語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Fabrication of Tissue Precursors Ind...
~
Akintewe, Olukemi O.
FindBook
Google Book
Amazon
博客來
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels./
作者:
Akintewe, Olukemi O.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2015,
面頁冊數:
128 p.
附註:
Source: Dissertations Abstracts International, Volume: 77-03, Section: B.
Contained By:
Dissertations Abstracts International77-03B.
標題:
Polymer chemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3714971
ISBN:
9781321928792
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels.
Akintewe, Olukemi O.
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels.
- Ann Arbor : ProQuest Dissertations & Theses, 2015 - 128 p.
Source: Dissertations Abstracts International, Volume: 77-03, Section: B.
Thesis (Ph.D.)--University of South Florida, 2015.
This item is not available from ProQuest Dissertations & Theses.
Scaffold based tissue reconstruction inherently limits regenerative capacity due to inflammatory response and limited cell migration. In contrast, scaffold-free methods promise formation of functional tissues with both reduced adverse host reactions and enhanced integration. Cell-sheet engineering is a well-known bottom-up tissue engineering approach that allows the release of intact cell sheet from a temperature responsive polymer such as poly-N-isopropylacrylamide (pNIPAAm). pNIPAAm is an ideal template for culturing cell sheets because it undergoes a sharp volume-phase transition owing to the hydrophilic and hydrophobic interaction around its lower critical solution temperature (LCST) of 32°C, a temperature close to physiological temperature. Compared to enzymatic digestion via trypsinization, pNIPAAm provides a non-destructive approach for tissue harvest which retains its basal surface extracellular matrix and preserves cell-to-cell junctions thereby creating an intact monolayer of cell sheet suitable for tissue transplantation. The overall thrust of this dissertation is to gain a comprehensive understanding of how tissue precursors are formed, harvested and printed from interactions with shape-changing pNIPAAm hydrogel. A simple geometrical microbeam pattern of pNIPAAm structures covalently bound on glass substrates for culturing mouse embryonic fibroblast and skeletal myoblast cell lines is presented. In order to characterize the cell-surface interactions, three main investigations were conducted: 1) the mechanism of cell detachment; 2) the feasibility of micro-contact printing tissue precursors onto target surfaces; and 3) the assembly of these tissues into three-dimensional (3D) constructs. Detachment of cells from the shape-changing hydrogel was found to correlate with the lateral swelling of the microbeams, which is induced by thermal activation, hydration and shape distortion of the patterns. The mechanism of cell detachment was primarily driven by strain, which occurred almost instantaneously above a critical strain of 25%. This shape-changing pNIPAAm construct allows water penetration from the periphery and beneath the attached cells, providing rapid hydration and detachment within seconds. Cell cultured microbeams were used as stamps for micro-contact printing of tissue precursors and their viability, metabolic activity, local and global organization were evaluated after printing. The formation and printing of intact tissues from the shape-changing hydrogel suggests that the geometric patterning of pNIPAAm directs spatial organization through physical guidance cues while preserving cell functioning. Tissue precursors were sequentially assembled into parallel and perpendicular configurations to demonstrate the feasibility of constructing dense tissues with different organizations such as interconnected cell lines that could induce vascularization to solve perfusion issues in regenerative therapies. The novel approach presented in this dissertation establishes an efficient method for harvesting and printing of tissue precursors that may be applicable for the modular, bottom up construction of complex tissues for organ models and regenerative therapies.
ISBN: 9781321928792Subjects--Topical Terms:
3173488
Polymer chemistry.
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels.
LDR
:04403nmm a2200349 4500
001
2206389
005
20190829083302.5
008
201008s2015 ||||||||||||||||| ||eng d
020
$a
9781321928792
035
$a
(MiAaPQ)AAI3714971
035
$a
(MiAaPQ)usf:13005
035
$a
AAI3714971
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Akintewe, Olukemi O.
$3
3433287
245
1 0
$a
Fabrication of Tissue Precursors Induced by Shape-changing Hydrogels.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2015
300
$a
128 p.
500
$a
Source: Dissertations Abstracts International, Volume: 77-03, Section: B.
500
$a
Publisher info.: Dissertation/Thesis.
500
$a
Toomey, Ryan G.;Gallant, Nathan D.
502
$a
Thesis (Ph.D.)--University of South Florida, 2015.
506
$a
This item is not available from ProQuest Dissertations & Theses.
506
$a
This item must not be sold to any third party vendors.
520
$a
Scaffold based tissue reconstruction inherently limits regenerative capacity due to inflammatory response and limited cell migration. In contrast, scaffold-free methods promise formation of functional tissues with both reduced adverse host reactions and enhanced integration. Cell-sheet engineering is a well-known bottom-up tissue engineering approach that allows the release of intact cell sheet from a temperature responsive polymer such as poly-N-isopropylacrylamide (pNIPAAm). pNIPAAm is an ideal template for culturing cell sheets because it undergoes a sharp volume-phase transition owing to the hydrophilic and hydrophobic interaction around its lower critical solution temperature (LCST) of 32°C, a temperature close to physiological temperature. Compared to enzymatic digestion via trypsinization, pNIPAAm provides a non-destructive approach for tissue harvest which retains its basal surface extracellular matrix and preserves cell-to-cell junctions thereby creating an intact monolayer of cell sheet suitable for tissue transplantation. The overall thrust of this dissertation is to gain a comprehensive understanding of how tissue precursors are formed, harvested and printed from interactions with shape-changing pNIPAAm hydrogel. A simple geometrical microbeam pattern of pNIPAAm structures covalently bound on glass substrates for culturing mouse embryonic fibroblast and skeletal myoblast cell lines is presented. In order to characterize the cell-surface interactions, three main investigations were conducted: 1) the mechanism of cell detachment; 2) the feasibility of micro-contact printing tissue precursors onto target surfaces; and 3) the assembly of these tissues into three-dimensional (3D) constructs. Detachment of cells from the shape-changing hydrogel was found to correlate with the lateral swelling of the microbeams, which is induced by thermal activation, hydration and shape distortion of the patterns. The mechanism of cell detachment was primarily driven by strain, which occurred almost instantaneously above a critical strain of 25%. This shape-changing pNIPAAm construct allows water penetration from the periphery and beneath the attached cells, providing rapid hydration and detachment within seconds. Cell cultured microbeams were used as stamps for micro-contact printing of tissue precursors and their viability, metabolic activity, local and global organization were evaluated after printing. The formation and printing of intact tissues from the shape-changing hydrogel suggests that the geometric patterning of pNIPAAm directs spatial organization through physical guidance cues while preserving cell functioning. Tissue precursors were sequentially assembled into parallel and perpendicular configurations to demonstrate the feasibility of constructing dense tissues with different organizations such as interconnected cell lines that could induce vascularization to solve perfusion issues in regenerative therapies. The novel approach presented in this dissertation establishes an efficient method for harvesting and printing of tissue precursors that may be applicable for the modular, bottom up construction of complex tissues for organ models and regenerative therapies.
590
$a
School code: 0206.
650
4
$a
Polymer chemistry.
$3
3173488
650
4
$a
Biomedical engineering.
$3
535387
650
4
$a
Chemical engineering.
$3
560457
690
$a
0495
690
$a
0541
690
$a
0542
710
2
$a
University of South Florida.
$b
Chemical Engineering.
$3
1685195
773
0
$t
Dissertations Abstracts International
$g
77-03B.
790
$a
0206
791
$a
Ph.D.
792
$a
2015
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3714971
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9382938
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入