Crystal forms of demethyleneberberine hydrochloride and preparation method therefor

Abstract

Provided are four crystal forms, A, B, C and D, of demethyleneberberine hydrochloride, and a preparation method therefor, and further provided are X-ray powder diffraction characteristic absorption peaks, infrared absorption peaks and DSC spectra of the four crystal forms. The X-ray powder diffraction characteristic diffraction peaks of the crystal forms are at about 8.205°, 8.805°, 10.817°, 14.835°, 15.479°, 16.668°, 17.492°, 18.529°, 20.656°, 21.536°, 23.538°, 25.657°, 26.192°, and 28.808°. A preparation method for the four crystal forms of the demethyleneberberine hydrochloride is also involved. The preparation method has a simple process, a high yield and a low cost; and has a high product purity and a stable quality.

Claims

1. A crystal form of demethyleneberberine hydrochloride selected from: A) a crystal form designated as crystal form A, characterized in that, it has characteristic diffraction peaks at 6.838, 8.300, 12.477, 13.667, 16.269, 16.642, 17.761, 18.247, 18.749, 20.389, 20.739, 21.926, 22.530, 23.983, 24.819, 25.774, 26.413, 26.592, 28.552, 30.333, and 38.312° in an X-ray powder diffraction spectrum represented by Cu-Kα radiation and 20±0.2° diffraction angle; one thermal absorption peak at 240±3° C. in a DSC thermogram; and characteristic infrared absorption peaks at 422.8 cm.sup.−1, 454.3 cm.sup.−1, 466.6 cm.sup.−1, 505.6 cm.sup.−1, 581.8 cm.sup.−1, 617.7 cm.sup.−1, 658.5 cm.sup.−1, 739.3 cm.sup.−1, 774.6 cm.sup.−1, 820.3 cm.sup.−1, 871.8 cm.sup.−1, 892.6 cm.sup.−1, 917.5 cm.sup.−1, 962.6 cm.sup.−1, 983.2 cm.sup.−1, 999.7 cm.sup.−1, 1,050.0 cm.sup.−1, 1,067.8 cm.sup.−1, 1,110.5 cm.sup.−1, 1,140.5 cm.sup.−1, 1,203.4 cm.sup.−1, 1,244.5 cm.sup.−1, 1,268.1 cm.sup.−1, 1,293.8 cm.sup.−1, 1,337.1 cm.sup.−1, 1,363.8 cm.sup.−1, 1,390.5 cm.sup.−1, 1,455.5 cm.sup.−1, 1,493.9 cm.sup.−1, 1,515.6 cm.sup.−1, 1,530.5 cm.sup.−1, 1,567.1 cm.sup.−1, 1,605.6 cm.sup.−1, 1,638.0 cm.sup.−1, 1,769.6 cm.sup.−1, 2,726.3 cm.sup.−1, 2,847.6 cm.sup.−1, 2,945.2 cm.sup.−1, 3,024.2 cm.sup.−1, 3,065.1 cm.sup.−1, 3,086.0 cm.sup.−1, and 3,150.6 cm.sup.−1; B) a crystal form designated as crystal form B, characterized in that, it has characteristic diffraction peaks at 6.838, 8.300, 12.477, 13.667, 16.269, 16.642, 17.761, 18.247, 18.749, 20.389, 20.739, 21.926, 22.530, 23.983, 24.819, 25.774, 26.413, 26.592, 28.552, 30.333, and 38.312° in an X-ray powder diffraction spectrum represented by Cu-Kα radiation and 20±0.2° diffraction angle; two thermal absorption peaks at 147±3° C. and 220±3° C. respectively in a DSC thermogram; and characteristic infrared absorption peaks at 421.5 cm.sup.−1, 448.0 cm.sup.−1, 464.4 cm.sup.−1, 506.1 cm.sup.−1, 523.9 cm.sup.−1, 543.5 cm.sup.−1, 568.8 cm.sup.−1, 583.9 cm.sup.−1, 618.9 cm.sup.−1, 649.1 cm.sup.−1, 676.8 cm.sup.−1, 718.3 cm.sup.−1, 742.1 cm.sup.−1, 777.5 cm.sup.−1, 833.0 cm.sup.−1, 859.8 cm.sup.−1, 878.7 cm.sup.−1, 924.5 cm.sup.−1, 960.4 cm.sup.