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研究生: 劉世明
Sh-Ming Liu
論文名稱: 幾丁聚醣與海藻膠複合被覆薄膜之相關物性與細胞貼覆
指導教授: 徐新興
Shin-Shing Shyu
口試委員:
學位類別: 碩士
Master
系所名稱: 工學院 - 化學工程與材料工程學系
Department of Chemical & Materials Engineering
畢業學年度: 89
語文別: 中文
論文頁數: 74
中文關鍵詞: 複合薄膜海藻膠幾丁聚醣
外文關鍵詞: alginate, chitosan
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  • 本實驗藉由幾丁聚醣與海藻膠的複合反應在兩高分子溶液以不同重量比例,pH值變化及鈣離子交聯時間等不同條件下來形成孔洞之板狀結構物以降低其剛性、增加吸收傷口滲出液及氧氣透過的能力。
    此幾丁聚醣/海藻膠複合薄膜在水含量測試有不錯的吸水值。其中又以改變pH值系列可得到較高的水含量,氣體透過實驗顯示由於薄膜具高孔洞結構而能完全透過,水氣透過值則約在1300~1400(g*m-2day-1)而不會使水分散失太快。經由3T3纖維母細胞生物體外毒性實驗(in vitro)顯示此複合薄膜不但不會釋放有毒物質,且其薄膜之立體結構可提供細胞生長的空間,有助於組織修復。
    包覆AgSD之幾丁聚醣/海藻膠複合薄膜其載藥率可達到87~91%,藥物可持續釋放達14天之久。藉由改變兩高分子溶液pH值讓複合反應的鍵結增強,使得此系列的藥物釋放速率較重量比例改變系列來的緩慢。抗菌實驗顯示經包覆AgSD的複合薄膜對於綠膿桿菌、金黃葡萄球菌都有明顯的抗菌能力,且其抗菌能力能維持至七天以上。


    Chitosan [β(1→4)-2-amino2-deoxy-D-glucan] is a nontoxic, biocomptible polymer and widely be used for wound dressing material. Three conditions of the experiment were employed: the different weight ratio and pH change of the polymer solution and crosslinking with calcium ion via different time. The homogeneous composite membrane consist of the porous structure which act as the water vapor barrier and is capable of absorbing wound exudate and provides a moist environment.
    Due to the porous sponge structure of the composite membrane, oxygen could pass membrane completely and the membrane had better water uptaking ability, especially in pH change series. In vitro experiment, the composite membrane was nontoxic to the fibroblast cells and provided three-dimensional structure for cell growth and tissue repiration.
    The release of AgSD from the composite membrane was slowly up to 14 days. Owing to the stronger bonding complex reaction the AgSD release of the pH series was slower than that the different weight ratio series. The antibacterial capacity of AgSD-impregnated wound dressing was examined in agar plate against Pseudomonas aeruginosa and Staphylococcus aureus. It was significantly found that the suppression of bacterial proliferation was effective within 7 days when compared with control group.

