(110) The results have showed that, compared with the model group, 0.8 g/kg and 1.6 g/kg of Paliurus ramosissimus (Lour.) Poir. extract effectively reduce hydroxyproline content in the lung of model rats, suggesting that it has good inhibition effect of pulmonary fibrosis.

(111) Pathological examination tests have showed that, rats in the model group appear obvious pulmonary fibrosis, with manifestation of a large number of interstitial lung fibroblasts, a large number of fibrous connective tissue deposition, structural damage in alveolar cells, and some alveolar space disappearance; compared with the model group, in Paliurus ramosissimus (Lour.) Poir. extract each dose group, fibrous connective tissue deposition in rats is less, and interstitial lung fibroblasts are also less, while the high-dose group is more significant, suggesting that the extract is a potential treatment of pulmonary fibrosis.

(112) 3. Effect of Paliurus ramosissimus (Lour.) Poir. Extract in Combination with Polyene Phosphatidylcholine on Liver Fibrosis in Rats

(113) Take 60 SD rats (200-240 g, male), randomly divide into blank control group, model control group, positive control group (dexamethasone, 1 mg/kg), Paliurus ramosissimus (Lour.) Poir. extract group (prepared according to Embodiment 1, 0.8 g/kg), Polyene phosphatidylcholine group, drug combination group (Paliurus ramosissimus (Lour.) Poir. Extract 0.8 g/kg+ Polyene phosphatidylcholine 1 ml/kg) with stratification of body weight. Except the blank control group, rats in other groups receive subcutaneous injection of 1 ml/kg of 40% carbon tetrachloride in vegetable oil solution, 2 times a week for 3 consecutive months, while receiving high-fat diet and 5% ethanol aqueous solution. Test substance is given via intragastric administration once daily for 3 consecutive months. On the next day after drug administration, draw abdominal aortic blood, separate plasma, determine the levels of alanine aminotransferase (ALT), III procollagen (PC-III), hyaluronic acid (HA) and laminin (LH); the sacrifice the animals, and take the liver for pathological examination. Serum biochemical test results are shown in Table 11.

(114) TABLE-US-00011 TABLE 11 Effect of drug combination on experimental hepatic fibrosis rat liver and blood biochemical indices (n = 10, x ± s) Group ALT (U/L) PC-III (μg/L) HA (μg/L) LN (μg/L) Normal control  42 ± 3**  9.7 ± 1.9** 129 ± 32** 11 ± 4** Model control 684 ± 114 31.7 ± 8.0 310 ± 63 87 ± 21 Positive control 478 ± 90** 20.6 ± 3.8** 285 ± 57 65 ± 23* Paliurus 423 ± 98** 24.5 ± 3.9* 271 ± 60 60 ± 18** ramosissimus (Lour.) Poir. Extract Polyene 443 ± 130** 27.0 ± 4.8 284 ± 78 63 ± 18* phosphatidylcholine Drug combination 315 ± 102**# 18.6 ± 5.1**## 186 ± 67**## 47 ± 11**# Compared with the model control group, *P < 0.05, **P < 0.01; compared with polyene phosphatidylcholine group, #P < 0.05, ##P < 0.01

(115) 4. Effect of Paliurus ramosissimus (Lour.) Poir. Extract in Combination with Ligustrazine on Pulmonary Fibrosis in Rats

(116) Take 60 SD rats (200-240 g, male), randomly divide into sham operation control group, model control group, positive control group (dexamethasone, 1 mg/kg), Paliurus ramosissimus (Lour.) Poir. extract group (prepared according to Embodiment 1, 0.8 g/kg.Math.op), Ligustrazine (40 mg/kg, ip) and drug combination group (Paliurus ramosissimus (Lour.) Poir. Extract 0.8 g/kg, op; Ligustrazine injection 40 mg/kg, ip) with stratification of body weight. All animals receive trachea separation under anesthesia by intraperitoneal injection of 10% chloral hydrate (350 mg/kg). Except the sham operation control group, rats in other groups receive injection of 5 mg/kg of bleomycin in 0.4 ml of normal saline solution, while rats in sham operation control group receive normal saline solution only. The next day after the surgery, give the test substance via intragastric administration or injection administration, test substance is given daily for 30 consecutive days. Sacrifice the animals by cervical dislocation, and take the lungs; some organs are homogenized for hydroxyproline content determination, and some are for pathological examination. The results of determined hydroxyproline content in lung tissue are shown in Table 12.

(117) TABLE-US-00012 TABLE 12 Effect of drug combination on hydroxyproline in the lungs of rats (n = 10, x ± s) Group Hydroxyproline content (mg/gpro) Sham operation control 10.1 ± 3.4** Model control 17.9 ± 4.3 Positive control 13.4 ± 3.7* Paliurus ramosissimus 12.9 ± 4.9* (Lour.) Poir. Extract Ligustrazine 14.6 ± 5.7 Drug combination  9.8 ± 2.9**# Compared with the model control group, *P < 0.05, **P < 0.01; Compared with the Ligustrazine group, #P < 0.05

(118) The results have showed that, 40 mg/kg of ligustrazine alone has no significant efficacy on experimental pulmonary fibrosis, while drug combination effectively reduces hydroxyproline content in lungs in model rats, which has significant differences when being compared with 40 mg/kg of ligustrazine, suggesting that Paliurus ramosissimus (Lour.) Poir. extract can effectively improve the efficacy of other pulmonary fibrosis therapeutic agents.

IV. Antifungal Activity of Paliurus ramosissimus (Lour.) Poir. Extract

(I) Embodiment Preparation of Paliurus ramosissimus (Lour.) Poir. Extract

(119) 1. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract

(120) (1) Take 1 kg of the whole plant of fresh Paliurus ramosissimus (Lour.) Poir., add 95% (volume concentration) ethanol of 8 times of the volume of Paliurus ramosissimus (Lour.) Poir., soak for 1-2 days, crush leaves, roots and stems, add 95% ethanol of 12 times of the volume of Paliurus ramosissimus (Lour.) Poir., soak for 3 days, collect the extract liquid, recover ethanol under reduced pressure, and freeze-dry the concentrated to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

(121) (2) Take 1 kg of the whole plant (or any part) of fresh Paliurus ramosissimus (Lour.) Poir., crush, add 95% ethanol of 8 times of the volume of Paliurus ramosissimus (Lour.) Poir., reflux to extract 3 times, collect the extract liquid, recover ethanol under reduced pressure, and freeze-dry the concentrated to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

(122) (3) Take 1 kg of the whole plant of fresh Paliurus ramosissimus (Lour.) Poir. (roots, stems, leaves, etc.), freeze-dry and then crush (or crush and then freeze-dry), add 95% ethanol of 10 times of the volume of Paliurus ramosissimus (Lour.) Poir., reflux to extract 3 times, collect the extract liquid, recover ethanol under reduced pressure, and freeze-dry the concentrated to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

(123) 2. Preparation of Paliurus ramosissimus (Lour.) Poir. Methanol Extract

(124) Take 1 kg of the whole plant of fresh Paliurus ramosissimus (Lour.) Poir., crush, add methanol of 6 times of the volume of Paliurus ramosissimus (Lour.) Poir., reflux to extract 3 times, collect the extract liquid, recover methanol under reduced pressure, and freeze-dry the concentrated to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract.

