博碩士論文 102222016 詳細資訊




以作者查詢圖書館館藏 以作者查詢臺灣博碩士 以作者查詢全國書目 勘誤回報 、線上人數:38 、訪客IP:18.119.134.171
姓名 許翔崴(Hsiang-Wei Hsu)  查詢紙本館藏   畢業系所 物理學系
論文名稱 以奈米黑色素螯合有毒金屬離子之物理研 究與應用開發
(Physics and application of the chelation of toxic metal ions by nano-melanin)
相關論文
★ GW準粒子於Mn3O4和GaN的激發態性質計算★ 混合物種與低溫冷凍原子團簇噴流的發展
★ 以雷射脈衝對磁性薄膜進行超快磁轉化及其動態時間解析★ 以脈衝雷射沈積製造FeBO3薄膜
★ 共焦拉曼與螢光顯微鏡之發展及其在材料診斷上之應用★ 以光激發黑色素來清除細胞環境中之活性氧之探討
★ 發展在電漿波導式雷射電漿波電子加速器中誘發電子注入與X 光產生之技術★ 莫斯堡光譜儀的建造以及其應用到FeCO3薄膜的診斷
★ 發展利用另一道脈衝雷射在脈衝雷射沉 積技術中成長碳薄膜的雷射同步過程進 行碳薄膜晶向之控制★ 研究以雷射進行基板之前置處理來達到控制脈衝雷射沉積的矽鍺量子點的尺寸分布的可行性
★ 以超短脈衝雷射沉積技術製作鍺/矽薄膜之研究★ 一百兆瓦雷射系統之建造與在結構化電漿波導之應用
★ 以基質輔助脈衝雷射蒸鍍法製備聚3-己基噻酚/(6,6)-苯基-C61-丁酸甲酯有機太陽能電池★ 藥物劑量與復原時間影響光動力療法疫苗之功效的系統性研究
★ 光控制實用的材料製程在PEM燃料電池及光電元件上的應用★ 以脈衝雷射沉積與脈衝雷射退火製造鍺/矽量子點與成長鍺薄膜於單晶矽上並應用於光偵測器的研究
檔案 [Endnote RIS 格式]    [Bibtex 格式]    [相關文章]   [文章引用]   [完整記錄]   [館藏目錄]   [檢視]  [下載]
  1. 本電子論文使用權限為同意立即開放。
  2. 已達開放權限電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。
  3. 請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。

摘要(中) 黑色素是人體內最普遍的生物聚合物之一,過去的研究顯示黑色素具有對抗自由基、活性含氧分子、腫瘤、蛇毒、病毒和重金屬離子等醫學應用的潛 力,
然而它在生物介質的不可溶解性大大的降低了它可能的療效。在先前的研 究裡,我們開發了用脈衝雷射來進行光粉碎以及長時間攪拌等方式,來進行黑 色素在生物介質中的奈米化和可分散化。經由這樣的方式,黑色素暴露的表面 積增加了好幾個數量級,大幅提升了它的化學與生物作用的效率。作為一個示 範,我們先前已經探究了奈米化黑色素對抗活性含氧分子而保護細胞的應用。 在這篇論文裡,我們將展現使用此奈米化黑色素作為對抗毒性金屬離子的螯合 劑的潛力。
本論文研究了使用奈米化黑色素來做為新型螯合劑的可能性。我們使用感應耦合電漿放射光譜儀 ( ICP-OES)來確認奈米化黑色素的螯合能力,並通過流式細胞儀和 ATP 測量來表現細胞活性。結果表明奈米化黑色素不僅可以螯合金
屬離子,更重要的是,它也可以使得受到鉛離子傷害的細胞進行修復。首先我
們確認了本製程的奈米黑色素確實具有螯合重金屬的能力,然後將奈米黑色素
進行細胞實驗,發現奈米黑色素可以治療已受金屬離子的傷害的細胞,但DMSA 不能,我們猜測奈米化黑色素可以進到細胞中使得細胞吐出已被細胞吞噬的鉛離子,並使得細胞的 ATP 產率上升,此結果表明,奈米化黑色素確實具有作為新型螯合劑的可能。
摘要(英) Melanin is one of the most ubiquitous biological polymer widespread in our body tissue, and it has been shown that melanin has potential
medical functions against free radicals, reactive oxygen species, tumor,
venin, virus, and heavy metal ions. However, its insolubility drastically
reduces its efficacy. We have shown previously that melanin can be
broken down to become nanometer-sized and water-dispersible by
pulsed-laser photo-fragmentation or by extended mechanical stir.
