Preparation method for extractive of jinxuan hemorrhoid washing powder botanicals

Abstract

A preparation method for extractive botanicals includes: (A) honeysuckle, schizonepeta, and purslane in a powder are mixed, ground, and passed through a mesh; the medicinal powder obtained from supercritical extraction is soaked in alcohol, then undergoes percolation extraction, and the percolate is collected; (B) the alcohol percolate is concentrated, left stand, and suction filtrated to obtain a filtrate; (C) the filtrate macroporously adsorbs to a resin column at a flow velocity, is then removed of impurity by water washing, and undergoes elution with alcohol to obtain an alcohol eluent; (D) alcohol is recovered from the eluent, the remaining liquid is concentrated, and the concentrated liquid is dried to obtain the extractive of botanicals. The total content of flavones, saponins, and organic acids exceeds 70%. The extractive has substantial anti-inflammatory and pain relieving effects.

Claims

1. A preparation method, comprising the following steps: mixing three ingredients including honeysuckle, schizonepeta, and purslane into a mixed powder at a weight ratio of 3:4:3, respectively; grinding and sifting the powder through a 30-50 mesh, performing a supercritical extraction of the powder, adding the powder after supercritical extraction to a first alcohol aqueous solution with a weight of 2-4 times that of said powder and a volume ratio of 30-90% and soaking the solution and the powder for 20-30 hours, and then an second alcohol aqueous solution with a volume ratio of 30-90% is added to make the weight of the first alcohol aqueous solution with a volume ratio of 30-90% equal to 6-14 times the weight of said powder; performing percolation extraction is with a flow velocity of the weight of 1-5 times that of said powder per hour, and collecting a resulting alcohol percolate; concentrating the alcohol percolate to a weight of 1-5 times that of said powder, leaving the alcohol percolate to stand for 2-10 hours, and suction filtering the alcohol percolate to obtain a filtrate; purifying the filtrate by macroporously absorbing the filtrate into a resin column at a flow velocity of a volume of 0.5-4 times that of the column per hour, by washing the resin column with water with a volume of 2-4 times that of the column, wherein the filtrate undergoes elution with an alcohol aqueous solution with a volume ratio of 40-95% and a flow velocity of a volume of 0.5-4 times that of the column per hour to obtain an alcohol eluent; and recovering alcohol from the alcohol eluent, concentrating any remaining liquid, and drying a resulting concentrated liquid to obtain an extractive of the ingredients.

2. The preparation method according to claim 1, wherein the powder obtained from mixing the three ingredients is added with an alcohol aqueous solution with a weight of 3 times that of said and a volume ratio of 50% and soaked for 24 hours, and then an alcohol aqueous solution with a volume ratio of 50% is added to make the weight of the alcohol aqueous solution with a volume ratio of 50% equal to 12 times the weight of said powder, percolation extraction is performed with flow velocity of the weight of 2 times that of said powder per hour, and then the resulting alcohol percolate is collected.

3. The preparation method according to claim 1, wherein the alcohol percolate obtained is concentrated to a weight of 3.3 times that of said powder.

4. The preparation method according to claim 1, wherein the filtrate macroporously absorbs into a resin column at a flow velocity of a volume of 1 time that of the column per hour, is then purified by washing with water with a volume of 3 times that of the column, and undergoes elution with an alcohol aqueous solution with a volume ratio of 70% and a flow velocity of a volume of 1 time that of the column per hour.

5. The preparation method according to claim 1, wherein drying the concentrated liquid is spray drying with conditions, including: inlet temperature of 170 C., outlet temperature of 90 C., and atomizing disk rotation speed of 20,000 R/M.

6. The preparation method according to claim 1, wherein said resin column is a medical type D101 type macroporous resin column.

7. The preparation method according to claim 1, wherein a diameter-height ratio of said resin column is 1:3-1:8.

8. The preparation method according to claim 1, wherein before mixing, the three ingredients are placed in a supercritical CO.sub.2 extraction device with extraction temperature of 45 C., extraction pressure of 25 MPa and extraction time of 90 min.

Description

DESCRIPTION OF THE ACCOMPANYING DRAWINGS

(1) FIG. 1 is the extracting and purifying process flow diagram of the extractive of Jinxuan Hemorrhoid Washing Powder botanicals.

