体内
PLGA公司
植入
分散性
生物相容性
微球
生物医学工程
药物输送
化学
细胞外基质
移植
生物物理学
材料科学
纳米技术
化学工程
外科
纳米颗粒
高分子化学
生物
医学
有机化学
生物技术
工程类
生物化学
作者
Jurjen Zandstra,Christine Hiemstra,Ansgar Petersen,Johan Zuidema,MM van Beuge,Sergio Rodríguez,AAR Lathuile,G.J. Veldhuis,Rob Steendam,R.A. Bank,ER Popa
摘要
Biodegradable poly-(DL-lactide-co-glycolide) (PLGA) microspheres (MSP) are attractive candidate vehicles for site-specific or systemic sustained release of therapeutic compounds.This release may be altered by the host's foreign body reaction (FBR), which is dependent on the characteristics of the implant, e.g.chemistry, shape or size.In this study, we focused on the characterisation of the influence of MSP size on the FBR.To this end we injected monodisperse MSP of defined size (small 5.8 µm, coefficient of variance (CV) 14 % and large 29.8 µm, CV 4 %) and polydisperse MSP (average diameter 34.1 µm, CV 51 %) under the skin of rats.MSP implants were retrieved at day 7, 14 and 28 after transplantation.The FBR was studied in terms of macrophage infiltration, implant encapsulation, vascularisation and extracellular matrix deposition.Although PLGA MSP of all different sizes demonstrated excellent in vitro and in vivo biocompatibility, significant differences were found in the characteristics of the FBR.Small MSP were phagocytosed, while large MSP were not.Large MSP occasionally elicited giant cell formation, which was not observed after implantation of small MSP.Cellular and macrophage influx and collagen deposition were increased in small MSP implants compared to large MSP.We conclude that the MSP size influences the FBR and thus might influence clinical outcome when using MSP as a drug delivery device.We propose that a rational choice of MSP size can aid in optimising the therapeutic efficacy of microsphere-based therapies in vivo.
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