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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 生化科技學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/20826
完整後設資料紀錄
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dc.contributor.advisor陳進庭
dc.contributor.authorHsiao-Chi Linen
dc.contributor.author林小琪zh_TW
dc.date.accessioned2021-06-08T03:05:31Z-
dc.date.copyright2017-08-29
dc.date.issued2017
dc.date.submitted2017-07-05
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46. Kato, I.T., et al., Antimicrobial photodynamic inactivation inhibits Candida albicans virulence factors and reduces in vivo pathogenicity. Antimicrob Agents Chemother, 2013. 57(1): p. 445-51.
47. Uppuluri, P., et al., Effects of fluconazole, amphotericin B, and caspofungin on Candida albicans biofilms under conditions of flow and on biofilm dispersion. Antimicrob Agents Chemother, 2011. 55(7): p. 3591-3.
48. Moor, A. C., Signaling pathways in cell death and survival after photodynamic therapy. Journal of Photochemistry and Photobiology B: Biology, 2000. 57(1): p. 1-13.
49. Alby, K. and Bennett, R. J., Stress-induced phenotypic switching in Candida albicans. Molecular Biology of the Cell, 2009. 20(14): p. 3178-91.
50. Temple, M. D., Perrone, G. G. and Dawes, I.W., Complex cellular responses to reactive oxygen species. Trends in Cell Biology, 2005. 15(6): p. 319-26.
51. 黃儀真, 結合光動力殺菌與Fluconazole在白色念珠菌的治療效果探討. 國立台灣大學, 2016.
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53. Jayatilake, J. A., Samaranayake, Y. H., Cheung, L. K. and Samaranayake, L. P., Quantitative evaluation of tissue invasion by wild type, hyphal and SAP mutants of Candida albicans, and non-albicans Candida species in reconstituted human oral epithelium. Journal of Oral Pathology & Medicine, 2006. 35(8): p. 484-91.
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59. Dovigo, L. N., Pavarina, A. C., Carmello, J. C., Machado, A. L,. Brunetti, I. L. and Bagnato, V. S., Susceptibility of Clinical Isolates of Candida to Photodynamic Effects of Curcumin. Biofouling, 2013. 29(9): p. 1057-67.
60. Mukherjee, P. K., Chandra, J., Kuhn, D. M. and Ghannoum, M. A., Mechanism of fluconazole resistance in Candida albicans biofilms: phase-specific role of efflux pumps and membrane sterols. Infection and Immunity, 2003. 71(8): p. 4333-40.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/20826-
dc.description.abstract白色念珠菌(Candida albicans)為院內感染的伺機性真菌之一,目前治療真菌感染主要還是以抗真菌藥物為主,但大多有副作用及抗藥性問題產生。光動力殺菌Photodynamic inactivation (PDI)是一種用來解決菌體產生抗藥性問題的治療方式,其作用方式為藉由光感物質在光激發下產生單態氧及自由基來破壞菌體,進而導致菌體死亡。
實驗室先前針對懸浮培養的白色念珠菌以光動力結合抗真菌藥物Fluconazole,發現可提高Fluconazole的藥物作用,但在白色念珠菌生物膜以相同模式進行殺菌,卻無法提升殺菌效果。於此,本研究分別分析光動力殺菌後的生物膜菌體生長曲線、菌絲的生成能力、胞外聚合物厚度,以及配合caspofungin,推論光動力殺菌結合抗真菌藥物對白色念珠菌的生物膜殺菌效果不佳,可能和光動力殺菌的效果與抗真菌藥物的性質有關。另外以5-Aminolevulinic acid (5-ALA)進行光動力殺菌,結合抗真菌藥物也可在懸浮菌體提高殺菌效果。未來將以5-ALA來探討是否因粒線體受損導致菌絲生成受到影響,再加入抗真菌藥物可以提升殺菌效果,以探討光動力殺菌結合抗真菌藥物的殺菌機制。
zh_TW
dc.description.abstractCandida albicans is an opportunistic fungus in hospital infection. Antifungal drugs are mainly used for the treatment of fungal infection nowadays. However, there are side effects and drug resistance problems. Photodynamic inactivation (PDI) is one of the alternative treatments used to overcome the problem of drug resistance. The principle of PDI is to combine photosensitizer and light to produce reactive oxygen species that are toxic to pathogens.