−1, 977.7 cm.sup.−1, 1,018.9 cm.sup.−1, 1,060.0 cm.sup.−1, 1,107.7 cm.sup.−1, 1,138.4 cm.sup.−1, 1,170.1 cm.sup.−1, 1,207.4 cm.sup.−1, 1,243.9 cm.sup.−1, 1,268.6 cm.sup.−1, 1,366.8 cm.sup.−1, 1,388.7 cm.sup.−1, 1,422.7 cm.sup.−1, 1,445.5 cm.sup.−1, 1,457.3 cm.sup.−1, 1,492.8 cm.sup.−1, 1,517.8 cm.sup.−1, 1,533.9 cm.sup.−1, 1,568.8 cm.sup.−1, 1,610.9 cm.sup.−1, 1,636.9 cm.sup.−1, 1,735.5 cm.sup.−1, 2,646.6 cm.sup.−1, 2,849.8 cm.sup.−1, 2,952.5 cm.sup.−1, 2,993.5 cm.sup.−1, 3,089.6 cm.sup.−1, and 3,364.3 cm.sup.−1; C) a crystal form designated as crystal form C, characterized in that, it has characteristic diffraction peaks at 3.260, 8.515, 9.715, 12.147, 13.219, 14.789, 17.607, 18.306, 20.728, 21.261, 24.633, 25.430, 25.837, 26.416, 27.606, 28.147, and 37.695° in an X-ray powder diffraction spectrum represented by Cu-Kα radiation and 20±0.2° diffraction angle; one thermal absorption peak at 253±3° C. in a DSC thermogram; and characteristic infrared absorption peaks at 422.8 cm.sup.−1, 441.6 cm.sup.−1, 452.2 cm.sup.−1, 505.0 cm.sup.−1, 526.2 cm.sup.−1, 584.6 cm.sup.−1, 637.3 cm.sup.−1, 652.0 cm.sup.−1, 665.7 cm.sup.−1, 699.9 cm.sup.−1, 723.4 cm.sup.−1, 742.0 cm.sup.−1, 774.1 cm.sup.−1, 814.2 cm.sup.−1, 828.2 cm.sup.−1, 869.6 cm.sup.−1, 891.7 cm.sup.−1, 915.6 cm.sup.−1, 964.5 cm.sup.−1, 980.6 cm.sup.−1, 998.8 cm.sup.−1, 1,065.8 cm.sup.−1, 1,108.5 cm.sup.−1, 1,139.7 cm.sup.−1, 1,192.2 cm.sup.−1, 1,216.5 cm.sup.−1, 1,241.0 cm.sup.−1, 1,273.9 cm.sup.−1, 1,287.4 cm.sup.−1, 1,308.2 cm.sup.−1, 1,343.5 cm.sup.−1, 1,356.5 cm.sup.−1, 1,389.3 cm.sup.−1, 1,420.2 cm.sup.−1, 1,437.9 cm.sup.−1, 1,456.1 cm.sup.−1, 1,510.2 cm.sup.−1, 1,565.5 cm.sup.−1, 1,580.9 cm.sup.−1, 1,604.3 cm.sup.−1, 1,618.6 cm.sup.−1, 1,633.2 cm.sup.−1, 2,697.9 cm.sup.−1, 2,842.7 cm.sup.−1, 2,946.1 cm.sup.−1, 3,005.3 cm.sup.−1, and 3,066.4 cm.sup.−1; and D) a crystal form designated as crystal form D, characterized in that, it has characteristic diffraction peaks at about 6.034, 8.699, 12.589, 18.108, 21.854, 24.224, 25.146 and 26.172° in an X-ray powder diffraction spectrum represented by Cu-Kα radiation and 2θ diffraction angle; two thermal absorption peaks at 131±3° C. and 190±3° C. respectively in a DSC thermogram; and characteristic infrared absorption peaks at 422.8 cm.sup.−1, 454.3 cm.sup.−1, 466.6 cm.sup.−1, 505.6 cm.sup.−1, 581.8 cm.sup.−1, 617.7 cm.sup.−1, 658.5 cm.sup.−1, 739.3 cm.sup.−1, 774.6 cm.sup.−1, 820.3 cm.sup.−1, 871.8 cm.sup.−1, 892.6 cm.sup.−1, 917.5 cm.sup.−1, 962.6 cm.sup.−1, 983.2 cm.sup.−1, 999.7 cm.sup.−1, 1,050.0 cm.sup.−1, 1,067.8 cm.sup.−1, 1,110.5 cm.sup.−1, 1,140.5 cm.sup.−1, 1,203.4 cm.sup.−1, 1,244.5 cm.sup.−1, 1,268.1 cm.sup.−1, 1,293.8 cm.sup.−1, 1,337.1 cm.sup.−1, 1,363.8 cm.sup.−1, 1,390.5 cm.sup.−1, 1,455.5 cm.sup.−1, 1,493.9 cm.sup.−1, 1,515.6 cm.sup.−1, 1,530.5 cm.sup.−1, 1,567.2 cm.sup.−1, 1,605.6 cm.sup.−1, 1,638.0 cm.sup.−1, 1,769.6 cm.sup.−1, 2,726.3 cm.sup.−1, 2,847.6 cm.sup.−1, 2,945.2 cm.sup.−1, 3,024.2 cm.sup.−1, 3,065.1 cm.sup.−1, 3,086.0 cm.sup.−1, and 3,150.6 cm.sup.−1.

