Effect of PEO surface density on long-circulating PLA-PEO nanoparticles which are very low complement activators

被引:164
作者
Vittaz, M
Bazile, D
Spenlehauer, G
Verrecchia, T
Veillard, M
Puisieux, F
Labarre, D
机构
[1] UNIV PARIS SUD,CNRS,URA 1218,LAB PHYSICOCHIM PHARMACOTECH BIOPHARM,F-92290 CHATENAY MALABRY,FRANCE
[2] RHONE POULENC RORER SA,DEPT PHARMACEUT SCI,F-94403 VITRY SUR SEINE,FRANCE
关键词
drug delivery; nanoparticles; complement system; poly(lactic acid coethylene oxide); PEO surface density;
D O I
10.1016/0142-9612(95)00322-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The rapid uptake of injected nanoparticles by cells of the mononuclear phagocytes system (MPS) is a major obstacle when a long blood circulation time is needed. Whereas nanoparticles made from PLA and stabilized by surfactants (PLA-F68) are rapidly phagocytized, the rate of phagocytosis is strongly reduced in case of nanoparticles made from a diblock copolymer (PLA-PEO). Because of the role of the complement system in opsonization, this difference of phagocytosis was hypothesized to be related to this system. An important complement consumption was obtained in 5 min in the presence of PLA-F68 particles. In the presence of a higher surface area of PLA-PEO particles possessing a high PEO surface density, the consumption remained very low. When the average PEO surface density was decreased on such particles below a given threshold, a fast and strong complement consumption occurred again. These experimental data support the concept of steric repulsion towards proteins, by surfaces covered with terminally attached PEO chains and emphasize the prime importance of PEO surface density in such an effect. The major, but probably not exclusive, role of complement as an opsonin capable of inducing a fast phagocytosis by MPS should be taken into account concerning the in vitro evaluation of nanoparticles as candidates for a long blood circulation. (C) 1996 Elsevier Science Limited
引用
收藏
页码:1575 / 1581
页数:7
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