(2) FIG. 2 is the leakage curve of the absorbed total flavones when the sample solution, which is prepared by 70% alcohol percolation extraction of the medicinal powder obtained from supercritical extraction of the three flavors of the botanicals in a Jinxuan Hemorrhoid Washing Powder prescription, goes through the D101 macroporous resin column.

(3) FIG. 3 is the eluting curve of the total flavones in an eluting resin column using 70% alcohol as its eluent.

(4) FIG. 4 is the eluting curve of the total saponins in an eluting resin column using 70% alcohol as its eluent.

(5) FIG. 5 is the eluting curve of the total organic acids in an eluting resin column using 70% alcohol as its eluent.

SPECIFIC EMBODIMENTS

(6) In combination with what is shown in FIG. 1, the present invention provides a preparation method for extractive of Jinxuan Hemorrhoid Washing Powder botanicals, comprising the following steps:

(7) (a) The three flavors of botanicalshoneysuckle, schizonepeta, and purslane in the prescription of Jinxuan Hemorrhoid Washing Powder are mixed at a weight ratio of 3:4:3, ground, and passed through a 40 mesh, the medicinal powder obtained from supercritical extraction (extraction conditions: put in supercritical CO.sub.2 extraction device, extraction temperature 45 C., extraction pressure 25 MPa, extraction time 90 min. Extraction purposes: to remove soluble ingredients) is added with an 3090% (volume ratio) alcohol aqueous solution with a weight of 24 times that of the medicinal powder (three flavors of botanicals) and soaked for 2030 hours, and then an 3090% (volume ratio) alcohol aqueous solution is added to make the weight of the 3090% (volume ratio) alcohol aqueous solution equal to 614 times the weight of the medicinal powder (three flavors of botanicals), the percolation extraction is underwent with a flow velocity of the weight of 15 times that of the medicinal powder (three flavors of botanicals) per hour, and the percolate is collected;

(8) (b) The alcohol percolate obtained in step (a) is concentrated to a weight of 15 times that of the medicinal powder (three flavors of botanicals), left stand (210 h), and suction filtrated to obtain a filtrate;

(9) (c) The filtrate macroporously adsorpts to a resin column at a flow velocity of a volume of 0.54 times that of the column per hour, is then removed of impurity by washing with water with a volume of 24 times that of the column, and undergoes elution with an 4095% (volume ratio) alcohol aqueous solution and a flow velocity of a volume of 0.54 times that of the column per hour to obtain an alcohol eluent; and

(10) (d) Alcohol is recovered from the alcohol eluent which is concentrated to a relative density (water=1) of 1.011.10, and the concentrated liquid is spray dried to obtain the extractive product of Jinxuan Hemorrhoid Washing Powder botanicals (extractive of the efficacy parts). The dried extraction is collected, sealed, weighed, and preserved in dry place. After determination, the total content of flavones, saponins, and organic acids in extractive of Jinxuan Hemorrhoid Washing Powder botanicals can exceed 70% of the weight of the extractive of Jinxuan Hemorrhoid Washing Powder botanicals.

(11) As shown in FIG. 1, the preparation method procedure of the extractive of Jinxuan Hemorrhoid Washing Powder botanicals in a more preferable example of the present invention is: 7.5 Kg medicinal powder obtained from supercritical extraction of the three flavors of Jinxuan Hemorrhoid Washing Powder botanicals (which is mixed at a ratio of 3:4:3, ground, and passed through a 40 mesh) is added with a 50% (volume ratio) alcohol aqueous solution with a weight of 3 times that of the medicinal powder (three flavors of botanicals) and soaked for 24 hours, and then a 50% (volume ratio) alcohol aqueous solution is added to make the weight of the 50% (volume ratio) alcohol aqueous solution equal to 12 times the weight of the medicinal powder (three flavors of botanicals), the percolation extraction is underwent with a flow velocity of the weight of 2 times that of the medicinal powder (three flavors of botanicals) per hour, and the percolate is collected; the percolate is concentrated to a certain volume to make the weight of the drug solution equal to 3.3 times that of said medicinal powder (25 L), left stand, and suction filtrated to obtain a sampling drug solution for future use. The sampling drug solution is absorbed at a flow velocity of 1 Bv/h (diameter-height ratio of the resin bed is 1:8), following absorption, it is washed with distilled water with a volume of 3 times that of the resin column at a flow velocity of 1 Bv/h and underwent elution with an 70% alcohol aqueous solution with a volume of 5 times that of the resin column at a flow velocity of 1 Bv/h to obtain the eluent. Alcohol is recovered from the eluent which is concentrated to a relative density of 1.03, and spray dried, the dried extraction is collected, sealed, weighed, and preserved in shade place.