Through this, the exposed surface area could be increased by many orders of magnitude, dramatically increasing the efficiency of chemical and biological interactions. As a demonstration, we have explored the
efficacy of using the nanonized melanin in protecting cells from reactive
oxygen species.In this master thesis , we will explore the utilization of the nanonized melanin as a chelation agent against toxic metal ions.
In this paper, the possibility of using melanin nanoparticles as a new
kind of chelation agent has been studied. The chelating ability was
characterized by using Inductively Coupled Plasma Optical Emission
Spectrometer ( ICP-OES). The cell viability activity were characterized by using flow cytometer and ATP measurement. Result shows the melanin nanoparticles not only can chelate metal ions, more importantly,
but also can recovery cells from harm of Pb2+ ion. First, the chelation
ability of melanin on Pb2+ was studied. Then nanolized melanin was been utilized to in-vitro experiment. it was found the melanin nanoparticles can cure cells from harm of metal ion, but DMSA can not. We hypothesize that the nanolized melanin could diffuse into the cells to spit out lead-ion which had been swallowed by cells, and increase cells ATP. This result indicates that the nanolized melanin did have the possibility of being a new chelating agent.
關鍵字(中) ★ 黑色素
★ 脈衝雷射
★ 自由基
★ 螯合劑
★ 活性氧
★ DMSA
★ ATP
關鍵字(英)
論文目次 中文摘要 ..................................................................................................... i
英文摘要 .................................................................................................... ii
誌謝 ........................................................................................................... iv
圖目錄 ...................................................................................................... vii
一、 緒論 .............................................................................................. 1
1.1. 重金屬的流行病學與病理學 ....................................................... 1
1.2. 螯合治療 ....................................................................................... 2
1.3. 黑色素 ........................................................................................... 3
1.4. 研究成果 ....................................................................................... 4
1.4.1. 本製程奈米黑色素確實可以螯合重金屬 ............................... 4
1.4.2. 奈米黑色素確實可以保護細胞不受重金屬傷害 ................... 4
二、 材料與方法 .................................................................................. 5
2.1. 奈米化黑色素的方法 ................................................................... 5
2.2. 感應耦合質譜分析儀 ( ICP-OES) .............................................. 6
2.2.1. 實驗步驟-無細胞實驗-奈米黑色素螯合能力 ........................ 7
2.3. 細胞培養 ....................................................................................... 7
2.4. 存活率量測 ................................................................................... 8
2.4.1. 實驗步驟-細胞試驗-鉛離子濃度對細胞的存活率影響 ........ 8
2.5. ATP 量測 ...................................................................................... 9
三、 結果與討論 ................................................................................ 11
3.1. 無細胞試驗 ................................................................................. 12
3.1.1. 奈米黑色素對 Pb2+的螯合能力 ............................................. 12
3.2. 體外細胞試驗 ............................................................................. 13
3.2.1. 鉛離子濃度對細胞的影響 ..................................................... 13
3.2.2. 奈米黑色素或 DMSA 與鉛離子對細胞的影響 ................... 15
四、 結論與未來展望 ........................................................................ 18
4.1. 結論 ............................................................................................. 18
4.2. 未來展望 ..................................................................................... 18
參 考 文 獻 ............................................................................................ 19
參考文獻 [1] Tchounwou PB Yedjou CG Petlolla AK Sutton DJ. Heavy metals
toxicity and the environment. NIH Public Access, 101:113–164, 2014.
[2] Lowry JA. Oral chelation therapy for patients with lead poisoning.
Am Acad Pediatr, 116: 1036-1046, 2010.
