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1.
J Biomater Appl ; 32(6): 800-812, 2018 01.
Article in English | MEDLINE | ID: mdl-29137495

ABSTRACT

Due to limited self-healing capacity in cartilages, there is a rising demand for an innovative therapy that promotes chondrocyte proliferation while maintaining its biofunctionality for transplantation. Chondrocyte transplantation has received notable attention; however, the tendencies of cell de-differentiation and de-activation of biofunctionality have been major hurdles in its development, delaying this therapy from reaching the clinic. We believe it is due to the non-stimulative environment in the injured cartilage, which is unable to provide sustainable physical and biological supports to the newly grafted chondrocytes. Therefore, we evaluated whether providing an appropriate matrix to the transplanted chondrocytes could manipulate cell fate and recovery outcomes. Here, we proposed the development of electrosprayed nanoparticles composed of cartilage specific proteins, namely collagen type II and hyaluronic acid, for implantation with pre-seeded chondrocytes into articular cartilage defects. The fabricated nanoparticles were pre-cultured with chondrocytes before implantation into injured articular cartilage. The study revealed a significant potential for nanoparticles to support pre-seeded chondrocytes in cartilage repair, serving as a protein delivery system while improving the survival and biofunctionality of transplanted chondrocytes for prolonged period of time.


Subject(s)
Cartilage, Articular , Chondrocytes , Nanoparticles , Tissue Scaffolds , Animals , Biocompatible Materials/chemistry , Collagen Type II/chemistry , Male , Nanoparticles/chemistry , Rabbits , Tissue Scaffolds/chemistry
2.
Article in English | MEDLINE | ID: mdl-24111272

ABSTRACT

Collagen I is the main component of protein in bone and exhibits many excellent applications in biomedical fields. Gellan gum possesses good biocompatible, biodegradable and good mechanical property, and shows great potentials as tissue engineering scaffold or cell culture substrate. Therefore, the aim of this study was to use collagen I, gellan gum and ß-TCP to prepare collagen I/gellan gum/ß-TCP microspheres by emulsion method as bone graft substitute materials. The preliminary results showed that collagen I/gellan gum/ß-TCP microspheres had particle size distribution between 500-1000 µP in diameter and exhibited better mechanical strength. These microspheres also showed good biocompatibility in cell activity test.


Subject(s)
Bone Substitutes/chemistry , Calcium Phosphates/chemistry , Collagen Type I/chemistry , Materials Testing , Microspheres , Polysaccharides, Bacterial/chemistry , Animals , Cells, Cultured , Osteoblasts/cytology , Osteoblasts/metabolism , Rats , Rats, Sprague-Dawley
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