Author:
Enright Elaine F.,Joyce Susan A.,Gahan Cormac G.M.,Taylor Lynne S.
Subject
Pharmaceutical Science,General Medicine,Biotechnology
Reference59 articles.
1. A win-win solution in oral delivery of lipophilic drugs: supersaturation via amorphous solid dispersions increases apparent solubility without sacrifice of intestinal membrane permeability;Miller;Mol. Pharm.,2012
2. The use of amorphous solid dispersions: a formulation strategy to overcome poor solubility and dissolution rate;Van den Mooter;Drug Discovery Today: Technol.,2012
3. Lipid digestion as a trigger for supersaturation: evaluation of the impact of supersaturation stabilization on the in vitro and in vivo performance of self-emulsifying drug delivery systems;Anby;Mol. Pharm.,2012
4. Lipid-based formulations and drug supersaturation: harnessing the unique benefits of the lipid digestion/absorption pathway;Williams;Pharm. Res.,2013
5. L. Almeida e Sousa, S.M. Reutzel-Edens, G.A. Stephenson, L.S. Taylor, Supersaturation potential of salt, co-crystal, and amorphous forms of a model weak base, Crystal Growth & Design, 16 (2016) 737–748.
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献