2. A method for preparing the crystal foil is of demethyleneberberine hydrochloride according to claim 1, comprising the following steps: (1) adding 4 g of phloroglucinol into 100 ml of 40%-60% sulfuric acid, and stirring, so that the phloroglucinol is dissolved; (2) adding 5 g of berberine hydrochloride into the solution obtained in the step (1), and stirring for 2 h at 80° C.-100° C.; (3) adding the solution obtained in the step (2) into 100 ml of saturated salt solution, and stirring for 2 h; (4) filtering the mixed solution obtained in the step (3) by suction-filtration, dissolving filter cake with 100 ml of methanol in water bath at 70° C., and recrystallizing; (5) filtering the solution obtained in the step (4) by suction-filtration, dissolving filter cake with 100 ml of methanol in water bath at 70° C., recrystallizing, and performing suction-filtration; (6) drying a yellow solid obtained in the step (5) by vacuum drying for 24 h at room temperature, so that a crystal form B of demethyleneberberine hydrochloride is obtained; (7) filtering the solution obtained in the step (4) by suction-filtration, dissolving filter cake with 100 ml of ethanol in water bath at 80° C., recrystallizing, and performing suction-filtration; (8) drying a yellow solid obtained in the step (7) by vacuum drying for 24 h at room temperature, so that a crystal form C of demethyleneberberine hydrochloride is obtained; (9) filtering the solution obtained in the step (4) by suction-filtration, dissolving 1 g of filter cake with 12 ml of ethanol in water bath at 80° C. while stirring, performing suction-filtration and collecting filter cake; (10) drying a yellow solid obtained in the step (9) by vacuum drying for 24 h at room temperature, so that a crystal form A of demethyleneberberine hydrochloride is obtained; (11) filtering the solution obtained in the step (4) by suction-filtration, dissolving 1 g of filter cake with 30 ml of deionized water in water bath at 74° C. while stirring, recrystallizing, and performing suction-filtration; and (12) drying a yellow solid obtained in the step (11) by vacuum freeze-drying for 48 h, so that a crystal form D of demethyleneberberine hydrochloride is obtained.

3. The method for preparing the crystal forms of demethyleneberberine hydrochloride according to claim 2, wherein the step (5) further comprises: adding a small amount of seed crystals, adding 10-20 vol. % of diethyl ether, adding 10-20 vol. % of xylene, and adding 10-20 vol. % of toluene.

