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Inthanon K, Daranarong D, Techaikool P, et al. Biocompatibility Assessment of PLCL-Sericin Copolymer Membranes Using Wharton's Jelly Mesenchymal Stem Cells. Stem Cells Int. 2015;2016:5309484doi: 10.1155/2016/5309484.
Inthanon, K., Daranarong, D., Techaikool, P., Punyodom, W., Khaniyao, V., Bernstein, A. M., & Wongkham, W. (2016). Biocompatibility Assessment of PLCL-Sericin Copolymer Membranes Using Wharton's Jelly Mesenchymal Stem Cells. Stem cells international, 20165309484. https://doi.org/10.1155/2016/5309484
Inthanon, Kewalin, et al. "Biocompatibility Assessment of PLCL-Sericin Copolymer Membranes Using Wharton's Jelly Mesenchymal Stem Cells." Stem cells international vol. 2016 (2016): 5309484. doi: https://doi.org/10.1155/2016/5309484
Inthanon K, Daranarong D, Techaikool P, Punyodom W, Khaniyao V, Bernstein AM, Wongkham W. Biocompatibility Assessment of PLCL-Sericin Copolymer Membranes Using Wharton's Jelly Mesenchymal Stem Cells. Stem Cells Int. 2016;2016:5309484. doi: 10.1155/2016/5309484. Epub 2015 Dec 29. PMID: 26839562; PMCID: PMC4709783.
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Stem Cells Int. 2016;2016:5309484. doi: 10.1155/2016/5309484. Epub 2015 Dec 29.

Biocompatibility Assessment of PLCL-Sericin Copolymer Membranes Using Wharton's Jelly Mesenchymal Stem Cells.

Stem cells international

Kewalin Inthanon, Donraporn Daranarong, Pimwalan Techaikool, Winita Punyodom, Vorathep Khaniyao, Audrey M Bernstein, Weerah Wongkham

Affiliations

  1. The Human and Animal Cell Technology Research Unit, Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
  2. Biomedical Polymers Technology Unit, Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
  3. The Graduate School, Chiang Mai University, Chiang Mai 50200, Thailand.
  4. Departments of Ophthalmology and Pharmacology and System Therapeutics, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, P.O. Box 1183, New York, NY 10029, USA.

PMID: 26839562 PMCID: PMC4709783 DOI: 10.1155/2016/5309484

Abstract

Stem cells based tissue engineering requires biocompatible materials, which allow the cells to adhere, expand, and differentiate in a large scale. An ideal biomaterial for clinical application should be free from mammalian products which cause immune reactivities and pathogen infections. We invented a novel biodegradable poly(L-lactic-co-ε-caprolactone)-sericin (PLCL-SC) copolymer membrane which was fabricated by electrospinning. Membranes with concentrations of 2.5 or 5% (w/v) SC exhibited qualified texture characteristics with a noncytotoxic release profile. The hydrophilic properties of the membranes were 35-40% higher than those of a standard PLCL and commercial polystyrene (PS). The improved characteristics of the membranes were due to an addition of new functional amide groups, C=O, N-H, and C-N, onto their surfaces. Degradation of the membranes was controllable, depending on the content proportion of SC. Results of thermogram indicated the superior stability and crystallinity of the membranes. These membranes enhanced human Wharton's jelly mesenchymal stem cells (hWJMSC) proliferation by increasing cyclin A and also promoted cell adhesion by upregulating focal adhesion kinase (FAK). On the membranes, hWJMSC differentiated into a neuronal lineage with the occurrence of nestin. These data suggest that PLCL-SC electrospun membrane represents some properties which will be useful for tissue engineering and medical applications.

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