(125) 3. Preparation of Paliurus ramosissimus (Lour.) Poir. Petroleum Ether Extract

(126) (1) Take Paliurus ramosissimus (Lour.) Poir. ethanol extract concentrate, extract with petroleum ether, recover petroleum ether, and dry.

(127) (2) Take Paliurus ramosissimus (Lour.) Poir. methanol extract dried sample, suspend with 10 times of water, extract with petroleum ether, recover petroleum ether, and dry.

(128) (3) Take Paliurus ramosissimus (Lour.) Poir. ethanol extract dried sample, reflux to extract with 10 times of petroleum ether, recover petroleum ether, and dry.

(129) 4. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethyl Acetate Extract

(130) (1) Take Paliurus ramosissimus (Lour.) Poir. ethanol extract concentrate, extract with 10 times of petroleum ether and then with 10 times of ethyl acetate, recover ethyl acetate, and dry.

(131) (2) Take Paliurus ramosissimus (Lour.) Poir. methanol extract dried sample, suspend with 10 times of water, extract with 10 times of petroleum ether and then with 10 times of ethyl acetate, recover ethyl acetate, and dry.

(132) (3) Take Paliurus ramosissimus (Lour.) Poir. ethanol extract dried sample, reflux to extract with 6 times of ethyl acetate 2 times, recover ethyl acetate, and dry.

(133) 5. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethyl Acetate Extract Tablets

(134) Take 300 g of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract, crush, pass through a 40-mesh sieve, add 100 g of microcrystalline cellulose, 57.5 g of lactose, 20 g of cross-linked sodium carboxymethyl cellulose, mix well, evenly spray appropriate amount of 95% (volume concentration) ethanol solution, granulate with wet extrusion, pass through a 24-mesh sieve, dry at 50° C., then add 20 g of cross-linked sodium carboxymethyl cellulose and 2.5 g of magnesium stearate, fully mix, compress to tablets to obtain Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract tablets;

(135) 6. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract Granules

(136) Take 1000 g of Paliurus ramosissimus (Lour.) Poir. ethanol extract, crush, pass through a 40-mesh sieve, add 4000 g of sugar powder, mix well, evenly spray appropriate amount of 95% (volume concentration) ethanol solution, granulate with wet extrusion, pass through a 24-mesh sieve, dry at 50° C., and uniform granules to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract granules;

(137) 7. Preparation of Paliurus ramosissimus (Lour.) Poir. Methanol Extract Ointments

(138) Weigh 115 g of octadecanol, 115 g of white petrolatum and 70 g of glyceryl monostearate, heat to melt to obtain the oil phase, add 40 g of Paliurus ramosissimus (Lour.) Poir. methanol extract; weigh 100 g of glycerol, 15 g of sodium lauryl sulfate and 0.01 g of cysteine hydrochloride, add 650 ml of water to dissolve to obtain the aqueous phase; heat separately to 75° C.-80° C., slowly add the water phase into the oil phase with stirring, then continue stirring for 15 minutes to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract ointments.

(139) 8. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract Gels

(140) Take 10 g of carbomer, pour into 420 ml of purified water, stir to swell, add 100 ml of propylene glycol and stir to dissolve, add 18 g of triethanolamine dropwise with stirring to prepare the gel matrix; take 100 g of Paliurus ramosissimus (Lour.) Poir. ethanol extract and 2 g of ethylparaben, dissolve in 350 ml of ethanol, add the gel matrix with stirring, and stir well.

(141) 9. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract Plastics

(142) Take 40 g of polyvinyl alcohol 124, swell in 400 ml of purified water; take 100 g of Paliurus ramosissimus (Lour.) Poir. ethanol extract, dissolve in 400 ml of ethanol, then add 100 ml of glycerin, stir well, slowly add into polyvinyl alcohol solution, stir well, filter, and add ethanol over a filter to 1000 ml.

(143) 10. Preparation of Paliurus ramosissimus (Lour.) Poir. Petroleum Ether Extract Liniment

(144) Take 100 g of Paliurus ramosissimus (Lour.) Poir. petroleum ether extract powder, place in a mortar, add 500 ml of peanut oil, grind well, then slowly add saturated calcium hydroxide aqueous solution to 1000 ml, and grind to homogeneous white milky substance.

(145) 11. Preparation of Paliurus ramosissimus (Lour.) Poir. Ethanol Extract Lotions

(146) Take 100 g of Paliurus ramosissimus (Lour.) Poir. ethanol extract powder, place in a mortar, add 50 ml of glycerol and appropriate amount of purified water, grind into a paste, and gradually add purified water until mix completely.

(II) Study on Antifungal Activity of Paliurus ramosissimus (Lour.) Poir. Extract

(147) Weigh 1 g of Paliurus ramosissimus (Lour.) Poir. ethanol extract prepared in Embodiment 1 (1), dissolve with 5% isopropanol solution to 10 ml, filter through a 0.22 μm membrane for sterilization. Take 1 ml of sterilized solution, add into 9 ml PDA medium which is melt and cooled to about 50° C., shake well, quickly pour into a Petri dish with diameter of 6 cm and allow to stand to make PDA of the culture plate containing 10 mg/ml Paliurus ramosissimus (Lour.) Poir. extract. Use same volume of 5% isopropyl alcohol solution to make the blank control PDA culture plate.

(148) Move bacterial inoculum which has been well cut, to the above drug-containing PDA culture plate, incubate at 25° C., when bacterial colonies in the control group are approaching the edge of the dish, determine colony diameter of all colonies on the culture plate with criss-cross method, and calculate fungus inhibition rate after correction.

(149) The results are shown in Table 13. Paliurus ramosissimus (Lour.) Poir. alcohol extract inhibits various types of tested fungi significantly. Because tested fungi are common pathogenic fungi with significant representation, the results suggest that Paliurus ramosissimus (Lour.) Poir. alcohol extract has strong antifungal activity, which is expected to be applied to the preparation of antifungal drugs.