(12) That is to say, the preferred extracting and purifying conditions of the preparation method of the extractive of Jinxuan Hemorrhoid Washing Powder botanicals in a more preferable example of the present invention are:

(13) In step (a), 7.5 Kg medicinal powder obtained from supercritical extraction of the three flavors of Jinxuan Hemorrhoid Washing Powder botanicals (which is mixed at a ratio of 3:4:3, ground, and passed through a 40 mesh) is added with a 50% (volume ratio) alcohol aqueous solution with a weight of 3 times that of the medicinal powder (three flavors of botanicals) and soaked for 24 hours, and then a 50% (volume ratio) alcohol aqueous solution is added to make the weight of the 50% (volume ratio) alcohol aqueous solution equal to 12 times the weight of the medicinal powder (three flavors of botanicals), the percolation extraction is underwent with a flow velocity of the weight of 2 times that of the medicinal powder (three flavors of botanicals) per hour, and the percolate is collected.

(14) In step (b), the concentrated drug solution of the alcohol percolate (100 L) has a weight of 3.3 times (25 L) that of the medicinal powder.

(15) In step (c), the filtrate macroporously adsorpts to a resin column at a flow velocity of a volume of 1 time that of the column per hour, is then removed of impurity by washing with water with a volume of 3 times that of the column, and continues to undergo elution with an 70% (volume ratio) alcohol aqueous solution and a flow velocity of a volume of 1 time that of the column per hour to elute the efficacy substances in the resin.

(16) In step (d), the conditions of spray drying are: inlet temperature of 170 C., outlet temperature of 90 C., and atomizing disk rotation speed of 20,000 R/M.

(17) The total content of flavones, saponins, and tannins in extractive of Jinxuan Hemorrhoid Washing Powder botanicals can be up to 71.1% of the weight of the extractive of Jinxuan Hemorrhoid Washing Powder botanicals.

(18) The concentration of the alcohol described in the present invention means the volume fragment of alcohol in 100 mL volume alcohol aqueous solution.

(19) The present invention also provides a pharmaceutical composition, i.e. total flavones, total saponins, and total organic acids, prepared with the extractive of Jinxuan Hemorrhoid Washing Powder botanicals, and the application of the extractive of the present invention in anti-inflammatory and pain relieving drugs.

(20) The aforementioned pharmaceutical composition of the present invention can be any medically accepted formulations which is comprised of: smoked lotions, tablets, sugar-coated tablets, film-coated tablets, enteric coated tablets, capsules, hard capsules, soft capsules, oral liquids, buccal tablets, granules, electuaries, pills, powders, ointments, sublimed preparations, suspensions, powders, solutions, injections, suppositories, soft ointments, hard ointments, creams, sprays, drops, and patches.

(21) A medically acceptable carrier can be added to the aforementioned pharmaceutical composition when it is prepared to a dosage form. Said pharmaceutically acceptable carrier can be: starch, sucrose, lactose, mannitol, silicon derivatives, cellulose and its derivatives, alginates, gelatin, polyvinylpyrrolidone, glycerol, polysorbate 80, agar, calcium carbonate, calcium bicarbonate, surfactant, polyethylene glycol, cyclodextrin, phospholipid material, kaolin, talc powder, calcium stearate, magnesium stearate, etc.

(22) The present invention will be further described below with reference to the examples.