4. The method for preparing the crystal form of demethyleneberberine hydrochloride according to claim 2, wherein the step (7) further comprises: adding a small amount of seed crystals, adding 10-20 vol. % of diethyl ether, adding 10-20 vol. % of xylene, and adding 10-20 vol. % of toluene.

5. A pharmaceutical composition comprising crystal form A, B, C and/or D of demethyleneberberine hydrochloride according claim 1.

6. The pharmaceutical composition, according to claim 5, formulated as a tablet, capsule, pill or as a sustained-release agent, or for injection, or as a microparticle administration system.

7. A method for treating liver fibrosis, acute and/or chronic alcoholic liver disease, ulcerative colitis, an immune liver injury and/or a nonalcoholic fatty liver disease, wherein said method comprises administering, to a subject in need of such treatment, a crystal form of demethyleneberberine hydrochloride according to claim 1.

8. A method for providing a hypoglycemic effect and/or for treating diabetes, wherein said method comprises administering, to a subject in need of such treatment, a crystal faun of demethyleneberberine hydrochloride according to claim 1.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 shows an X-ray powder diffraction pattern of the crystal form A of demethyleneberberine hydrochloride according to the present invention;

(2) FIG. 2 shows a differential scanning calorimetry (DSC) thermogram of the compound in FIG. 1;

(3) FIG. 3 shows an infrared spectrum of the compound in FIG. 1;

(4) FIG. 4 shows an X-ray powder diffraction pattern of the crystal form B of demethyleneberberine hydrochloride according to the present invention;

(5) FIG. 5 shows a differential scanning calorimetry (DSC) thermogram of the compound in FIG. 4;

(6) FIG. 6 shows an infrared spectrum of the compound in FIG. 4;

(7) FIG. 7 shows an X-ray powder diffraction pattern of the crystal form C of demethyleneberberine hydrochloride according to the present invention;

(8) FIG. 8 shows a differential scanning calorimetry (DSC) thermogram of the compound in FIG. 7;

(9) FIG. 9 shows an infrared spectrum of the compound in FIG. 7;

(10) FIG. 10 shows an X-ray powder diffraction pattern of the crystal form D of demethyleneberberine hydrochloride according to the present invention;

(11) FIG. 11 shows a differential scanning calorimetry (DSC) thermogram of the compound in FIG. 10;

(12) FIG. 12 shows an infrared spectrum of the compound in FIG. 10;

(13) FIG. 13 shows solubility curves of the compounds in FIGS. 1, 4, 7 and 10 in water system;

(14) FIG. 14 shows solubility curves of the compounds in FIGS. 1, 4, 7 and 10 in methanol system;

(15) FIG. 15 shows solubility curves of the compounds in FIGS. 1, 4, 7 and 10 in ethanol system;

(16) FIG. 16 shows blood concentration and time curves of the compounds in FIGS. 1, 4,7 and 10.

EMBODIMENTS

(17) The following examples can help those skilled in the art to understand the present invention more comprehensively, without constituting any limitation to the present invention in any way.

(18) X-ray powder diffraction, differential scanning calorimetry and infrared spectrum are used for structural characterization of the crystal forms of demethyleneberberine hydrochloride in the present invention.

Example 1. Synthesis of Crystal Form a of Demethyleneberberine Hydrochloride

(19) 5 g of phloroglucinol is added into 100 ml of 60% H.sub.2SO.sub.4 system at 90° C. and stirred to dissolve fully; 6 g of berberine hydrochloride is added; under the catalysis of phloroglucinol, the reaction is held for 2 h, so that methylene is removed and demethyleneberberine hydrochloride is obtained. After the reaction is completed, the reaction solution is poured into 100 ml of saturated salt solution and the mixture is stirred for 2 h. The solution is suction-filtered and a filter cake is obtained; 100 ml of methanol is added into the filter cake, and the filter cake is dissolved fully in water bath at 70° C., the solution is placed in a beaker for recrystallization, or a small amount of xylene or toluene or diethyl ether is added for recrystallization utilizing the mixed solvent. The crystallization solution obtained in the previous step is suction-filtered, and the filter cake is collected and weighed. 1 g of filter cake is taken and added into 12 ml of ethanol, the mixture is placed in water bath at 80° C. and stirred for 20 min., and then is suction-filtered; the filter cake is collected and dried, so that a crystal form A of demethyleneberberine hydrochloride is obtained; then the product is weighed and tested. An X-ray powder diffraction diagram of the obtained solid is shown in FIG. 1, a DSC thermogram is shown in FIG. 2, and an infrared spectrum is shown in FIG. 3.

