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  2. Morphology-Mediated Tumor Deep Penetration for Enhanced Near Infrared II Photothermal and Chemotherapy of Colorectal Cancer

Morphology-Mediated Tumor Deep Penetration for Enhanced Near Infrared II Photothermal and Chemotherapy of Colorectal Cancer

  • ACS Nano. 2024 Oct 15;18(41):28038-28051. doi: 10.1021/acsnano.4c07085.
Zhenyu Wang 1 2 Qianyi Su 1 Wenjia Deng 1 Xiao Wang 1 Huimin Zhou 1 Miaomiao Zhang 1 Wenbin Lin 3 Jisheng Xiao 1 2 Xiaopin Duan 1
Affiliations

Affiliations

  • 1 Department of General Surgery, Zhujiang Hospital; Cancer Research Institute, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • 2 Department of Cardiology, Heart Center, Guangdong Provincial Biomedical Engineering Technology Research, Center for Cardiovascular Disease, Translational Medicine Research Center, Zhujiang Hospital, Southern Medical University, Guangzhou 510280, China.
  • 3 Departments of Chemistry and Radiation and Cellular Oncology and the Ludwig Center for Metastasis Research, The University of Chicago, Chicago, Illinois 60637, United States.
Abstract

The low permeability and heterogeneous distribution of drugs (including nanomedicines) have limited their deep penetration into solid tumors. Herein we report the design of gold nanoparticles with virus-like spikes (AuNVs) to mimic viral shapes and facilitate tumor penetration. Mechanistic studies revealed that AuNVs mainly entered cells through macropinocytosis, then transported to the Golgi/endoplasmic reticulum system via Rab11-regulated pathway, and finally exocytosed through recycling endosomes, leading to high cellular uptake, effective transcytosis, and deep tumor penetration compared to gold nanospheres (AuNPs) and gold nanostars (AuNSs). The high tumor accumulation and deep tumor penetration of mitoxantrone (MTO) facilitated by AuNVs endowed effective chemophotothermal therapy when exposed to a near-infrared II laser, significantly reducing tumor sizes in a mouse model of colorectal Cancer. This study reveals a potent mechanism of viral-like structures in tissue penetration and highlights their potential as effective drug delivery carriers.

Keywords

cancer treatment; intracellular trafficking; transcytosis; tumor infiltration; virus-like nanoparticles.

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  • HY-D0938
    99.01%, Cell Proliferation Fluorescent Probe