光热治疗
适体
化学
纳米棒
化疗
光热效应
癌症治疗
癌症研究
癌细胞
乳腺癌
纳米技术
癌症
药理学
内科学
分子生物学
医学
材料科学
生物
作者
Hui Xu,Lu Zhao,Xiaoliang Chen,Zhiqiang Bai,Yanjun Li,Nianping Zhang,Yunfeng Bai,Feng Feng
标识
DOI:10.1021/acs.bioconjchem.5c00348
摘要
The failure of chemotherapy to effectively target cancer cells is a major problem in cancer treatment. Herein, an acidic/near-infrared (NIR) dual-triggered drug release nanoplatform, AuNR/Apt-P@DOX, based on aptamer-functionalized gold nanorods (AuNRs) was reported for actively targeted combined chemo-photothermal therapy. The nanoplatform was prepared by functionalizing AuNRs with the PD-L1 aptamer (Apt-P) and loading DOX, which could be triggered to release under weak acidic conditions and NIR stimulation. Meanwhile, the chemotherapy effect coming from DOX and AuNRs played a vital role in photothermal therapy. The MTT results showed that the fatality rate of MCF-7 cancer cells was up to 80% under the targeting effect of Apt-P. Furthermore, the tumors in mice were almost completely cured under the combined action of photothermal and chemotherapy. This targeted combination therapeutic approach could offer novel insights into the advancement of antitumor strategies for clinical translation.
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