Example 2. Synthesis of Crystal Form B od Demethyleneberberine Hydrochloride

(20) 5 g of phloroglucinol is added into 100 ml of 60% H.sub.2SO.sub.4 system at 90° C. and stirred to dissolve fully; 6 g of berberine hydrochloride is added; under the catalysis of phloroglucinol, the reaction is held for 2 h, so that methylene is removed and demethyleneberberine hydrochloride is obtained. After the reaction is completed, the reaction solution is poured into 100 ml of saturated salt solution and the mixture is stirred for 2 h for exchange. The solution is suction-filtered and a filter cake is obtained; 100 ml of methanol is added, the filter cake is dissolved fully in water bath at 70° C., the solution is placed in a beaker for recrystallization, or a small amount of xylene or toluene or diethyl ether is added for recrystallization utilizing the mixed solvent. The crystallization solution obtained in the previous step is suction-filtered, and the filter cake is collected and weighed. 70 ml of methanol is added, and the filter cake is dissolved fully in water bath at 70° C.; the solution is placed in a beaker, and recrystallization is carried out at room temperature, utilizing a single-component solvent; or a small amount of xylene or toluene or diethyl ether is added, and recrystallization is carried out, utilizing a mixed solvent, so that a crystal form B of demethyleneberberine hydrochloride is obtained. The product is suction-filtered, dried, weighed and tested. An X-ray powder diffraction pattern of the obtained solid is shown in FIG. 4, a DSC thermogram is shown in FIG. 5, and an infrared spectrum is shown in FIG. 6.

Example 3. Synthesis of Crystal Form C of Demethyleneberberine Hydrochloride

(21) 5 g of phloroglucinol is added into 100 ml of 60% H.sub.2SO.sub.4 system at 90° C. and stirred to dissolve fully; 6 g of berberine hydrochloride is added; under the catalysis of phloroglucinol, the reaction is held for 2 h, so that methylene is removed and demethyleneberberine hydrochloride is obtained. After the reaction is completed, the reaction solution is poured into 100 ml of saturated salt solution and the mixture is stirred for 2 h. The solution is suction-filtered and a filter cake is obtained; 100 ml of methanol is added to the filter cake, and the filter cake is dissolved fully in water bath at 70° C., the solution is placed in a beaker for recrystallization, or a small amount of xylene or toluene or diethyl ether is added for recrystallization utilizing the mixed solvent. The crystallization solution obtained in the previous step is suction-filtered, and the filter cake is collected and weighed. 120 ml of ethanol is added, and the filter cake is dissolved fully in water bath at 80° C.; the solution is placed in a beaker, and recrystallization is carried out overnight at 4° C.; then the product is suction-filtered and dried, so that a crystal form C of demethyleneberberine hydrochloride is obtained; then the obtained product is weighed and tested. An X-ray powder diffraction pattern of the obtained solid is shown in FIG. 7, a DSC thermogram is shown in FIG. 8, and an infrared spectrum is shown in FIG. 9.