Example 1

(23) Percolation Extraction Process Test of Active Ingredients of the Three Flavors of BotanicalsHoneysuckle, Schizonepeta, and Purslane in Jinxuan Hemorrhoid Washing Powder Prescription Using Alcohol as Solvent

(24) (1) Alcohol percolation extraction process test: percolation extraction process studies have been done to the effective substances contained in the medicinal powder (50 g) obtained from supercritical CO.sub.2 extraction of the three flavors of Jinxuan Hemorrhoid Washing Powder botanicals (which is mixed at a ratio of 3:4:3, ground, and passed through a 40 mesh) in the present test. Four factors and three levels orthogonal table experimental method is employed, the alcohol concentration in the solvent, the dose of alcohol, the percolation rate and other affecting factors in the percolation extraction process are preferably selected, its examining indicators are yield rates of total flavones and dry paste of the main efficacy substances in the extractive, and experimental results are shown in Table 4 to Table 7.

(25) TABLE-US-00004 TABLE 4 Pilot factor level table A Alcohol B Alcohol dose D percolation rate Level concentration (%) (times) C Blank (BV/H) 1 50 8 2 2 60 10 4 3 70 12 6

(26) TABLE-US-00005 TABLE 5 Orthogonal Experimental Design and Result Analysis Amount of Dry total paste flavones yield Test in Jinzuan rate no. A B C D (mg) (%) 1 1 1 1 1 1178.441 19.69 2 1 2 2 2 1204.917 19.86 3 1 3 3 3 1286.992 20.35 4 2 1 2 3 1133.432 18.14 5 2 2 3 1 1239.336 18.98 6 2 3 1 2 1268.459 19.16 7 3 1 3 2 1085.775 17.28 8 3 2 1 3 1173.146 17.27 9 3 3 2 1 1318.763 18.71 aK1 1223.45 1132.55 1206.68 1245.51 aK2 1213.74 1205.8 1219.04 1186.38 aK3 1192.56 1291.41 1204.03 1197.86 aR 30.889 158.856 15.003 59.129 bK1 19.967 18.37 18.707 19.127 bK2 18.76 18.703 18.903 18.767 bK3 17.753 19.407 18.87 18.587 bR 2.214 1.037 0.196 0.54

(27) TABLE-US-00006 TABLE 6 Variance Analysis of Total Flavones Sum of squares of Degree of Mean F Factor deviations freedom square value P A 1496.98 2 3.891 B 37928.844 2 98.579 <0.05 D 5899.105 2 15.332 Blank (error) 384.75 2 F0.05(2,2) = 19.00

(28) TABLE-US-00007 TABLE 7 Variance Analysis of Dry Paste Yield Rate Sum of squares of Degree Mean F Rate deviations of freedom square value P A 7.368 2 111.636 <0.05 B 1.680 2 25.455 <0.05 D 0.454 2 6.879 Blank (error) 0.07 2 F0.05(2,2) = 19.00 F0.01(2,2) = 99.00

(29) Experimental results show that the biggest affecting factor is the dose of alcohol, followed by alcohol concentration, percolation rate is of no significant impact, and combining visual analysis and variance analysis, the optimum process condition A.sub.1B.sub.3D.sub.1, i.e. 12 times the amount of 50% alcohol is added and percolation is conducted at a rate of 2 BV/H, is preferred.

(30) (2) Verification test: In accordance with the optimum condition preferably selected with the orthogonal design test, repeatable tests are conducted in 3 times, and the experimental results are shown in Table 8.

(31) TABLE-US-00008 TABLE 8 Verification Test Results of Percolation Extraction Amount of total Medicine flavones in Jinxuan Dry paste yield Test no. dosage (g) (mg) rate (%) 1 50 1381.77 20.80 2 50 1331.77 20.45 3 50 1334.896 20.60

(32) Verification results show that the extraction process preferably selected is stable and plausible.

Example 2

(33) Macroporous Resin Purification Process Test in the Preparation Method of Alcohol Extractive of the Three Flavors of Botanicals in the Jinxuan Hemorrhoid Washing Powder Prescription

(34) The following purification test is conducted to the percolate extracting solution of the three flavors of botanicals of Jinxuan Hemorrhoid Washing Powder obtained through the aforementioned extracting conditions:

(35) (1) D101 Macroporous Resin Purification Process Test

(36) {circle around (1)} Preferable Selection of Absorption Conditions

(37) Orthogonal test method is employed, using sampling flow velocity, drug solution concentration (by the original medicinal material amount contained in the sample, namely drug solution concentration=medicinal powder weight/filtrate volume100%) and the diameter-height ratio as investigated factors, and the test is arranged applying L.sub.9 (3.sup.4) orthogonal table with factor and level arrangements shown in Table 6. Contents of total flavones, total saponins, and total organic acid in the following 9 groups are measured respectively, its ratio of adsorption is measured, and comprehensive evaluation is conducted. Analysis results are shown in Tables 913.

