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2-N, 6-O-sulfated chitosan-assisted BMP-2 immobilization of PCL scaffolds for enhanced osteoinduction.
Cao, Lingyan; Yu, Yuanman; Wang, Jing; Werkmeister, Jerome A; McLean, Keith M; Liu, Changsheng.
Afiliação
  • Cao L; Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China; Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China; CSIR
  • Yu Y; Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China; Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China.
  • Wang J; Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China; Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China. Elec
  • Werkmeister JA; CSIRO Manufacturing, Bayview Avenue, Clayton, Victoria 3168, Australia.
  • McLean KM; CSIRO Manufacturing, Bayview Avenue, Clayton, Victoria 3168, Australia. Electronic address: Keith.McLean@csiro.au.
  • Liu C; Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China; Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, PR China. Elec
Mater Sci Eng C Mater Biol Appl ; 74: 298-306, 2017 May 01.
Article em En | MEDLINE | ID: mdl-28254298
ABSTRACT
The aim of this study was to develop a 2-N, 6-O-sulfated chitosan (26SCS) modified electrospun fibrous PCL scaffold for bone morphogenetic protein-2 (BMP-2) delivery to improve osteoinduction. The PCL scaffold was modified by an aminolysis reaction using ethylenediamine (ED) and 26SCS was immobilized via electrostatic interactions (PCL-N-S). Scaffolds were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle measurements. In vitro BMP-2 adsorption and release kinetics indicated that modified PCL-N-S scaffolds showed higher levels of binding of BMP-2 (about 30-100 times), moderative burst release (about one third), and prolonged releasing time compared to the unmodified PCL scaffold. The bioactivity of released BMP-2 determined by alkaline phosphatase (ALP) activity assay was maintained and improved 8-12 times with increasing concentration of immobilized 26SCS on the scaffolds. In vitro studies demonstrated that bone marrow mesenchymal stem cells (BMSCs) attached more readily to the PCL-N-S scaffolds with increased spreading. In conclusion, 26SCS modified PCL scaffolds can be a potent system for the sustained and bioactive delivery of BMP-2.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Materiais Biocompatíveis / Quitosana / Alicerces Teciduais / Proteína Morfogenética Óssea 2 Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Materiais Biocompatíveis / Quitosana / Alicerces Teciduais / Proteína Morfogenética Óssea 2 Idioma: En Ano de publicação: 2017 Tipo de documento: Article