Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage

Abstract Exposure to ultraviolet (UV) radiation compromises both the aesthetic and functional properties of the skin, accelerates aging, increases the risk of skin cancer, and significantly impairs quality of life. Exosomes derived from human umbilical cord mesenchymal stem cells (hUMSC-Exo) and nat...

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Published in:Journal of Nanobiotechnology
Main Authors: Chenhui He, Zeqian Wang, Zhaoting Jiang, Yuqi Zhou, Xiaoqi Chen, Jia Zhang, Bo Wang, Qi Wang, Tong Wu, Chunying Li, Zhe Jian
Format: Article
Language:English
Published: BMC 2025-10-01
Subjects:
Online Access:https://doi.org/10.1186/s12951-025-03735-x
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author Chenhui He
Zeqian Wang
Zhaoting Jiang
Yuqi Zhou
Xiaoqi Chen
Jia Zhang
Bo Wang
Qi Wang
Tong Wu
Chunying Li
Zhe Jian
author_facet Chenhui He
Zeqian Wang
Zhaoting Jiang
Yuqi Zhou
Xiaoqi Chen
Jia Zhang
Bo Wang
Qi Wang
Tong Wu
Chunying Li
Zhe Jian
author_sort Chenhui He
collection DOAJ
container_title Journal of Nanobiotechnology
description Abstract Exposure to ultraviolet (UV) radiation compromises both the aesthetic and functional properties of the skin, accelerates aging, increases the risk of skin cancer, and significantly impairs quality of life. Exosomes derived from human umbilical cord mesenchymal stem cells (hUMSC-Exo) and natural compounds such as epigallocatechin gallate (EGCG) show great therapeutic potential for UV-induced skin damage. However, their efficacy is often limited by poor stability, low bioavailability, and inefficient skin penetration. In this study, we show that hUMSC-Exo and EGCG act synergistically to reduce oxidative stress and exert potent anti-inflammatory effects. By incorporating these agents into a microneedle-based delivery system, we achieved efficient transdermal co-delivery, which significantly enhanced the repair of UV-induced skin injury. The treatment markedly attenuated inflammatory responses, reduced DNA damage, and promoted tissue regeneration. These findings suggest that hUMSC-Exo/EGCG-loaded microneedles provide a simple yet effective strategy for treating UV-induced skin damage and aging, with potential applicability to a broader range of inflammatory skin conditions.
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spelling doaj-art-820fcceedde44ffdbe45e5f14941deff2025-10-12T11:48:18ZengBMCJournal of Nanobiotechnology1477-31552025-10-0123111910.1186/s12951-025-03735-xMicroneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damageChenhui He0Zeqian Wang1Zhaoting Jiang2Yuqi Zhou3Xiaoqi Chen4Jia Zhang5Bo Wang6Qi Wang7Tong Wu8Chunying Li9Zhe Jian10Department of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityDepartment of Dermatology, Xijing Hospital, Fourth Military Medical UniversityAbstract Exposure to ultraviolet (UV) radiation compromises both the aesthetic and functional properties of the skin, accelerates aging, increases the risk of skin cancer, and significantly impairs quality of life. Exosomes derived from human umbilical cord mesenchymal stem cells (hUMSC-Exo) and natural compounds such as epigallocatechin gallate (EGCG) show great therapeutic potential for UV-induced skin damage. However, their efficacy is often limited by poor stability, low bioavailability, and inefficient skin penetration. In this study, we show that hUMSC-Exo and EGCG act synergistically to reduce oxidative stress and exert potent anti-inflammatory effects. By incorporating these agents into a microneedle-based delivery system, we achieved efficient transdermal co-delivery, which significantly enhanced the repair of UV-induced skin injury. The treatment markedly attenuated inflammatory responses, reduced DNA damage, and promoted tissue regeneration. These findings suggest that hUMSC-Exo/EGCG-loaded microneedles provide a simple yet effective strategy for treating UV-induced skin damage and aging, with potential applicability to a broader range of inflammatory skin conditions.https://doi.org/10.1186/s12951-025-03735-xMicroneedlesExosomesEGCGSkin photodamage
spellingShingle Chenhui He
Zeqian Wang
Zhaoting Jiang
Yuqi Zhou
Xiaoqi Chen
Jia Zhang
Bo Wang
Qi Wang
Tong Wu
Chunying Li
Zhe Jian
Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
Microneedles
Exosomes
EGCG
Skin photodamage
title Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
title_full Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
title_fullStr Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
title_full_unstemmed Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
title_short Microneedles combining delivery of hUMSC-derived exosomes and EGCG mitigate UV-induced skin damage
title_sort microneedles combining delivery of humsc derived exosomes and egcg mitigate uv induced skin damage
topic Microneedles
Exosomes
EGCG
Skin photodamage
url https://doi.org/10.1186/s12951-025-03735-x
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