[3] Pombeiro-Sponchiado SR Goncalves RDR. Antioxidant activity of
the melanin pigment extracted from aspergillus nidulans. Biol Pharm
Bull, 28(6):1129–1131, 2005.
[4] Niwano Y Tada M, Kohno M. Scavenging or quenching effect
of melanin on superoxide anion and singlet oxygen. J. Clin.
Biochem. Nutr., 46(3):224–228, 2010.
[5] Sichel G Brai M Palminteri MC, Sciuto S. Seasonal dependence
of ESR feature of frog melanins. Comp. Comparative Biochemistry
and Physiology Part B: Comparative Biochemistry, 70(3):611-613,
1981.
[6] Geremia E et al. Vanella A, Sichel, G. Eumelanins as free
radicals trap and superoxide dismutase activities in Amphibia.
Comparative Biochemistry and Physiology Part B: Comparative
Biochemistry, 79(1): 67-69, 1984.
[7] Sarna T Pilas B Land EJ, Truscott TG. Interaction of radicals
from water radiolysis with melanin. Biochimica et Biophysica Acta
22
(BBA)-General Subjects, 883(1): 162-167, 1986.
[8] Scalia M Geremia E Corsaro C Santoro C Baratta D, Sichel G.
Lipid peroxidation in pigmented and unpigmented liver tissues:
protective role of melanin. Pigment Cell Research, 3(2): 115-119,
1990.
[9] Burkhart CN Burkhart CG. The mole theory: primary function
of melanocytes and melanin may be antimicrobial defense
and immunomodulation (not solar protection). Int. J. Dermatol.,
44(4):340–342, 2005.
[10] Mackintosh JA. The antimicrobial properties of melanocytes,
melanosomes and melanin and the evolution of black skin. J.
Theor. Biol., 211(2):101–113, 2001.
[11] Garger SJ Dousman L Grill LK Tus’ e D Mohagheghpour N,
Waleh N. Synthetic melanin suppresses production of proinflammatory
cytokines. Cell. Immunol., 199(1):25–36, 2000.
[12] Michel M et al. Ball V, Frari DD. Deposition mechanism and
properties of thin polydopamine films for high added value applications
in surface science at the nanoscale. BioNanoSci., 2(1):16–
34, 2012.
[13] Irimia-Vladu M Mostert AB Schwenn PE Meredith P, Bettinger
CJ. Electronic and optoelectronic materials and devices
inspired by nature. Rep. Prog. Phys., (034501):1–36, 2013.
[14] Sivakumar K Kim S-K Manivasagan P, Venkatesan J.
Actinobacterial melanins: current status and perspective for the
future. World J. Microbiol. Biotechnol., 29:1737–1750, 2013.
[15] Gasyna EM Kobori Y Rezaei KA-Norris JR Jr. Seagle BL,
Rezai KA. Time-resolved detection of melanin free radicals quenching
reactive oxygen species. Journal of the American Chemical
Society, 127(32):11220–11221, 2005.
[16] Potts AM Au PC. The affinity of melanin for inorganic ions. Exp.
Eye, 22(5): 487–491, 1976.
[17] Lee J-K Kim DJ, Ju K-Y. The synthetic melanin nanoparticles
having an excellent binding capacity of heavy metal ions. Bull. Korean
Chem. Soc., 33(11): 3788–3792, 2012.
[18] Chu P et al. Schweitzer AD, Revskaya E. Melanin-covered
nanoparticles for protection of bone marrow during radiation therapy
of cancer. Int. J. Radiat. Oncol. Biol. Phys., 78(5): 1494–1502, 2010.
[19] Mikirova N Casciari J, Hunninghake R. Efficacy of oral DMSA
and intravenous EDTA in chelation of toxic metals and improvement
of the number of stem/progenitor cells in circulation. Translational
Biomedicine, 2(2), 2011.
指導教授 陳賜原 審核日期 2017-1-11
推文 facebook   plurk   twitter   funp   google   live   udn   HD   myshare   reddit   netvibes   friend   youpush   delicious   baidu   
網路書籤 Google bookmarks   del.icio.us   hemidemi   myshare   

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明