STEALTH ME.PEG-PLA NANOPARTICLES AVOID UPTAKE BY THE MONONUCLEAR PHAGOCYTES SYSTEM

被引:522
作者
BAZILE, D
PRUDHOMME, C
BASSOULLET, MT
MARLARD, M
SPENLEHAUER, G
VEILLARD, M
机构
[1] RHONE POULENC RORER,INST BIOPHARM,DEPT PHARMACOTECHNY,F-92160 ANTONY,FRANCE
[2] RHONE POULENC RORER,INST BIOPHARM,DEPT ANAL,F-92160 ANTONY,FRANCE
[3] RHONE POULENC RORER,INST BIOPHARM,DEPT BIODYNAM,F-92160 ANTONY,FRANCE
[4] RHONE POULENC RECH,CTR RECH CARRIERES,F-69192 ST FONS,FRANCE
关键词
D O I
10.1002/jps.2600840420
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Nanoparticles were prepared from methoxy poly(ethylene glycol)poly(d,l-lactic acid) block copolymers (Me.PEG-PLA) or blends of Me.PEG-PLA and PLA by the precipitation-soivent diffusion method. These nanoparticles, labeled by introducing [C-14]PLA in the formulation, were shown to be more slowly captured by cultured THP-1 monocytes than F68-coated PLA nanoparticles, in a PEG chain-length-dependent manner. In vivo, the half-life in plasma of the Me.PEG-PLA nanoparticles that were intravenously administered to rats is increased by a factor 180 compared with the F68-coated PLA nanoparticles. This mononuclear phagocytes system avoidance was explained according to a conformation model in which the PEG density at the surface of the particles is a key parameter.
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页码:493 / 498
页数:6
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