Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
    • 指導教授
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  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/123456789/15967
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor謝銘鈞(Ming-Jium Shieh)
dc.contributor.authorJui-An Paien
dc.contributor.author白芮安zh_TW
dc.date.accessioned2021-06-07T17:56:42Z-
dc.date.copyright2020-08-06
dc.date.issued2020
dc.date.submitted2020-08-05
dc.identifier.citation[1] 久保明良著, 1996,胃腸病症狀的發現與治療,初版,益群出版, 222-232.
[2] 廖繼鼎, 2003,臨床腫瘤學,初版,合記圖書出版社, 513-571.
[3] Colorectal Cancer - American Cancer Society.
[4] Magrini R, Bhonde MR, Hanski M-L, et al. (2002) Cellular effects of CPT-11 on colon carcinoma cells: Dependence on p53 and hMLH1 status. International Journal of Cancer. 101:23-31.
[5] Bala V, Rao S, Boyd BJ, et al. (2013) Prodrug and nanomedicine approaches for the delivery of the camptothecin analogue SN38. Journal of Controlled Release. 172:48-61.
[6] Gabriella F, Alessandra di M, Viviana T, et al. (2012) Human serum albumin: From bench to bedside, Molecular Aspects of Medicine, Volume 33, Issue 3, Pages 209-290, ISSN 0098-2997
[7] Kouchakzadeh H, Safavi MS, Shojaosadati SA. (2015) Efficient delivery of therapeutic agents by using targeted albumin nanoparticles. Adv Protein Chem Struct Biol. 98:121-43.
[8] Ding D, Tang X, Cao X, et al. (2014) Novel self-assembly endows human serum albumin nanoparticles with an enhanced antitumor efficacy. AAPS PharmSciTech.15(1):213–222.
[9] Elsadek B, Kratz F. (2012) Impact of albumin on drug delivery-new applications on the horizon. J Control Release. 157(1):4–28.
[10] Frei E. (2011) Albumin binding ligands and albumin conjugate uptake by cancer cells. Diabetol Metab Syndr. 3(1):11.
[11] Kim TH, Jiang HH, Youn YS, et al. (2011) Preparation and characterization of watersoluble albumin-bound curcumin nanoparticles with improved antitumor activity. Int J Pharm. 403(1–2):285–291.
[12] Quan Q, Xie J, Gao H, et al. (2011) HSA coated iron oxide nanoparticles as drug delivery vehicles for cancer therapy. Mol Pharm. 8(5):1669–1676.
[13] Sheng Z, Hu D, Zheng M, et al. (2014) Smart human serum albumin indocyanine green nanoparticles generated by programmed assembly for dual-modal imaging-guided cancer synergistic phototherapy. ACS Nano. 8(12):12310–12322.
[14]Tirkey B, Bhushan B, Uday Kumar S, et al. (2017) Prodrug encapsulated albumin nanoparticles as an alternative approach to manifest anti-proliferative effects of suicide gene therapy. Mater Sci Eng C Mater Biol Appl. 73:507-515.
[15] Lee S, Lee C, Park S, et al. (2018) Facile fabrication of highly photothermal-effective albumin-assisted gold nanoclusters for treating breast cancer. Int J Pharm. 553(1-2):363-374.
[16] Yin T, Wang G, He S, Liu Q, Sun J, Wang Y. (2016) Human cancer cells with stem celllike phenotype exhibit enhanced sensitivity to the cytotoxicity of IL-2 and IL-15 activated natural killer cells. Cell Immunol. 300:41-5.
[17] Cadete A, Alonso MJ. (2016) Targeting cancer with hyaluronic acid-based nanocarriers: recent advances and translational perspectives. Nanomedicine (Lond). 11(17):2341-57.
[18] Golden EB, Chhabra A, Chachoua A, Adams S, Donach M, Fenton-Kerimian M, Friedman K, Ponzo F, Babb JS, Goldberg J, Demaria S, Formenti SC. (2015) Local radiotherapy and granulocyte-macrophage colony-stimulating factor to generate abscopal responses in patients with metastatic solid tumours: a proof-of-principle trial. Lancet Oncol. 16(7):795- 803.
