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Polyplex-Loaded Hydrogels for Local Gene Delivery to Human Dermal Fibroblasts
Author(s) -
José Antonio Durán,
Júlia Quintanas Yani,
Benjamin D. Almquist,
Salvador Borrós,
Nuria Oliva
Publication year - 2021
Publication title -
acs biomaterials science and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.082
H-Index - 50
ISSN - 2373-9878
DOI - 10.1021/acsbiomaterials.1c00159
Subject(s) - wound healing , self healing hydrogels , genetic enhancement , chronic wound , in vivo , wound care , medicine , transfection , debridement (dental) , population , gene delivery , plga , amputation , surgery , cell culture , materials science , gene , nanotechnology , microbiology and biotechnology , chemistry , biology , nanoparticle , genetics , environmental health , polymer chemistry , biochemistry
Impaired cutaneous healing leading to chronic wounds affects between 2 and 6% of the total population in most developed countries and it places a substantial burden on healthcare budgets. Current treatments involving antibiotic dressings and mechanical debridement are often not effective, causing severe pain, emotional distress, and social isolation in patients for years or even decades, ultimately resulting in limb amputation. Alternatively, gene therapy (such as mRNA therapies) has emerged as a viable option to promote wound healing through modulation of gene expression. However, protecting the genetic cargo from degradation and efficient transfection into primary cells remain significant challenges in the push to clinical translation. Another limiting aspect of current therapies is the lack of sustained release of drugs to match the therapeutic window. Herein, we have developed an injectable, biodegradable and cytocompatible hydrogel-based wound dressing that delivers poly(β-amino ester)s (pBAEs) nanoparticles in a sustained manner over a range of therapeutic windows. We also demonstrate that pBAE nanoparticles, successfully used in previous in vivo studies, protect the mRNA load and efficiently transfect human dermal fibroblasts upon sustained release from the hydrogel wound dressing. This prototype wound dressing technology can enable the development of novel gene therapies for the treatment of chronic wounds.

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