利用负载阿霉素的介孔二氧化硅光热触发控制药物传递系统有效杀伤人肝癌细胞

Ming Li, Yu Han Huang, Yingqiang Qin, Bo Ren, Hong Yu Song, Yanhai Qi
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摘要

设计并制备了光热-温度响应的[Ag纳米颗粒-中空介孔二氧化硅纳米球-聚(n -异丙基丙烯酰胺-丙烯酸)](Ag@HMSN@PNIPAM-AA)纳米颗粒,并利用Ag纳米颗粒(AgNPs)与[聚(n -异丙基丙烯酰胺-丙烯酸)](PNIPAM-AA)的组合作为光热-温度效应的开关来控制药物释放。体外细胞培养结果表明,[介孔二氧化硅纳米球-聚(n -异丙基丙烯酰胺-丙烯酸)](MSN@PNIPAM-AA)和Ag@HMSN@PNIPAM-AA纳米颗粒在808 nm近红外光下具有良好的生物相容性和较小的细胞毒性,Ag@HMSN@PNIPAM-AA纳米颗粒在808 nm近红外光下具有较高的细胞抑制作用。近红外光联合阿霉素对HepG2细胞的释放效率更高,抑制作用更强。这些特征表明Ag@HMSN@PNIPAM-AA纳米颗粒具有很大的治疗潜力。该研究也证明了Ag@HMSN@PNIPAM-AA纳米颗粒的普遍适用性。不同的模型药物和纳米颗粒可以发挥不同的作用,具有开发潜力。
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Photothermally Triggered Control of the Drug Delivery System Using Doxorubicin-Loaded Mesoporous Silica for Effective Killing of Human Hepatoma Cells
Photothermal-temperature responsive [Ag nanoparticles-hollow mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (Ag@HMSN@PNIPAM-AA) nanoparticles were designed and prepared, and the combination of Ag nanoparticles (AgNPs) and [poly (N-isopropyl acrylamide-acrylic acid)] (PNIPAM-AA) was used as a switch of the photothermal-temperature effect to control drug release. The results of cell culture in vitro showed that [mesoporous silica nanospheres–poly (N-isopropyl acrylamide-acrylic acid)] (MSN@PNIPAM-AA) and Ag@HMSN@PNIPAM-AA nanoparticles had good biocompatibility and less cytotoxicity, and Ag@HMSN@PNIPAM-AA nanoparticles had higher cell inhibition under 808 nm near-infrared light. The combination of near-infrared light and doxorubicin showed higher drug release efficiency and a stronger inhibitory effect on HepG2 cell growth. These characteristics indicate that Ag@HMSN@PNIPAM-AA nanoparticles have great potential for treatment. This study also proved the universal applicability of Ag@HMSN@PNIPAM-AA nanoparticles. Different model drugs and nanoparticles can play different roles and have development potential.
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