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http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/53612完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 謝銘鈞 | |
| dc.contributor.author | Zong-Ping Hsu | en |
| dc.contributor.author | 徐宗平 | zh_TW |
| dc.date.accessioned | 2021-06-16T02:26:22Z | - |
| dc.date.available | 2020-08-12 | |
| dc.date.copyright | 2015-08-12 | |
| dc.date.issued | 2015 | |
| dc.date.submitted | 2015-08-05 | |
| dc.identifier.citation | REFERENCE
1. Luo, Y., M.R. Ziebell, and G.D. Prestwich, A Hyaluronic Acid−Taxol Antitumor Bioconjugate Targeted to Cancer Cells. Biomacromolecules, 2000. 1(2): p. 208-218. 2. Denet, A.R., R. Vanbever, and V. Preat, Skin electroporation for transdermal and topical delivery. Adv Drug Deliv Rev, 2004. 56(5): p. 659-74. 3. Subramaniam, V., et al., CD44 regulates cell migration in human colon cancer cells via Lyn kinase and AKT phosphorylation. Exp Mol Pathol, 2007. 83(2): p. 207-15. 4. Cai, S., et al., Intralymphatic chemotherapy using a hyaluronan-cisplatin conjugate. The Journal of surgical research, 2008. 147(2): p. 247-252. 5. Degim, I.T., D.J. Burgess, and F. Papadimitrakopoulos, Carbon nanotubes for transdermal drug delivery. J Microencapsul, 2010. 27(8): p. 669-81. 6. Zhao, Q.H., et al., Anticancer effect of realgar nanoparticles on mouse melanoma skin cancer in vivo via transdermal drug delivery. Med Oncol, 2010. 27(2): p. 203-12. 7. El-Dakdouki, M.H., et al., A simple method for the synthesis of hyaluronic acid coated magnetic nanoparticles for highly efficient cell labelling and in vivo imaging. RSC Advances, 2011. 1(8): p. 1449-1452. 8. Giri, A., et al., Polymer hydrogel from carboxymethyl guar gum and carbon nanotube for sustained trans-dermal release of diclofenac sodium. Int J Biol Macromol, 2011. 49(5): p. 885-93. 9. Kong, M., X. Chen, and H. Park, Design and investigation of nanoemulsified carrier based on amphiphile-modified hyaluronic acid. Carbohydrate Polymers, 2011. 83(2): p. 462-469. 10. Pissuwan, D., et al., A solid-in-oil dispersion of gold nanorods can enhance transdermal protein delivery and skin vaccination. Small, 2011. 7(2): p. 215-20. 11. Nose, K., et al., Gold nanorods in an oil-base formulation for transdermal treatment of type 1 diabetes in mice. Nanoscale, 2012. 4(12): p. 3776-80. 12. Yang, J.A., et al., Transdermal delivery of hyaluronic acid -- human growth hormone conjugate. Biomaterials, 2012. 33(25): p. 5947-54. 13. Shahini, M. and J.T. Yeow, Cell electroporation by CNT-featured microfluidic chip. Lab Chip, 2013. 13(13): p. 2585-90. 14. Shiozuka, M., Y. Nonomura, and R. Matsuda, Transdermal delivery of adriamycin to transplanted ehrlich ascites tumor in mice. Pharmaceutics, 2013. 5(3): p. 385-91. 15. Tsai, S.W., et al., Hyaluronan-cisplatin conjugate nanoparticles embedded in Eudragit S100-coated pectin/alginate microbeads for colon drug delivery. Int J Nanomedicine, 2013. 8: p. 2399-407. 16. Zorec, B., et al., Skin electroporation for transdermal drug delivery: the influence of the order of different square wave electric pulses. Int J Pharm, 2013. 457(1): p. 214-23. 17. Arpicco, S., et al., Hyaluronic acid conjugates as vectors for the active targeting of drugs, genes and nanocomposites in cancer treatment. Molecules, 2014. 19(3): p. 3193-230. 18. Gao, Y., et al., Transdermal delivery of 10,11-methylenedioxycamptothecin by hyaluronic acid based nanoemulsion for inhibition of keloid fibroblast. Carbohydr Polym, 2014. 112: p. 376-86. 19. Jung, H.S., et al., Nanographene Oxide–Hyaluronic Acid Conjugate for Photothermal Ablation Therapy of Skin Cancer. ACS Nano, 2014. 8(1): p. 260-268. 20. Mero, A. and M. Campisi, Hyaluronic Acid Bioconjugates for the Delivery of Bioactive Molecules. Polymers, 2014. 6(2): p. 346-369. 21. Mizrahy, S., et al., Tumor targeting profiling of hyaluronan-coated lipid based-nanoparticles. Nanoscale, 2014. 6(7): p. 3742-52. 22. Siu, K.S., et al., Non-covalently functionalized single-walled carbon nanotube for topical siRNA delivery into melanoma. Biomaterials, 2014. 35(10): p. 3435-42. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/53612 | - |
| dc.description.abstract | 皮膚癌為一種東方人較少的癌症病變,然而在國外則是併發率極高的癌症之一,分為基底細胞瘤,鱗狀細胞瘤,黑色素瘤.而我們的實驗則是以黑色素瘤作為實驗的細胞,主要是因為雖然他病發率低僅占皮膚癌中的百分之五左右,但因為其高轉移性導致死亡率極高,所以我們選擇以這組細胞最為實驗組.一般來說皮膚癌最常見的治療方式為手術切除,但因為黑色素瘤(melanoma)容易轉移及深入的特性,導致常常手術無法清除乾淨,所以我們希望能使用經皮傳輸將藥物以塗抹的方式進行療,如此不僅可以降低患者對於治療的恐懼,也比較不會承受那麼大的痛苦,並且接受率也較高.