(150) TABLE-US-00013 TABLE 13 Effect of Paliurus ramosissimus (Lour.) Poir. alcohol extract on inhibition of various fungi (n = 3, x ± s) Strains Fungus inhibition rate (%) Candida albicans 87.53 ± 8.36 Trichophyton rubrum 80.46 ± 10.24 Trichophyton mentagrophytes 72.69 ± 11.53 Trichophyton violaceum 90.16 ± 14.36 Trichophyton tonsurans 54.39 ± 8.67 Trichophyton verrucosum 42.63 ± 12.81 Microsporum nanum 60.54 ± 10.33 Microsporum canis 61.32 ± 7.65 Sporothrix schenckii 76.87 ± 15.69 Phialophora compactum 66.63 ± 17.65 Exophiala dermatitidis 62.65 ± 8.87 Hormodendrum pedrosei 53.13 ± 10.08

V. Paliurus ramosissimus (Lour.) Poir. Leaf Extract in the Treatment of Immune Dysfunction or (and) Autoimmune Diseases

(151) (I) Preparation of Paliurus ramosissimus (Lour.) Poir. Extract

(152) 1. Preparation of Whole Plant Ethanol Extract

(153) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add 95% ethanol of 8 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight, soak for 2 days, collect the extract liquid, recover ethanol at 50° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

(154) 2. Preparation of Stem and Leaf Ethanol, Petroleum Ether and Ethyl Acetate Extracts

(155) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. stems and leaves, add 95% ethanol of 10 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight for reflux extraction, collect the extract liquid, recover ethanol at 60° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. ethanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

(156) 3. Preparation of Whole Plant Petroleum Ether and Ethyl Acetate Extracts

(157) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add methanol of 10 times the weight, soak for one day, then crush, add methanol of 8 times the weight, soak for 2 days, collect the extract liquid, recover methanol at 40° C. under reduced pressure, and dry to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. methanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

(158) 4. Ingredient Quantitative Analysis

(159) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 23 g of triterpenoids.

(160) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 103 mg of flavonoids.

(161) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 21 g of alkaloids.

(162) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 10.2 mg of coumarins.

(163) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 108 mg of triterpenoids.

(164) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 497 mg of flavonoids.

(165) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 107 mg of alkaloids.

(166) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 186 mg of coumarins.

(167) (II) Preparation of Paliurus ramosissimus (Lour.) Poir. Preparations

(168) 1. Preparation of Tablets

(169) Take 300 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethanol extract, add suitable excipient, such as: 100 g of microcrystalline cellulose, 57.5 g of lactose, 20 g of cross-linked sodium carboxymethyl cellulose, etc., and compress into tablets.

(170) 2. Preparation of Capsules

(171) Take Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, add suitable excipient, such as: lactose, compressible starch, carboxymethyl starch, microcrystalline cellulose, etc., to make capsules.

(172) 3. Preparation of Granules

(173) Take Paliurus ramosissimus (Lour.) Poir. whole plant methanol extract, add suitable excipient, such as: lactose, starch, methyl cellulose, hydroxymethyl cellulose, hydroxypropylmethyl cellulose, hydroxypropyl cellulose, polyvinylpyrrolidone, silica powder etc., to make granules.

(174) 4. Preparation of Ointments

(175) Take Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, add suitable excipient, such as: octadecanol, glycerol monostearate, glycerin, stearic acid etc., to make ointments.

(176) 5. Preparation of Suppositories

(177) Take Paliurus ramosissimus (Lour.) Poir. whole plant ethanol extract, add suitable excipient, such as: mixed fatty acid glycerides, PEG, beeswax etc., to make suppositories.

(III) In Vitro Cytological Studies

(178) 1. Effect of Paliurus ramosissimus (Lour.) Poir. Extract on Spleen Lymphocyte in Vitro Proliferation in Mice

(179) 1.1 Preparation of Mouse Spleen Lymphocytes

(180) Take spleen of Kunming mice in a sterile manner, place in a dish filled with appropriate amount of RPMI1640 culture medium, remove the connective tissue, grind with a syringe needle, filter through a 200 mesh screen, transfer to a centrifuge tube, wash with RPMI1640, collect cells, and add 1 ml of erythrocyte lysate. After standing at 4° C. for 5-10 min, centrifuge at 1500 r/min for 5 min, discard the supernatant, wash twice with RPMI1640 medium, and finally suspend the cells in 1 ml RPMI1640 complete medium. Determine survival rate by trypan blue, and the results have showed that the spleen cell survival rate is greater than 95%. Appropriately dilute the above spleen cell suspension, and adjust cell density to 2×10.sup.6 cells/ml for future use.

(181) 1.2. Effect of Paliurus ramosissimus (Lour.) Poir. Extract on Spleen Lymphocyte in Vitro Proliferation in Mice

(182) On a 96-well plate, to each well, add 100 μl of spleen cell suspension of 2×10.sup.6 cells/ml. Set blank group, control group and Paliurus ramosissimus (Lour.) Poir. extract groups. For the control group, to each well, add 100 μl of RPMI1640 complete medium; for Paliurus ramosissimus (Lour.) Poir. extract group, to each well, add 100 μl of RPMI1640 complete medium solution containing various concentration of Paliurus ramosissimus (Lour.) Poir. extract; and the blank group contains medium only. Place the 96-well plate in 37° C., 5% CO.sub.2 incubator for 60 h. Take out the plate, draw the liquids in wells, wash three times with PBS, add 100 μl of culture medium and 20 μl of MTT buffer (5 mg.Math.ml.sup.−1), and place in 37° C., 5% CO.sub.2 incubator for 4 h. Take out the plate, carefully draw the supernatant, add 150 μl of dimethylsulfoxide, place the plate on a microplate shaker, shake for 10 min so that the formed formazan particles are fully dissolved, and determine absorbance with microplate reader at wavelength of 490 nm. Record the results and calculate the average in vitro survival rate of mouse spleen cells by Paliurus ramosissimus (Lour.) Poir. extract, according to formula (1).

(183) $\begin{array}{cc}\mathrm{Average}\mathrm{in}\mathrm{vitro}\mathrm{survival}\mathrm{rate}\left(\%\right)=\frac{\mathrm{Experiment}\mathrm{group}A\mathrm{value}\text{-}\mathrm{Blank}\mathrm{group}A\mathrm{value}}{\mathrm{Control}\mathrm{group}A\mathrm{value}\text{-}\mathrm{Blank}\mathrm{group}A\mathrm{value}}\times 100\%& \left(1\right)\end{array}$

(184) The results have showed that, when the concentration of Paliurus ramosissimus (Lour.) Poir. extract is 0.004 mg/ml, 0.02 mg/ml, and 0.2 mg/ml, the average survival rate of mouse spleen cells is 117.85%, 107.21% and 77.46%. The results have indicated that low concentration Paliurus ramosissimus (Lour.) Poir. extract can promote the proliferation of mouse spleen cells in vitro, while high concentration Paliurus ramosissimus (Lour.) Poir. extract inhibits the proliferation of spleen cells.

