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基于金纳米壳的白桦脂酸脂质体用于协同化-光热治疗。

Gold nanoshell-based betulinic acid liposomes for synergistic chemo-photothermal therapy.

机构信息

Hebei Key Laboratory of Applied Chemistry, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao, PR China; State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao, PR China.

Hebei Key Laboratory of Applied Chemistry, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao, PR China.

出版信息

Nanomedicine. 2017 Aug;13(6):1891-1900. doi: 10.1016/j.nano.2017.03.012. Epub 2017 Mar 29.

Abstract

A novel synthesis approach is first developed to fabricate a multifunctional smart nanodrug delivery system: gold nanoshell-coated betulinic acid liposomes (AuNS-BA-Lips) mediated by a glutathione. The AuNS-BA-Lips exhibited good size distribution (149.4±2.4nm), preferable photothermal conversion ability and synergistic chemo-photothermal therapy. Additionally, the absorption wavelength of AuNS-BA-Lips showed a significantly red-shifted to near infrared (NIR) region, which can strongly absorbed NIR laser and efficiently convert it into localized heat, thus providing controlled drug release and antitumor thermotherapy. Moreover, the nanocarriers excited by NIR light significantly promoted cell uptake compared to those without irradiation, resulting in an enhanced intracellular drug accumulation. Upon NIR irradiation, the AuNS-BA-Lips showed highly efficient antitumor effects on tumor-bearing mice with an inhibition rate of 83.02%, thus demonstrating a remarkable synergistic therapeutic effect of chemotherapy and thermotherapy. Therefore, this work provides new insight into developing a multifunctional antitumor drug.

摘要

本文首次开发了一种新的合成方法,用于构建多功能智能纳米药物递送系统:谷胱甘肽介导的金纳米壳包裹白桦脂酸脂质体(AuNS-BA-Lips)。AuNS-BA-Lips 表现出良好的粒径分布(149.4±2.4nm)、优异的光热转换能力和协同化学-光热治疗。此外,AuNS-BA-Lips 的吸收波长明显红移至近红外(NIR)区域,可强烈吸收 NIR 激光并将其高效转化为局部热,从而提供受控的药物释放和抗肿瘤热疗。此外,与未辐照的纳米载体相比,近红外光激发的纳米载体显著促进了细胞摄取,从而导致细胞内药物积累增加。在近红外照射下,AuNS-BA-Lips 对荷瘤小鼠表现出高效的抗肿瘤作用,抑制率为 83.02%,从而显示出化疗和热疗的协同治疗效果显著。因此,这项工作为开发多功能抗肿瘤药物提供了新的思路。

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