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Research Article

Simulation of Physiological pH - Time Profile in In Vitro Dissolution Study: Relationship Between Dissolution Rate and Bioavailability of Controlled Release Dosage Form

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Pages 537-544 | Published online: 20 Oct 2008
 

Abstract

An in vitro batch dissolution method, simulating the in vivo pH-time profile was developed, using the USP XX dissolution apparatus. Significant correlation between in vitro dissolution data and bioavailability of the drug from the controlled release dosage form was obtained.

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