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载吲哚菁绿的可生物降解肿瘤靶向纳米探针的体外与体内成像研究。

Indocyanine green-loaded biodegradable tumor targeting nanoprobes for in vitro and in vivo imaging.

机构信息

CAS Key Lab of Health Informatics, Shenzhen Key Laboratory of Cancer Nanotechnology, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.

出版信息

Biomaterials. 2012 Aug;33(22):5603-9. doi: 10.1016/j.biomaterials.2012.04.044. Epub 2012 May 9.

DOI:10.1016/j.biomaterials.2012.04.044
PMID:22575835
Abstract

Indocyanine green (ICG) is a near-infrared (NIR) fluorescence dye for extensive biological application, but limited by its poor aqueous stability in vitro, concentration-dependent aggregation, rapid elimination from the body, and lack of target specificity. In this paper, to overcome these limitations, folate receptor-targeted, ICG dye-doped poly(d,l-lactide-co-glycolide) (PLGA) lipid nanoparticles (FA-ICG-PLGA-lipid NPs) were constructed by a single-step self-assemble and nanoprecipitation method. The prepared FA-ICG-PLGA-lipid NPs exhibited good biocompatibility, monodispersity, excellent NIR penetration ability, significant stability against photobleaching and long circulation time. The intracellular uptake experiment proved the targeting efficacy of the FA-ICG-PLGA-lipid NPs was more effective in folate receptor over-expressing MCF-7 cells than folate receptor negative A549 cells. Furthermore, the in vivo experiments showed the FA-ICG-PLGA-lipid NPs were specifically targeted to the tumor, and its circulation time was much longer than free ICG. These biocompatible and biodegradable NIR-NPs prove a potential application in tumor diagnosis and targeted imaging due to its high aqueous stability, excellent NIR optical properties and significantly targeting property in vivo.

摘要

吲哚菁绿(ICG)是一种近红外(NIR)荧光染料,广泛应用于生物学领域,但由于其在体外的水稳定性差、浓度依赖性聚集、从体内迅速消除以及缺乏靶向特异性等限制了其应用。在本文中,为了克服这些限制,采用一步自组装和纳米沉淀法构建了叶酸受体靶向、吲哚菁绿染料掺杂的聚(D,L-乳酸-共-乙醇酸)(PLGA)脂质纳米粒(FA-ICG-PLGA-脂质 NPs)。所制备的 FA-ICG-PLGA-脂质 NPs 表现出良好的生物相容性、单分散性、优异的近红外穿透能力、对光漂白的显著稳定性和长循环时间。细胞内摄取实验证明,FA-ICG-PLGA-脂质 NPs 在叶酸受体过表达的 MCF-7 细胞中的靶向效果优于叶酸受体阴性的 A549 细胞。此外,体内实验表明,FA-ICG-PLGA-脂质 NPs 特异性地靶向肿瘤,其循环时间比游离 ICG 长得多。这些具有生物相容性和可生物降解性的近红外 NPs 由于其高的水稳定性、优异的近红外光学性质和体内显著的靶向特性,证明了其在肿瘤诊断和靶向成像方面有潜在的应用。

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