Preparation and comparison of tacrolimus-loaded solid dispersion and self-microemulsifying drug delivery system by in vitro/in vivo evaluation

Author:

Huo Taotao,Tao Chun,Zhang Minxin,Liu Qinghong,Lin Bing,Liu Zhihong,Zhang Jialiang,Zhang Meijing,Yang Haiyue,Wu Jue,Sun Xinrong,Zhang Qian,Song HongtaoORCID

Funder

Natural Science Foundation of Fujian Province

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference59 articles.

1. Taste-masked tacrolimus-phospholipid nanodispersions: dissolution enhancement, taste masking and reduced gastric complications;Ahmed;Pharm. Dev. Technol.,2017

2. Contribution of P-glycoprotein to the enhancing effects of dimethyl-b-cyclodextrin on oral bioavailability of tacrolimus;Arima;J. Pharmacol. Exp. Ther.,2001

3. Improved drug delivery using microemulsions: rationale, recent progress, and new horizons;Bagwe;Crit. Rev. Ther. Drug Carrier Syst.,2001

4. Design and evaluation of self-microemulsifying drug delivery system (smedds) of tacrolimus;Borhade;AAPS Pharm. Sci.Tech.,2008

5. Supersaturating drug delivery systems: the answer to solubility-limited oral bioavailability;Brouwers;J. Pharm. Sci.,2009

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