PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
March 15, 2026ACS Nano2 citations

Bioorthogonal Click-Engineered Microneedle Patch Enables Adeno-Associated Virus-Mediated Dermal Acidic Fibroblast Growth Factor Expression for Hair Loss Treatment

View Full Paper
AZAnwei ZhouYZYu ZhangCollaborative Innovation Center of Advanced MicrostructuresWCWeiwei ChenCollaborative Innovation Center of Advanced Microstructures

Key Points

  • The research investigates a novel microneedle patch designed for effective hair loss treatment through gene therapy.
  • Developed a bioorthogonal click-engineered microneedle patch for drug delivery.
  • Used adeno-associated virus (AAV) encoding aFGF for localized therapy.
  • Evaluated in murine models of alopecia for efficacy on hair follicle regeneration.
  • The microneedle patch improved hair-follicle regeneration significantly compared to controls.
  • Enhanced dermal angiogenesis was observed following treatment with the patch.
  • A single treatment maintained prolonged aFGF expression and supportive follicular architecture.

Abstract

Hair loss is a prevalent dermatological disorder with limited durable therapies. Although acidic fibroblast growth factor (aFGF) promotes hair regeneration, its poor bioavailability and rapid degradation constrain efficacy. Here, we report a bioorthogonal click-engineered microneedle patch (ClickMNP) that enables efficient intradermal delivery of adeno-associated virus encoding aFGF (AAV-aFGF) for localized, sustained transgene expression. ClickMNP is constructed by synthesizing dibenzocyclooctyne-modified hyaluronic acid (HA-DBCO) that undergoes strain-promoted azide-alkyne cycloaddition (SPAAC) with an azide-functionalized poly(lactide-co-glycolide) (PLGA-N3) microneedle matrix, forming a cross-linked hydrogel network on the microneedle surface that immobilizes AAV while retaining infectivity, thereby creating a chemically robust, biologically active microneedle-virus interface for dermal gene transfer. Following intradermal application, ClickMNP breaches the stratum corneum and establishes a sustained viral depot that drives prolonged aFGF expression, addressing the low exposure and rapid clearance inherent to protein administration. In murine alopecia models, a single ClickMNP administration accelerates hair-follicle regeneration, enhances dermal angiogenesis, and prolongs anagen, outperforming free AAV-aFGF and recombinant aFGF controls. The platform preserves follicle viability and sustains regrowth across repeated depilation cycles, yielding native-like follicular architecture with increased indices of de novo folliculogenesis. Biocompatibility assessment indicates favorable local tolerability, and transcriptomic analysis reveals upregulation of pathways associated with fibroblast proliferation, angiogenesis, and follicular cycling, consistent with the observed phenotype. Collectively, ClickMNP establishes a versatile bioorthogonal microneedle-virus interface strategy that combines chemical engineering with gene therapy, offering a transformative solution for hair loss and broader cutaneous indications.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Zhou et al. (2026) studied this question.

synapsesocial.com/papers/69b5ff6e83145bc643d1bfcbhttps://doi.org/10.1021/acsnano.5c21849
Ask AI
Helpful
Bookmark
Share
View Full Paper