Prediction of the changes in drug dissolution from an immediate-release tablet containing two active pharmaceutical ingredients using an accelerated stability assessment program (ASAPprime®)-Reference-Cited by-同舟云学术

Prediction of the changes in drug dissolution from an immediate-release tablet containing two active pharmaceutical ingredients using an accelerated stability assessment program (ASAPprime®)

Published:2016-11-03 Issue:1 Volume:2 Page:
ISSN:2364-9534
Container-title:AAPS Open
language:en
Short-container-title:AAPS Open

Author:

Li Hanlin^ORCID,Nadig David,Kuzmission Andrew,Riley Christopher M.

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1186/s41120-016-0010-5.pdf

Reference11 articles.

1. Baertschi S (2007) Pharmaceutical Stress Testing: Predicting Drug Degradation. Informa Healthcare, New York

2. Colgan S, Hofer R, Vuoviski K, Waterman K, Norris (2015) Lean Stability, AAPS Newsmagazine, 14-18 Sept. The Timmerman. vol 220 (1–3)

3. Huynh-Ba K (2008) Handbook of Stability Testing on Pharmaceutical Development: Regulations, Methodologies and Best Practices. Spirnger, New York

4. Karstensen J (1990) Drug Stability: Principles and Practices. Marcel Dekker, New York

5. MacDonald KW (2010) Package selection for moisture protection for solid, oral drug products. J Pharm Sci 99:4437–4452

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