    目 錄 第一章緒論-----------------------------------------------------------------1 第二章文獻回顧----------------------------------------------------------3 2.1 前言-------------------------------------------------------------------------3 2.2 被覆物質的起源及分類-------------------------------------------------3 2.2.1 傳統式被覆物質--------------------------------------------------------4 2.2.2 生物性被覆物質--------------------------------------------------------5 2.2.3 人工合成被覆物質-----------------------------------------------------6 2.3 幾丁聚醣與海藻膠的相關性質與應用-----------------------------13 2.3.1 安全性、酵素分解性及可被生物降解之物質------------------13 2.3.2 血液相容性與止血性------------------------------------------------14 2.3.3 組織及傷口癒和的促進---------------------------------------------14 2.3.4 金屬離子及蛋白質的分離技術------------------------------------16 2.3.5 幾丁聚醣與其他高分子之相容性---------------------------------17 2.3.6 海藻膠之相關性質---------------------------------------------------19 第三章實驗---------------------------------------------------------------21 3.1 實驗目的-----------------------------------------------------------------21 3.2 實驗藥品-----------------------------------------------------------------21 3.3 實驗儀器-----------------------------------------------------------------22 3.4 實驗步驟-----------------------------------------------------------------23 3.4.1 FTIR實驗---------------------------------------------------------------26 3.4.2水氣透過實驗----------------------------------------------------------26 3.4.3動態水含量實驗-----------------------------------------------26 3.4.4製作氣體透過檢量線-----------------------------------------28 3.4.5氣體透過實驗--------------------------------------------------28 3.4.6掃瞄式電子顯微鏡(SEM)實驗觀察------------------------29 3.4.7細胞毒性及貼覆之測試實驗--------------------------------29 3.4.8薄膜藥物包覆之實驗-----------------------------------------30 3.4.9 Silver sulfadiazine檢量線之製作---------------------------30 3.4.10 AgSD載藥率測定--------------------------------------------32 3.4.11藥物釋放實驗方法-------------------------------------------32 3.4.12抗菌實驗-------------------------------------------------------33 第四章結果與討論----------------------------------------------34 4.1 FTIR分析-----------------------------------------------------------------34 4.2 SEM之型態觀察分析--------------------------------------------------38 4.3動態水含量探討---------------------------------------------------------43 4.4 水氣透過實驗-----------------------------------------------------------50 4.5 氣體透過分析-----------------------------------------------------------50 4.6細胞毒性及細胞貼覆分析--------------------------------52 4.7載藥率實驗------------------------------------------------------------58 4.8 AgSD釋放分析------------------------------------------------------59 4.9抗菌實驗結果之分析--------------------------------------------64 第五章 結論-----------------------------------------------------------------69 參考文獻------------------------------------------------------------------------71

    參考文獻
    【1】Winter G. D., “Formation of the scab and the rate of epithelialization of Superficial wounds in skin of young domestic pig”, Nature, 193, 293, (1963).
    【2】Wong P., “Physical evaluation of hydrogel as a burn wound dressing”, MSc Thesis, (1980).
    【3】Muir I. F. K., Barclay T. U., “Burns and Their Treatment”, London., Lloyd Luke., (1962).
    【4】Norton L. and Chvapil M., “Comparison of newer synthetic and biological wound dressing”, J. Trauma , 21, 463, (1981).
    【5】Sabolinsly M. L., Alvarez O., Auletta M., Mulder G., Parenteau N. L., “Cultured skin as a smart material for healing wounds: experience in venous ulcers”, Biomaterials, 17, 311, (1996).
    【6】Platt A. J., Phipps A., Judkins K., “A comparative study of silicone net dressing and paraffin gauze dressing in skin-grafted sites”, Burns., 22, 543, (1996).
    【7】Queen D., Evans J. H., Gaylor J. S. D., Courtney J. M. et al ., “Burn wound dressings-a review”, Burns, 13, 218, (1987).
    【8】Barlett R. H., “Skin substitutes”, J. Trauma, 21, 731, (1981).
    【9】Pruitt B. A. and Levine N. S., “Characteristics and uses of biological dressings and skin substitutes”, Arch. Surg., 119, 312, (1984).
    【10】Quinn K. J., Courtney J. M., Evans J. H. et al., “Principles of burn dressings”, Biomaterial, 6, 369, (1985).
    【11】Rahman M. M., “in vitro Assessment of polymeric burn wound converings”, MSc Thesis, (1985).
    【12】Townsend P. L. G., “The guest for a deep and painless donor site dressing”, Burns, 2, 82, (1975).
    【13】Tavis M. J., Thornton J., Danet R. et al., “A new composite skin prosthesis”, Burns, 7, 123, (1978).
    【14】Lawrence J. C. Laboratory, “Studies of dressings in wound healing symposium”, Lawrence J. C. (Institute of accident surgery) Birmingham in England, 115, (1982).
