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载有脂质体的阿霉素/金纳米颗粒用于化疗-光热协同抗肿瘤治疗。

Doxorubicin/gold nanoparticles coated with liposomes for chemo-photothermal synergetic antitumor therapy.

机构信息

Applying Chemistry Key Lab of Hebei Province, Department of Bioengineer, Yanshan University, No.438 Hebei Street, Qinhuangdao, 066004, People's Republic of China. Hebei Province Asparagus Industry Technology Research Institute, Qinhuangdao, People's Republic of China.

出版信息

Nanotechnology. 2018 Oct 5;29(40):405101. doi: 10.1088/1361-6528/aad358. Epub 2018 Jul 13.

Abstract

Hybrid liposome/metal nanoparticles are promising candidate drug-carriers for therapy of various diseases due to their unique photothermal effect. In this study, self-crystallized gold nanoparticles (Au NPs) and doxorubicin (DOX) were co-encapsulated within liposomes (Au/DOX-Lips) by thin film hydration and gel separation technology. The surface plasmon resonance bands of drug-carriers were controllable in the near-infrared (NIR) zone. When the complex liposome/metallic hybrids were irradiated by NIR light, they displayed higher endocytosis efficiency following the fracture of liposomal membranes and the release of Au NPs. Then, the Au NPs penetrated further into deeper tumor tissue to accomplish photothermal treatment. The Au/DOX-Lips showed an excellent antitumor effect, whose inhibition rate for tumor cells was up to 78.28%. In experiments on mice bearing tumors, the Au/DOX-Lips treated mice exhibited superior tumor suppression. This novel drug system provides huge potential for biomedical application.

摘要

载药杂化脂质体/金属纳米颗粒由于其独特的光热效应,有望成为治疗各种疾病的候选药物载体。本研究采用薄膜水化和凝胶分离技术,将自结晶金纳米颗粒(Au NPs)和阿霉素(DOX)共包封于脂质体(Au/DOX-Lips)中。药物载体的表面等离子体共振带可在近红外(NIR)区进行调控。当复合脂质体/金属杂化物受到近红外光照射时,脂质体膜破裂,Au NPs 释放,载药杂化脂质体显示出更高的内吞效率。然后,Au NPs 进一步穿透到更深的肿瘤组织中,完成光热治疗。Au/DOX-Lips 表现出优异的抗肿瘤效果,对肿瘤细胞的抑制率高达 78.28%。在荷瘤小鼠实验中,经 Au/DOX-Lips 处理的小鼠表现出优异的肿瘤抑制作用。这种新型药物系统为生物医学应用提供了巨大的潜力。

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