Helodermin-loaded nanoparticles:: Characterization and transport across an in vitro model of the follicle-associated epithelium

被引:49
作者
des Rieux, Anne
Fievez, Virginie
Momtaz, Maryani
Detrembleur, Christophe
Alonso-Sande, Maria
Van Gelder, Jan
Cauvin, Annick
Schneider, Yves-Jacques
Preat, Veronique
机构
[1] Catholic Univ Louvain, Unite Pharm Galen, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Inst Sci Vie, Biochim Cellulaire Lab, B-1348 Louvain, Belgium
[3] Catholic Univ Louvain, Lab Chim Med, B-1348 Louvain, Belgium
[4] Univ Liege, Ctr Etud & Rech Macromol, B-4000 Liege, Belgium
[5] Univ Santiago de Compostela, Dept Pharmaceut Technol, Santiago De Compostela, Spain
[6] Lily Dev Ctr, B-1348 Mont St Guibert, Belgium
关键词
peptide; M cells; in vitro model of the human follicle-associated epithelium (FAE); polymeric nanoparticles; oral delivery; helodermin;
D O I
10.1016/j.jconrel.2006.12.023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
M cells represent a potential portal for oral delivery of peptides and proteins due to their high endocytosis abilities. An in vitro model of human FAE (co-cultures) was used to evaluate the influence of M cells on the transport of free and encapsulated helodermin - a model peptide - across the intestinal epithelium. M cells enhanced transport of intact helodermin (18-fold, Papp 3 X 10(-6) cm s(-1)). As pegylation increased nanoparticle transport by M cells, helodermin was encapsulated in 200 mu nanoparticles containing PEG-b-PLA:PLGA 1:1. Stability of the selected formulation was demonstrated in simulated gastric and intestinal fluids. M cells increased the transport of helodermin encapsulated in these nanoparticles by a factor of 415, as compared to Caco-2 cells. Transport of free and encapsulated helodermin occurred most probably by endocytosis. In conclusion, M cells improved helodermin transport across the intestinal epithelium, confirming their high potential for oral delivery of peptides. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:294 / 302
页数:9
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