[19] Kanegasaki S, Matsushima K, Shiraishi K, Nakagawa K, Tsuchiya T. (2014) Macrophage inflammatory protein derivative ECI301 enhances the alarmin-associated abscopal benefits of tumor radiotherapy. Cancer Res. 74(18):5070-8.
[20] Demaria S, Golden EB, Formenti SC. (2015) Role of Local Radiation Therapy in Cancer Immunotherapy. JAMA Oncol. 1(9):1325-32.
[21] Song, G., Chao, Y., Chen, Y., Liang, C., Yi, X., Yang, G., Yang, K., Cheng, L., Zhang, Q. and Liu, Z. (2016), All‐in‐One Theranostic Nanoplatform Based on Hollow TaOx for Chelator‐Free Labeling Imaging, Drug Delivery, and Synergistically Enhanced Radiotherapy. Adv. Funct. Mater., 26: 8243-8254. doi:10.1002/adfm.201603845
[22] Wang Y, Yang L, Zhang J, Zhou M, Shen L, Deng W, Liang L, Hu R, Yang W, Yao Y, Zhang H1, Zhang Z. (2018) Radiosensitization by irinotecan is attributed to G2/M phase arrest, followed by enhanced apoptosis, probably through the ATM/Chk/Cdc25C/Cdc2 pathway in p53-mutant colorectal cancer cells. Int J Oncol. 53(4):1667-1680.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15967-
dc.description.abstract大腸直腸癌目前已是全球人類死亡的重大疾病之一,而國內隨著經濟之進步、飲食 習慣之西化,大腸直腸癌之發生率亦隨之增加,且約有三分之一的大腸直腸癌患者 於診斷時即已發生轉移。而本計畫即是利用人類血清白蛋白(Human serum albumin, HSA)分子所帶有的疏水官能基將化療藥物7-乙基-10-羥基喜樹鹼(7-Ethyl- 10-hydroxycamptothecin,SN-38) 包覆於內,並在此藥物載體摻入透明質酸 (Hyaluronic acid, HA)以作為有效標靶大腸直腸癌治療之藥物載體。其中,HSA可 增加此奈米藥物載體於血液中之相容性,有效增加此奈米藥物載體在血液中的半衰 期,而HA則可提高腫瘤與腫瘤幹細胞之標靶效益,提高整體治療效果與降低化療 藥物的毒性。而包覆於奈米藥物載體中的SN-38除了作為化療藥物外,也可作為放 射線療法時之放射增敏劑以有效殺死腫瘤細胞。最後。藉由化療與放射線治療所殺 死的細胞則會更進一步引起自體的免疫反應以攻擊未接受放射線治療之腫瘤病灶或 是轉移的腫瘤細胞,進而提高大腸直腸癌治療之效果。zh_TW
dc.description.abstractColorectal cancer (CRC) is now one of the major diseases in the world. With westernized diet in Taiwan, the incidence of colorectal cancer increases. In about 30% of original colorectal cancer, diagnoses metastasizes has occurred. In this study, the 7-Ethyl-10-hydroxycamptothecin (SN-38) molecules could be loaded in human serum albumin (HSA)-hyaluronic acid (HA) based nanoparticles (SN-38/HSA/HA NPs) by the hydrophobic side groups of amino acid in HSA. Herein, HSA could be used to increase the compatibility and half-life of nanoparticles in the blood, while HA can improve the target benefit to CRC and cancer stem cells (CSCs) and the overall treatment effect and reduce the side effect. In addition to being used as a chemotherapeutic agent, SN-38 in the designed nanoparticles can also be used as a radiosensitizer during radiation therapy to effectively kill tumor cells. At last, cancer cells killed by chemotherapy and radiation will further induce the immune response to attack tumor lesions or metastatic tumor cells without direct radiation exposure. Therefore, the use of this designed nanoparticle could be significantly more efficacious than the chemotherapy alone for colorectal cancer therapy.en