(38) TABLE-US-00009 TABLE 9 Factor and Level Table A Sampling B Absorption D concentration flow velocity C Diameter-height Level (g .Math. mL.sup.1) (BV/H) Blank ratio 1 0.1 2 1:3 2 0.3 4 1:8 3 0.5 6 1:12

(39) TABLE-US-00010 TABLE 10 Percolate Extracting Solution of Jinxuan Hemorrhoid Washing Powder Absorption Orthogonal Test Design and Result Analysis Table Ratio absorptiom Ratio absorptiom Ratio absorptiom amount of total amount of total amount of total Test flavones saponins organic acid no. A B C D (mg .Math. g.sup.1) (mg .Math. g.sup.1) (mg .Math. g.sup.1) 1 1 1 1 1 27.9802 3.4808 6.4768 2 1 2 2 2 25.6412 4.4925 6.677 3 1 3 3 3 24.7292 5.507 5.8394 4 2 1 2 3 30.0425 6.083 13.1014 5 2 2 3 1 31.1506 8.9516 12.1938 6 2 3 1 2 29.9781 9.77 22.828 7 3 1 3 2 33.6501 14.9129 20.8562 8 3 2 1 3 31.1507 13.8162 8.033 9 3 3 2 1 30.2089 13.1321 8.7032 aK1 26.117 30.558 29.703 29.780 aK2 30.390 29.314 28.631 29.756 aK3 31.670 28.305 29.843 28.641 aR 5.553 2.253 1.212 1.139 bK1 4.493 8.159 9.022 8.521 bK2 8.268 9.087 7.903 9.725 bK3 13.954 9.470 9.790 8.469 bR 9.461 1.311 1.887 1.256 cK1 6.331 13.478 12.446 9.125 cK2 16.041 8.968 9.494 16.787 cK3 12.531 12.457 12.963 8.991 R 9.710 4.510 3.469 7.796

(40) TABLE-US-00011 TABLE 11 Variance Analysis of Ratio Absorption Amount of Total Flavones of Jinxuan Hemorrhoid Washing Powder Sum of squares of Degree of Factor deviations freedom F value Significance Sampling 50.736 2 19.225 <0.05 concentration Absorption flow 7.636 2 2.894 velocity Diameter-height 2.543 2 0.964 ratio Error 2.64 2 F0.05(2,2) = 19, F0.01(2,2) = 99.00

(41) TABLE-US-00012 TABLE 12 Variance Analysis of Ratio Absorption Amount of Total Saponins of Jinxuan Hemorrhoid Washing Powder Degree Sum of squares of F Factor of deviations freedom value Significance Sampling 136.071 2 25.161 <0.05 concentration Absorption flow 2.726 2 0.504 velocity Diameter-height 3.030 2 0.560 ratio Error 5.41 2 F0.05(2,2) = 19, F0.01(2,2) = 99.00

(42) TABLE-US-00013 TABLE 13 Variance Analysis of Ratio Absorption Amount of Total Organic Acids of Jinxuan Hemorrhoid Washing Powder Sum of squares of Degree of F Factor deviations freedom value Significance Sampling 145.043 2 6.901 concentration Absorption 33.558 2 1.597 flow velocity Diameter-height 119.506 2 5.686 ratio Error 21.02 2 F0.05(2,2) = 19, F0.01(2,2) = 99.00

(43) The variance analysis results show that sampling concentration (A) has significant effect in the absorption process of alcohol extractivetotal flavones, total saponins, and total organic acids, of the three flavors of botanicals in the prescription of Jinxuan Hemorrhoid Washing Powder. Visual analysis shows that absorption flow velocity and diameter-height ratio are of no significant impact, and the optimum process parameter obtained by comprehensive analysis is: A.sub.3B.sub.1D.sub.2, i.e. sampling concentration is 0.5 g/ml, absorption flow velocity is 2 BV/H, and diameter-height ratio is 1:8.