    【15】Purna S., Mary B., “Collagen based dressing-a review”, Burns, 26, 54, (2000).
    【16】Wokalck H., Ruh H., Vaubel E. et al., “Theoretical aspects and clinical experience on a new hydrogel wound dressing material”, In: Woods H. F., Cottier D., (eds), Geliperm: Alear Advance In Healing., Proceedings of a Conference Held at The John Radcliffe Hospital, Oxford, (1985).
    【17】Gilchrist T., Martin A. M., “Wound treatment with sorbsan-an alginate fibre dressing”, Biomaterials, 4, 4, (1983).
    【18】Biagini G. et al., “Wound management with N-carboxybutyl chitosan”, Biomaterials, 12, 281, (1991).
    【19】Rao S. B., Sharma P., “Use of chitosan as a biomaterial: Studies on its safety and hemostatic potential”, J. Biomed. Mater. Res., 34, 21, (1997).
    【20】Kojima K., Okamoto Y., Miyatale K., Kitamura Y., Minamis , “Collagen typing of granulation tissue induced by chitin and chitosan”, Carbohyd . Polym., 37, 109, (1998).
    【21】Gokoo C., Burhop K., “A comparative study of wound dressings on full thickness wounds in micropigs”, Decubitus, 6, 42, (1993).
    【22】Su C. H. et al., “Fungal mycelia as the source of chitin and polysaccharides and their applications as skin substitutes”, Biomaterials, 18, 1169, (1997).
    【23】Onishi H., Machida Y., “Biodegradation and distribution of water-soluble chitosan in mice”, Biomaterials, 20, 175, (1999).
    【24】Hirano S., Noishiki Y., “The blood compatibility of chitosan and N-acylchitosans”, J. Biomed. Mater. Res. 19, 413, (1985).
    【25】Xu J., McCarthy P., Gross R. A. Kaplan D. L., “Chitosan film acylation and effects on biodegradability”, Macromulecules, 29, 3436, (1996).
    【26】Muzzarelli R. A. A. et al., “Stimulatory effect on bone formation exerted by a modified chitosan”, Biomaterials, 15, 1075, (1994).
    【27】Minami S., Okamoto Y., Miyatake K., Matsuhashi A., Kitamura Y., Tanigawa T., Tanaka Y., Shigemasa Y., “Chitin induces type IV collagen and elastic fiber in implanted nonwoven fabric of polyester”, Carbohyd. Polym., 29, 295, (1996).
    【28】Demo H., Yamada H., Tanaka I., kaba N., Matsuura M., Okumura M., Kadosawa T., Fujinaga., “Accelerating effects of chitosan for healing at early phase of experimental open wound in dogs”, Biomaterials, 20, 1407, (1999).
    【29】Wan W. S., Liang K. H., “Adsorption of gold(III)ions onto chitosan and N-carboxymethyl chitosan: Equilibrium Studies”, Ind. Eng. Chem. Res., 38, 1411,(1999).
    【30】Modrzejewska Z., Kaminski W., “Separation of Cr(VI)on chitosan membrane”, Ind. Rng. Chem. Res., 38, 4996, (1999).
    【31】Zeng X., Ruckenstein E., “Cross-linked macroporos chitosan anion-exchange membranes for prutein separations”, J. Membrane. Sci ., 148, 195, (1998).
    【32】Guibal E., Larkin A., Vincent T., Tobin J. M., “Chitosan sorbents for platinum sorption from dilute solutions”, Ind. Rng. Chem. Res., 38, 4011, (1999).
    【33】Lasko C. L., Hurst M. P., “An investigation into the use of chitosan for the removal of soluble silver from industrial wastewater”, Environ. Sci. Technol., 33, 3622, (1999).
