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
相关论文
共 36 条
[1]   STEALTH ME.PEG-PLA NANOPARTICLES AVOID UPTAKE BY THE MONONUCLEAR PHAGOCYTES SYSTEM [J].
BAZILE, D ;
PRUDHOMME, C ;
BASSOULLET, MT ;
MARLARD, M ;
SPENLEHAUER, G ;
VEILLARD, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (04) :493-498
[2]   Comparative uptake studies of bioadhesive and non-bioadhesive nanoparticles in human intestinal cell lines and rats: The effect of mucus on particle adsorption and transport [J].
Behrens, I ;
Pena, AIV ;
Alonso, MJ ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 2002, 19 (08) :1185-1193
[3]   NMR spectroscopic evidence that helodermin, unlike other members of the secretin/VIP family of peptides, is substantially structured in water [J].
Blankenfeldt, W ;
Nokihara, K ;
Naruse, S ;
Lessel, U ;
Schomburg, D ;
Wray, V .
BIOCHEMISTRY, 1996, 35 (19) :5955-5962
[4]   Transport of nanoparticles across an in vitro model of the human intestinal follicle associated epithelium [J].
des Rieux, A ;
Ragnarsson, EGE ;
Gullberg, E ;
Préat, V ;
Schneider, YJ ;
Artursson, P .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 25 (4-5) :455-465
[5]   Nanoparticles as potential oral delivery systems of proteins and vaccines: A mechanistic approach [J].
des Rieux, Anne ;
Fievez, Virginie ;
Garinot, Marie ;
Schneider, Yves-Jacques ;
Preat, Veronique .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (01) :1-27
[6]   Gastrointestinal uptake of biodegradable microparticles: Effect of particle size [J].
Desai, MP ;
Labhasetwar, V ;
Amidon, GL ;
Levy, RJ .
PHARMACEUTICAL RESEARCH, 1996, 13 (12) :1838-1845
[7]  
DESRIEUX A, IN PRESS EUR J PHARM
[8]   In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs [J].
Dressman, JB ;
Reppas, C .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 11 :S73-S80
[9]   CONTROLLED VACCINE RELEASE IN THE GUT-ASSOCIATED LYMPHOID-TISSUES .1. ORALLY-ADMINISTERED BIODEGRADABLE MICROSPHERES TARGET THE PEYERS PATCHES [J].
ELDRIDGE, JH ;
HAMMOND, CJ ;
MEULBROEK, JA ;
STAAS, JK ;
GILLEY, RM ;
TICE, TR .
JOURNAL OF CONTROLLED RELEASE, 1990, 11 (1-3) :205-214
[10]   NANOCAPSULE FORMATION BY INTERFACIAL POLYMER DEPOSITION FOLLOWING SOLVENT DISPLACEMENT [J].
FESSI, H ;
PUISIEUX, F ;
DEVISSAGUET, JP ;
AMMOURY, N ;
BENITA, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 55 (01) :R1-R4