Development of a Polymeric Patch Impregnated with Naproxen as a Model of Transdermal Sustained Release System

被引:14
|
作者
Argemi, Anna [1 ]
Ellis, Jeffrey L. [2 ]
Saurina, Javier [1 ]
Tomasko, David L. [2 ]
机构
[1] Univ Barcelona, Dept Analyt Chem, E-08028 Barcelona, Spain
[2] Ohio State Univ, Dept Chem & Biomol Engn, Columbus, OH 43210 USA
关键词
controlled delivery; transdermal drug delivery; processing; in vitro models; polymeric drug carrier; supercritical fluids; SUPERCRITICAL CARBON-DIOXIDE; ACETATE COPOLYMERS FILMS; SMALL MOLECULES; DRUG-DELIVERY; FLUIDS; CO2; MICROSPHERES; FORMULATIONS; TECHNOLOGY; STABILITY;
D O I
10.1002/jps.22346
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This paper describes the preparation and characterization of transdermal patches impregnated with naproxen. A mixture of ethylene vinyl acetate and Eudragit (R) E100 (80:20, w/w) is used as a polymeric matrix to obtain a thin membrane to be impregnated. Drug impregnation is carried out under pressurized CO(2) as a processing medium according to a two-step procedure. The patch is first soaked at 1000 psi and 22 degrees C for 2 h, and then foamed as a result of the rapid release of CO(2) pressure in order to increase the porosity of the surface. Subsequently, the naproxen solution is placed in contact with the membrane and then soaked in CO(2) at 450 psi and 37 degrees C for 2.5 h to enhance the mass transfer of drug into the polymer matrix. The characterization of the resulting samples by liquid chromatography, microscopy, and calorimetry provides information on naproxen content and distribution. Patches synthesized in this way are loaded with about 1% naproxen. The drug release and diffusion process through a membrane have been studied chromatographically using a Franz diffusion cell. Results have shown that a sustained delivery for more than 24 h is obtained. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:992-1000, 2011
引用
收藏
页码:992 / 1000
页数:9
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