Correlation of dissolution and disintegration results for an immediate-release tablet

Author:

Nickerson Beverly,Kong Angela,Gerst Paul,Kao Shangming

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference15 articles.

1. ICH Harmonised Tripartite Guideline, Specifications: Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products: Chemical Substances: Q6A. October 1999. http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html.

2. Dissolution Testing and Specification Criteria for Immediate-Release Solid Oral Dosage Forms Containing Biopharmaceutics Classification System Class 1 and 3 Drugs;FDA Draft Guidance for Industryy,2015

3. Correlation between tablet disintegration and in vitro dissolution;Carstensen;Drug Dev. Ind. Pharm.,1980

4. The effect of low- and high-humidity aging on the hardness, disintegration time and dissolution rate of tribasic calcium phosphate-based tablets;Chowhan;Drug Dev. Ind. Pharm.,1979

5. Disintegration of highly soluble immediate release tablets: a surrogate for dissolution;Gupta;AAPS PharmSciTech,2009

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