Dissolution specifications based on release rates-Reference-Cited by-同舟云学术

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Dissolution specifications based on release rates

Published:1999-04 Issue:4 Volume:88 Page:434-444
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Elkoshi Zeev

Publisher

American Geophysical Union (AGU)

Subject

Pharmaceutical Science

Reference7 articles.

1. Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations,1991

2. The United States Pharmacopeia (USP 23),1995

3. Biopharmaceutical characterization of oral controlled/modified-release drug products. In vitro/in vivo correlation of roxatidine;Frick;Eur. J. Pharm. Biopharm.,1998

4. Pharmacokinetics;Gibaldi,1982

5. Sensitivity of indirect metrics for assessing “rate” in bioequivalence studies-moving the “goalposts” or changing the “game”;Rostami-Hodjegan;J. Pharm. Sci.,1994

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. In Vitro/In Vivo Correlations;Developing Solid Oral Dosage Forms;2017

2. In Vitro- In Vivo Correlation’s Dissolution Limits Setting;Pharmaceutical Research;2014-03-28

3. Dissolution Testing of Solid Products;Developing Solid Oral Dosage Forms;2009

4. In Vitro–In Vivo Correlations;Developing Solid Oral Dosage Forms;2009

5. A new principal component analysis-based approach for testing “similarity” of drug dissolution profiles;European Journal of Pharmaceutical Sciences;2008-05

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