dc.description.provenanceMade available in DSpace on 2021-06-07T17:56:42Z (GMT). No. of bitstreams: 1
U0001-3107202016412300.pdf: 2292206 bytes, checksum: 73c9b02d13258e209af6b3f30c786108 (MD5)
Previous issue date: 2020
en
dc.description.tableofcontents目錄
誌謝 i
中文摘要 ii
Abstract iii
List of Schemes vii
List of Table viii
List of Figures ix
Chapter 1 Introduction 1
1.1 Research background and its importance 1
1.2 Chemotherapy and its limitation 3
1.3 Human serum albumin (HSA) 4
1.4 Hyaluronic acid (HA) 6
1.5 The Abscopal effect 6
1.6 Radiotherapy 7
1.7 Development of nano-carrier combined chemotherapy and radiotherapy 8
Chapter 2 Materials and Methods 10
2.1 Materials 10
2.2 Preparation of SH nanoparticles and SH/HA nanoparticles 10
2.3 Characterization of nanoparticles 10
2.4 Cell culture 12
2.5 Cellular uptake 12
2.6 CD44 expression of colon cancer cell line 13
2.7 In vitro cytotoxicity of chemotherapy and radiotherapy 13
2.8 Cell cycle analysis 14
2.9 Biodistribution 14
2.10 In vivo anticancer efficacy 15
2.11 Tumor metastasis model 16
2.12 Anti-tumor immune response evaluation 16
2.13 Statistic analysis 17
Chapter 3 Results and Discussion 18
3.1 Synthesis and characterization of SH NPs and SH/HA NPs 18
3.2 CD44 expression of colon cancer cell line 19
3.3 Cellular uptake 20
3.4 In vitro cytotoxicity of chemotherapy and radiotherapy 21
3.5 Cell cycle analysis 22
3.6 Biodistribution 23
3.7 In vivo anticancer efficacy 24
3.8 Tumor metastasis model and immune response evaluation 25
Chapter 4 Conclusion 27
Reference 28
Schemes 32
Table 32
Figures 33
dc.language.isoen
dc.subject7-乙基-10-羥基喜樹鹼zh_TW
dc.subject大腸直腸癌zh_TW
dc.subject轉移zh_TW
dc.subject人類血清白蛋白zh_TW
dc.subject透明質酸zh_TW
dc.subject化學治療zh_TW
dc.subject放射線治療zh_TW
dc.subjecthyaluronic aciden
dc.subject7-Ethyl-10-hydroxycamptothecinen
dc.subjectradiotherapyen
dc.subjectchemotherapyen
dc.subjectcolorectal canceren
dc.subjectmetastasisen
dc.subjecthuman serum albuminen
dc.subjectcancer stem cellsen
dc.subjectradiosensitizeren
dc.title結合化療與放射線療法之大腸直腸癌奈米藥物載體開發zh_TW
dc.titleThe development of nano-carrier for colorectal cancer by the combination of chemotherapy and radiotherapyen
dc.typeThesis
dc.date.schoolyear108-2
dc.description.degree碩士
dc.contributor.oralexamcommittee楊台鴻(Tai-Horng Young),林文澧(Win-Li Lin),張富雄,駱俊良(Chun-Liang Lo)
dc.subject.keyword大腸直腸癌,轉移,人類血清白蛋白,透明質酸,化學治療,放射線治療,7-乙基-10-羥基喜樹鹼,zh_TW
dc.subject.keywordcolorectal cancer,metastasis,human serum albumin,hyaluronic acid,cancer stem cells,chemotherapy,radiotherapy,7-Ethyl-10-hydroxycamptothecin,radiosensitizer,en
dc.relation.page39
dc.identifier.doi10.6342/NTU202002173
dc.rights.note未授權
dc.date.accepted2020-08-05
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept醫學工程學研究所zh_TW
顯示於系所單位:醫學工程學研究所

文件中的檔案:
檔案 大小格式 
U0001-3107202016412300.pdf
  未授權公開取用
2.24 MBAdobe PDF
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved