TY - JOUR
T1 - Polyplex-Loaded Hydrogels for Local Gene Delivery to Human Dermal Fibroblasts
AU - Duran-Mota, Jose Antonio
AU - Yani, Júlia Quintanas
AU - Almquist, Benjamin D.
AU - Borrós, Salvador
AU - Oliva, Nuria
N1 - Funding Information:
N.O. acknowledges funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement 712949 (TECNIOspring PLUS) and from the Agency for Business Competitiveness of the Government of Catalonia, along with funding from an Imperial College Research Fellowship and a British Skin Foundation Small Grant Award 005/BSFSG/20. S.B. acknowledges funding from the Ministerio de Ciencia, Innovación y Universidades, project RTI2018-094734-B-C22. B.D.A acknowledges funding from the Engineering and Physical Sciences Research Council, project EP/R041628/1. We thank Dr. Meysam Keshavarz from the Hamlyn Centre at Imperial College London for assistance with SEM imaging, Jessica Rowley and Larissa Zarate-Garcia from the SAFB Flow Cytometry Core Facility for their assistance with the cytometer, and Miguel Hermida Ayala from the Department of Bioengineering at Imperial College London and Cristina Fornaguera Puigvert from the Department of Bioengineering at Institut Químic de Sarrià for assistance with confocal microscopy imaging. We also want to thank Núria Agulló Chaler for her knowledge and assistance with the rheometry experiments and Marta Guerra Rebollo for assistance with the luciferase mRNA transfection experiments.
Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/9/13
Y1 - 2021/9/13
N2 - 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 previousin vivostudies, 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.
AB - 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 previousin vivostudies, 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.
KW - gene delivery
KW - human dermal fibroblasts
KW - hydrogel
KW - nanoparticles
KW - poly(β-amino ester)s
KW - polyethylene glycol
KW - skin
KW - wound healing
UR - http://www.scopus.com/inward/record.url?scp=85108550378&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000696370300019&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1021/acsbiomaterials.1c00159
DO - 10.1021/acsbiomaterials.1c00159
M3 - Article
C2 - 34081451
AN - SCOPUS:85108550378
SN - 2373-9878
VL - 7
SP - 4347
EP - 4361
JO - ACS Biomaterials Science and Engineering
JF - ACS Biomaterials Science and Engineering
IS - 9
ER -