Example 4. Synthesis of Crystal Form D of Demethyleneberberine Hydrochloride

(22) 5 g of phloroglucinol is added into 100 ml of 60% H.sub.2SO.sub.4 system at 90° C. and stirred to dissolve fully; 6 g of berberine hydrochloride is added; under the catalysis of phloroglucinol, the reaction is held for 2 h, so that methylene is removed and demethyleneberberine hydrochloride is obtained. After the reaction is completed, the reactant solution is poured into 100 ml of saturated salt solution and the mixture is stirred for 2 h. The solution is suction-filtered, and the filter cake is collected; 100 ml of methanol is added, and the filter cake is dissolved fully in water bath at 70° C.; then the solution is placed in a beaker and recrystallization is carried out. The crystallization solution obtained in the previous step is suction-filtered, the filter cake is collected and weighed; thus, a crude product of demethyleneberberine hydrochloride is obtained. 1 g of crude product is taken, 30 ml of deionized water is added to the crude product, and the crude product is dissolved fully in water bath at 74° C.; the solution is placed in a beaker, and recrystallization is carried out at room temperature; then the solution is suction-filtered, and the obtained product is vacuum freeze-dried; thus, a crystal form D of demethyleneberberine hydrochloride is obtained; then the obtained product is weighed and tested. An X-ray powder diffraction pattern of the obtained solid is shown in FIG. 10, a DSC thermogram is shown in FIG. 11, and an infrared spectrum is shown in FIG. 12.

Example 5. Study on Stability of Demethyleneberberine Hydrochloride Crystals in High-Temperature Experiment

(23) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and placed in plates numbered as A1, B1, C1 and D1 respectively, and then the plates are placed in a high-temperature environment at 60±2° C. respectively for stability test. The experimental results are shown as follows. The demethyleneberberine hydrochloride crystals A, B and C are relatively stable in the high-temperature environment, while the demethyleneberberine hydrochloride crystal D is unstable in the long-term high-temperature environment, and undergoes crystal transformation.

(24) TABLE-US-00001 Sample Test Time Content Content of Relevant X-Ray Powder No. (day) (%) Substance (%) Diffraction A1 0 99.62 0.38 Unchanged 5 99.63 0.37 Unchanged 10 99.61 0.39 Unchanged B1 0 99.82 0.18 Unchanged 5 99.62 0.38 Unchanged 10 99.67 0.33 Unchanged C1 0 99.18 0.82 Unchanged 5 99.21 0.79 Unchanged 10 99.19 0.81 Unchanged D1 0 99.78 0.22 Unchanged 5 99.83 0.17 Unchanged 10 99.71 0.29 Changed

Example 6. Study on Stability of Demethyleneberberine Hydrochloride Crystals in High-Humidity Experiment

(25) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and placed in plates numbered as A2, B2, C2 and D2 respectively, and then the plates are placed in a high-humidity environment at RH90±5% respectively for stability test. The experimental results are shown in the following table. The demethyleneberberine hydrochloride crystals A, B, C and D are relatively stable in the high-humidity environment.

(26) TABLE-US-00002 Sample Test Time Content Content of Relevant X-Ray Powder No. (day) (%) Substance (%) Diffraction A2 0 99.62 0.38 Unchanged 5 99.58 0.42 Unchanged 10 99.60 0.40 Unchanged B2 0 99.58 0.42 Unchanged 5 99.60 0.40 Unchanged 10 99.56 0.44 Unchanged C2 0 99.77 0.23 Unchanged 5 99.72 0.28 Unchanged 10 99.57 0.43 Unchanged D2 0 99.48 0.52 Unchanged 5 99.41 0.59 Unchanged 10 99.32 0.68 Unchanged

Example 7. Study on Stability of Demethyleneberberine Hydrochloride Crystals in Strong Light Irradiation Experiment

(27) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and placed in plates numbered as A3, B3, C3 and D3 respectively, and then the plates are placed in a strong light irradiation environment at 4,500 lx±500 lx respectively for stability test. The experimental results are shown in the following table. The demethyleneberberine hydrochloride crystals A, B and C are relatively stable in the strong light irradiation environment, while the demethyleneberberine hydrochloride crystal D is unstable in the long-term strong light irradiation environment, and undergoes crystal transformation.

