Nanofiber matrix formulations for the delivery of Exendin-4 for tendon regeneration:

Halloysite nanotubes Nanofiber matrix formulation Protein delivery Soft tissue regeneration

Journal

Bioactive materials
ISSN: 2452-199X
Titre abrégé: Bioact Mater
Pays: China
ID NLM: 101685294

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 11 11 2022
revised: 16 01 2023
accepted: 16 01 2023
entrez: 3 2 2023
pubmed: 4 2 2023
medline: 4 2 2023
Statut: epublish

Résumé

Tendon and ligament injuries are the most common musculoskeletal injuries, which not only impact the quality of life but result in a massive economic burden. Surgical interventions for tendon/ligament injuries utilize biological and/or engineered grafts to reconstruct damaged tissue, but these have limitations. Engineered matrices confer superior physicochemical properties over biological grafts but lack desirable bioactivity to promote tissue healing. While incorporating drugs can enhance bioactivity, large matrix surface areas and hydrophobicity can lead to uncontrolled burst release and/or incomplete release due to binding. To overcome these limitations, we evaluated the delivery of a peptide growth factor (exendin-4; Ex-4) using an enhanced nanofiber matrix in a tendon injury model. To overcome drug surface binding due to matrix hydrophobicity of poly(caprolactone) (PCL)-which would be expected to enhance cell-material interactions-we blended PCL and cellulose acetate (CA) and electrospun nanofiber matrices with fiber diameters ranging from 600 to 1000 nm. To avoid burst release and protect the drug, we encapsulated Ex-4 in the open lumen of halloysite nanotubes (HNTs), sealed the HNT tube endings with a polymer blend, and mixed Ex-4-loaded HNTs into the polymer mixture before electrospinning. This reduced burst release from ∼75% to ∼40%, but did not alter matrix morphology, fiber diameter, or tensile properties. We evaluated the bioactivity of the Ex-4 nanofiber formulation by culturing human mesenchymal stem cells (hMSCs) on matrix surfaces for 21 days and measuring tenogenic differentiation, compared with nanofiber matrices in basal media alone. Strikingly, we observed that Ex-4 nanofiber matrices accelerated the hMSC proliferation rate and elevated levels of sulfated glycosaminoglycan, tendon-related genes (Scx, Mkx, and Tnmd), and ECM-related genes (Col-I, Col-III, and Dcn), compared to control. We then assessed the safety and efficacy of Ex-4 nanofiber matrices in a full-thickness rat Achilles tendon defect with histology, marker expression, functional walking track analysis, and mechanical testing. Our analysis confirmed that Ex-4 nanofiber matrices enhanced tendon healing and reduced fibrocartilage formation versus nanofiber matrices alone. These findings implicate Ex-4 as a potentially valuable tool for tendon tissue engineering.

Identifiants

pubmed: 36733930
doi: 10.1016/j.bioactmat.2023.01.013
pii: S2452-199X(23)00013-0
pmc: PMC9876843
doi:

Types de publication

Journal Article

Langues

eng

Pagination

42-60

Subventions

Organisme : NIBIB NIH HHS
ID : R01 EB020640
Pays : United States

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

All authors have been involved in writing of the review article and each of the authors has read and concurs with the content in the review article. All authors and co-authors accept the submission of the review article without any conflict of interest.

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Auteurs

Sama Abdulmalik (S)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.

Jack Gallo (J)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.

Jonathan Nip (J)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.

Sara Katebifar (S)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.

Michael Arul (M)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.

Amir Lebaschi (A)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.

Lucas N Munch (LN)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.

Jenna M Bartly (JM)

Department of Immunology, Center on Aging, University of Connecticut Health, Farmington, CT, USA.

Shilpa Choudhary (S)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.

Ivo Kalajzic (I)

Department of Reconstructive Sciences, University of Connecticut Health, Farmington, CT, USA.

Yeshavanth Kumar Banasavadi-Siddegowdae (YK)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Syam P Nukavarapu (SP)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.
Department of Materials Science and Engineering, University of Connecticut, Storrs, CT, USA.

Sangamesh G Kumbar (SG)

Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT, USA.
Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.
Department of Materials Science and Engineering, University of Connecticut, Storrs, CT, USA.

Classifications MeSH