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Showing 1 to 2 of 2 for “"Modified dissolution testing apparatus 2"”.
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Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2
Dissolution tests are routinely carried out in the pharmaceutical industry to determine the dissolution rate of solid dosage forms. Dissolution testing serves as a surrogate for drug bioavailability through in vitro-in vivo correlation (IVIVR), and it additionally helps in guiding the development …
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Dissolution of different commercial aspirin tablets using a novel off-center paddle impeller (OPI) dissolution testing system
Dissolution testing is routinely conducted in the pharmaceutical industry to provide in vitro drug release information for quality control purposes. The most common dissolution testing system for solid dosage forms is the United States Pharmacopeia (USP) Dissolution Testing Apparatus 2. In this …