(28) TABLE-US-00003 Sample Test Time Content Content of Relevant X-Ray Powder No. (day) (%) Substance (%) Diffraction A3 0 99.62 0.38 Unchanged 5 99.61 0.39 Unchanged 10 99.60 0.40 Unchanged B3 0 99.58 0.42 Unchanged 5 99.77 0.23 Unchanged 10 99.67 0.33 Unchanged C3 0 99.57 0.43 Unchanged 5 99.49 0.51 Unchanged 10 99.55 0.45 Unchanged D3 0 99.78 0.22 Unchanged 5 99.58 0.42 Unchanged 10 99.64 0.36 Changed

Example 8. Study on Solubility of Demethyleneberberine Hydrochloride Crystals A, B, C and D in Water System

(29) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and the solubility of demethyleneberberine hydrochloride crystals A, B, C and D at different temperatures in a water system is studied respectively. 20 μl of sample is taken at each temperature node and detected by HPLC. The experimental results are shown in FIG. 13. Solubility of crystal form C of demethyleneberberine hydrochloride>solubility of crystal form B of demethyleneberberine hydrochloride>solubility of crystal form A of demethyleneberberine hydrochloride>solubility of crystal form D of demethyleneberberine hydrochloride.

Example 9. Study on Solubility of Demethyleneberberine Hydrochloride Crystals A, B, C and D in Methanol System

(30) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and the solubility of demethyleneberberine hydrochloride crystals A, B, C and D at different temperatures in a methanol system is studied respectively. 20 μl of sample is taken at each temperature node and detected by HPLC. The experimental results are shown in FIG. 14. Solubility of crystal form C of demethyleneberberine hydrochloride>solubility of crystal form B of demethyleneberberine hydrochloride>solubility of crystal form A of demethyleneberberine hydrochloride>solubility of crystal form D of demethyleneberberine hydrochloride.

Example 10. Study on Solubility of Demethyleneberberine Hydrochloride Crystals A, B, C and D in Ethanol System

(31) Demethyleneberberine hydrochloride crystals A, B, C and D are taken in an appropriate amount and the solubility of demethyleneberberine hydrochloride crystals A, B, C and D at different temperatures in an ethanol system is studied respectively. 20 μl of sample is taken at each temperature node and detected by HPLC. The experimental results are shown in FIG. 15. Solubility of crystal form C of demethyleneberberine hydrochloride>solubility of crystal form B of demethyleneberberine hydrochloride>solubility of crystal form A of demethyleneberberine hydrochloride>solubility of crystal form D of demethyleneberberine hydrochloride.

Example 11. Determination of Blood Concentration of Demethyleneberberine

(32) Hydrochloride Crystals A, B, C and D

(33) Male SD rats are adaptively bred for 3 days, and rats having (220±20) g body weight are selected and divided into 5 groups, namely, blank group, demethyleneberberine hydrochloride crystal form A group, demethyleneberberine hydrochloride crystal form B group, demethyleneberberine hydrochloride crystal form C group and demethyleneberberine hydrochloride crystal form D group. Food supply is stopped for 12 h for gastric emptying before the experiment. For the rats in the experimental groups, ig (intragastric) administration dosage is 200 mg/kg. 0.2 ml of blood is taken from the orbits of the rats at 5 min., 15 min., 30 min., 1 h, 2 h, 6 h and 12 h respectively after ig administration, the whole blood is centrifuged, and 100 μl of plasma is taken and frozen at −20° C. for use later. 100 μl of plasma sample is taken, 200 μl of methanol is added into the plasma sample, the mixture is vortexed for 5 min., and then centrifuged at 10,000 r/min. for 15 min. in a centrifuge; the supernatant is taken and tested by HPLC. The experimental results are shown in FIG. 16. For crystal form A of demethyleneberberine hydrochloride, C.sub.max=0.292 μg×ml.sup.−1, t.sub.max=2 h; for crystal form B of demethyleneberberine hydrochloride, C.sub.max=0.642 μg×ml.sup.−1, t.sub.max=1 h; for crystal form C of demethyleneberberine hydrochloride, C.sub.max=1.262 μg×ml.sup.−1, t.sub.max=0.5 h; for crystal form D of demethyleneberberine hydrochloride, C.sub.max=1.234 μg×ml.sup.−1, t.sub.max=2 h. Through calculation on the basis of the experimental results, it is determined: D.sub.AUC=3.675 μg×ml.sup.−1×h>A.sub.AUC=1.247 μg×ml.sup.−1×h>B.sub.AUC=1.150 μg×ml.sup.−1×h>C.sub.AUC=1.077 μg×ml.sup.−1×h.