(44) {circle around (2)} Sampling Amount Examination

(45) 0.5 g/ml Jinxuan percolate is added to the upper end of the 20 g handled D101 resin column, and absorbed according to the optimum adsorption conditions, and the effluent is collected with every 10 mL as one flow fraction. As verified by the pre-test, flavones is first leaked, so the total flavones amount is measured and the leakage curve is drawn with fraction number as the horizontal axis and the absorbance of total flavones as the vertical axis. The result is shown in FIG. 2. It can be seen in the figure that when the sampling amount is 30 mL (about 1.5 times the amount of resin), the total flavones starts to leak, and when the sampling amount is 160 mL (about 8 times the amount of resin), the adsorption reaches its saturation.

(46) {circle around (3)} Washing Condition Examination

(47) Sampling adsorption is conducted according to the aforementioned optimum adsorption conditions with a sampling amount of 30 mL, then washed with water, every 10 mL out-let solution is collected as one flow fraction and identified with molish reaction and Liebermann reaction examination knowledge, the dry paste weight is simultaneously determined, after 60 mL washing, molish reaction and Liebermann reaction are negative, the dry paste weight stops changing, and results show that after washing with 60 mL water (about three times the resin column volume) the sugars in the resin column can be substantially removed.

(48) {circle around (4)} Alcohol Elution Concentration Examination

(49) Another five parts of 20 g resin are loaded, absorbed and removed impurity according to the aforementioned absorption conditions and washing conditions, then eluted with 90 mL 30%, 50%, 70%, and 90% alcohol respectively at the same flow velocity, contents and the desorption rate of the total flavones, total saponins, and total organic acids are calculated, and the results are shown in Tables 14, 15 and 16.

(50) TABLE-US-00014 TABLE 14 Alcohol Elution Concentration Examination Results of Total Flavones of Jinxuan Hemorrhoid Washing Powder Alcohol Desorption rate of Dry paste Total concentration total flavones Desorption weight flavones (%) (mg) rate (%) (mg) purity (%) 30 130.02 40.79 625.1 20.8 50 285 78.5 785.2 36.3 70 288.1 80.3 807 35.7 90 299.6 85 886.4 33.8

(51) TABLE-US-00015 TABLE 15 Alcohol Elution Concentration Examination Results of Total Saponins of Jinxuan Hemorrhoid Washing Powder Alcohol Desorption rate Dry paste Total concentration of total Desorption rate weight saponins (%) saponins (mg) (%) (mg) purity (%) 30 40.3 33.81 625.1 6.45 50 85.6 71.5 785.2 10.9 70 95.5 80.12 807 11.83 90 98.3 82.47 886.4 11.08

(52) TABLE-US-00016 TABLE 16 Alcohol Elution Concentration Examination Results of Total Organic Acids of Jinxuan Hemorrhoid Washing Powder Desorption Alcohol rate of total Dry paste Total saponins concentration organic acids Desorption weight acids purity (%) (mg) rate (%) (mg) (%) 30 40.63 60.3 625.1 6.5 50 70.67 73.5 785.2 9 70 126 78.1 807 15.71 90 101.9 80 886.4 11.5

(53) The above test results show that both the desorption rate and content of the total flavones, total saponins, and total organic acids are relatively high when the concentration of the alcohol is above 50%, wherein the desorption rate of total flavones, total saponins, and total organic acids in 90% alcohol elution is the highest, while the purity of total saponins, and total organic acids in 70% alcohol elution is the highest. After comprehensive analysis, taking into account that the desorption rate of 70% alcohol differentiates not that much from that of 90% alcohol, and the production costs are relatively low, therefore 70% alcohol is selected as the eluent of the present test.

(54) {circle around (5)} Elution Rate Examination

(55) Dynamic adsorption is conducted according to the above conditions, with 70% alcohol as eluent, eluted at a velocity of 1 BV.Math.H.sup.1, 2 BV.Math.H.sup.1, 4 BV.Math.H.sup.1, and 6 BV.Math.H.sup.1 respectively, the amount of total flavones, total saponins, total organic acids and dry paste weight are measured and the desorption rate and purity are calculated, and the results are shown in Tables 17, 18, and 19.

