Synergistic ferroptosis‐starvation therapy for bladder cancer based on hyaluronic acid modified metal–organic frameworks

Author:

Wang Yu1ORCID,Xie Kunfeng1,Chen Wei2,Fang Yunze1,Mo Qixin1,Zhang Henghui1,Zhao Xinlei1,Li Dongqing1,Tan Wanlong1,Zhao Peng3,Li Fei1

Affiliation:

1. Department of Urology Nanfang Hospital, Southern Medical University Guangzhou Guangdong 510515 People's Republic of China

2. Department of Urology Zigong Fourth People's Hospital Zigong Sichuan People's Republic of China

3. Guangdong Provincial Key Laboratory of New Drug Screening, NMPA Key Laboratory for Research and Evaluation of Drug Metabolism, Guangdong Provincial Key Laboratory of Cardiac Function and Microcirculation School of Pharmaceutical Sciences, Southern Medical University Guangzhou 510515 People's Republic of China

Abstract

AbstractBladder cancer (BCa) is one of the most common malignancies of the urinary tract. Metastasis and recurrence of BCa are the leading causes of poor prognosis, and only a few patients can benefit from current first‐line treatments such as chemotherapy and immunotherapy. It is urgent to develop more effective therapeutic method with low side effects. Here, a cascade nanoreactor, ZIF‐8/PdCuAu/GOx@HA (ZPG@H), is proposed for starvation therapy and ferroptosis of BCa. The ZPG@H nanoreactor was constructed by co‐encapsulation of PdCuAu nanoparticles and glucose oxidase into zeolitic imidazolate framework‐8 (ZIF‐8) modified by hyaluronic acid. The vitro results indicated that ZPG@H enhanced intracellular reactive oxygen species levels and reduced mitochondrial depolarization in the tumor microenvironment. Therefore, the integrated advantages of starvation therapy and chemodynamic therapy endow ZPG@H with a perfect ferroptosis inducing ability. This effectiveness, combined with its excellent biocompatibility and biosafety, means that ZPG@H could make a critical contribution to the development of novel BCa treatments.

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biotechnology

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