Development and Evaluation of a Novel Mucus Diffusion Test System Approved by Self-Nanoemulsifying Drug Delivery Systems

被引:155
作者
Friedl, Heike [1 ]
Duennhaupt, Sarah [1 ]
Hintzen, Fabian [2 ]
Waldner, Claudia [1 ]
Parikh, Shruti [3 ]
Pearson, Jeffrey P. [3 ]
Wilcox, Matthew D. [3 ]
Bernkop-Schnuerch, Andreas [2 ]
机构
[1] ThioMatrix GmbH, Res Ctr Innsbruck, A-6020 Innsbruck, Austria
[2] Leopold Franzens Univ Innsbruck, Inst Pharm, Dept Pharmaceut Technol, A-6020 Innsbruck, Austria
[3] Newcastle Univ, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
diffusion; nanoparticles; particle size; self-emulsifying; solubility; surfactants; GASTROINTESTINAL MUCUS; MUCIN; PERMEATION; ABSORPTION; THICKNESS; TRANSPORT; BARRIER; LAYER; GELS;
D O I
10.1002/jps.23757
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this study was the development of a novel mucus diffusion model and the approval thereof by self-nanoemulsifying drug delivery systems (SNEDDSs). For diffusion experiments, various SNEDD formulations were developed, spiked with fluorescein diacetate, and evaluated for their mucus diffusion behavior through an intestinal mucus layer within the novel setup. In brief, SNEDD formulations resulting in particle sizes of 12.0nm produced 70.3% of diffused model drug through the mucus layer. In comparison, SNEDDSs with particle sizes of 455.5nm led to a permeation of 8.3% only. Apart from this size dependence, two SNEDDS excipients namely Cremophor RH40 and triacetin were identified to strongly affect the permeation through mucus. Hence, it could be demonstrated that particle size and single excipients can positively influence mucus diffusion of SNEDDSs. Furthermore, it could be shown that the developed mucus diffusion model is a promising tool for pharmaceutical research in comparison with already established systems as it allows an easy handling coupled with the possibility to test different kinds of mucus in parallel within one setup. (c) 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:4406-4413, 2013
引用
收藏
页码:4406 / 4413
页数:8
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