(56) TABLE-US-00017 TABLE 17 Alcohol Elution Rate Examination of Total Flavones of Jinxuan Hemorrhoid Washing Powder Elution Elution amount of Total flavones Dry paste flow total flavones Desorption purity in the dry weight velocity (mg) rate (%) paste (%) (mg) 1BV/H 311.2 81 37 841.1 2BV/H 296.17 80.49 36.7 807 4BV/H 240.76 79.1 30.69 784.5 6BV/H 202.2 59 28.8 702.1

(57) TABLE-US-00018 TABLE 18 Alcohol Elution Rate Examination of Total Saponins of Jinxuan Hemorrhoid Washing Powder Elution Elution amount of Total saponins Dry paste flow total sanopins Desorption purity in the dry weight velocity (mg) rate (%) paste (%) (mg) 1BV/H 96.4 82 11.46 841.1 2BV/H 95.03 79.8 11.78 807 4BV/H 93.7 75.3 11.94 784.5 6BV/H 80.35 63.7 11.4 702.1

(58) TABLE-US-00019 TABLE 19 Alcohol Elution Rate Examination of Total Organic Acids of Jinxuan Hemorrhoid Washing Powder Total organic Dry Elution amount of acids purity in paste Elution flow total organic acids Desorption the dry paste weight velocity (mg) rate (%) (%) (mg) 1BV/H 130.25 77.2 15.49 841.1 2BV/H 121.41 75 15.04 807 4BV/H 110.05 73.8 14.03 784.5 6BV/H 80.49 69 11.46 702.1

(59) Results show that at the flow velocity of 1 BV/H, the elution effect is relatively good, the purity and desorption rate are both relatively high. After comprehensive analysis, an elution flow velocity of 1 BV/H is selected.

(60) {circle around (6)} Alcohol Elution Amount Examination

(61) Dynamic adsorption is conducted according to the above conditions, with 70% alcohol as eluent, eluted at a velocity of 1 BV.Math.H.sup.1, the amount of total flavones, the out-let solution is collected at a certain volume and total saponins, total organic acids are measured, and elution curve is drawn. The results are shown in FIG. 3, FIG. 4 and FIG. 5.

(62) Results show that flavonoids compositions absorbed by 20 g resin can be completely eluted with 100 mL (about 5 times the amount of resin) 70% alcohol; saponins compositions absorbed by 20 g resin can be completely eluted with 90 mL (about 4.5 times the amount of resin) 70% alcohol; organic acids compositions absorbed by 20 g resin can be completely eluted with 100 mL (about 5 times the amount of resin) 70% alcohol. So using 100 mL (5 times the amount of resin) 70% alcohol at a flow velocity of 1 Bv/h can make flavonoids, saponins and organic acids compositions absorbed by 20 g resin completely eluted.

(63) The final preferred purification process condition parameters are: Resin Model: D101; sampling volume: the ratio between the medicinal powder amount and the resin amount is 0.75:1; sampling concentration: relatively more precipitate is produced and the loss is relatively large when sampling at a concentration of 0.5 g/ml, so the sampling concentration of 0.3 g/ml is finally selected. Adsorption rate: 2 BV/H; diameter-height ratio: 1:8; water washing amount: 3 BV; alcohol wash concentration: 70%; alcohol washing speed: 1 BV/H; alcohol washing amount: 5 BV.

Example 3

(64) Pilot Plant Enlargement Test

(65) 7.5 Kg medicinal powder obtained from supercritical CO.sub.2 extraction of the three flavors of Jinxuan Hemorrhoid Washing Powder botanicals (which is mixed at a ratio of 3:4:3, ground, and passed through a 40 mesh) is added with a 50% alcohol aqueous solution with a weight of 3 times that of the medicinal powder and soaked for 24 hours, and then a 50% alcohol aqueous solution is added to make the weight of the 50% alcohol aqueous solution equal to 12 times the weight of the medicinal powder, the percolation extraction is underwent with a flow velocity of the weight of 2 times that of the medicinal powder per hour, and the percolate is collected; the percolate is concentrated to a certain volume to make the weight of the drug solution equal to 3.3 times that of said medicinal powder (25 L), and suction filtrated to obtain a sampling drug solution.

(66) 10 Kg medical grade D101 macroporous resin is soaked with an appropriate amount of alcohol, wet packed and handled for future use.

