体内分布
PLGA公司
Zeta电位
纳米颗粒
体内
结合
荧光
分散性
化学
聚乙烯醇
生物物理学
离体
共轭体系
临床前影像学
荧光显微镜
荧光寿命成像显微镜
材料科学
纳米技术
体外
聚合物
有机化学
生物化学
数学分析
物理
生物技术
数学
量子力学
生物
作者
Regina Reul,Nicolas Tsapis,Hervé Hillaireau,Lucie Sancey,Simona Mura,Marion Recher,Julien Nicolas,Jean‐Luc Coll,Elias Fattal
出处
期刊:Polymer Chemistry
[Royal Society of Chemistry]
日期:2012-01-01
卷期号:3 (3): 694-694
被引量:43
摘要
To introduce optical imaging among methods available to follow nanoparticle biodistribution, we have evaluated the concept of covalently labeling poly(lactide-co-glycolide) (PLGA) with a near-infrared (NIR) dye to obtain stable NIR fluorescent nanoparticles. PLGA was coupled with the NIR dye (DY-700, Dyomics) by an amide bond with 38% efficiency. Incorporating 1% of this conjugate into PLGA nanoparticles stabilised by polyvinyl alcohol (PVA) leads to stable nanoparticles (NPs) without affecting their colloidal characteristics (average diameter, polydispersity and zeta potential). In addition, nanoparticles remain strongly fluorescent and display good storage stability for 4 weeks at 4 °C or over one week at 37 °C. Nanoparticle cytotoxicity evaluated using HUVEC, NIH/3T3 and J774.A1 cell lines was similar for unlabeled or labeled NPs. Fluorescent nanoparticles and free dye were injected intravenously into mice and their biodistribution was followed for 24 h by NIR imaging, in vivo and ex vivo. Nanoparticles were found mainly in the liver whereas the free dye was not accumulating preferentially in this organ. The DY-700 NIR conjugate incorporated into PLGA NPs shows good performance both in vitro and in vivo, thus paving the way to finely traceable PLGA nanosystems for in vivo administration.
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