(2018) Bulk Synthesis of Monodisperse and Highly Biocompatible Poly(ɛ-caprolactone)-diol by Transesterification Side-Reactions. Polymer - Plastics Technology and Engineering. pp. 492-499. ISSN 03602559 (ISSN)
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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 ε-caprolactone was performed at 130°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(ε-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. © 2018 Taylor & Francis.
Item Type: | Article |
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Keywords: | Biocompatible MTT assay polycaprolactone diol transesterification Biocompatibility Cell culture Deionized water Molecular weight Polycaprolactone Stem cells Human mesenchymal stem cells MTT assays Narrow distribution Poly (epsiloncaprolactone) Polycaprolactone diols Polydispersity indices Stannous octoate Ring opening polymerization |
Divisions: | |
Page Range: | pp. 492-499 |
Journal or Publication Title: | Polymer - Plastics Technology and Engineering |
Journal Index: | Scopus |
Volume: | 57 |
Number: | 6 |
Identification Number: | https://doi.org/10.1080/03602559.2016.1211690 |
ISSN: | 03602559 (ISSN) |
Depositing User: | مهندس مهدی شریفی |
URI: | http://eprints.bmsu.ac.ir/id/eprint/653 |
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