Author:
Bergstrand Martin,Söderlind Erik,Eriksson Ulf G,Weitschies Werner,Karlsson Mats O
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology
Reference49 articles.
1. Tong C, Lozano R, Mao Y, Mirza T, Löbenberg R, Nickerson B, et al. The value of in Vitro dissolution in drug development: a position paper from the AAPS in Vitro release and dissolution focus group. Pharm Technol. 2009;33(4):52–64.
2. Azarmi S, Roa W, Löbenberg R. Current perspectives in dissolution testing of conventional and novel dosage forms. Int J Pharm. 2007;328(1 SPEC. ISS):12–21.
3. Siewert M. FIP guidelines for dissolution testing of solid oral products. Joint report of the section for official laboratories and medicines control services and the section of industrial pharmacists of the F.I.P. Drugs Made in Germany. 1997;40(4):123–9
4. Jorgensen ED, Bhagwat D. Development of dissolution tests for oral extended-release products. Pharm Sci Tech Today. 1998;1(3):128–35.
5. Garbacz G, Golke B, Wedemeyer RS, Axell M, Söderlind E, Abrahamsson B, et al. Comparison of dissolution profiles obtained from nifedipine extended release once a day products using different dissolution test apparatuses. Eur J Pharm Sci. 2009;38(2):147–55.
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