Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/21256
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    CNU IR > Chna Nan Annual Bulletin > No.34 (2008) >  Item 310902800/21256
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/21256


    Title: 甲基安非他命生物共軛物之合成及其多株抗體之生產
    Studies on the Synthesis of Methamphetamine-Protein Bioconjugates and Production of Polyclonal Antibodies against Methamphetamine
    Authors: 周淑芬
    陳美吟
    黃國旭
    楊朝成
    Contributors: 生物科技系
    化妝品科技研究所
    Keywords: 甲基安非他命
    生物共軛物
    多株抗體
    酵素連結免疫吸附分析法
    Methamphetamine
    Bioconjugate
    Polyclonal antibodies
    Enzyme-linked immunsorbent assay (ELISA)
    Date: 2008
    Issue Date: 2009-05-01 15:10:51 (UTC+8)
    Abstract: 本研究目的在於自行合成甲基安非他命(methamphetamine; Meth)與蛋白質之生物共軛物(bioconjugates)來腹腔免疫ICR小鼠,以生產Meth 之多株抗體(P olyclonal antibodies against methamphetamine : anti-Meth PAbs)。由於Meth之分子量很小(約149.233 g/mol)不易在小鼠體內引起免疫反應,故本研究選用牛血清白蛋白(bovine serum albumin;BSA)以及絲膠蛋白(Sericin ; Ser),分別與Meth 形成生物共軛物,藉由大分子蛋白誘導小鼠體內產生Meth 之抗體。多株抗體製作過程為將高度免疫hyperimmune)中之ICR小鼠,注射0.5 mL pristane 後,再間隔兩週注射106l個NS-1 骨髓癌細胞。待小鼠腹腔漲大至行動困難時,收集ICR 小鼠所產生之腹水及血清,利用HitrapTM rProtein A column 來進行多株抗體之初步純化,並進一步測定anti-Meth PAbs 之效價(titer)以及進行蛋白質定量工作。本實驗工作首先成功合成出藥物與蛋白質之生物共軛物,其中Meth 與BSA 之生物共軛物(Meth-BSA)當作免疫原(immunogen)進行小鼠免疫工作;另外,Meth 與Ser 之生物共軛物(Meth-ser)當作酵素連結免疫吸附分析法(Enzyme-linked immunosorbent assay ; ELISA)檢測系統中所用之抗原(antige),以避免測到腹水中anti-BSA 抗體效價,而造成誤差• 最後生產並初步純化5.68mg /mL多株抗體(含anti-Meth and anti-BSA PAbs),並加以冷凍乾燥保存。
    The aim of this study was to synthesize methaphetamine (Meth) - protein bioconjugates and produce polyclonal antibodies (PAbs) against Meth (anti-Meth PAbs ) . ICR mice were intraperitoneally immunized with Meth-protein bioconjugates every two weeks. Because the molecular weight of Meth is very small , it is difficult to induce production of mice antibodies The Meth molecules were conjugated with bovine serum albumin ( BSA ) and sericin (Ser), respectively. Hyperimmune ICR mice produced anti-Meth PAbs after injected with 0.5 mL pristane, and injected with NS-1 rnyeloma cells two weeks later. Ascites and serum were collected from ICR mice, but before the rnice had difficulty moving, and anti-Moth PAbs was Purified by using HitrapTM rProtein A column. In this study, the drug-proteins bioconjugates had been successfully produced. Meth-BSA bioconjugates were as the immunogen for mice immunization and Meth-Ser bioconjugates were as the antigen for Enzyme-Link Immunosorbent Assay (ELISA). Finally the production and primary purification of a anti-Meth PAbs were performed The concentration of PAbs obtained was 5.68 mg / mL. Then, the anti-Meth PAbs were stored by freeze-dry method .
    Relation: 嘉南學報(科技類)34期:p.73-85
    Appears in Collections:[Chna Nan Annual Bulletin] No.34 (2008)
    [Dept. of Biotechnology (including master's program)] Periodical Articles
    [Dept. of Cosmetic Science and institute of cosmetic science] Periodical Articles

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