Literature DB >> 16409397

Evaluation of biodegradable polyesters modified by type II collagen and Arg-Gly-Asp as tissue engineering scaffolding materials for cartilage regeneration.

Shan-Hui Hsu1, Shih-Hau Chang, Hung-Jen Yen, Shu Wen Whu, Ching-Lin Tsai, David Chanhen Chen.   

Abstract

Synthetic biodegradable polyesters poly(L-lactide) (PLLA) and poly(D,L-lactide-coglycolide) (PLGA) (50:50) modified by porcine type II collagen and an Arg-Gly-Asp (RGD)-containing protein were evaluated as scaffolds for cartilage regeneration in this study. Cytocompatibility of the polymer films was tested using immortalized chondrocytes. Neocartilage formation in vitro on cell-seeded scaffolds was further examined using primary porcine chondrocytes. The inflammatory response of the scaffolds was evaluated subcutaneously in rats. A pilot animal study was conducted, in which rabbit allogeneic chondrocyte-seeded scaffolds were implanted to repair the defected rabbit knee cartilage. The results demonstrated that PLGA as well as its blends with PLLA had better cell growth than pure PLLA, and that type II collagen enhanced, but RGD inhibited cell proliferation. Scaffolds made of blended PLLA/PLGA had larger dynamic compressive modulus compared to scaffolds made of PLLA or PLGA single polymer. Chondrocyte-seeded scaffolds modified by type II collagen without RGD had the greater number of cells as well as higher glycosaminoglycan (GAG) and collagen contents compared to scaffolds without type II collagen modification or scaffolds further modified with RDG. Type II collagen modification prevented infiltration by host tissue and capsule formation. Unmodified PLLA and PLLA/PLGA constructs demonstrated persisting inflammatory response after 6 months, while all type II collagen-modified PLLA/PLGA constructs showed complete repair and no inflammation. Partial or full repair was observed after 2 months of postimplantation in type II collagen-modified PLLA/PLGA constructs, with equal cellularity and 75-80% matrix contents of a normal rabbit articular cartilage. It was concluded that PLLA/PLGA blended scaffolds modified by type II collagen were a potential tissue engineering scaffold for cartilage regeneration.

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Year:  2006        PMID: 16409397     DOI: 10.1111/j.1525-1594.2006.00179.x

Source DB:  PubMed          Journal:  Artif Organs        ISSN: 0160-564X            Impact factor:   3.094


  7 in total

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Authors:  Guillaume R Ragetly; Dominique J Griffon; Hae-Beom Lee; Yong Sik Chung
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2.  The effects of laser irradiation of cartilage on chondrocyte gene expression and the collagen matrix.

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Journal:  Lasers Surg Med       Date:  2009-09       Impact factor: 4.025

3.  Poly(ε-caprolactone)-based substrates bearing pendant small chemical groups as a platform for systemic investigation of chondrogenesis.

Authors:  Min Chen; Lei Xu; Yan Zhou; Yan Zhang; Meidong Lang; Zhaoyang Ye; Wen-Song Tan
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Review 4.  Engineering cartilage tissue.

Authors:  Cindy Chung; Jason A Burdick
Journal:  Adv Drug Deliv Rev       Date:  2007-10-05       Impact factor: 15.470

5.  Matrix-assisted autologous chondrocyte transplantation for remodeling and repair of chondral defects in a rabbit model.

Authors:  Markus T Berninger; Gabriele Wexel; Ernst J Rummeny; Andreas B Imhoff; Martina Anton; Tobias D Henning; Stephan Vogt
Journal:  J Vis Exp       Date:  2013-05-21       Impact factor: 1.355

6.  Positively and negatively modulating cell adhesion to type I collagen via peptide grafting.

Authors:  Gary A Monteiro; Anthony V Fernandes; Harini G Sundararaghavan; David I Shreiber
Journal:  Tissue Eng Part A       Date:  2009-01-27       Impact factor: 3.845

Review 7.  Extracellular matrix production in vitro in cartilage tissue engineering.

Authors:  Jie-Lin Chen; Li Duan; Weimin Zhu; Jianyi Xiong; Daping Wang
Journal:  J Transl Med       Date:  2014-04-05       Impact factor: 5.531

  7 in total

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