Dissolution and oral bioavailability enhancement of praziquantel by solid dispersions
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmaceutical Science
Link
http://link.springer.com/article/10.1007/s13346-018-0487-7/fulltext.html
Reference36 articles.
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2. Dinora GE, Julio R, Nelly C, Lilian YM, Cook HJ. In vitro characterization of some biopharmaceutical properties of praziquantel. Int J Pharm. 2005;295(1–2):93–9. https://doi.org/10.1016/j.ijpharm.2004.01.033.
3. Passerini N, Albertini B, Perissutti B, Rodriguez L. Evaluation of melt granulation and ultrasonic spray congealing as techniques to enhance the dissolution of praziquantel. Int J Pharm. 2006;318(1–2):92–102. https://doi.org/10.1016/j.ijpharm.2006.03.028 .
4. Cheng L, Lei L, Guo SR. In vitro and in vivo evaluation of praziquantel loaded implants based on PEG/PCL blends. Int J Pharm. 2010;387(1–2):129–38. https://doi.org/10.1016/j.ijpharm.2009.12.010.
5. Parrot-Lopez H, Perret F, Bertino-Ghera B. Les cyclodextrines amphiphiles et leurs applications. Élaboration de nanoparticules de cyclodextrines amphiphiles pour des applications biomédicales. Ann Pharm Fr. 2010;68(1):12–26. https://doi.org/10.1016/j.pharma.2009.12.002 .
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