The in vitro cell association of invasin coated polylactide-co-glycolide nanoparticles

被引:51
作者
Dawson, GF [1 ]
Halbert, GW [1 ]
机构
[1] Univ Strathclyde, Dept Pharmaceut Sci, Glasgow G4 0NR, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
invasin; PLGA; nanoparticles; phagocytosis; in vitro;
D O I
10.1023/A:1007503123620
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. To determine the effect of particle size and ligand surface density on the cellular association of poly lactide-co-glycolide nanoparticles covalently coated with bacterial invasin. Methods. Poly lactide-co-glycolide nanoparticles containing a flourescent probe were prepared at four diameters 155nm, 200nm, 375nm and 600nm using standard techniques. Bacterial invasin was covalently coupled to the particles surface at varying surface concentrations using a water soluble carbodiimide. The modified particle's cellular association with HEp2 2B cells in tissue culture was determined using flow cytometry. Results. Cellular association of modified nanoparticles was time dependent, abolished at low temperature, competitively inhibited by free invasin or the RGD peptide ligand and saturable. Increased cell association was produced by increasing the particle's surface invasin concentration however, this effect was size dependent. Small particles (155 nm and 200 nm) exhibiting a maximal association with increasing invasin concentration whilst the larger particles (375 nm and 600 nm) provide a minimum at low invasin concentrations. Conclusions Modified particle cell association provided results commensurate with a receptor dependent uptake mechanism related to the presence of invasin. The size and surface concentration dependency however illustrate that application of these ligands to particulate drug delivery or targeting systems will be controlled by their natural cellular association properties.
引用
收藏
页码:1420 / 1425
页数:6
相关论文
共 24 条
[1]   VECTORS THAT FACILITATE THE EXPRESSION AND PURIFICATION OF FOREIGN PEPTIDES IN ESCHERICHIA-COLI BY FUSION TO MALTOSE-BINDING PROTEIN [J].
DIGUAN, C ;
LI, P ;
RIGGS, PD ;
INOUYE, H .
GENE, 1988, 67 (01) :21-30
[2]   The oral absorption of micro- and nanoparticulates: Neither exceptional nor unusual [J].
Florence, AT .
PHARMACEUTICAL RESEARCH, 1997, 14 (03) :259-266
[3]   Lectins and bacterial invasion factors for controlling endo- and transcytosis of bioadhesive drug carrier systems [J].
Haltner, E ;
Easson, JH ;
Lehr, CM .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1997, 44 (01) :3-13
[4]   Utilizing bacterial mechanisms of epithelial cell entry: Invasin-induced oral uptake of latex nanoparticles [J].
Hussain, N ;
Florence, AT .
PHARMACEUTICAL RESEARCH, 1998, 15 (01) :153-156
[5]  
ISBERG RR, 1994, ANNU REV GENET, V28, P395, DOI 10.1146/annurev.ge.28.120194.002143
[6]   CULTURED MAMMALIAN-CELLS ATTACH TO THE INVASIN PROTEIN OF YERSINIA-PSEUDOTUBERCULOSIS [J].
ISBERG, RR ;
LEONG, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6682-6686
[7]   A SINGLE GENETIC-LOCUS ENCODED BY YERSINIA-PSEUDOTUBERCULOSIS PERMITS INVASION OF CULTURED ANIMAL-CELLS BY ESCHERICHIA-COLI K-12 [J].
ISBERG, RR ;
FALKOW, S .
NATURE, 1985, 317 (6034) :262-264
[8]   NANOPARTICLE UPTAKE BY THE RAT GASTROINTESTINAL MUCOSA - QUANTITATION AND PARTICLE-SIZE DEPENDENCY [J].
JANI, P ;
HALBERT, GW ;
LANGRIDGE, J ;
FLORENCE, AT .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1990, 42 (12) :821-826
[9]   FURTHER HISTOLOGICAL EVIDENCE OF THE GASTROINTESTINAL ABSORPTION OF POLYSTYRENE NANOSPHERES IN THE RAT [J].
JANI, PU ;
FLORENCE, AT ;
MCCARTHY, DE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 84 (03) :245-252
[10]   IDENTIFICATION OF THE INTEGRIN BINDING DOMAIN OF THE YERSINIA-PSEUDOTUBERCULOSIS INVASIN PROTEIN [J].
LEONG, JM ;
FOURNIER, RS ;
ISBERG, RR .
EMBO JOURNAL, 1990, 9 (06) :1979-1989