Transport mechanism of lipid covered saquinavir pure drug nanoparticles in intestinal epithelium-Reference-Cited by-同舟云学术

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Transport mechanism of lipid covered saquinavir pure drug nanoparticles in intestinal epithelium

Published:2018-01 Issue: Volume:269 Page:159-170
ISSN:0168-3659
Container-title:Journal of Controlled Release
language:en
Short-container-title:Journal of Controlled Release

Author:

Xia Dengning,He Yuan,Li Qiuxia,Hu Cunde,Huang Wei,Zhang Yunhai,Wan Feng,Wang Chi,Gan Yong

Funder

National Natural Science Foundations of China

China Postdoctoral Science Foundations

Chinese Academy of Sciences

Youth Innovation Promotion Association-CAS

Shanghai Science and Technology Innovation Action Plan for Basic Research

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference57 articles.

1. Effect of crystal size on the in vitro dissolution and oral absorption of Nitrendipine in rats;Xia;Pharm. Res.,2010

2. Twenty years of drug nanocrystals: where are we, and where do we go?;Muller;Eur. J. Pharm. Biopharm.,2012

3. Enhanced transport of nanocage stabilized pure nanodrug across intestinal epithelial barrier mimicking listeria monocytogenes;Xia;Biomaterials,2015

4. Enhancement of cellular uptake, transport and oral absorption of protease inhibitor saquinavir by nanocrystal formulation;He;Acta Pharmacol. Sin.,2015

5. Nimodipine nanocrystals for oral bioavailability improvement: role of mesenteric lymph transport in the oral absorption;Fu;Int. J. Pharm.,2013

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