(185) 2. Effect of Paliurus ramosissimus (Lour.) Poir. Extract on ConA-Induced In Vitro Proliferation of Splenocytes

(186) On a 96-well plate, to each well, add 100 μl of spleen cell suspension of 2×10.sup.6 cells/ml. Set blank group, control group, ConA group and Paliurus ramosissimus (Lour.) Poir. extract groups. For the control group, to each well, add 100 μl of RPMI1640 complete medium; For the ConA group, to each well, add 100 μl of RPMI1640 complete medium solution containing 25 μg/ml ConA; for Paliurus ramosissimus (Lour.) Poir. extract group, to each well, add 100 μl of RPMI1640 complete medium solution containing various concentration of Paliurus ramosissimus (Lour.) Poir. extract (the solution also contains 25 μg/ml ConA); and the blank group contains medium only. Place the 96-well plate in 37° C., 5% CO.sub.2 incubator for 60 h. Take out the plate, draw the liquids in wells, wash three times with PBS, add 100 μl of culture medium and 20 μl of MTT buffer (5 mg.Math.ml.sup.−1), and place in 37° C., 5% CO.sub.2 incubator for 4 h. Take out the plate, carefully draw the supernatant, add 150 μl of dimethylsulfoxide, place the plate on a microplate shaker, shake for 10 min so that the formed formazan particles are fully dissolved, and determine absorbance with microplate reader at wavelength of 490 nm. Record the results and calculate the average in vitro survival rate of mouse spleen cells by ConA group and Paliurus ramosissimus (Lour.) Poir. Extract group, according to formula (1); Calculate proliferation rate of ConA-induced in vitro proliferation of splenocytes by Paliurus ramosissimus (Lour.) Poir. extract, according to formula (2).

(187) $\begin{array}{cc}\mathrm{Relative}\mathrm{proliferation}\mathrm{rate}\left(\%\right)=\frac{\left(\mathrm{Experimental}\mathrm{group}-1\right)}{\mathrm{ConA}\mathrm{Control}\mathrm{group}}\times 100\%& \left(2\right)\end{array}$

(188) The results have showed that, when the concentration of Paliurus ramosissimus (Lour.) Poir. extract is 0.004 mg/ml, 0.02 mg/ml, and 0.2 mg/ml, the relative proliferation rate to ConA group is 15.11%, 5.69% and −14.35%, indicating that low concentration Paliurus ramosissimus (Lour.) Poir. extract can promote the ConA-induced in vitro proliferation of splenocytes, while high concentration Paliurus ramosissimus (Lour.) Poir. extract inhibits the proliferation.

(189) 3. Effect of Paliurus ramosissimus (Lour.) Poir. Extract on LPS-Induced In Vitro Proliferation of Splenocytes

(190) On a 96-well plate, to each well, add 100 μl of spleen cell suspension of 2×10.sup.6 cells/ml. Set blank group, control group, LPS group and Paliurus ramosissimus (Lour.) Poir. extract groups. For the control group, to each well, add 100 μl of RPMI1640 complete medium; For the LPS group, to each well, add 100 μl of RPMI1640 complete medium solution containing 20 μg/ml LPS; for Paliurus ramosissimus (Lour.) Poir. extract group, to each well, add 100 μl of RPMI1640 complete medium solution containing various concentration of Paliurus ramosissimus (Lour.) Poir. extract (the solution also contains 20 μg/ml LPS); and the blank group contains medium only. Place the 96-well plate in 37° C., 5% CO.sub.2 incubator for 60 h. Take out the plate, draw the liquids in wells, wash three times with PBS, add 100 μl of culture medium and 20 μl of MTT buffer (5 mg.Math.ml.sup.−1), and place in 37° C., 5% CO.sub.2 incubator for 4 h. Take out the plate, carefully draw the supernatant, add 150 μl of dimethylsulfoxide, place the plate on a microplate shaker, shake for 10 min so that the formed formazan particles are fully dissolved, and determine absorbance with microplate reader at wavelength of 490 nm. Record the results and calculate the average in vitro survival rate of mouse spleen cells by LPS group and Paliurus ramosissimus (Lour.) Poir. Extract group, according to formula (1); Calculate proliferation rate of LPS-induced in vitro proliferation of splenocytes by Paliurus ramosissimus (Lour.) Poir. extract, according to formula (2).

(191) The results have showed that, when the concentration of Paliurus ramosissimus (Lour.) Poir. extract is 0.004 mg/ml, 0.02 mg/ml, and 0.2 mg/ml, the relative proliferation rate to LPS group is 34.37%, 20.48% and −15.60%, indicating that low concentration Paliurus ramosissimus (Lour.) Poir. extract can promote the LPS-induced in vitro proliferation of splenocytes, while high concentration Paliurus ramosissimus (Lour.) Poir. extract inhibits the proliferation, which is consistent with the conclusion drawn from the above study of ConA-induced in vitro proliferation of splenocytes that Paliurus ramosissimus (Lour.) Poir. extract has bi-directional immunomodulatory effect.

(IV) Pharmacological Verification

(192) 1. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on Nonspecific Immune Function of Immunocompromised Mice (Peritoneal Macrophages Method)

(193) Take 80 KM mice, randomly divide into 8 groups with stratification of body weight, namely suspension control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (coriolus versicolor polysaccharide), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. In all groups, mice receive test substance or suspension via intragastric administration once a day for 14 consecutive days. Except suspension control group, mice in other groups receive intraperitoneal injection of 25 mg/kg cyclophosphamide in normal saline solution at day 8, 10 and 12 to introduce immunosuppression. At day 13 and 14, apply intraperitoneal injection of 6% starch solution respectively. 1 h after the last administration at day 14, apply intraperitoneal injection of 1 ml of 5% chicken erythrocytes in saline suspension; 30 min later, sacrifice the mice by cervical dislocation, apply intraperitoneal injection of 2 ml saline, and gently massage the abdomen. 1 min later, cut open abdomen, draw 1 ml of peritoneal washings, evenly drop on two slides, place in a wet box, and incubate at 37° C. for 30 min. Rinse in saline, dry, fix with 1:1 acetone-methanol solution, stain with 4% (v/v) Giemsa-PBS for 3 min, rinse with distilled water and dry, perform microscopic examination, and calculate the percentage of phagocytosis.

(194) TABLE-US-00014 TABLE 14 Effect of Paliurus ramosissimus (Lour.) Poir. extracts on peritoneal macrophage phagocytosis of immunocompromised mice (n = 10, x ± s) Percentage of Group Dose phagocytosis Suspension control — 0.40 ± 0.09** Model control — 0.17 ± 0.07  Positive control (coriolus versicolor 0.4 g/kg 0.36 ± 0.11** polysaccharide) Ethyl acetate extract low-dose 0.1 g/kg 0.26 ± 0.08** Ethyl acetate extract high-dose 0.4 g/kg 0.32 ± 0.10** Methanol extract 1.2 g/kg 0.32 ± 0.11** Petroleum ether extract 1.2 g/kg 0.31 ± 0.07** Ethanol extract 1.2 g/kg 0.36 ± 0.11** Compared with the model control group, *P < 0.05, **P < 0.01

(195) The results are shown in Table 14. Intragastric administration of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract of 0.1 g/kg and above for 14 days can significantly improve the phagocytic activity of peritoneal macrophages of immunocompromised mice, and the strength of 0.4 g/kg dose group does not show significant difference with that of coriolus versicolor polysaccharide group; 1.2 g/kg of ethanol, methanol, petroleum ether extracts can effectively enhance phagocytic activity of peritoneal macrophages of immunocompromised mice, suggesting that the four extracts have good immune enhancement activity.

(196) 2. Effect of ethanol, methanol, petroleum ether extracts and ethyl acetate extract on specific immune function of immunocompromised mice (2,4-difluorophenyl nitrate-induced ear edema method).

