Esnaashari, S., Javadzadeh, Y., Batchelor, Hannah and Conway, Barbara R (2005) The use of microviscometry to study polymer dissolution from solid dispersion drug delivery systems. International Journal of Pharmaceutics, 292 (1-2). pp. 227-230. ISSN 0378-5173Metadata only available from this repository.
Solid dispersions can be used to improve dissolution of poorly soluble drugs and PVP is a common polymeric carrier in such systems. The mechanisms controlling release of drug from solid dispersions are not fully understood and proposed theories are dependent on an understanding of the dissolution behaviour of both components of the dispersion. This study uses microviscometry to measure small changes in the viscosity of the dissolution medium as the polymer dissolves from ibuprofen-PVP solid dispersions. The microviscometer determines the dynamic and kinematic viscosity of liquids based on the rolling/falling ball principle. Using a standard USP dissolution apparatus, the dissolution of the polymer from the solid dispersion was easily measured alongside drug release. Drug release was found to closely follow polymer dissolution at the molecular weights and ratios used. The combination of sensitivity and ease of use make microviscometry a valuable technique for the elucidation of mechanisms governing drug release from polymeric delivery systems.
|Subjects:||Q Science > Q Science (General)
Q Science > QD Chemistry
|Schools:||School of Applied Sciences
School of Human and Health Sciences > Institute for Skin Integrity and Infection Prevention
|Depositing User:||Sharon Beastall|
|Date Deposited:||04 Nov 2010 13:29|
|Last Modified:||29 Mar 2016 15:06|
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