黑色素瘤細胞目前已經有許多一線藥物,例如Doxorubicin .Oxaliplatin和Cisplatin等等,其中又以鉑類藥物最常使用,所以我們選用Oxaliplatin 的active form DACHPt作為化療藥,為了增加經皮傳輸的穿透效果,且提升對於腫瘤細胞的targeting效果,我們選用了玻尿酸(Hyaluronic acid, HA)作為藥物載體不僅僅能提升穿透效果,其較高的生物相容性也可使患者不會有副作用的疑慮. 人類皮膚分為三層,分別是表皮層.真皮層.皮下組織,其中表皮層最外層的角質層排列緊緻保護著全身,導致許多藥物無法穿透,所以僅僅是利用玻尿酸本身濕潤增加通透度的能力還是不夠,所以我們利用電穿孔(Electroporation)來增加一條穿透的途徑,然而電穿孔需要較高的福特數才能使細胞產生孔洞,我們選擇搭配多壁奈米碳管(MWNT)來解決這部分的問題,因為奈米碳管極高的長徑比可使其有放大電場的效果,使我們不用用高福特數仍能達到使細胞打開孔洞的效果. 本論文是使用玻尿酸接枝鉑類藥物後搭配奈米碳管提升電穿孔的效果對於皮膚癌進行治療,而我們也發現我們的材料對於有CD44受器的細胞有較好得毒殺效果,並且確實碳管配合電穿孔會有更好的藥物傳輸效果,因此希望將玻尿酸接枝藥物配合電穿孔的方式可以在不同的領域有貢獻,不管在治療或是醫美等等. | zh_TW |
| dc.description.abstract | Skin cancer is a cancer lesion that Oriental less, but in foreign countries is complicated by high rates of cancer, into basal cell tumor, squamous cell tumors, melanoma. Our experiment is based on the melanoma cells as experimental, mainly because the disease is low, although he was only five percent of skin cancer in the left and right, but because of its high metastatic cause high mortality rate, so we choose in this group were the most experimental groups.
