Difference between revisions of "Dissolution testing"

Latest revision as of 21:25, 19 September 2022

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This article is a direct transclusion of the Wikipedia article and therefore may not meet the same editing standards as LIMSwiki.

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-In the pharmaceutical industry, drug '''dissolution testing''' is routinely used to provide critical in vitro drug release [[information]] for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict [[in vivo]] drug release profiles.<ref name="Bai1">{{cite journal|author=Ge Bai, Yimin Wang and Piero M. Armenante |title=Velocity profiles and shear strain rate variability in the USP Dissolution Testing Apparatus 2 at Different Impeller Agitation Speeds |journal=International Journal of Pharmaceutics |volume=403 |issue=1–2 |pages=1–14 |year=17 January 2011 |doi=10.1016/j.ijpharm.2010.09.022}}</ref>
+{{wikipedia::Dissolution testing}}
+==Notes==
-==References==
+This article is a direct transclusion of [https://en.wikipedia.org/wiki/Dissolution_testing the Wikipedia article] and therefore may not meet the same editing standards as LIMSwiki.
-{{reflist}}
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+[[Category:Articles transcluded from other wikis]]
 [[Category:Testing terminology]]