Piezocatalytic 2D WS2 Nanosheets for Ultrasound‐Triggered and Mitochondria‐Targeted Piezodynamic Cancer Therapy Synergized with Energy Metabolism‐Targeted Chemotherapy

Author:

Truong Hoang Quan1,Huynh Kim Anh2,Nguyen Cao Thuy Giang1,Kang Ji Hee3,Dang Xuan Nghia2,Ravichandran Vasanthan1,Kang Han Chang4,Lee Minjong5,Kim Jong‐Eun6,Ko Young Tag3,Lee Tae Il2,Shim Min Suk1ORCID

Affiliation:

1. Department of Nano‐Bioengineering Incheon National University Incheon 22012 Republic of Korea

2. Department of Materials Science and Engineering Gachon University Seongnam Gyeonggi‐Do 13306 Republic of Korea

3. College of Pharmacy Gachon University Incheon 21936 Republic of Korea

4. Department of Pharmacy Integrated Research Institute of Pharmaceutical Sciences and BK21 PLUS Team for Creative Leader Program for Pharmacomics‐based Future Pharmacy College of Pharmacy The Catholic University of Korea Gyeonggi‐do 14662 Republic of Korea

5. Department of Internal Medicine Ewha Womans University College of Medicine Seoul 07804 Republic of Korea

6. Department of Prosthodontics Yonsei University College of Dentistry Seoul 03722 Republic of Korea

Abstract

AbstractPiezoelectric nanomaterials that can generate reactive oxygen species (ROS) by piezoelectric polarization under an external mechanical force have emerged as an effective platform for cancer therapy. In this study, piezoelectric 2D WS2 nanosheets are functionalized with mitochondria‐targeting triphenylphosphonium (TPP) for ultrasound (US)‐triggered, mitochondria‐targeted piezodynamic cancer therapy. In addition, a glycolysis inhibitor (FX11) that can inhibit cellular energy metabolism is loaded into TPP‐ and poly(ethylene glycol) (PEG)‐conjugated WS2 nanosheet (TPEG‐WS2) to potentiate its therapeutic efficacy. Upon US irradiation, the sono‐excited electrons and holes generated in the WS2 are efficiently separated by piezoelectric polarization, which subsequently promotes the production of ROS. FX11‐loaded TPEG‐WS2 (FX11@TPEG‐WS2) selectively accumulates in the mitochondria of human breast cancer cells. In addition, FX11@TPEG‐WS2 effectively inhibits the production of adenosine triphosphate . Thus, FX11@TPEG‐WS2 exhibits outstanding anticancer effects under US irradiation. An in vivo study using tumor‐xenograft mice demonstrates that FX11@TPEG‐WS2 effectively accumulated in the tumors. Its tumor accumulation is visualized using in vivo computed tomography . Notably, FX11@TPEG‐WS2 with US irradiation remarkably suppresses the tumor growth of mice without systemic toxicity. This study demonstrates that the combination of piezodynamic therapy and energy metabolism‐targeted chemotherapy using mitochondria‐targeting 2D WS2 is a novel strategy for the selective and effective treatment of tumors.

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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