Dissolution testing - Revision history

Shawndouglas: Turned into a transclusion

2022-09-19T21:25:28Z

Turned into a transclusion

← Older revision		Revision as of 21:25, 19 September 2022
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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]]		[[Category:Testing terminology]]

Shawndouglas: Changed cat

2014-08-06T19:31:14Z

Changed cat

← Older revision		Revision as of 19:31, 6 August 2014
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	[[Category:~~Scientific techniques~~]]		[[Category:Testing terminology]]

Shawndouglas: Added cat

2014-08-06T17:39:33Z

Added cat

← Older revision		Revision as of 17:39, 6 August 2014
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	==References==		==References==
	{{reflist}}		{{reflist}}

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			[[Category:Scientific techniques]]

Shawndouglas: Internal link.

2013-09-13T22:14:06Z

Internal link.

← Older revision		Revision as of 22:14, 13 September 2013
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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>		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>

	==References==		==References==
	{{reflist}}		{{reflist}}

Shawndouglas: Recreated article due to necessary redirect.

2011-10-26T22:50:36Z

Recreated article due to necessary redirect.

New page

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>

==References==
{{reflist}}