4.8 Article

Fully armed photodynamic therapy with spear and shear for topical deep hypertrophic scar treatment

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 343, Issue -, Pages 408-419

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2022.01.043

Keywords

Hypertrophic scar; Microneedle; Hyaluronidase; Photodynamic therapy; Autophagy

Funding

  1. National Natural Science Foundation of China [82104071]
  2. Fundamental Research Funds for the Central Universities [21620356]
  3. Key Areas Research and Development Pro-gram of Guangdong Province [2019B020204002]
  4. Key Areas Research and Development Program of Guangzhou [202007020006]
  5. Basic and Applied Basic Research Project of Guangzhou Basic Research Program [202102020703]
  6. Natural Science Foundation of Guangdong Province [2021A1515012525]

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This study proposes a novel photodynamic therapy that utilizes hyaluronidase and metformin to enhance therapeutic efficacy. By improving the stiffness and permeability of dissolving microneedles, the photosensitizer can penetrate deep lesions more effectively. Meanwhile, metformin can intervene in cellular respiration and autophagy process, amplifying the effectiveness of photodynamic therapy.
5-aminolevulinic acid (ALA)-mediated photodynamic therapy (PDT) has emerged as a promising therapy for hypertrophic scar (HS). However, the poor permeability of ALA across biological barriers and pro-survival autophagy of fibroblasts largely restricted the efficacy of PDT. Herein, PDT was well equipped with spear and shear to overcome the therapeutic resistance. Specifically, hyaluronidase (HAase) based dissolving microneedles (MN)with improved stiffness and permeability were developed as a spear to deliver ALA into deep lesions by combating the dual barriers of stratum corneum and dense extracellular matrix (ECM). Besides, metformin (Met) MN was applied as a shear to intervene the respiration and autophagic process for amplified PDT. HAase significantly enhanced the in vitro and in vivo transdermal delivery efficiency of ALA, while the combination of HAase and Met successfully amplified the anti-scarring efficacy of PDT by elevating cytotoxicity, promoting permeation, activating signal pathways, and interdicting the autophagy process simultaneously. The pharmacodynamics study revealed that the combination therapy achieved the lowest scar elevation index (SEI), downregulated expression of collagen I and TGF-131, and decreased LC3 II/I ratio, showing excellent therapeutic efficacy. Therefore, such a fully armed PDT integrating double-prolonged attack on the physiological and pathological barriers offers a promising topical treatment for deep HS.

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