Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy

博士 === 義守大學 === 電機工程學系 === 106 === In general, Porous 3D scaffold has merits of providing larger surface and interconnection for cell growth and thereafter to generate tissues. The properties, pore size, pore geometry and the interconnection of pores all affect the cellular growth and differentiatio...

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Main Authors: Yi-Jhen Wu, 吳宜真
Other Authors: Shyh Ming Kuo
Format: Others
Language:zh-TW
Published: 2018
Online Access:http://ndltd.ncl.edu.tw/handle/zu5u26
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spelling ndltd-TW-106ISU054420102019-11-14T05:35:52Z http://ndltd.ncl.edu.tw/handle/zu5u26 Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy 調控支架孔洞性於血管增生應用暨肝纖維化修復治療之研究 Yi-Jhen Wu 吳宜真 博士 義守大學 電機工程學系 106 In general, Porous 3D scaffold has merits of providing larger surface and interconnection for cell growth and thereafter to generate tissues. The properties, pore size, pore geometry and the interconnection of pores all affect the cellular growth and differentiation of culture cells. Till today, It is very difficulty to prepare big pore size (>300 µm)and good interconnection 3D porous scaffolds, especially for collagen biomaterials. In this present study, we prepared collagen scaffolds with various pore sizes and geometries and to evaluate the effects on cultured cells, angiogenesis and liver fibrosis repair. The obtained results indicated that we could produce average 80 µm pore size and good interconnection 3D collagen scaffold. Furthermore, we could produce more large pore size, about 500 µm, collagen scaffold by using alginate microspheres as porogen materials. The prepared collagen scaffolds all with good interconnection and with 99% water content. The porosity could be varied by using different alginate microspheres porogen and with a range of 70% -90%. The cell culture results showed that ADSCs grew well on large pore size collagen scaffolds. The ADSCs number did not change significantly after ultrasound stimulus. From SEM observation, the cell number increased obviously on ADSCs/Liver cell/HUVECs co-culture groups after ultrasound stimulus. The co-cultured cells grew better on the small pore size/mixed pore size collagen scaffolds; besides, ultrasound stimulus would influence the growth of cells. From confocal microscopy observation, the ADSCs expressed un-differentiated CD49d protein expression after 28-d culturing. The SD rats had obvious angiogenesis on the collagen scaffolds that implanted in the dorsal site after 4-w ultrasound stimulus. The liver repair and angiogenesis also appealed on rats that fibrotic liver implanted with small pore size collagen scaffolds. Shyh Ming Kuo 郭士民 2018 學位論文 ; thesis 115 zh-TW
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description 博士 === 義守大學 === 電機工程學系 === 106 === In general, Porous 3D scaffold has merits of providing larger surface and interconnection for cell growth and thereafter to generate tissues. The properties, pore size, pore geometry and the interconnection of pores all affect the cellular growth and differentiation of culture cells. Till today, It is very difficulty to prepare big pore size (>300 µm)and good interconnection 3D porous scaffolds, especially for collagen biomaterials. In this present study, we prepared collagen scaffolds with various pore sizes and geometries and to evaluate the effects on cultured cells, angiogenesis and liver fibrosis repair. The obtained results indicated that we could produce average 80 µm pore size and good interconnection 3D collagen scaffold. Furthermore, we could produce more large pore size, about 500 µm, collagen scaffold by using alginate microspheres as porogen materials. The prepared collagen scaffolds all with good interconnection and with 99% water content. The porosity could be varied by using different alginate microspheres porogen and with a range of 70% -90%. The cell culture results showed that ADSCs grew well on large pore size collagen scaffolds. The ADSCs number did not change significantly after ultrasound stimulus. From SEM observation, the cell number increased obviously on ADSCs/Liver cell/HUVECs co-culture groups after ultrasound stimulus. The co-cultured cells grew better on the small pore size/mixed pore size collagen scaffolds; besides, ultrasound stimulus would influence the growth of cells. From confocal microscopy observation, the ADSCs expressed un-differentiated CD49d protein expression after 28-d culturing. The SD rats had obvious angiogenesis on the collagen scaffolds that implanted in the dorsal site after 4-w ultrasound stimulus. The liver repair and angiogenesis also appealed on rats that fibrotic liver implanted with small pore size collagen scaffolds.
author2 Shyh Ming Kuo
author_facet Shyh Ming Kuo
Yi-Jhen Wu
吳宜真
author Yi-Jhen Wu
吳宜真
spellingShingle Yi-Jhen Wu
吳宜真
Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
author_sort Yi-Jhen Wu
title Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
title_short Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
title_full Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
title_fullStr Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
title_full_unstemmed Effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
title_sort effects of scaffold porosity on angiogenesis and its potential application on hepatic fibrosis therapy
publishDate 2018
url http://ndltd.ncl.edu.tw/handle/zu5u26
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