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Mesoscopic Metal Nanoparticles Doubly Functionalized with Natural and Engineered Lipidic Dispersants for Therapeutics

机译:介观金属纳米粒子双重功能化与天然和工程脂质分散剂的治疗。

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摘要

Surface engineering of mesoscopic metal nanoparticles to increase biocompatibility and cell interaction is important for improvement of their therapeutic properties. Here, we describe a strategy to stabilize mesoscopic metal nanoparticles and to enhance their cell interaction by stepwise addition of (Z)-9-octadecenoate (oleate) and a cell-penetrating peptide-fused high-density lipoprotein (cpHDL). Oleate replaces a cytotoxic dispersant on the surface of gold nanorods (AuNRs), which enables subsequent cpHDL binding without causing aggregation. Notably, these two lipidic dispersants are probably intercalated on the surface. This procedure was also used to stabilize 20 nm spherical gold nanoparticles and 40 nm aggregates of 10 nm magnetite nanoparticles. cpHDL-bound AuNRs were internalized greater than 80 times more efficiently than poly(ethylene glycol)-conjugated AuNRs and were able to elicit cancer cell photoablation.
机译:介观金属纳米颗粒的表面工程化以提高生物相容性和细胞相互作用对于改善其治疗性能很重要。在这里,我们描述了一种策略,通过逐步添加(Z)-9-十八烯酸酯(油酸酯)和细胞穿透肽融合的高密度脂蛋白(cpHDL)来稳定介观金属纳米颗粒并增强其细胞相互作用。油酸替代了金纳米棒(AuNRs)表面上的细胞毒性分散剂,从而使后续cpHDL结合而不会引起聚集。值得注意的是,这两种脂质分散剂可能插入在表面上。该程序还用于稳定20 nm球形金纳米颗粒和10 nm磁铁矿纳米颗粒的40 nm聚集体。与结合了聚乙二醇的AuNRs相比,与cpHDL结合的AuNRs的内在化效率高80倍以上,并且能够引发癌细胞的光消融。

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