Evaluations of the Effect of Sodium Metabisulphite on the Stability and Dissolution Rates of Various Model Drugs from the Extended Release Polyethylene Oxide Matrices
Author:
Funder
University of Sussex
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmaceutical Science
Link
http://link.springer.com/article/10.1007/s12247-017-9286-9/fulltext.html
Reference36 articles.
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2. Khan MZ. Dissolution testing for sustained or controlled release oral dosage forms and correlation with in vivo data: challenges and opportunities. Int J Pharm. 1996;140:131–43.
3. Khan GM. Controlled release oral dosage forms: some recent advantages in matrix type drug delivery systems. The Sciences. 2001;1(5):350–4.
4. Rane M, et al. Hydrophilic matrices for oral extended release. Pharma Times. 2012;42(4):41–5.
5. Maderuelo C, et al. Critical factors in the release of drugs from sustained release hydrophilic matrices. J Control Release. 2011;154:2–19.
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