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首页> 外文期刊>Food analytical methods >Simultaneous Determination of Flumequine and Oxolinic Acid Residues in Aquatic Products Using Pressurized Capillary Electrochromatography
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Simultaneous Determination of Flumequine and Oxolinic Acid Residues in Aquatic Products Using Pressurized Capillary Electrochromatography

机译:加压毛细管电色谱法同时测定水产品中的氟喹啉和草酸残留量

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摘要

A rapid method for detection of flumequine (FQ) and oxolinic acid (OA) residues from fish tissues was established using pressurized capillary electrochromatography (pCEC). Residual FQ and OA were extracted from fish tissue samples with acidified acetonitrile and purified on an Oasis HLB C-18 solid-phase extraction column. The extract was then analyzed by pCEC with the mobile phase (pH = 3) consisting of acetonitrile and 15 mM ammonium acetate (45: 55, v/v, respectively) at the flow rate of 0.07 mL/min, detection wavelength of 324 nm, and applied voltage of -10 kV. Baseline separation of FQ and OA was achieved in 10 min; both drugs showed good linearity in the range of 0.2-5 mu g/mL. The recoveries of FQ and OA were between 82 and 92 % (relative standard deviation = 3.63-5.96). The limits of detection for FQ and OA were 0.1 and 0.08 mg/kg, respectively.
机译:建立了使用加压毛细管电色谱法(pCEC)建立的快速检测鱼组织中的氟啶胺(FQ)和草酸(OA)残留的方法。用酸化的乙腈从鱼组织样品中提取残留的FQ和OA,并在Oasis HLB C-18固相提取柱上纯化。然后将提取物用pCEC分析,流动相(pH = 3)由乙腈和15 mM乙酸铵(分别为45:55,v / v)组成,流速为0.07 mL / min,检测波长为324 nm ,施加的电压为-10 kV。 FQ和OA的基线分离在10分钟内完成;两种药物在0.2-5μg / mL的范围内均显示出良好的线性。 FQ和OA的回收率在82%至92%之间(相对标准偏差= 3.63-5.96)。 FQ和OA的检出限分别为0.1和0.08 mg / kg。

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