PD-L1 Aptamer-Functionalized Gold Nanorods for Targeted Combined Chemo-Photothermal Therapy in Breast Cancer

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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Publication Details

Journal
Bioconjugate Chemistry
Published
2025-08-11
DOI
https://doi.org/10.1021/acs.bioconjchem.5c00348
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.00

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article

PD-L1 Aptamer-Functionalized Gold Nanorods for Targeted Combined Chemo-Photothermal Therapy in Breast Cancer

Hui Xu, Lu Zhao, Yunfeng Bai, Nianping Zhang et al.
Bioconjugate Chemistry
Nanoplatforms for cancer theranostics
article

PD-L1 Aptamer-Functionalized Gold Nanorods for Targeted Combined Chemo-Photothermal Therapy in Breast Cancer

Hui Xu, Lu Zhao, Yunfeng Bai, Nianping Zhang, Yanjun Li, Feng Feng, Xiaoliang Chen, Zhiqiang Bai
article en

Abstract

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.

Bioconjugate ChemistryVol. 36(8)
Kochi Medical School Hospital (JP), Shanxi Datong University (CN), Shanxi Normal University (CN)
National Natural Science Foundation of China, Shanxi Datong University, Shanxi Normal University, Program for the Scientific Activities of Selected Returned Overseas Professionals in Shaanxi Province
Good health and well-being
Openalex Percentile: Top 81%
Nanoplatforms for cancer theranostics
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