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  1. NTU Theses and Dissertations Repository
  2. 工學院
  3. 醫學工程學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/31600
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor黃義侑
dc.contributor.authorYu-Ching Huangen
dc.contributor.author黃郁晴zh_TW
dc.date.accessioned2021-06-13T03:15:35Z-
dc.date.available2008-08-01
dc.date.copyright2006-08-01
dc.date.issued2006
dc.date.submitted2006-07-31
dc.identifier.citation[1]Kas H. S., Chitosan: properties, preparations and application to microparticulate systems. J Microencap ,1997. 14 (6) :689-711.
[2]Francis J. K., Matthew H. W.T., Application of Chitosan-Based Polysaccharide Biomaterial in Cartilage Tissue Engineering: a Review. Biomaterials 2000. 21 :2589–2598.
[3]Khor E., Lim L.Y., Implantable Application of Chitin and Chitosan. Biomaterials 2003. 24 : 2339-2349.
[4]Hirano S., Tsuchida H., Nagao N., N-acetylation in chitosan and the rate of its enzymic hydrolysis. Biomaterials 1989.10 (8) :574-576.
[5]Dixon M., Edwin C., et al., Enzymes, 3rd ed., Academic Press, New York 1976.
[6]Errington N., Harding S. E. et al., Hydrodynamic characterization of chitosans varying in molecular weight and degree of acetylation. Int J Biol Macromol 1993. 15 :119-117.
[7]Illum L., Chitosan and its use as a pharmaceutical excipient. Pharm Res 1998.15 (9) :1326-1331.
[8]Sanflord P. A., Chitosan and algimate: new forms of commercial interest. Am Chem Soc Div Polym Chem 1990. 31 :628.
[9] Wendy Amass, Allan Amass, Brian Tighe., A review of biodegradable polymers: uses, current developments in the synthesis and characterization of biodegradable polyesters, blends of biodegradable polymers and recent advances in biodegradation studies. polymer international 1998. 47 (2) :89-144.
[10]Sania Mansouri, Patrick Lavigne, Karin Corsi, et al., Chitosan-DNA nanoparticles as non-viral vectors in gene therapy:strategies to improve transfection efficacy. European Journal of Pharmaceutics and Biopharmaceutics 2004. 57 :1–8.
[11]Malcolm P. Stevens., POLYMER CHEMISTRY 3rd ed. New York Oxford 1999 :350.
[12]Yabin Zhu, Changyou Gao, Xingyu Liu, and Jiacong Shen, Surface Modification of Polycaprolactone Membrane via Aminolysis and Biomacromolecule Immobilization for Promoting Cytocompatibility of Human Endothelial Cells. Biomacromolecules 2002. 3 (6) :1312-1319
[13]Kurita K, Ikeda H, Yoshida Y, Shimojoh M, Harata M., Chemoselective Protection of the Amino Groups of Chitosan by Controlled Phthaloylation:Facile Preparation of a Precursor Useful for Chemical Modifications. Biomacromolecules 2002. 3 :1–4
[14]Li Liu, Yu Li, Hao Liu, Yue’e Fang., European Polymer Journal 2004. 40 : 2739–2744
[15]Chin-San Wu., A comparison of the structure, thermal properties, and biodegradability of polycaprolactone/chitosan and acrylic acid grafted polycaprolactone/chitosan. Polymer 2005. 46 :47–155
[16]Li Liu, Yusong Wang, Xiaofeng Shen, Yue’e Fang., Preparation of chitosan-g-polycaprolactone copolymers through ring-opening polymerization of -caprolactone onto phthaloyl-protected chitosan. Biopolymers 2005. 78 (4) :163–170.
[17]Aparna Sarasam, Sundararajan V. Madihally., Characterization of chitosan–polycaprolactone blends for tissue engineering applications. Biomaterials 2005. 26 (27) :5500–5508
[18]Na Mei, Guang Chen, Ping Zhou, Xin Chen, et al., Biocompatibility of Poly(e-caprolactone) Scaffold Modified by Chitosan—The Fibroblasts Proliferation in vitro. Journal of Biomaterial Applications 2005. 19 :323-339
[19]廖峻德, 王明誠, 電漿技術在生物醫學上的應用. 化工資訊月刊 第八期 2002/8/6.
[20]Deepak Sehgal and Inder K. Vijay., A Methid for the High Efficiency of Water-Soluble Carbodiimide-Mediated Amidation. Analytical biochemistry 1994. 218 :87-91
[21]Rickerby D. S., Matthews A., Advanced Surface Coatings: a Habdbook of Surface Engineering, Blackie & Son Ltd., London 1991. :196.
[22]Ferencz Denes. Synthesis and Surface Modification by Macromolecular Plasma Chemistry. TRIP 1997. 5 (1) :23-31.
[23]Zuwei Ma., Wei He, Thomas Yong, Ramakrishna S., .Grafting of Gelatin on Electrospun Poly(caprolactone) Nanofibers to Improve Endothelial Cell Spreading and Proliferation and to Control Cell Orientation. Tissue Engineering 2005. 11 (7/8) :1149-1158.
