Thread Size and Polymer Composition of 3D Printed and Electrospun Wound Dressings Affect Wound Healing Outcomes in an Excisional Wound Rat Model.


Journal

Biomacromolecules
ISSN: 1526-4602
Titre abrégé: Biomacromolecules
Pays: United States
ID NLM: 100892849

Informations de publication

Date de publication:
12 10 2020
Historique:
pubmed: 10 9 2020
medline: 22 6 2021
entrez: 9 9 2020
Statut: ppublish

Résumé

Thread size and polymer composition are critical properties to consider for achieving a positive healing outcome with a wound dressing. Three-dimensional (3D) printed scaffolds and electrospun mats both offer distinct advantages as replaceable wound dressings. This research aims to determine if the thread size and polymer compositions of the scaffolds affect skin wound healing outcomes, an aspect that has not been adequately explored. Using a modular polymer platform, four polyester direct-write 3D printed scaffolds and electrospun mats were fabricated into wound dressings. The dressings were applied to splinted, full thickness skin wounds in an excisional wound rat model and evaluated against control wounds to which no dressing was applied. Wound closure rates and reduction of the wound bed width were not affected by the thread size or polymer composition. However, epidermal thickness was larger in wounds treated with electrospun dressings and was slightly affected by the polymer composition. Two of the four tested polymer compositions lead to delayed reorganization of granulation tissues. Moreover, enhanced angiogenesis was seen in wounds treated with 3D printed dressings compared to those treated with electrospun dressings. The results from this study can be used to inform the choice of dressing architecture and polymer compositions to achieve positive wound healing outcomes.

Identifiants

pubmed: 32902971
doi: 10.1021/acs.biomac.0c00801
doi:

Substances chimiques

Polyesters 0
Polymers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

4030-4042

Subventions

Organisme : NIDCR NIH HHS
ID : R01 DE026117
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States

Auteurs

Nicholas Nun (N)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

Megan Cruz (M)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

Tanmay Jain (T)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

Yen-Ming Tseng (YM)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

Josh Menefee (J)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

Samreen Jatana (S)

Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44106, United States.

Pritam S Patil (PS)

Department of Chemical, Biomolecular and Corrosion Engineering, The University of Akron, Akron, Ohio 44325, United States.

Nic D Leipzig (ND)

Department of Chemical, Biomolecular and Corrosion Engineering, The University of Akron, Akron, Ohio 44325, United States.

Christine McDonald (C)

Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44106, United States.

Edward Maytin (E)

Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland Ohio 44106, United States.
Department of Dermatology, Dermatology and Plastic Surgery Institute, Cleveland Clinic, Cleveland, Ohio 44106, United States.

Abraham Joy (A)

Department of Polymer Science, The University of Akron, Akron, Ohio 44325, United States.

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Classifications MeSH