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作 者:杜寒春[1] 冯德芬[2] 叶赛芳 黄泽军[2] 艾晨昊 罗燕妮[2] 谭学才[2] DU Hanchun;FENG Defen;YE Saifang;HUANG Zejun;AI Chenhao;LUO Yanni;TAN Xuecai(Guangxi Zhuang Autonomous Region Center for analysis and Test Research,Nanning 530022, China;School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Key Laboratory of Guangxi Colleges and Universities for Food Safety and Pharmaceutical Analytical Chemistry, Nanning 530008, China)
机构地区:[1]广西壮族自治区分析测试研究中心,广西南宁530022 [2]广西民族大学化学化工学院,广西高校食品安全与药物分析化学重点实验室,广西南宁530008
出 处:《化工技术与开发》2016年第12期30-34,48,共6页Technology & Development of Chemical Industry
基 金:国家自然科学基金项目(21365004);广西直属公益性科研院所基本科研业务费专项项目(2013ACZ04)
摘 要:本文利用青霉素酶与青霉素发生水解反应生成青霉噻唑酸,该酸电离出H+,促使溶液中的氧化苏木精发生还原反应,产生电流信号。以玻碳电极为工作电极,建立一种检测青霉素的电化学方法。在最佳的实验条件下,青霉素浓度在10-9~10-5 mol·L^(-1)范围内与其相对电流强度呈良好的线性关系(r2=0.9973),最低检出限(S/N=3)为1.661×10-8 mol·L^(-1)。连续平行测定1×10-6 mol·L^(-1)的青霉素溶液3次,相对电流强度的RSD为2.50%,表明该方法具有良好的稳定性。将该方法用于牛奶样品的实际测定,回收率为99.70%~102.69%,结果较为理想。The penicillinase catalyzed the hydrolysis of penicillin to penicilloic acid, which H+ was liberated. H+ promoted the reduction reaction of hematein, thereby generated a current signal. Based on the principle, a new electrochemical method was established for the determination of penicillin at the glass carbon electrode. Under the optimum conditions, the GCE/hematein/penicillinase exhibited excellent performance for penicillin in PBS with a wide range of 10-9~10-5 mol/L and the detect limit was 1.661×10-8 mol/L(S/N=3). The RSD for 1×10-6 mol/L penicillin was 2.50%, which indicated that the method had good stability. The detection of penicillin concentration in real sample (milk) had acceptable accuracy with the assay system, which the recovery was 99.70%~102.69%.
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