Docetaxel‐Encapsulated Catalytic Pt/Au Nanotubes for Synergistic Chemo‐Photothermal Therapy of Triple‐Negative Breast Cancer

Author:

Yang Haiyan123,Zhang Qian4,Dai Liwei2,Wang Yazi2,Zheng Guangrong5,Zhang Xinyue2,Zheng Di2,Ji Xiaojuan16,Sang Yutao2ORCID,Nie Zhihong2ORCID

Affiliation:

1. Department of Ultrasound Chongqing General Hospital Chongqing University Chongqing 401147 P. R. China

2. State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecule Science Fudan University Shanghai 200438 P. R. China

3. State Key Laboratory of Ultrasound in Medicine and Engineering Chongqing Medical University Chongqing 400146 P. R. China

4. Department of Materials Science and Engineering University of Maryland College Park 20742 USA

5. Department of Radiology Yan'an Hospital Affiliated to Kunming Medical University Kunming 650051 P. R. China

6. Department of ultrasound Children's Hospital of Chongqing Medical University National Clinical Research Center for Child Health and Disorders Ministry of Education Key Laboratory of Child Development and Disorders Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity Chongqing 400015 P. R. China

Abstract

AbstractThe combination of photothermal therapy with chemotherapy has emerged as a promising therapeutic modality for addressing triple‐negative breast cancer (TNBC). This manuscript describes a novel hybrid nanoplatform comprising ultrathin catalytic platinum/gold (Pt/Au) nanotubes encapsulated with docetaxel and phase‐change materials (PCMs) for the photoacoustic imaging‐guided synergistic chemo‐photothermal therapy of TNBC. Upon irradiation of near‐infrared laser, the photothermal heating of nanotubes converts solid‐state PCM into liquid, triggering the controlled release of the encapsulated docetaxel. The thin Pt layer within nanotubes enhances the nanotube's thermal stability, thus prolonging the photothermal ablation of tumors. Furthermore, platinum effectively mitigates tumor hypoxia by catalyzing the decomposition of hydrogen peroxides to generate oxygen in the tumor microenvironment, thus improving the efficiency of chemotherapy. It is demonstrated that the drug‐loaded nanotubes achieve significant tumor inhibition rates of 75.4% in vivo on 4T1 tumor‐bearing mice, significantly surpassing control groups. These nanotubes also notably extend survival, attributable to the synergistic effects of prolonged photothermal therapy facilitated by platinum and oxygenation‐enhanced chemotherapy. This combination leverages the unique properties of the Pt/Au NTs‐DTX/PCM nanoplatform, optimizing therapeutic outcomes. It is envisioned that this nanoplatform may find important applications in managing superficial malignant solid tumors in general.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

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