    【34】C. P. Sharma, T. Chandy, “Protein blended Chitosan membranes for an improved hemodialysis”, Trans. Soc. Biomat., 10, 31, (1987).
    【35】C. V. Claramma, T. Chandy, C. P. Sharma, “Phosphoryl choline bilayer immobilized on albumin blended chitosan membrane-permeability properties”, Trans. Soc. Biomat., 11, 477, (1988).
    【36】T. Chandy and C. P. Sharma, “Prostaglandin El-immobilized poly(vinyl-alcohol)-blended chitosan membranes: blood compatibility and permeability properties”, J. Appli. Polym. Sci., 44, 2145, (1992).
    【37】S. Nakatsuka and A. L. Andrandy, “Permeability of vitamin B-12 in chitosan membrane, effect of blending with poly( vinyl-alcohol )on permeability”, J. Appl. Polym. Sci., 44, 17, (1992).
    【38】J. H. Kim., J. Y. Kim., Y. M. Lee and K.Y. Kim., “Controlled release riboflavin and insulin through crosslinked poly(vinyl-alcohol)/chitosan blend membrane”, J. Appl. Polym. Sci., 1823, (1992).
    【39】T. Chandy and C. P. Sharma, “Polyelectrolyte membranes from chitosan”, Acta Polym., 41, 198, (1990).
    【40】M. N. Taravel and A. Domard., “Competition between gel and polyanion-polycation complex formation in a collagen-chitosan binary system”, Macromolecular, Reports, A31, 1237, (1994).
    【41】K. D. Yao., T. Peng., M. F. Goosen., J. M. Min and Y. Y. He., “pH-sensitinity of hydrogels based on complex forming chitosan: Polyether interpetrating polymer network”, J. Appl. Polym. Sci., 48, 343, (1993).
    【42】K. D. Yao., T. Peng., H. B. Feng and Y. Y. He., “Swelling kineticsand release characteristic of crosslinked chitosan: Polyether Polymer Network(Semi-INP)Hydrogels”, J. Appl. Polym. Sci.: Polym. Chem., 32, 1213, (1994).
    【43】Sennerby L., Rostlund T., Albrektsson , B. and Albrektsson T., “acute tissue recations to potassium alginate with and without colour / flavour addeitives” Biomaterials, 8, 49, (1987).
    【44】Cohen S., Bernstein H., Hewes C., Chow M. and Langer R., “The pharmacokinetics of and humoral responses to antigen delivered by microencapsulated liposomes”, Proc. Natl. Acad. Sci. U.S.A., 88, 1040, (1991).
    【45】M. M. Meshali and K. E. Gabr., “Effect of interpolymer complex formation of chitosan with pectin or acacia on the release behaviour of chlorpromazine HCI”, Int. J. Pharm., 89, 177, (1993).
    【46】M. D. Daly., D. Knorr., “Chitosan-alginate complex coacervate capsules: effect of calcium chloride ,plasticizers and polyelectrolytes on mechanical stability”, Biotechol. Prog., 4, 76, (1988).
    【47】K. D. Yao., T. Peng., Y. J. Yin., M. X. Xu and M. F. A. Goosen., “Microcapsules / Microspheres related to chitosan”, J. M. S. Rev. Macromol. Chem. Phys., C35, 150, (1995).
    【48】L. F. Tay., L. K. Khoh., C. S. Loh., and E. Khor., “Alginate-chitosan coacervation in production of artificial seeds”, Biotechnol . Bioeng., 42, 449, (1993).
    【49】S. Overgand, J. M. Scharer., m. Moo-Young and N. C. Bols., “Immobilization of hybridoma cells in chitosan alginate beads”, Canda. J. Chem. Eng., 69, 439, (1992).
    【50】M. L. Hugnat., A. Groboillot., R. J. Neufeld., D. Poncelet and E. Dellacherie, “Hemoglobin encapsulation in chitosan / calcium alginate beads”, J. Appl. Polym. Sci., 1427, (1994).

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