4.5 Article

Mechanism of Mucosal Permeability Enhancement of CriticalSorb® (Solutol® HS15) Investigated In Vitro in Cell Cultures

期刊

PHARMACEUTICAL RESEARCH
卷 32, 期 2, 页码 516-527

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-014-1481-5

关键词

absorption enhancers; calu-3 cells; mucosal protein delivery; solutol (R) HS15; surfactants

资金

  1. BBSRC
  2. Critical Pharmaceuticals

向作者/读者索取更多资源

Purpose CriticalSorb (TM), with the principal component Solutol (R) HS15, is a novel mucosal drug delivery system demonstrated to improve the bioavailability of selected biotherapeutics. The intention of this study is to elucidate mechanism(s) responsible for the enhancement of trans-mucosal absorption of biological drugs by Solutol (R) HS15. Methods Micelle size and CMC of Solutol (R) HS15 were determined in biologically relevant media. Polarised airway Calu-3 cell layers were used to measure the permeability of a panel of biological drugs, and to assess changes in TEER, tight junction and F-actin morphology. The rate of cell endocytosis was measured in vitro in the presence of Solutol (R) HS15 using a membrane probe, FM 2-10. Results This work initially confirms surfactant-like behaviour of Solutol (R) HS15 in aqueous media, while subsequent experiments demonstrate that the effect of Solutol (R) HS15 on epithelial tight junctions is different from a 'classical' tight junction opening agent and illustrate the effect of Solutol (R) HS15 on the cell membrane (endocytosis rate) and F-actin cytoskeleton. Conclusion Solutol (R) HS15 is the principle component of CriticalSorb (TM) that has shown an enhancement in permeability of medium sized biological drugs across epithelia. This study suggests that its mechanism of action arises primarily from effects on the cell membrane and consequent impacts on the cell cytoskeleton in terms of actin organisation and tight junction opening.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据