(197) Take 80 KM mice, randomly divide into 8 groups with stratification of body weight, namely suspension control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (coriolus versicolor polysaccharide), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. In all groups, mice receive test substance or suspension via intragastric administration once a day for 14 consecutive days. Except suspension control group, mice in other groups receive intraperitoneal injection of 25 mg/kg cyclophosphamide in normal saline solution at day 8, 10 and 12 to introduce immunosuppression. At day 9 of administration, smear 25 μl of 1% 2,4-difluorophenyl nitrate (DNFB) solution (take 100 mg of DNFB, add to the 1:1 acetone-vegetable oil mixture, mix well, and volume to 10 ml) on the abdomen of mice; 1 h after the administration at day 13, smear 10 μl of 1% DNFB solution on the left ear of mice; 24 hours of the smear, i.e., 1 hour after last administration, sacrifice the mice by cervical dislocation, weigh the ear and calculate the degree of ear edema.

(198) TABLE-US-00015 TABLE 15 Effect of Paliurus ramosissimus (Lour.) Poir. extract on ear edema induced by DNFB of immunocompromised mice (n = 10, x ± s) Group Dose Ear edema (mg) Suspension control — 11.05 ± 1.72** Model control — 6.06 ± 0.63  Positive control (coriolus versicolor 0.4 g/kg  7.11 ± 1.73** polysaccharide) Ethyl acetate extract low-dose 0.1 g/kg 7.20 ± 1.32* Ethyl acetate extract high-dose 0.4 g/kg  8.04 ± 1.55** Methanol extract 1.2 g/kg  8.31 ± 1.45** Petroleum ether extract 1.2 g/kg 7.31 ± 1.56* Ethanol extract 1.2 g/kg 7.09 ± 1.06* Compared with the model control group, *P < 0.05, **P < 0.01

(199) The results are shown in Table 15. Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract can improve ear edema induced by DNFB of immunocompromised mice, suggesting that it has activity of enhancing cellular immune function for immunocompromised animals; the effect of 1.2 g/kg of ethanol, methanol, petroleum ether extracts is similar to that of ethyl acetate extract, suggesting that the four extracts have good enhancing effect on specific immune of immunocompromised animals.

(200) 3. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on Nonspecific Immune Function of Normal Mice (Peritoneal Macrophages Method)

(201) Take 80 KM mice, randomly divide into 8 groups with stratification of body weight, namely suspension control group (0.5% mucilage tragacanth), enhancement effect positive control group (coriolus versicolor polysaccharide), Inhibition effect positive control group (Cyclophosphamide), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. Except that the mice in inhibition effect positive control group receive one dose of subcutaneous injection at day 13, mice in other groups receive test substance or suspension via intragastric administration once a day for 14 consecutive days. At day 13 and 14, apply intraperitoneal injection of 6% starch solution respectively. 1 h after the last administration at day 14, apply intraperitoneal injection of 1 ml of 5% chicken erythrocytes in saline suspension; 30 min later, sacrifice the mice by cervical dislocation, apply intraperitoneal injection of 2 ml saline, and gently massage the abdomen. 1 min later, cut open abdomen, draw 1 ml of peritoneal washings, evenly drop on two slides, place in a wet box, and incubate at 37° C. for 30 min. Rinse in saline, dry, fix with 1:1 acetone-methanol solution, stain with 4% (v/v) Giemsa-PBS for 3 min, rinse with distilled water and dry, perform microscopic examination, and calculate the percentage of phagocytosis.

(202) TABLE-US-00016 TABLE 16 Effect of Paliurus ramosissimus (Lour.) Poir. extracts on peritoneal macrophage phagocytosis of normal mice (n = 10, x ± s) Percentage of Group Dose phagocytosis Blank control — 0.49 ± 0.11 Enhancement effect positive control 0.4 g/kg 0.47 ± 0.19 (Coriolus versciclor polysaccharides) Inhibition effect positive control 0.1 g/kg 0.12 ± 0.03** (Cyclophosphamide) Ethyl acetate extract low-dose 0.1 g/kg 0.41 ± 0.13 Ethyl acetate extract high-dose 0.4 g/kg 0.37 ± 0.08* Methanol extract 1.2 g/kg 0.33 ± 0.07** Petroleum ether extract 1.2 g/kg 0.36 ± 0.12* Ethanol extract 1.2 g/kg 0.36 ± 0.10** Compared with the suspension control group, *P < 0.05, **P < 0.01

(203) The results are shown in Table 16. Intragastric administration of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract of 0.4 g/kg for 14 days can improve the phagocytic activity of peritoneal macrophages of normal mice, while dose of 0.1 g/kg dose group does not show obvious effect; 1.2 g/kg of ethanol, methanol, petroleum ether extracts show inhibitory effect of varying degrees, suggesting that the four extracts have mild immune inhibitory effect on normal animals.

(204) 4. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on Specific Immune Function of Normal Mice (2,4-Difluorophenyl Nitrate-Induced Ear Edema Method)

(205) Take 80 KM mice, randomly divide into 8 groups with stratification of body weight, namely suspension control group (0.5% mucilage tragacanth), enhancement effect positive control group (coriolus versicolor polysaccharide), Inhibition effect positive control group (Cyclophosphamide), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. Except that the mice in inhibition effect positive control group receive one dose of subcutaneous injection at day 13, mice in other groups receive test substance or suspension via intragastric administration once a day for 14 consecutive days. At day 9 of administration, smear 25 μl of 1% 2,4-difluorophenyl nitrate (DNFB) solution (take 100 mg of DNFB, add to the 1:1 acetone-vegetable oil mixture, mix well, and volume to 10 ml) on the abdomen of mice; 1 h after the administration at day 13, smear 10 μl of 1% DNFB solution on the left ear of mice; 24 hours of the smear, i.e., 1 hour after last administration, sacrifice the mice by cervical dislocation, weigh the ear and calculate the degree of ear edema.

(206) TABLE-US-00017 TABLE 17 Effect of Paliurus ramosissimus (Lour.) Poir. extract on ear edema induced by DNFB of normal mice (n = 10, x ± s) Group Dose Ear edema (mg) Suspension control — 10.78 ± 1.19   Model control 0.4 g/kg 10.59 ± 1.33   Positive control (coriolus 0.1 g/kg 5.66 ± 0.72** versicolor polysaccharide) Ethyl acetate extract low-dose 0.1 g/kg 9.54 ± 1.21*  Ethyl acetate extract high-dose 0.4 g/kg 7.28 ± 0.98** Methanol extract 1.2 g/kg 7.15 ± 1.17** Petroleum ether extract 1.2 g/kg 9.12 ± 1.34** Ethanol extract 1.2 g/kg 8.52 ± 1.63** Compared with the suspension control group, *P < 0.05, **P < 0.01

(207) The results are shown in Table 17. 0.1 g/kg of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract can inhibit ear edema induced by DNFB of normal mice, suggesting that it has certain inhibitory effect of cellular immune function on normal animals; the effect of 1.2 g/kg of ethanol, methanol, petroleum ether extracts is similar to that of ethyl acetate extract, suggesting that the four extracts have certain specific immune inhibitory effect.