Melanoma cells has many first-line drugs, such as Doxorubicin .Oxaliplatin and Cisplatin, etc., among which the most commonly used platinum-based drugs, so we use the active form DACHPt Oxaliplatin as chemotherapy drugs, in order to increase the penetration effect of percutaneous transmission and to enhance the effect for targeting tumor cells, we use hyaluronic acid (Hyaluronic acid, HA) not only as a drug carrier can enhance the penetration effect, its high biocompatibility also allows patients will not have adverse effects concerns. Human skin is divided into three layers, namely the epidermis. Dermis subcutaneous tissue, wherein the outermost layer of the epidermis cuticle compact arrangement protects the body, causing many drugs can not penetrate, so just increase the use of hyaluronic acid itself moist transparent ability degree is not enough, so we use electroporation (Electroporation) a way to increase the penetration, however electroporation Ford needs a higher number of cells in order to make the holes, we choose with multi-walled carbon nanotubes (MWNT) to this part of the problem, because the high aspect ratio of carbon nanotubes can amplify it has the effect of an electric field, so that we do not use a high number of Ford still achieve the effect of the cells to open pores. This paper is the use of hyaluronic acid after graft carbon nanotubes with platinum drugs to enhance the effect of electroporation treatment for skin cancer, and we have found our material for CD44 by the cells had better get toxic effect, and indeed carbon tubes with electroporation have better drug delivery effect, it is desirable to coordinate the way electroporation grafted hyaluronic acid drugs can contribute in different areas, whether in health or beauty treatment and so on. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-16T02:26:22Z (GMT). No. of bitstreams: 1 ntu-104-R02548065-1.pdf: 1981535 bytes, checksum: 259cbc5caeb53e5ab981553d7577e4c5 (MD5) Previous issue date: 2015 | en |
| dc.description.tableofcontents | CONTENT
ABSTRACT II CONTENT IV LIST of SCHEMES VI LIST of FIGURES VII Chapter 1 Introduction 1 Chapter 2 Materials and methods 4 Experiments procedure 4 2.1 Material 4 2.2 Synthesis of HA-DACHPt 5 2.3 Synthesis of HA-FITC and HA-Cy5.5 5 2.4 Oxidation of Carbon nanotube(CNT) 6 2.5. In vitro serum stability test of HA-DACHPt conjugate 6 2.6 In vitro drug release profile of DACHPt from HA-DACHPt with and without electroporation 6 2.7 In vitro cellular uptake 7 2.8 In vitro cytotoxicity 7 2.9 In vitro transdermal delivery of drug 8 2.10 animals and tumor model 9 2.11 In vivo tumor accumulation and imaging 10 2.12 In vivo and In vitro application of electroporation treatment 10 Chapter 3 Result and discussions 11 3.1 Synthesis and characterization of HA-DACHPt and HA-FITC 11 3.2 Oxidation of multiwall carbon nanotube(MWNT) 13 3.3 Expression level of CD44 surface marker on melanoma cells 14 3.4 Cellular uptake of HA-DACHPt 15 3.5 In vitro cytotoxicity 15 3.6 In vitro penetration of skin 16 3.7 HA penetration through the stratum corneum 17 3.8 In Vivo Transdermal Therapy of Skin Cancer 18 Chapter 4 Conclusions 20 REFERENCE 21 SCHEME 25 FIGURE 29 LIST of SCHEMES Scheme 1. Mechanism 24 Scheme 2 .Synthesis of HA-DACHPt 25 Scheme 3. Synthesis of HA-FITC 26 Scheme 4. Spectrum of HA-FITC 27 LIST of FIGURES Figure1. HA-DACHPt , L.E.&D.C. 28 Figure2. L.E. and D.C.. of HA-DACHPt 29 Figure3. TEM of MWNT , Oxidation for (a)7h(b)14h(c)24H 30 Figure4. Flow cytometer & Western blot 31 Figure5. Binding test 32 Figure6. Cellular uptake of HA-FITC 33 Figure7. Cellular uptake of HA-FITC & HA-DACHPt 34 Figure8. Cell viability (a).(b) pure HA treat B16-F10 , B16-F10(K.O.) 35 (c),(d) DACHPt treat B16-F10 , B16-F10(K.O.) 36 (e),(f) Oxaliplatin treat B16-F10 , B16-F10(K.O.) 37 (g),(h) HA-DACHPt treat B16-F10 , B16-F10(K.O.) 38 Figure9. LD50 39 Figure10. Ex vivo penetration 40 Figure11. Ex vivo transdermal penetration 41 Figure12. Animal model schedule 42 Figure13. Tumor 43 Figure14. HA-EDA conjugation ratio -44 Figure15. ICP-MS 45 | |
| dc.language.iso | en | |
| dc.subject | 玻尿酸 | zh_TW |
| dc.subject | 經皮傳輸 | zh_TW |
| dc.subject | 奈米碳管 | zh_TW |
| dc.subject | 電穿孔 | zh_TW |
| dc.subject | transdermal | en |
| dc.subject | Electroporation | en |
| dc.subject | melanoma | en |
| dc.subject | DACHPt | en |
| dc.subject | hyaluronic acid | en |
| dc.title | 玻尿酸接枝鉑類藥物結合奈米碳管之製備藉由電穿孔經皮傳輸應用於黑色素細胞瘤之治療 | zh_TW |
| dc.title | Electroporation Enhanced Transdermal Drug Delivery for
Melanoma Skin Cancer Therapy by Using DACH-Platinum Conjugated Hyaluronic Acid/Multi-walled Carbon Nanotube Mixtures. | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 103-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 駱俊良,林文澧 | |
| dc.subject.keyword | 玻尿酸,經皮傳輸,奈米碳管,電穿孔, | zh_TW |
| dc.subject.keyword | melanoma,hyaluronic acid,DACHPt,transdermal,Electroporation, | en |
| dc.relation.page | 46 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2015-08-05 | |
| 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 | |
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