(67) 3.2.1 Adjustment of Test Parameters

(68) During pilot plant enlargement, both the sampling amount and flow velocity are enlarged by 1000 times, thus test parameters need to be timely adjusted according to the test results. Different absorption and water washing rates are employed to examine its purification effect, and the results are shown in Table 20.

(69) TABLE-US-00020 TABLE 20 Flow Velocity Examination Table Transfer Transfer Transfer Extract rate Total rate of Total rate of Total Coagulant collection of total flavones total saponins total acids Velocity dose Extractive rate flavones purity saponins purity organic purity (BV/H) (Kg) (mg) (%) (%) (%) (%) (%) acids (%) (%) 4 7.5 262.5 3.5 59.2 30.5 60.6 12.2 57.7 14.8 2 7.5 315 4.2 67.5 33.1 71.6 15.7 69.1 18.6 1 7.5 375 5 78 34.8 79.3 13.1 73.4 19.7 0.5 7.5 412.5 5.5 80 36.7 81.4 17.4 78 21.3

(70) Results show that the content and transfer rate of total flavones, total saponins, and total organic acids are relatively high when the flow velocity is 1 time the column volume per hour. Therefore, the sampling and water washing flow velocity is determined to be 1 BV.Math.H.sup.1.

(71) 3.2.2 Experimental Method and Results

(72) An appropriate amount of the three flavors of botanicalshoneysuckle, schizonepeta, and purslane in the prescription of Jinxuan Hemorrhoid Washing Powder are mixed at a weight ratio of 3:4:3, ground, passed through a 40 mesh, and supercritically CO.sub.2 extracted to obtain the medicinal powder. 7.5 Kg medicinal powder is added with 50% alcohol and soaked for 24 hours, 50% alcohol with a weight of 12 times the weight of the medicinal powder is added, the percolation extraction is underwent at a flow velocity of 2 BV/H, the percolate is collected, alcohol is recovered by reduced pressure to a certain volume, and suction filtrated to obtain the sampling drug solution.

(73) 10 Kg medical grade D101 macroporous resin is soaked with an appropriate amount of alcohol, wet packed and washed with a large amount of alcohol, out-let solution is constantly detected until when mixed with water white precipitation is not exhibited. Then alcohol is washed with a large amount of distilled water for future use.

(74) The absorption is conducted at a sampling flow velocity of 1 Bv/h with resin bed diameter-height ratio of 1:8, washed with 3 BV distilled water after the completion of absorption at a flow velocity of 1 Bv/h till the molish reaction exhibiting negative, and then underwent elution with 70% alcohol with a volume of 5 times that of the resin column at a flow velocity of 1 Bv/h to obtain the eluent; the eluent is concentrated to a relative density of 1.03, and spray dried (at inlet temperature of 170 C., outlet temperature of 90 C., and atomizing disk rotation speed of 20,000 RIM). The dried extraction is collected, sealed, weighed, and preserved in shade place.

(75) Ultravioletvisible spectrophotometry is employed to measure the amount of total flavones in the extractive, Transfer rate (transfer rate=the amount of total flavones in the extractive/he amount of total flavones in the raw medical material100%) and cream collection rate (cream collection rate=total extractive weight/total raw medical material weight100%) are calculated. The results are shown in Table 21.

(76) TABLE-US-00021 TABLE 21 Pilot Plant Test Results Transfer Transfer Transfer Extract rate Total rate of Total rate of Total Coagulant collection of total flavones total saponins total acids Test dose Extractive rate flavones purity saponins purity organic purity batch (Kg) (mg) (%) (%) (%) (%) (%) acids (%) (%) 1 7.5 330 4.4 75.2 34.8 80.2 15.2 72.7 19.8 2 7.5 352.5 4.7 78.5 35.1 79.6 15.5 76.1 20.6 3 7.5 397.5 5.3 81.0 35.8 82.3 15.7 78.4 20.7 Average 7.5 360 4.8 78.2 35.2 80.7 15.5 75.7 20.4

(77) Results show that the total content of flavones, saponins, and organic acids in the extractives of the three batches can exceed 70%, which shows that the present experimental research has plausible process parameters and can be transited to industrialized production after further pilot plant adjustment of the process conditions.