(208) 5. The Therapeutic Effect on Mice Experimental Lupus and Effect on Cellular Immunity of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract

(209) Take 80 KM mice, randomly divide into 8 groups with stratification of body weight, namely suspension control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (tripterygium glycosides), ethyl acetate extract low-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. Except the suspension control group, mice in other groups receive intraperitoneal injection of 0.5 ml/body pristine, and test substance or suspension via intragastric administration once a day for 30 consecutive days. 24 h after last administration, draw 20 μl of orbital blood, centrifuge at 4° C. to separate the serum, and determine nti-dsDNA antibody level in serum by ELISA.

(210) Take another group of animals, group in the same way and replicate the model. Day 24 after the injection of pristane, except the suspension control group, mice in other groups receive intraperitoneal injection of 0.2 ml/body 5% chicken erythrocytes in saline suspension, continue the drug administration until day 30 after the injection of pristine. 24 h after last administration, draw 20 μl of orbital blood, add 1 ml of saline, then 0.5 ml of 4% chicken erythrocytes in saline suspension and 0.5 ml of 10% guinea pig serum respectively, after mixing, incubate at 37° C. for 0.5 h, centrifuge at 3000 rpm for 10 min, draw 1 ml of the supernatant, add 3 ml of Drabkin's reagent, and perform colorimetry at 540 nm.

(211) TABLE-US-00018 TABLE 18 Effect of Paliurus ramosissimus (Lour.) Poir. extract on experimental lupus in mice (n = 10, x ± s) Serum dsdna Hemolysin Group Dose content (OD) (OD × 10.sup.−1) Suspension control — 0.26 ± 0.028** 1.70 ± 0.19** Model control 0.4 g/kg 2.56 ± 0.381 2.52 ± 0.29 Positive control 0.03 g/kg  1.63 ± 0.101** 0.82 ± 0.17** (Tripterygium glycosides) Ethyl acetate extract 0.1 g/kg 2.23 ± 0.285 2.09 ± 0.31* low-dose Ethyl acetate extract 0.4 g/kg 2.08 ± 0.452* 1.82 ± 0.26** high-dose Methanol extract 1.2 g/kg 2.25 ± 0.309 2.00 ± 0.24** Petroleum ether extract 1.2 g/kg 2.10 ± 0.347* 2.12 ± 0.25* Ethanol extract 1.2 g/kg 2.11 ± 0.251* 2.04 ± 0.30** Compared with the model control group, *P < 0.05, **P < 0.01

(212) The results are shown in Table 18. 0.4 g/kg of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract can effectively reduce dsDNA antibody level in serum of mice with experimental lupus, suggesting that it may be used to treat lupus; the effect of 1.2 g/kg of ethanol, methanol, and petroleum ether extracts is similar to that of ethyl acetate extract, suggesting that the four extracts have some effects on lupus. Lupus may manifest as abnormally elevated humoral immunity, and in the study, hemolysin level in model animals is significantly higher than that in normal animals, and 0.1 g/kg of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract can effectively reduce such abnormally elevated hemolysin level, and 1.2 g/kg of ethanol, methanol, and petroleum ether extracts are similar to that of ethyl acetate extract, suggesting that the four extracts have significant inhibitory effect on abnormal immune hyperthyroidism.

VI. The Treatment of Oral and Gastrointestinal Inflammation and Ulcer by Paliurus Ramosissimus (Lour.) Poir. Extract

(213) (I) Preparation of Paliurus ramosissimus (Lour.) Poir. Extract

(214) 1. Preparation of Whole Plant Ethanol Extract

(215) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add 95% ethanol of 8 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight, soak for 2 days, collect the extract liquid, recover ethanol at 50° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract.

(216) 2. Preparation of Stem and Leaf Ethanol, Petroleum Ether and Ethyl Acetate Extracts

(217) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. stems and leaves, add 95% ethanol of 10 times the weight, soak for one day, then crush, add 95% ethanol of 10 times the weight for reflux extraction, collect the extract liquid, recover ethanol at 60° C. under reduced pressure until no ethanol smell and dry to obtain Paliurus ramosissimus (Lour.) Poir. ethanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. ethanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

(218) 3. Preparation of Whole Plant Petroleum Ether and Ethyl Acetate Extracts

(219) Take 1 kg of Paliurus ramosissimus (Lour.) Poir. whole plant, add methanol of 10 times the weight, soak for one day, then crush, add methanol of 8 times the weight, soak for 2 days, collect the extract liquid, recover methanol at 40° C. under reduced pressure, and dry to obtain Paliurus ramosissimus (Lour.) Poir. methanol extract. Disperse Paliurus ramosissimus (Lour.) Poir. methanol extract in water, and extract with petroleum ether and ethyl acetate in sequence, to obtain petroleum ether extract and ethyl acetate extract.

(220) 4. Ingredient Quantitative Analysis

(221) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 23 g of triterpenoids.

(222) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 103 mg of flavonoids.

(223) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 21 g of alkaloids.

(224) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 10.2 mg of coumarins.

(225) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, place in 10-ml volumetric flasks, add ethyl acetate to the mark, then precisely pipette 4 ml, and transfer to 10-ml volumetric flasks. After evaporating the solvent, add 0.4 ml of 5% vanillin-glacial acetic acid, 1.6 ml of perchloric acid, mix well, dilute with ethyl acetate to the mark, place in a 70° C. water bath for 15 min, cool to room temperature, transfer to 10-ml volumetric flasks, add ethyl acetate to the mark, shake well, determine absorbance at wavelength of 540 nm, and calculate total triterpenoids content in sample test solution (triterpenoids as ceanothic acid). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir extract contains 108 g of triterpenoids.

(226) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add water to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 510 nm, and calculate total flavonoids content in sample test solution (flavonoids as rutin). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 497 mg of total flavonoids.

(227) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract, precisely weigh, place in stoppered Erlenmeyer flasks, soak in 2 ml of 18% ammonia for 1 hour, add 30 ml of mixed solvent of ether 2-chloroform 2-ethanol (25:8:2.5), extract with ultrasound for 20 min, and pour the supernatant to a small conical flask, then add 30 ml of the above mixed solvent, cold soak for half an hour, then extract with ultrasound for 20 min, filter, wash the residues and filter paper with 15 ml of the same solvent in three times, combine the filtrates in a conical flask, evaporate in a 60° C. water bath, accurately add 10 ml of chloroform for complete dissolution, accurately pipette 5 ml, transfer to a small separating funnel, and add 6 ml of chloroform and 2 ml of buffer (pH=5.0, 0.2 M potassium hydrogen phthalate buffer). Titrate with 1 mmol.Math.L−1 bromothymol blue solution, and continue shaking; when approaching the end, separate chloroform layer, add 5 ml of fresh chloroform, continue titration and shaking, allow to stand and separate layers, until the water layer appears slight yellow. Calculate total alkaloids content in sample test solution (alkaloids as paliurine B). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 107 mg of alkaloids.

