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Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation

BACKGROUND: The best solvent type and ratio for grafting of poly-n-isopropylacrylamide (PNIPAAm) on the surface of polystyrene is obtained under ultraviolet radiation. In this study, the effects of solvents, such as water, methanol, and their combinations, under ultraviolet radiation were investigat...

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Autores principales: Biazar, Esmaeil, Khorasani, MT, Daliri, M
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044182/
https://www.ncbi.nlm.nih.gov/pubmed/21383854
http://dx.doi.org/10.2147/IJN.S15371
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author Biazar, Esmaeil
Khorasani, MT
Daliri, M
author_facet Biazar, Esmaeil
Khorasani, MT
Daliri, M
author_sort Biazar, Esmaeil
collection PubMed
description BACKGROUND: The best solvent type and ratio for grafting of poly-n-isopropylacrylamide (PNIPAAm) on the surface of polystyrene is obtained under ultraviolet radiation. In this study, the effects of solvents, such as water, methanol, and their combinations, under ultraviolet radiation were investigated successfully. METHOD AND RESULTS: Attenuated total reflection Fourier transform infrared analysis showed the existence of the graft PNIPAAm on the substrate for all samples resolved in solvents. The best solvent ratio and NIPAAm concentration for grafting was obtained with 40% NIPAAm concentrations resolved in a solvent of 9:1 (v/v) water/methanol (120%). Scanning electron microscopic and atomic force microscopic images clearly showed that a 10% increase of methanol to water would increase the amount of grafting. Surface topography and graft thickness in atomic force microscopic images of the grafted samples showed that the thickness of these grafts was about 600 nm. The drop water contact angles of the best grafted sample at 37°C and 4°C were 43.3° and 60.4°, respectively, which demonstrated the hydrophilicity and hydrophobicity of the grafted surfaces. Differential scanning calorimetric analysis also revealed the low critical solution temperature of the grafted sample to be 32°C. Thermoresponsive polymers were grafted to dishes covalently, which allowed epithelial cells to attach and proliferate at 37°C. The cells were also detached spontaneously without using enzymes when the temperature dropped below 4°C. CONCLUSION: MTT analysis also showed good viability of cells on the grafted samples, suggesting that this type of grafted material had potential as a biomaterial for cell sheet engineering.
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spelling pubmed-30441822011-03-07 Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation Biazar, Esmaeil Khorasani, MT Daliri, M Int J Nanomedicine Original Research BACKGROUND: The best solvent type and ratio for grafting of poly-n-isopropylacrylamide (PNIPAAm) on the surface of polystyrene is obtained under ultraviolet radiation. In this study, the effects of solvents, such as water, methanol, and their combinations, under ultraviolet radiation were investigated successfully. METHOD AND RESULTS: Attenuated total reflection Fourier transform infrared analysis showed the existence of the graft PNIPAAm on the substrate for all samples resolved in solvents. The best solvent ratio and NIPAAm concentration for grafting was obtained with 40% NIPAAm concentrations resolved in a solvent of 9:1 (v/v) water/methanol (120%). Scanning electron microscopic and atomic force microscopic images clearly showed that a 10% increase of methanol to water would increase the amount of grafting. Surface topography and graft thickness in atomic force microscopic images of the grafted samples showed that the thickness of these grafts was about 600 nm. The drop water contact angles of the best grafted sample at 37°C and 4°C were 43.3° and 60.4°, respectively, which demonstrated the hydrophilicity and hydrophobicity of the grafted surfaces. Differential scanning calorimetric analysis also revealed the low critical solution temperature of the grafted sample to be 32°C. Thermoresponsive polymers were grafted to dishes covalently, which allowed epithelial cells to attach and proliferate at 37°C. The cells were also detached spontaneously without using enzymes when the temperature dropped below 4°C. CONCLUSION: MTT analysis also showed good viability of cells on the grafted samples, suggesting that this type of grafted material had potential as a biomaterial for cell sheet engineering. Dove Medical Press 2011 2011-02-02 /pmc/articles/PMC3044182/ /pubmed/21383854 http://dx.doi.org/10.2147/IJN.S15371 Text en © 2011 Biazar et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Biazar, Esmaeil
Khorasani, MT
Daliri, M
Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title_full Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title_fullStr Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title_full_unstemmed Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title_short Cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
title_sort cell sheet engineering: solvent effect on nanometric grafting of poly-n-isopropylacrylamide onto polystyrene substrate under ultraviolet radiation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044182/
https://www.ncbi.nlm.nih.gov/pubmed/21383854
http://dx.doi.org/10.2147/IJN.S15371
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