Previous studies in our laboratory found that combination of PDI and Fluconazole could increase the antifungal activity against suspension of C. albicans; however, the effect is not significant against C. albicans biofilm. In this study, we analyzed the growth curves of biofilm, the ability of hyphae formation and the thickness of extracellular polymeric substances (EPS) after PDI. Meanwhile, another antifungal drug, caspofungin was used to combine with PDI to study the antifungal activity against suspension and biofilm of C. albicans. We found the ineffectiveness of PDI combined with fluconazole against biofilm might relate to the effect of PDI and the action mechanism of antifungal drugs. Furthermore, we found that the combination of a photosensitizer precursor, 5-Aminolevulinic acid (5-ALA), and antifungal drugs could also increase the antifungal effect against the suspension of C. albicans.
en
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en
dc.description.tableofcontents第一章 緒論 1
1.1 微生物與人類 1
1.1.1正常菌叢 1
1.1.2伺機性感染 1
1.1.3院內感染 2
1.2白色念珠菌 3
1.2.1白色念珠菌感染疾病 3
1.2.2白色念珠菌生物膜 4
1.2.3白色念珠菌生物膜生成過程 4
1.2.4白色念珠菌生物膜抗藥性機制 5
1.3抗真菌藥物 7
1.3.1抗真菌藥物種類 7
1.3.2抗真菌藥物的抗藥性 8
1.4光動力治療 11
1.4.1光動力治療發展與歷史 11
1.4.2光動力治療作用機轉 11
1.4.3光感物質 12
1.4.4光動力殺菌 13
1.5研究動機與目的 14
1.6研究架構 15
第二章 材料與方法 16
2. 1藥品 16
2.2儀器 16
2.3菌種來源、保存與活化 17
2.3.1菌種來源 17
2.3.2菌種保存 17
2.3.3菌種活化 17
2.4實驗方法 18
2.4.1藥物配置 18
2.4.2白色念珠菌懸浮菌體培養 18
2.4.3白色念珠菌生物膜培養 18
2.4.4光動力殺菌於白色念珠菌生物膜 18
2.4.5白色念珠菌生物膜生長曲線 18
2.4.6光動力殺菌於白色念珠菌懸浮菌體 19
2.4.7誘導白色念珠菌菌絲生成分析 19
2.4.8生物膜胞外聚合物觀察 19
2.4.9光動力殺菌結合抗真菌藥物於白色念珠菌生物膜 19
2.4.10以5-ALA進行光動力殺菌結合抗真菌藥物於白色念珠菌懸浮
菌體 19
2.4.11統計分析 20
第三章 結果 21
3.1光動力殺菌後白色念珠菌生物膜之生長曲線 21
3.2光動力殺菌後白色念珠菌菌絲生成能力分析 21
3.3光動力殺菌後白色念珠菌生物膜胞外聚合物厚度分析 22
3.4光動力殺菌結合caspofungin對白色念珠菌生物膜影響 22
3.5光動力殺菌結合posaconazole對白色念珠菌生物膜影響 23
3.6以不同濃度5-ALA進行光動力殺菌之效果 23
3.7 5-ALA進行光動力殺菌結合不同濃度抗真菌藥物之效果 24
第四章 討論 25
4.1光動力殺菌後白色念珠菌生物膜之生長曲線探討 25
4.2光動力殺菌後白色念珠菌菌絲生成能力分析 25
4.3光動力殺菌後白色念珠菌生物膜胞外聚合物厚度分析 26
4.4光動力殺菌結合caspofungin對白色念珠菌生物膜效果探討 27
4.5光動力殺菌結合posaconazole對白色念珠菌生物膜效果探討 28
4.6 5-ALA進行光動力殺菌結合不同濃度抗真菌藥物之效果探討 28
4.7生物膜狀態之探討 29
第五章 結論與未來研究方向 31
結果圖表 32
附錄 41
參考文獻 43
dc.language.isozh-TW
dc.subject生物膜zh_TW
dc.subject光動力殺菌zh_TW
dc.subject白色念珠菌zh_TW
dc.subject氟康唑zh_TW
dc.subject5-氨基乙?丙酸zh_TW
dc.subject卡泊芬淨zh_TW
dc.subject甲苯胺藍zh_TW
dc.subjectBiofilmen
dc.subjectCandida albicansen
dc.subjectPhotodynamic inactivationen
dc.subjectToluidine blue Oen
dc.subjectFluconazoleen
dc.subject5-Aminolevulinic aciden
dc.subjectCaspofunginen
dc.title結合光動力殺菌與抗真菌藥物於白色念珠菌的生物效應探討zh_TW
dc.titleInvestigate the biological consequences of combining photodynamic inactivation and antifungal agents against Candida albicansen
dc.typeThesis
dc.date.schoolyear105-2
dc.description.degree碩士
dc.contributor.oralexamcommittee林晉玄,吳?承,簡雄飛
dc.subject.keyword白色念珠菌,光動力殺菌,甲苯胺藍,氟康唑,5-氨基乙?丙酸,卡泊芬淨,生物膜,zh_TW
dc.subject.keywordCandida albicans,Photodynamic inactivation,Toluidine blue O,Fluconazole,5-Aminolevulinic acid,Caspofungin,Biofilm,en
dc.relation.page50
dc.identifier.doi10.6342/NTU201701341
dc.rights.note未授權
dc.date.accepted2017-07-06
dc.contributor.author-college生命科學院zh_TW
dc.contributor.author-dept生化科技學系zh_TW
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