(228) Take three portions of 0.1 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethyl acetate extract, precisely weigh, place in 50-ml volumetric flasks, add appropriate amount of ethanol, dissolve with ultrasound, cool, add ethanol to the mark, and shake well. Precisely pipette 1 ml, and transfer to 10-ml volumetric flasks, add 70% ethanol to the mark, and shake well. Precisely pipette 3 ml, and transfer to 25-ml volumetric flasks, determine absorbance at wavelength of 340 nm, and Calculate total coumarins content in sample test solution (coumarins as umbelliferone). The calculation has showed that 1 g of Paliurus ramosissimus (Lour.) Poir. extract contains 186 mg of coumarins.

(229) (II) Preparation of Paliurus ramosissimus (Lour.) Poir. Preparations

(230) 1. Preparation of Tablets

(231) Take 300 g of Paliurus ramosissimus (Lour.) Poir. whole plant ethanol extract, add suitable excipient, such as: 100 g of microcrystalline cellulose, 57.5 g of lactose, 20 g of cross-linked sodium carboxymethyl cellulose, etc., and compress into tablets.

(232) 2. Preparation of Capsules

(233) Take Paliurus ramosissimus (Lour.) Poir. stem and leaf ethyl acetate extract, add suitable excipient, such as: lactose, compressible starch, carboxymethyl starch, microcrystalline cellulose, etc., to make capsules.

(234) 3. Preparation of Granules

(235) Take Paliurus ramosissimus (Lour.) Poir. whole plant methanol extract, add suitable excipient, such as: lactose, starch, methyl cellulose, hydroxymethyl cellulose, hydroxypropylmethyl cellulose, hydroxypropyl cellulose, polyvinylpyrrolidone, silica powder etc., to make granules.

(236) 4. Preparation of Ointments

(237) Take Paliurus ramosissimus (Lour.) Poir. stem and leaf petroleum ether extract, add suitable excipient, such as: octadecanol, glycerol monostearate, glycerin, stearic acid etc., to make ointments.

(238) 5. Preparation of Suppositories

(239) Take Paliurus ramosissimus (Lour.) Poir. whole plant ethanol extract, add suitable excipient, such as: mixed fatty acid glycerides, PEG, beeswax etc., to make suppositories.

(240) (III) Pharmacology Verification of Uses of Paliurus ramosissimus (Lour.) Poir. Extract

(241) 1. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on Pylorus Ligation Induced Experimental Gastric Ulcer in Rats.

(242) Take 80 SD mice, randomly divide into 8 groups with stratification of body weight, namely model control group (0.5% mucilage tragacanth), positive control group (ranitidine), ethyl acetate extract low-dose group, ethyl acetate extract middle-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. In all groups, mice receive test substance via intragastric administration once a day for 3 consecutive days. 1 h after the last administration, perform pylorus ligation, 15 hours after the surgery, sacrifice the animals by cervical dislocation, take out the stomach, fix with 1% formaldehyde for 20 min, then dissect, observe the extent of mucosal damage by stereoscopic microscope, and calculate ulcer index and ulcer inhibition rate.

(243) TABLE-US-00019 TABLE 19 Effect of Paliurus ramosissimus (Lour.) Poir. extracts on pylorus ligation induced experimental gastric ulcer in rats (n = 10, x ± s) Inhibition Group Dose Ulcer index rate (%) Model control — 4.7 ± 1.7 — Positive control (ranitidine)  60 mg/kg 1.5 ± 0.4** 68.1 Ethyl acetate extract low-dose 0.1 g/kg 3.7 ± 1.4 21.3 Ethyl acetate extract middle dose 0.2 g/kg 2.8 ± 0.7* 40.4 Ethyl acetate extract high-dose 0.4 g/kg 2.0 ± 1.0** 57.4 Methanol extract 1.2 g/kg 1.9 ± 0.6** 59.6 Petroleum ether extract 1.2 g/kg 2.0 ± 0.6** 57.4 Ethanol extract 1.2 g/kg 2.2 ± 0.8** 53.2 Compared with the model control group, *P < 0.05, **P < 0.01

(244) The results are shown in Table 19. Intragastric administration of 0.2 g/kg and higher doses of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract 3 times can significantly inhibit the degree of pyloric ligation induced gastric ulcers in rats, and the strength of 0.4 g/kg dose group has no significant difference with that of 60 mg/kg ranitidine group; 1.2 g/kg of ethanol, methanol, petroleum ether extracts can also effectively inhibit ulcer degree, suggesting that the four extracts have good anti-ulcer effect.

(245) 2. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on 2,4,6-Trinitrotoluene Sulfonic Acid (TNBS) Induced Colitis in Rats

(246) Take 90 SD mice, randomly divide into 9 groups with stratification of body weight, namely sham operation group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (dexamethasone), ethyl acetate extract low-dose group, ethyl acetate extract middle-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. After the animals are fasted for 24 h, perform anesthesia with sodium pentobarbital. Except the sham operation group, perform coloclysis with TNBS and 40% ethanol, and replicate experimental colitis model; 6 h after model construction, administer test substance. At the day 5 of administration, draw tail vein blood and count leukocyte. At day 6, perform urethane anesthesia, draw abdominal aortic blood and sacrifice the animals by cervical dislocation. Cut 9 cm colon from the anus, in an ice bath, cut intestine along the mesenteric edge, wash out the contents, measure the ulcer area, calculate the percentage of ulcer area; weigh the colon, scrap colonic mucosa, and determine tumor necrosis factor (TNF-α) concentration with ELISA method.

(247) TABLE-US-00020 TABLE 20 Effect of Paliurus ramosissimus (Lour.) Poir. extracts on TNBS induced experimental colitis in rats (n = 10, x ± s) Leukocyte Ratio of ulcer TNF-α Group Dose count (10.sup.9/L) area (%) (ng/gpro) Sham operation — 17.5 ± 1.2**  5.0 ± 2.3**  28.1 ± 5.0** Model control — 22.9 ± 1.1 42.3 ± 13.8 234.9 ± 67.3 Positive control   2 mg/kg  8.4 ± 0.9** 28.6 ± 10.5*  73.2 ± 19.6** (dexamethasone) Ethyl acetate extract low-dose 0.1 g/kg 21.5 ± 1.9 32.7 ± 12.1 189.6 ± 52.7 Ethyl acetate extract middle 0.2 g/kg 18.6 ± 1.1** 27.9 ± 15.3* 137.3 ± 45.9** dose Ethyl acetate extract 0.4 g/kg 18.2 ± 0.8** 20.4 ± 9.3** 102.8 ± 37.5** high-dose Methanol extract 1.2 g/kg 18.6 ± 0.6** 18.8 ± 8.0** 132.7 ± 39.9** Petroleum ether extract 1.2 g/kg 18.0 ± 0.9** 25.3 ± 6.8** 169.0 ± 78.3* Ethanol extract 1.2 g/kg 18.5 ± 0.12** 23.8 ± 10.6** 121.6 ± 44.0** Compared with the model control group, *P < 0.05, **P < 0.01

(248) The results are shown in Table 21. TNBS induced experimental colitis in rats may manifest as increased inflammatory cells, increased levels of inflammatory cytokines and ulcer on colon surface. 0.2 g/kg and higher doses of Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract can inhibit the increase of leukocyte and proinflammatory cytokines TNF-α, and reduce the formation of ulcers; the effect of 1.2 g/kg of ethanol, methanol, petroleum ether extracts is similar to that of ethyl acetate extract, suggesting that the four extracts have good anti-colitis effect.

