Ni–Cu Bimetallic Nanozyme and Minoxidil Co-Loaded Dissolving Microneedles Reshape Hair Follicle Microenvironment for Androgenic Alopecia Treatment

Androgenetic alopecia (AGA) is a prevalent dermatological disorder. Conventional minoxidil (MXD)-based therapies suffer from limitations such as low bioavailability and frequent dosing, necessitating the development of safer and more effective treatment strategies. Herein, we developed a dissolvable microneedle system (NC&MXD MNs) coloaded with nickel–copper nanozymes (NC) and MXD, which remodels the hair follicle microenvironment through synergistic dual-functional reactive oxygen species (ROS) scavenging and mechanostimulation-enhanced angiogenesis. The NC nanozymes demonstrated remarkable SOD-like and CAT-like activities, efficiently decomposing H2O2 into O2, while the microneedles achieved rapid drug release with a transdermal efficiency of 83.4% (penetration depth: 200–300 μm). Moreover, the mechanical stimulation from microneedles promoted angiogenesis and improved local blood flow. In AGA mouse models, NC&MXD MNs enhanced hair regeneration coverage to 93.7% (vs 85.1% for MXD alone), increased Ki67+ cell proliferation by 1.9-fold, and significantly thickened regenerated hair diameter. Additionally, this system reduced ROS levels by 2.3-fold and increased CD31+ vascular density by 40%, markedly improving the microenvironment. The proposed nanozyme-microneedle combinatorial strategy offers a safe, minimally invasive, and highly effective therapeutic approach for AGA.

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Publication Details

Journal
ACS Applied Nano Materials
Published
2025-04-28
DOI
https://doi.org/10.1021/acsanm.5c01140
Citations
7
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
5.54

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article

Ni–Cu Bimetallic Nanozyme and Minoxidil Co-Loaded Dissolving Microneedles Reshape Hair Follicle Microenvironment for Androgenic Alopecia Treatment

Xiangdong Kong, Yongjia Zhang, Ruibo Zhao, Xianan Li et al.
7 citations
ACS Applied Nano Materials
Advancements in Transdermal Drug Delivery
5.54
article

Ni–Cu Bimetallic Nanozyme and Minoxidil Co-Loaded Dissolving Microneedles Reshape Hair Follicle Microenvironment for Androgenic Alopecia Treatment

Xiangdong Kong, Yongjia Zhang, Ruibo Zhao, Xianan Li, Han Zhang, Beibei Wang, Shibo Wang, Xiaoli Zhou, Mengcheng Tang
article en
7 citations

Abstract

Androgenetic alopecia (AGA) is a prevalent dermatological disorder. Conventional minoxidil (MXD)-based therapies suffer from limitations such as low bioavailability and frequent dosing, necessitating the development of safer and more effective treatment strategies. Herein, we developed a dissolvable microneedle system (NC&MXD MNs) coloaded with nickel–copper nanozymes (NC) and MXD, which remodels the hair follicle microenvironment through synergistic dual-functional reactive oxygen species (ROS) scavenging and mechanostimulation-enhanced angiogenesis. The NC nanozymes demonstrated remarkable SOD-like and CAT-like activities, efficiently decomposing H2O2 into O2, while the microneedles achieved rapid drug release with a transdermal efficiency of 83.4% (penetration depth: 200–300 μm). Moreover, the mechanical stimulation from microneedles promoted angiogenesis and improved local blood flow. In AGA mouse models, NC&MXD MNs enhanced hair regeneration coverage to 93.7% (vs 85.1% for MXD alone), increased Ki67+ cell proliferation by 1.9-fold, and significantly thickened regenerated hair diameter. Additionally, this system reduced ROS levels by 2.3-fold and increased CD31+ vascular density by 40%, markedly improving the microenvironment. The proposed nanozyme-microneedle combinatorial strategy offers a safe, minimally invasive, and highly effective therapeutic approach for AGA.

ACS Applied Nano MaterialsVol. 8(18)
Zhejiang Sci-Tech University (CN), Smart Material (Germany) (DE), Division of Materials Science and Engineering (AU)
National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province
Zero hunger
Openalex Percentile: Top 4%
Advancements in Transdermal Drug Delivery
5.54
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