(2018) Bulk Synthesis of Monodisperse and Highly Biocompatible Poly(-caprolactone)-diol by Transesterification Side-Reactions. Polymer-Plastics Technology and Engineering. pp. 492-499. ISSN 0360-2559
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Bulk Synthesis of Monodisperse and Highly Biocompatible Poly(ɛ-caprolactone)-diol by Transesterification Side-Reactions.pdf Download (1MB) |
Abstract
Ring-opening polymerization of epsilon-caprolactone was performed at 130 degrees C, under partial vacuum in the presence of stannous octoate as the catalyst and 1,4-butanediol as the initiator. After the termination of polymerization by deionized water, a hydroxyl group formed at the end of the polymer chains. Structure of the synthetic poly(epsilon-caprolactone)-diols (PCL-diol), molecular weight, polydispersity index, and Cell viability were evaluated. Very narrow distribution in the molecular weight obtained for PCL-diols is due to a new method for synthesis. It was shown that by the increase in PCL-diols, the compatibility of human mesenchymal stem cells grew up. GRAPHICS .
Item Type: | Article |
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Keywords: | Biocompatible MTT assay polycaprolactone diol transesterification ring-opening polymerization poly-epsilon-caprolactone mechanical-properties polycaprolactone scaffolds tissue chitosan blends degradation composites behavior Polymer Science |
Divisions: | |
Page Range: | pp. 492-499 |
Journal or Publication Title: | Polymer-Plastics Technology and Engineering |
Journal Index: | ISI |
Volume: | 57 |
Number: | 6 |
Identification Number: | https://doi.org/10.1080/03602559.2016.1211690 |
ISSN: | 0360-2559 |
Depositing User: | مهندس مهدی شریفی |
URI: | http://eprints.bmsu.ac.ir/id/eprint/4058 |
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