Literature DB >> 12809780

Rat costochondral cell characteristics on poly (L-lactide-co-epsilon-caprolactone) scaffolds.

M Honda1, N Morikawa, K Hata, T Yada, S Morita, M Ueda, K Kimata.   

Abstract

This study was designed to examine the adhesion, proliferation, and morphology of chondrocytes on new scaffolds; and to examine these cells histologically for the ability of the chondrocytes to maintain chondrogenic properties after subcutaneous implantation into nude mice. Both 75:25 poly (L-lactide-co-epsilon-caprolactone) (75PLC) and 50:50 poly (L-lactide-co-epsilon-capro-lactone) scaffold (50PLC) were tested as a scaffold for rat costochondral resting zone chondrocytes in comparison with a type I collagen sponge scaffold (collagen scaffold). Both of the poly (L-lactide-co-epsilon-caprolactone) scaffolds (75PLC and 50PLC) were coated with type I collagen solution and the effects of the collagen coat (hybrid-PLC) were also examined. The hybrid-75PLC bound the same number of cells as the collagen scaffold, whereas the 75PLC and the 50PLC bound 60% and 50% fewer cells than the collagen scaffold, respectively. The cell growth on the scaffolds progressed with culture time in all scaffolds. Cell morphology was assessed by scanning electron microscopy for differences in the structure of cellular interaction. Chondrocytes on every scaffold maintained a spherical shape. The hybrid-PLCs were superior to the PLCs with respect to the number of cells attached. The PLCs had an advantageous degradation characteristic in that they retained their original shape better than the collagen scaffold. Additionally, in the PLCs seeded, the cells retained their integrity 4 weeks after implantation, although the volume of collagen scaffold decreased by 50%.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12809780     DOI: 10.1016/s0142-9612(03)00210-2

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  6 in total

Review 1.  Functional tooth regenerative therapy: tooth tissue regeneration and whole-tooth replacement.

Authors:  Masamitsu Oshima; Takashi Tsuji
Journal:  Odontology       Date:  2014-07-23       Impact factor: 2.634

2.  Novel osteoconductive β-tricalcium phosphate/poly(L-lactide-co-e-caprolactone) scaffold for bone regeneration: a study in a rabbit calvarial defect.

Authors:  Hanna Pihlman; Pauli Keränen; Kaarlo Paakinaho; Jere Linden; Markus Hannula; Iida-Kaisa Manninen; Jari Hyttinen; Mikko Manninen; Outi Laitinen-Vapaavuori
Journal:  J Mater Sci Mater Med       Date:  2018-10-08       Impact factor: 3.896

3.  Local regeneration of dentin-pulp complex using controlled release of fgf-2 and naturally derived sponge-like scaffolds.

Authors:  Chiaki Kitamura; Tatsuji Nishihara; Masamichi Terashita; Yasuhiko Tabata; Ayako Washio
Journal:  Int J Dent       Date:  2011-11-17

4.  RGD peptide and graphene oxide co-functionalized PLGA nanofiber scaffolds for vascular tissue engineering.

Authors:  Yong Cheol Shin; Jeonghyo Kim; Sung Eun Kim; Su-Jin Song; Suck Won Hong; Jin-Woo Oh; Jaebeom Lee; Jong-Chul Park; Suong-Hyu Hyon; Dong-Wook Han
Journal:  Regen Biomater       Date:  2017-02-07

Review 5.  Advances in Biodegradable 3D Printed Scaffolds with Carbon-Based Nanomaterials for Bone Regeneration.

Authors:  Sara Lopez de Armentia; Juan Carlos Del Real; Eva Paz; Nicholas Dunne
Journal:  Materials (Basel)       Date:  2020-11-11       Impact factor: 3.623

6.  A biodegradable, sustained-released, prednisolone acetate microfilm drug delivery system effectively prolongs corneal allograft survival in the rat keratoplasty model.

Authors:  Yu-Chi Liu; Yan Peng; Nyein Chan Lwin; Subbu S Venkatraman; Tina T Wong; Jodhbir S Mehta
Journal:  PLoS One       Date:  2013-08-05       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.