[24]E. Mangala, T. Suresh Kumar, et al., Development of Chitosan/ Poly (vinyl alcohol) Blend Membranes as Burn Dressing. Trends Biomater. Artif. Organs. 2003 . 17 (1) :34-40.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/31600-
dc.description.abstract聚酯類中,例如:聚乳酸polylactide (PLA)、polyglycolide (PGA)、poly(ε-caprolactone) (PCL),由於具備良好的生物相容性及生物可分解性,所以,不論是材料本身或其共聚合物皆已被廣泛地使用在生醫領域,但其本身之疏水性及缺乏提供細胞辨識貼附的官能基,有時會使其用途受限,因此,為增加其效能,與其他生物性分子共同混合或形成共聚合物是常採取的策略,其中又以結合親水性高分子,形成兩性高分子更吸引了研究者的注意。
在本篇研究中選擇了疏水的聚己內酯(PCL)及親水的天然高分子幾丁聚醣作為基材,有別於化學合成的方式,嘗試使用非高溫、步驟簡單的處理方式完成聚己內酯膜的表面改質,包括:紫外光輻射及輝光電漿。再以測量基材表面親疏水性、傅立葉轉換紅外線光譜及ninhydrin assay確認接合情形。並在基材表面培養細胞,探討其生物相容性。
zh_TW
dc.description.abstractpolyesters,such as polylactide (PLA)、polyglycolide (PGA)、 poly ε-caprolactone(PCL),and their copolymers,like polylactide-co-glycolide(PLAGA),have been widely studied and extensively applied in biomedical field, since they have the good biocompatibility and biodegradability。However, because of their hydrophobicity and lack of functional groups,they need modification inevitably to make them more usable。Among the strategies, combining the hydrophilic segments and the hydrophobic polyesters to make amphiphilic copolymer attracts most attentions。
In this study,we choose PCL and chitosan as our materials,and try to use simple methods, for instance,ultraviolet radiation and plasma, to make the grafting of chitosan on PCL membrane。
The hydrophilicity of film was investigated by contact angle,the formation and the depletion of functional groups were examined by FTIR,and the changes of surface element on film were analyzed by ninhydrin assay。 Besides, the attachment and proliferation of cells on the film evidence the cytocompatiability of our material。
en
dc.description.provenanceMade available in DSpace on 2021-06-13T03:15:35Z (GMT). No. of bitstreams: 1
ntu-95-R93548003-1.pdf: 1410752 bytes, checksum: a592c9bfe14d5fbf7da994c40e9de1c1 (MD5)
Previous issue date: 2006
en
dc.description.tableofcontents目錄-------------------------------------------------------------------------1
圖目錄------------------------------------------------------------------------------4
表目錄--------------------------------------------------------------------------6

第一章 前言-----------------------------------------------------------------------7
第二章 文獻回顧---------------------------------------------------------------8
2.1 幾丁聚醣--------------------------------------------------------------------8
2.2 聚己內酯--------------------------------------------------------------------11
2.3 幾丁聚醣與聚己內酯-----------------------------------------------------13
2.4 表面改質--------------------------------------------------------------------16
2.4.1 交聯劑---------------------------------------------------------------------17
2.4.2 輝光電漿------------------------------------------------------------------18
第三章 實驗材料與方法------------------------------------------------------22
3.1實驗藥品與器材------------------------------------------------------------22
3.1.1 實驗藥品------------------------------------------------------------------22
3.1.2 實驗儀器------------------------------------------------------------------23
3.2 實驗溶液與培養液配製--------------------------------------------------25
3.3 實驗方法--------------------------------------------------------------------27
3.3.1製備聚己內酯膜----------------------------------------------------------27
3.3.2製底層塗佈上PDMS的培養皿----------------------------------------27
3.3.3製chitosan-PCL混合(blend)溶液之膜--------------------------------28
3.3.4 Plasma之操作------------------------------------------------------------28
3.3.5 UV之操作----------------------------------------------------------------28
3.3.6 羧基密度測定------------------------------------------------------------29
3.3.7 EDCNHS交聯系統------------------------------------------------------29
3.3.8 胺基密度測定------------------------------------------------------------30
3.3.9 細胞培養------------------------------------------------------------30
3.3.10 MTS測試------------------------------------------------------------30
第四章 初步結果與討論------------------------------------------------------33
4.1聚己內酯膜之製備---------------------------------------------------------33
4.2 改質方法處理後之結果--------------------------------------------------35
4.2.1 親水性測定---------------------------------------------------------------35
4.2.2 FT-IR測定-----------------------------------------------------------------36
4.2.3 羧基密度測定------------------------------------------------------------42
4.2.4 韌帶細胞活性測定------------------------------------------------------45
第五章 結論---------------------------------------------------------------------46
第六章 參考文獻---------------------------------------------------------------48
dc.language.isozh-TW
dc.subject聚己內酯zh_TW
dc.subject表面改植zh_TW
dc.subject幾丁聚醣zh_TW
dc.subjectchitosanen
dc.subjectpoly ε-caprolactoneen
dc.subjectsurface modificationen
dc.title以紫外光及電漿方式接枝幾丁聚醣於聚己內酯薄膜之研究zh_TW
dc.titleThe Grafting of Chitosan on polyε-caprolactone membrane with UV Irradiation and Plasma methodsen
dc.typeThesis
dc.date.schoolyear94-2
dc.description.degree碩士
dc.contributor.oralexamcommittee鍾次文,劉得任,梁有志
dc.subject.keyword表面改植,聚己內酯,幾丁聚醣,zh_TW
dc.subject.keywordsurface modification,poly ε-caprolactone,chitosan,en
dc.relation.page51
dc.rights.note有償授權
dc.date.accepted2006-07-31
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept醫學工程學研究所zh_TW
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