The effect of amorphous and crystal sodium warfarin and its content uniformity on bioequivalence of tablets-Reference-Cited by-同舟云学术

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The effect of amorphous and crystal sodium warfarin and its content uniformity on bioequivalence of tablets

Published:2018-12 Issue: Volume:125 Page:120-129
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Franc Aleš,Muselík Jan,Zeman Jiří,Lukášová Ivana,Kurhajec Slavomír,Bartoníčková Eva,Galvánková Lucie,Mika Filip,Dominik Martin,Vetchý David

Funder

IGA

University of Veterinary and Pharmaceutical Sciences Brno

Ministry of Education, Youth and Sports

Czech Academy of Sciences

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference42 articles.

1. Pharmaceutical quality of warfarin sodium tablets. A multinational postmarket comparative study;Ali;Pharm. Ind.,1999

2. An evaluation of fit factors and dissolution efficiency for the comparison of in vitro dissolution profiles;Anderson;J. Pharm. Biomed. Anal.,1998

3. Raman spectroscopy as a complementary tool to assess the content uniformity of dosage units in break-scored warfarin tablets;Arruabarrena;Int. J. Pharm.,2014

4. Effect of superdisintegrants on dissolution of cationic drugs;Balasubramaniam;Dissol. Technol.,2008

5. Modeling and comparison of dissolution profiles;Costa;Eur. J. Pharm. Sci.,2001

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1. Quality by Design Considerations for Drop-on-Demand Point-of-Care Pharmaceutical Manufacturing of Precision Medicine;Molecular Pharmaceutics;2024-04-25

2. A Comparison of Methods for Computing Relative Anhydrous–Hydrate Stability with Molecular Simulation;Crystal Growth & Design;2022-11-29

3. Warfarin Sodium Stability in Oral Formulations;Molecules;2021-11-01

4. Structural Changes of Sodium Warfarin in Tablets Affecting the Dissolution Profiles and Potential Safety of Generic Substitution;Pharmaceutics;2021-08-30

5. Molecular Insights into Warfarin Sodium 2-Propanol Solvate Solid Form Changes and Disproportionation Using a Low Volume Two-Stage Dissolution Approach;Molecular Pharmaceutics;2021-03-09

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