A propofol microemulsion with low free propofol in the aqueous phase: Formulation, physicochemical characterization, stability and pharmacokinetics-Reference-Cited by-同舟云学术

A propofol microemulsion with low free propofol in the aqueous phase: Formulation, physicochemical characterization, stability and pharmacokinetics

Published:2012-10 Issue:1-2 Volume:436 Page:536-544
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Cai WeiHui,Deng WanDing,Yang HuiHui,Chen XiaoPing,Jin Fang

Funder

Science and Technology Commission of Shanghai Municipality

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference38 articles.

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3. Relationship between free propofol concentrations of different delivery systems for injection and in vitro hemolytic activities;Cai;Chinese J. Pharm.,2008

4. Formulation and evaluation of an alternative triglyceride-free propofol microemulsion;Cho;Arch. Pharm. Res.,2010

5. The pharmacokinetics and pharmacodynamics of propofol in a modified cyclodextrin formulation (Captisol) versus propofol in a lipid formulation (Diprivan): an electroencephalographic and hemodynamic study in a porcine model;Egan;Anesth. Analg.,2003

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