Smart Microneedle Arrays Integrating Cell‐Free Therapy and Nanocatalysis to Treat Liver Fibrosis

Author:

Xu Yanteng1,Zhang Yixin1,Tian Hao12,Zhong Qingguo1,Yi Ke1,Li Fenfang1,Xue Tiantian1,Wang Haixia1,Lao Yeh‐Hsing3,Xu Yingying45,Li Yinxiong45,Long Ling2,Li Kai1,Tao Yu16,Li Mingqiang16ORCID

Affiliation:

1. Laboratory of Biomaterials and Translational Medicine Center for Nanomedicine and Department of Ultrasound The Third Affiliated Hospital Sun Yat‐sen University Guangzhou 510630 China

2. Department of Neurology The Third Affiliated Hospital Sun Yat‐sen University Guangzhou 510630 China

3. Department of Pharmaceutical Sciences University at Buffalo The State University of New York Buffalo NY 14214 USA

4. Center for Health Research Guangzhou Institutes of Biomedicine and Health Chinese Academy of Sciences Guangzhou 510530 China

5. University of China Academy of Sciences Beijing 100049 China

6. Guangdong Provincial Key Laboratory of Liver Disease Guangzhou 510630 China

Abstract

AbstractLiver fibrosis is a chronic pathological condition lacking specific clinical treatments. Stem cells, with notable potential in regenerative medicine, offer promise in treating liver fibrosis. However, stem cell therapy is hindered by potential immunological rejection, carcinogenesis risk, efficacy variation, and high cost. Stem cell secretome‐based cell‐free therapy offers potential solutions to address these challenges, but it is limited by low delivery efficiency and rapid clearance. Herein, an innovative approach for in situ implantation of smart microneedle (MN) arrays enabling precisely controlled delivery of multiple therapeutic agents directly into fibrotic liver tissues is developed. By integrating cell‐free and platinum‐based nanocatalytic combination therapy, the MN arrays can deactivate hepatic stellate cells. Moreover, they promote excessive extracellular matrix degradation by more than 75%, approaching normal levels. Additionally, the smart MN arrays can provide hepatocyte protection while reducing inflammation levels by ≈70–90%. They can also exhibit remarkable capability in scavenging almost 100% of reactive oxygen species and alleviating hypoxia. Ultimately, this treatment strategy can effectively restrain fibrosis progression. The comprehensive in vitro and in vivo experiments, supplemented by proteome and transcriptome analyses, substantiate the effectiveness of the approach in treating liver fibrosis, holding immense promise for clinical applications.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Primary Health Care Foundation

Recruitment Program of Global Experts

Guangdong Provincial Pearl River Talents Program

Publisher

Wiley

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