Poly (lactide-co-glycolide) particles of different physicochemical properties and their uptake by Peyer's patches in mice

被引:127
作者
Shakweh, M [1 ]
Besnard, M [1 ]
Nicolas, V [1 ]
Fattal, E [1 ]
机构
[1] Univ Paris Sud, CNRS, UMR 8612, Sch Pharm, F-92296 Chatenay Malabry, France
关键词
poly (lactide-co-glycolide); polyethyleneimine; gastro-intestinal uptake; Peyer's patches; hydrophobically modified hydroxyethylcellulose; electron spectroscopy for chemical analysis; zeta potential;
D O I
10.1016/j.ejpb.2005.04.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nano-and microparticles of poly(lactide-co-glycolide) (PLGA) were formulated using poly(vinyl alcohol) (PVA) or hydrophobically modified hydroxyethylcellulose (HMHEC) or polyethyleneimine (PEI) as stabilizers. The uptake by murine Peyer's patches (PPs) and the binding to Peyer's patches-free tissue (PPFT) of these particles was investigated using fluorescence microscopy providing qualitative information about the tissue distribution of particles. Observations of intestinal cryo-sections showed significant discrimination in the uptake by PP of nano-and microparticles. The uptake by PPs of PLGA-PVA and PLGA-HMHEC nano-and microparticles, of negative and neutral zeta potential, respectively, was comparable, whereas a smaller number was observed in the case of nano-and microparticles of PLGA-PEI, positively charged. Moreover, particle uptake by PPs appeared to be strongly size-dependent. The number of particles of mean diameter around 0.3 and 1 mu m observed in PPs was much greater than that of particles of diameter average close to 3 mu m. However, in all cases, particles were found in the PPFT for at least 48 h. In conclusion, regarding the tissue samples we have observed, it appeared that the uptake of particles by PPs and binding to PPFT could be influenced by the physicochemical properties of the particles but this may not have been true at all sites of the intestine and may differ between animals. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 28 条
[1]   DYNAMIC PROPERTIES OF POLY(DL-LACTIDE) AND POLYVINYL-ALCOHOL MONOLAYERS AT THE AIR-WATER AND DICHLOROMETHANE WATER INTERFACES [J].
BOURY, F ;
IVANOVA, T ;
PANAIOTOV, I ;
PROUST, JE ;
BOIS, A ;
RICHOU, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1995, 169 (02) :380-392
[2]   Quantitative determination of pneumococcal capsular polysaccharide serotype 14 using a modification of phenol-sulfuric acid method [J].
Cuesta, G ;
Suarez, N ;
Bessio, MI ;
Ferreira, F ;
Massaldi, H .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 52 (01) :69-73
[3]   Ileal uptake of polyalkylcyanoacrylate nanocapsules in the rat [J].
Damgé, C ;
Aprahamian, M ;
Humbert, W ;
Pinget, M .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2000, 52 (09) :1049-1056
[4]   Biodegradable microparticles for the controlled delivery of oligonucleotides [J].
De Rosa, G ;
Quaglia, F ;
La Rotonda, MI ;
Besnard, M ;
Fattal, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :225-228
[5]   Evaluation of nano- and microparticle uptake by the gastrointestinal tract [J].
Delie, F .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 34 (2-3) :221-233
[6]  
ELDRIDGE JH, 1989, ADV EXP MED BIOL, V251, P191
[7]   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
[8]   Biodegradable microparticles for the mucosal delivery of antibacterial and dietary antigens [J].
Fattal, E ;
Pecquet, S ;
Couvreur, P ;
Andremont, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :15-24
[9]   The oral absorption of micro- and nanoparticulates: Neither exceptional nor unusual [J].
Florence, AT .
PHARMACEUTICAL RESEARCH, 1997, 14 (03) :259-266
[10]   Preparation of biodegradable, surface engineered PLGA nanospheres with enhanced lymphatic drainage and lymph node uptake [J].
Hawley, AE ;
Illum, L ;
Davis, SS .
PHARMACEUTICAL RESEARCH, 1997, 14 (05) :657-661