Berberine hydrochloride co-amorphous drug and preparation method thereof
The invention discloses a berberine hydrochloride co-amorphous drug and a preparation method thereof, and the preparation method comprises the following steps: blending berberine hydrochloride and chlorogenic acid, adding into a solvent, grinding, then washing and dissolving by using the solvent, and separating out a solid by using a vacuum rotary evaporation method to obtain the berberine hydrochloride co-amorphous drug. According to the prepared berberine hydrochloride co-amorphous medicine, the solubility of berberine hydrochloride in a 0.1 mol/L HCl buffer solution and water is improved in a co-amorphous mode, and reference is provided for development of oral preparations and external preparations for treating stomach diseases through berberine hydrochloride; the dissolution rate and bioavailability of berberine hydrochloride are improved, and reference is provided for development of a berberine hydrochloride quick-release preparation; in addition, the preparation method disclosed by the invention is simple and easy to implement, mild in condition, easy to control, good in reproducibility, easy to realize large-scale industrial production and low in production cost, and has great commercial application value..
Medienart: |
Patent |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Europäisches Patentamt - (2024) vom: 12. Jan. Zur Gesamtaufnahme - year:2024 |
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Sprache: |
Englisch |
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Beteiligte Personen: |
SHEN XIANGCHUN [VerfasserIn] |
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Links: |
Volltext [kostenfrei] |
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Themen: |
Sonstige Themen: |
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Anmerkungen: |
Source: www.epo.org (no modifications made), First posted: 2024-01-12, Last update posted on www.tib.eu: 2024-03-25, Last updated: 2024-03-29 |
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Patentnummer: |
CN117379558 |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
EPA001289527 |
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520 | |a The invention discloses a berberine hydrochloride co-amorphous drug and a preparation method thereof, and the preparation method comprises the following steps: blending berberine hydrochloride and chlorogenic acid, adding into a solvent, grinding, then washing and dissolving by using the solvent, and separating out a solid by using a vacuum rotary evaporation method to obtain the berberine hydrochloride co-amorphous drug. According to the prepared berberine hydrochloride co-amorphous medicine, the solubility of berberine hydrochloride in a 0.1 mol/L HCl buffer solution and water is improved in a co-amorphous mode, and reference is provided for development of oral preparations and external preparations for treating stomach diseases through berberine hydrochloride; the dissolution rate and bioavailability of berberine hydrochloride are improved, and reference is provided for development of a berberine hydrochloride quick-release preparation; in addition, the preparation method disclosed by the invention is simple and easy to implement, mild in condition, easy to control, good in reproducibility, easy to realize large-scale industrial production and low in production cost, and has great commercial application value. | ||
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