The Core‐Shell Microneedle with Probiotic Extracellular Vesicles for Infected Wound Healing and Microbial Homeostasis Restoration

Author:

Qi Fangfang1,Xu Yujie1,Zheng Bowen2,Li Yue1,Zhang Jiarui1,Liu Zhen1,Wang Xusheng3,Zhou Zhiyang4,Zeng Dongqiang5,Lu Feng1,Zhang Chunhua1,Gan Yuyang1,Hu Zhiqi1,Wang Gaofeng16ORCID

Affiliation:

1. Department of Plastic and Aesthetic Surgery Nanfang Hospital of Southern Medical University Guangzhou 510515 China

2. Center of Plastic and Reconstructive Surgery Department of Plastic and Reconstructive Surgery Zhejiang Provincial People's Hospital of Hangzhou Medical College Hangzhou 314408 China

3. School of Pharmaceutical Sciences (Shenzhen) Shenzhen Campus of Sun Yat‐sen University Sun Yat‐sen University Shenzhen 518107 China

4. The First School of Clinical Medicine Southern Medical University Guangzhou 510515 China

5. Department of Oncology Nanfang Hospital of Southern Medical University Guangzhou Guangdong 510515 China

6. Department of Dermatology Johns Hopkins University School of Medicine Baltimore MD 21210 USA

Abstract

AbstractWound healing is a dynamic process involving the timely transition of organized phases. However, infected wounds often experience prolonged inflammation due to microbial overload. Thus, addressing the viable treatment needs across different healing stages is a critical challenge in wound management. Herein, a novel core‐shell microneedle (CSMN) patch is designed for the sequential delivery of tannic acid‐magnesium (TA‐Mg) complexes and extracellular vesicles from Lactobacillus druckerii (LDEVs). Upon application to infected sites, CSMN@TA‐Mg/LDEV releases TA‐Mg first to counteract pathogenic overload and reduce reactive oxygen species (ROS), aiding the transition to proliferative phase. Subsequently, the sustained release of LDEVs enhances the activities of keratinocytes and fibroblasts, promotes vascularization, and modulates the collagen deposition. Notably, dynamic track of microbial composition demonstrates that CSMN@TA‐Mg/LDEV can both inhibit the aggressive pathogen and increase the microbial diversity at wound sites. Functional analysis further highlights the potential of CSMN@TA‐Mg/LDEV in facilitating wound healing and skin barrier restoration. Moreover, it is confirmed that CSMN@TA‐Mg/LDEV can accelerate wound closure and improve post‐recovery skin quality in the murine infected wound. Conclusively, this innovative CSMN patch offers a rapid and high‐quality alternative treatment for infected wounds and emphasizes the significance of microbial homeostasis.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Guangzhou Municipal Science and Technology Bureau

Publisher

Wiley

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