In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing

Chronic wounds are an increasing source of morbidity and mortality, especially diabetic ulcers which affects roughly 15% of diabetic patients. With technological advances in nanoparticles and biocomposite nanofibers, this in-vitro study looked into the possibility of using a combination of poly(lact...

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Main Author: Chong, Daniel Kaijun
Other Authors: Chinnasamy Gandhimathi
Format: Final Year Project
Language:English
Published: 2017
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Online Access:http://hdl.handle.net/10356/72622
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-726222020-11-01T05:32:41Z In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing Chong, Daniel Kaijun Chinnasamy Gandhimathi Lee Kong Chian School of Medicine (LKCMedicine) Srinivasan Dinesh Kumar DRNTU::Science::Medicine Chronic wounds are an increasing source of morbidity and mortality, especially diabetic ulcers which affects roughly 15% of diabetic patients. With technological advances in nanoparticles and biocomposite nanofibers, this in-vitro study looked into the possibility of using a combination of poly(lactic-co-glycolic-acid) (PLGA) and a TGF-β core to augment and assist wound healing. PLGA/TGF-β was tested against a plain cover slip (negative control) and PLGA. The rate of cell proliferation, amount of collagen secretion, structural studies via 5-chloromethylfluorescein diacetate (CMFDA) staining were compared between the 3 groups. PLGA/TGF-β was superior to PLGA and the cover slip in the rate of cell proliferation seen by an absorbance value of 3.30 units on the MTS assay against 2.61 and 2.62 on PLGA and the cover slip respectively. Based on the images taken after the sirius red staining, PLGA/TGF-β again demonstrated increased cell proliferation and collagen secretion. Lastly, the CMFDA dye showed normal cell morphology reflecting that PLGA/TGF-β gave rise to a suitable environment for the cells to grow in. Results of both the immunofluorescence analysis for expression of F-actin and also the scanning electron microscope (SEM) images are still underway and results will be analysed on a later date. From the above results there is potential for clinical relevance and application of this TGF-β imbued scaffold to assist treatment of diabetic ulcers. Although the current findings are suggestive of a positive correlation between the use of the scaffold and improved wound healing, however further studies such as in-vivo studies including a battery of test have to be carried out first. Bachelor of Medicine and Bachelor of Surgery 2017-08-30T08:27:27Z 2017-08-30T08:27:27Z 2017 Final Year Project (FYP) http://hdl.handle.net/10356/72622 en 8 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Medicine
spellingShingle DRNTU::Science::Medicine
Chong, Daniel Kaijun
In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
description Chronic wounds are an increasing source of morbidity and mortality, especially diabetic ulcers which affects roughly 15% of diabetic patients. With technological advances in nanoparticles and biocomposite nanofibers, this in-vitro study looked into the possibility of using a combination of poly(lactic-co-glycolic-acid) (PLGA) and a TGF-β core to augment and assist wound healing. PLGA/TGF-β was tested against a plain cover slip (negative control) and PLGA. The rate of cell proliferation, amount of collagen secretion, structural studies via 5-chloromethylfluorescein diacetate (CMFDA) staining were compared between the 3 groups. PLGA/TGF-β was superior to PLGA and the cover slip in the rate of cell proliferation seen by an absorbance value of 3.30 units on the MTS assay against 2.61 and 2.62 on PLGA and the cover slip respectively. Based on the images taken after the sirius red staining, PLGA/TGF-β again demonstrated increased cell proliferation and collagen secretion. Lastly, the CMFDA dye showed normal cell morphology reflecting that PLGA/TGF-β gave rise to a suitable environment for the cells to grow in. Results of both the immunofluorescence analysis for expression of F-actin and also the scanning electron microscope (SEM) images are still underway and results will be analysed on a later date. From the above results there is potential for clinical relevance and application of this TGF-β imbued scaffold to assist treatment of diabetic ulcers. Although the current findings are suggestive of a positive correlation between the use of the scaffold and improved wound healing, however further studies such as in-vivo studies including a battery of test have to be carried out first.
author2 Chinnasamy Gandhimathi
author_facet Chinnasamy Gandhimathi
Chong, Daniel Kaijun
format Final Year Project
author Chong, Daniel Kaijun
author_sort Chong, Daniel Kaijun
title In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
title_short In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
title_full In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
title_fullStr In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
title_full_unstemmed In-vitro study of TGF-β loaded PLGA nanofibrous scaffold in promoting diabetic wound healing
title_sort in-vitro study of tgf-β loaded plga nanofibrous scaffold in promoting diabetic wound healing
publishDate 2017
url http://hdl.handle.net/10356/72622
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