The role of PEG on the stability in digestive fluids and in vivo fate of PEG-PLA nanoparticles following oral administration

被引:295
作者
Tobío, M
Sánchez, A
Vila, A
Soriano, I
Evora, C
Vila-Jato, JL
Alonso, MJ
机构
[1] Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Santiago De Compostela 15706, Spain
[2] Univ La Laguna, Sch Pharm, Dept Pharmaceut Technol, Tenerife, Spain
关键词
nanoparticles; PLA; PLA-PEG; oral administration; tetanus toxoid;
D O I
10.1016/S0927-7765(99)00157-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The aim of the present work was to evaluate if the presence of a polyethylenglycol (PEC) coating around PLA nanoparticles would affect their interaction with biological surfaces, following oral administration to rats. For this purpose, a model antigen, I-125-radiolabeled tetanus toroid, was encapsulated in PLA and PLA-PEG nanoparticles by a modified water-in-oil-water solvent evaporation technique. Firstly, the stability of the nanoparticles in simulated gastrointestinal fluids was evaluated. Results showed an interaction between the nanoparticles and the enzymes of the digestive fluids, this interaction being considerably reduced by the PEG coating around the particles. On the other hand, the PLA forming the nanoparticles was found to be only slightly degraded (9% converted to lactate for PLA nanoparticles and 3% for PLA-PEG nanoparticles) and that the encapsulated tetanus toroid remained mostly associated to the nanoparticles upon incubation in the digestive fluids for up to 4 h. Finally, the in vivo experiments showed that, after oral administration to rats, the levels of encapsulated radioactive antigen in the blood stream and lymphatics were higher for PLA-PEG nanoparticles than for PLA nanoparticles. In conclusion, the PLA-PEC nanoparticles have a promising future as protein delivery systems for oral administration. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:315 / 323
页数:9
相关论文
共 27 条
[1]   THE TRANSPORT OF MICROSPHERES FROM THE GASTROINTESTINAL-TRACT TO INFLAMMATORY AIR POUCHES IN THE RAT [J].
ALPAR, HO ;
FIELD, WN ;
LEWIS, DA .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1989, 41 (03) :194-196
[2]  
BLANCO MD, 1997, EUR J PHARM BIOPHARM, V43, P285
[3]   MUCOADHESION OF POLY(2-HYDROXYETHYL METHACRYLATE) IS IMPROVED WHEN LINEAR POLY(ETHYLENE OXIDE) CHAINS ARE ADDED TO THE POLYMER NETWORK [J].
DEASCENTIIS, A ;
DEGRAZIA, JL ;
BOWMAN, CN ;
COLOMBO, P ;
PEPPAS, NA .
JOURNAL OF CONTROLLED RELEASE, 1995, 33 (01) :197-201
[4]   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
[5]   EFFECTS OF POLYMERIZATION VARIABLES ON PLGA PROPERTIES - MOLECULAR-WEIGHT, COMPOSITION AND CHAIN STRUCTURE [J].
DORTA, MJ ;
MUNGUIA, O ;
LLABRES, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 100 (1-3) :9-14
[6]  
DUNN SE, 1994, INT S CONTROL REL BI, V21, P210
[7]  
ERMAK TH, 1995, CELL TISSUE RES, V279, P433, DOI 10.1007/BF00318501
[8]   The oral absorption of micro- and nanoparticulates: Neither exceptional nor unusual [J].
Florence, AT .
PHARMACEUTICAL RESEARCH, 1997, 14 (03) :259-266
[9]   Comparative degradation study of biodegradable microspheres of poly(DL-lactide-co-glycolide) with poly(ethyleneglycol) derivates [J].
Garcia, JT ;
Fariña, JB ;
Munguía, O ;
Llabrés, M .
JOURNAL OF MICROENCAPSULATION, 1999, 16 (01) :83-94
[10]   THE CONTROLLED INTRAVENOUS DELIVERY OF DRUGS USING PEG-COATED STERICALLY STABILIZED NANOSPHERES [J].
GREF, R ;
DOMB, A ;
QUELLEC, P ;
BLUNK, T ;
MULLER, RH ;
VERBAVATZ, JM ;
LANGER, R .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :215-233