English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1505260      線上人數 : 358
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    主頁登入上傳說明關於CMUR管理 到手機版
    請使用永久網址來引用或連結此文件: http://ir.cmu.edu.tw/ir/handle/310903500/6943


    題名: 牙科用金屬材料對人類口腔細胞毒性之評估
    其他題名: Evaluation of the Cytotoxicity of Metallic Dental Materials on Human Oral Epithelial Cells and Gigival Fibroblasts
    作者: (林常申);涂明君(Tu,Ming-Gene);(陳振陽);陳三餘(Chen,San-Yue)
    貢獻者: 醫學院牙醫學系
    關鍵詞: 細胞毒性;牙科用金屬;人類口腔上皮細胞;cytotoxicity;dental alloys;human oral epithelial cells
    日期: 2006-12
    上傳時間: 2009-08-26 16:05:48 (UTC+8)
    摘要: 目的 因牙科用金屬材料長期使用於口腔之溼潤環境下,故本研究欲探討其在液體中之溶出物,對人類口腔上皮細胞之生物親和性與生物效應之影響。方法 將金合金、欽合金、鈀合金、鎳合金及銀粉五種牙科臨床上最常用之材料製作成直徑15mm厚2mm之圓板,經高溫滅菌處理之後,放入內含5mL細胞培養液之塑膠管內於37℃,5% CO2之培養箱內放置24小時,再以其培養液放入內含大約5×10^4個細胞之24孔培養皿中於37℃,5% CO2之條件下培養24小時後,用位相差顯微鏡觀察其形態變化,並進行MTT試驗來測定細胞存率以評估細胞毒性。其中細胞毒性較大之銀粉再利用流式細胞儀來作細胞周J明與細胞凋亡的觀察,並輔以分析培養液中lactate dehydrogenase (LDH)的活性來測試細胞壞死情形,並進一步分析細胞之p53及NF-kB活性,以及利用BrdU-incorporation測其對DNA複製的影響。結果 細胞形態學之觀察及MTr測試顯示4種鑄造用合金未見對細胞有明顯之影響而銀粉則呈現明顯之毒性刺激反應。針對銀粉材料作更進一步的調查顯示銀粉材料未引起細胞凋亡,而LDH測試証明與細胞壞死有關係。P53及NF-kB活性測試顯示經銀粉處理的細胞會產生發炎與逆境反應,BrdU-incorporation測試發現銀粉處理會抑制DNA的複製。結論 根據本次實驗之結果得知使用鑄造合金比銀粉合金更安全。
    Purpose. We examinated the cytotoxicity of metallic dental material eluates on human oral epithelium cells and gingival fibroblasts. Methods. A total of five common metallic alloys, including Amalgam, Gold, Nickel, Titanium, and Platinum were tested. Five discs of each alloy were prepared, and each disc was 15 mm diameter and 2 mm thick. After being autoclaved, these alloy discs were incubated with 5 ml of culture medium at 37℃, with 5% CO2 for 24 hours. The medium was then used to grow KB and HGF-1 cells. MTT assay examined the cytotoxicity of alloy eluates after 24-hour incubation. The effects of toxic alloy on cell cycle, necrosis, p53 and NF-kB activity, and DNA synthesis were further examined by flow cytometry, lactate dehydrogenase releasing assay, luciferase assay, and BrdU-incorporation, respectively. Results. Morphologic observation and the MTT test revealed that only the amalgam alloy was cytotoxic. Although flow cytometry showed no apoptotic cells after amalgam alloy treatment, high lactate dehydrogenase activity was found in culture medium. These results suggested that amalgam alloy induced breakdown of the cell membrane, a characteristic of necrosis. In addition, elevated p53 and NF-kB activity after amalgam alloy treatment supported that this alloy could cause inflammatory and stress responses. Finally, BrdU incorporation showed that amalgam alloy inhibited DNA synthesis. Conclusions. Based on the results of this experiment, casting metal alloys are safer than amalgam alloy.
    關聯: Mid-Taiwan Journal of Medicine 11(4 )236 ~242
    顯示於類別:[牙醫學系暨碩博士班、口腔醫學產業碩士班] 期刊論文

    文件中的檔案:

    檔案 大小格式瀏覽次數
    200612236242.pdf4718KbAdobe PDF313檢視/開啟


    在CMUR中所有的資料項目都受到原著作權保護.

    TAIR相關文章

     


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