In vitro and in vivo evaluations of Loofah (Luffa cylindrica) micro- and PHBV nanofiber-integrated hydrogel scaffolds for meniscus regeneration


Baysan G., AKDOĞAN E. K., Gunes O. C., Yilmaz P. A., Ozenler A. K., Husemoglu R. B., ...Daha Fazla

Journal of Materials Science, cilt.60, 2025 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 60
  • Basım Tarihi: 2025
  • Doi Numarası: 10.1007/s10853-025-11127-7
  • Dergi Adı: Journal of Materials Science
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Applied Science & Technology Source, Chemical Abstracts Core, Chimica, Communication Abstracts, Compendex, Computer & Applied Sciences, INSPEC, MEDLINE, Metadex, Public Affairs Index, Civil Engineering Abstracts
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

This study focuses on developing a composite hydrogel scaffold for meniscus regeneration by integrating loofah (Luffa cylindrica) microfibers and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanofibers as cell adhesion sites and mechanical reinforcements into a biomimetic collagen/chitosan matrix Scaffolds were chemically cross-linked with a natural cross-linker genipin (0.1%, 0.3%, 0.5%) and fabricated via freeze-drying to achieve optimal porosity and mechanical stability. The 0.3% genipin-cross-linked composite hydrogel scaffold (PL/ChtCol-3) demonstrated the highest compressive strength, damping capacity, and water absorption, and was selected for biocompatibility evaluation. In vitro studies using rabbit bone marrow-derived mesenchymal stem cells (rMSCs) confirmed the scaffold’s nontoxicity and biocompatibility, promoting cell attachment, proliferation, and type II collagen expression. In vivo analysis was conducted using a standardized meniscus defect model in 24 New Zealand rabbits, divided into three groups: empty defect, cell-free scaffold, and cell-laden scaffold. Postimplantation assessments, including Micro-CT, biomechanical, histological, and immunohistochemical analyses showed that the cell-laden PL/ChtCol-3 scaffold significantly enhanced meniscus regeneration. Notably, it reduced defect volume and restored compressive modulus to levels comparable with native tissue. These findings demonstrate that the PL/ChtCol-3 scaffold, particularly when combined with rMSCs, holds strong potential as a biomimetic and regenerative platform for meniscus tissue engineering.