(249) 3. Effect of Ethanol, Methanol, Petroleum Ether Extracts and Ethyl Acetate Extract on Ammonia Induced Chronic Gastritis in Rats

(250) Take 120 SD mice, randomly divide into 10 groups with stratification of body weight, namely normal control group (0.5% mucilage tragacanth), model control group (0.5% mucilage tragacanth), positive control group (Sanjiuweitai particle), ethyl acetate extract low-dose group, ethyl acetate extract middle-dose group, ethyl acetate extract high-dose group, ethanol extract group, methanol extract group, and petroleum ether extract group. All animals receive intragastric administration of 0.02% ammonia once daily for 90 consecutive days; meanwhile, animals receive intragastric administration of test substance once daily for 90 consecutive days. On the next day after the last drug administration, sacrifice the animals by cervical dislocation, Take stomach wall of the lesser curvature, fix with 10% formalin, paraffin-embed, slice, HE and PAS stain. On HE staining slice, observe inflammatory reactions and score, and measure mucosal thickness of the gastric body; on PAS staining slice, measure the thickness of positive layer and characteristic mucus layer.

(251) TABLE-US-00021 TABLE 21 Effect of Paliurus ramosissimus (Lour.) Poir. extracts on ammonia induced experimental chronic gastritis in rats (n = 12, x ± s) Thickness of Inflammation Thickness of mucous mucus layer Group Dose score layer (mm × 10.sup.−1) (mm × 10.sup.−2) Normal control — 0.20 ± 0.12** 5.13 ± 0.62** 9.60 ± 2.56** Model control — 3.23 ± 1.04 3.18 ± 0.54 3.28 ± 0.69 Positive 0.5 g/kg 1.56 ± 0.75** 3.51 ± 0.48 6.72 ± 1.93** control (Sanjiuweitai particle) Ethyl acetate 0.1 g/kg 2.07 ± 1.12* 3.29 ± 0.47 6.08 ± 1.71** extract low-dose Ethyl acetate 0.2 g/kg 1.62 ± 0.63** 3.72 ± 0.83 7.29 ± 2.05** extract middle dose Ethyl acetate 0.4 g/kg 1.08 ± 0.55** 4.67 ± 1.04** 7.38 ± 1.36** extract high-dose Combined Ethyl acetate extract 1.45 ± 0.69** 4.28 ± 0.61**# 7.33 ± 1.59** application 0.2 g/kg + Sanjiuweitai 0.5 g/kg Methanol extract 1.2 g/kg 1.58 ± 0.69** 4.75 ± 1.00** 7.12 ± 1.15** Petroleum ether 1.2 g/kg 1.39 ± 0.47** 4.44 ± 0.86** 6.33 ± 0.92** extract Ethanol extract 1.2 g/kg 1.28 ± 0.48** 4.38 ± 0.96** 7.05 ± 1.14** Compared with the model control group, *P < 0.05, **P < 0.01; Compared with the positive control group (Sanjiuweitai particle group), #P < 0.05

(252) The results are shown in Table 21. For ammonia induced experimental chronic gastritis, Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract has effects in inhibiting inflammation and increasing layer thickness of mucous layer and mucus layer, especially in inhibiting inflammation and increasing thickness of mucus layer; the effect of 1.2 g/kg of ethanol, methanol, petroleum ether extracts is similar to that of ethyl acetate extract, suggesting that the four extracts have good effect against chronic gastritis.

(253) 4. Effect of Ethyl Acetate Extract in Combination of Sanjiuweitai on Pylorus Ligation Induced Experimental Gastric Ulcer in Rats

(254) Take 50 SD mice, randomly divide into 5 groups with stratification of body weight, namely model control group (0.5% mucilage tragacanth), positive control group (ranitidine), ethyl acetate extract group, Sanjiuweitai particle group and combined application group. In all groups, mice receive test substance via intragastric administration once a day for 3 consecutive days. 1 h after the last administration, perform pylorus ligation, 15 hours after the surgery, sacrifice the animals by cervical dislocation, take out the stomach, fix with 1% formaldehyde for 20 min, then dissect, observe the extent of mucosal damage by stereoscopic microscope, and calculate ulcer index and ulcer inhibition rate.

(255) TABLE-US-00022 TABLE 22 Effect of ethyl acetate extract in combination of Sanjiuweitai on pylorus ligation induced experimental gastric ulcer in rats (n = 10, x ± s) Ulcer inhibition rate Group Dose Ulcer index (%) Model control — 4.5 ± 1.3 — Positive control 60 mg/kg 1.8 ± 0.6** 60.0 (ranitidine) Ethyl acetate extract 0.2 g/kg 3.0 ± 0.9* 33.3 Sanjiuweitai particle 1 g/kg 4.2 ± 1.7 6.7 Combined application Ethyl acetate 2.7 ± 1.1**## 40.0 extract 0.2 g/kg + Sanjiuweitai 1 g/kg Compared with the model control group, *P < 0.05, **P < 0.01; Compared with the Sanjiuweitai particle group, #P < 0.05, ##P < 0.01.

(256) The results are shown in Table 22. The intragastric administration of 0.2 g/kg Paliurus ramosissimus (Lour.) Poir. ethyl acetate extract three times can significantly inhibit the degree of pyloric ligation induced gastric ulcers in rats; Sanjiuweitai alone does not have effect in the model, but when being applied in combination with the extract of the present invention, it can significantly enhance the efficacy of anti-ulcer, suggesting that it has synergistic effect with anti-ulcer drugs or drug combinations.

(257) 5. Effect of Ethyl Acetate Extract in Combination of Sanjiuweitai on Ammonia Induced Experimental Chronic Gastritis in Rats

(258) This experiment is carried out with pharmacodynamics experiment 2, and the results showed in Table 21, with shared normal control group and model control group. The results have showed that Sanjiuweitai can significantly increase mucus layer thickness, reduce inflammation, but does not have significant effect on mucous layer thickness. And the combination with the extract of the present invention can enhance the effects by Sanjiuweitai and also effectively increase mucous layer thickness, suggesting that it has synergistic effect with chronic gastritis drugs or drug combinations.

(259) In summary, Paliurus ramosissimus (Lour.) Poir. extract and the raw medicine material, Paliurus ramosissimus (Lour.) Poir., have significant anti-tumor activity, antifungal activity, anti-fibrotic activity and, bi-directional immunomodulatory effects, as well as the effects in treatment of oral and gastrointestinal inflammation or/and ulcer.