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Determination of fluoroquinolones in edible animal tissue samples by high performance liquid chromatography after solid phase extraction

机译:固相萃取-高效液相色谱法测定食用动物组织样品中的氟喹诺酮类药物

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In the present work, a rapid, accurate, and sensitive method has been developed for the quantitative determination of five fluoroquinolones (enoxacin, ofloxacin, norfloxacin, ciprofloxacin, and enrofloxacin) in edible animal tissues (muscle tissue, liver, kidney, and eggs). The separation was accomplished on an Inertsil (250 x 4 mm) C-8, 5 mu m, analytical column, at ambient temperature within 15 min. The mobile phase consisted of a mixture of citric acid (0.4 mol L-1)-CH3OH-CH3CN (87:9:4% v/v). UV detection at 275 nm yielded the following limits of detection: 100 pg per 20 mu L injected volume for enoxacin, norfloxacin, and ciprofloxacin, 20 pg for ofloxacin, and 200 pg for enrofloxacin. Peaks in real samples were identified by means of a photodiode array detector. The method was validated in terms of intra-day (n = 8) and inter-day (n = 8) precision and accuracy. Tissue samples were purified from endogenous interference by solid-phase extraction using Oasis HLB cartridges. The solid-phase extraction protocol was optimized in terms of retention and elution. Recovery rates at fortification levels of 40, 60, and 80 ng/g ranged from 82.5% to 111.1%. The applicability of the method was examined using real samples from a chicken treated orally with the five studied fluoroquinolones.
机译:在当前的工作中,已经开发了一种快速,准确和灵敏的方法,用于定量测定食用动物组织(肌肉组织,肝,肾和卵)中的五种氟喹诺酮类药物(依诺沙星,氧氟沙星,诺氟沙星,环丙沙星和恩诺沙星)。 。分离是在环境温度下15分钟内在5微米Inertsil(250 x 4 mm)C-8分析柱上完成的。流动相由柠檬酸(0.4 mol L-1)-CH3OH-CH3CN(87:9:4%v / v)的混合物组成。 275 nm处的UV检测产生以下检测限:依诺沙星,诺氟沙星和环丙沙星每20 ul注射体积100 pg,对氧氟沙星为20 pg,对恩氟沙星为200 pg。实际样品中的峰通过光电二极管阵列检测器鉴定。该方法已通过日内(n = 8)和日间(n = 8)精度和准确性进行了验证。使用Oasis HLB柱通过固相萃取从内源性干扰中纯化组织样品。在保留和洗脱方面对固相萃取方案进行了优化。设防水平为40、60和80 ng / g时,回收率介于82.5%至111.1%之间。使用经五个研究的氟喹诺酮类药物口服治疗的鸡肉的真实样品,检验了该方法的适用性。

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