首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of olaquindox, oxytetracycline and chlorotetracycline in feeds by high performance liquid chromatography with ultraviolet and fluorescence detection adopting online synchronous derivation and separation
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Simultaneous determination of olaquindox, oxytetracycline and chlorotetracycline in feeds by high performance liquid chromatography with ultraviolet and fluorescence detection adopting online synchronous derivation and separation

机译:用高效液相色谱法同时测定含紫外线液相色谱法在紫外线和荧光检测喂养饲料中的含量含量。

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摘要

Olaquindox, oxytetracycline and chlorotetracycline were widely used in feed as antibiotics and growth promoter to improve feed conversion efficiency and increase the rate of weight gain for animals. However, the use of these antibiotics in feed was gradually prohibited because of concerns about contamination and resistance in animals. A quantitative and confirmatory method for determining the presence of olaquindox, oxytetracycline and chlorotetracycline in feed by high performance liquid chromatography equipped with ultraviolet detector in series with fluorescence detector (HPLC-UVD-FLD) was developed, optimized, and validated in three different matrices (compound, concentrated and premix feed). The analytes extraction was performed with a mixture of acetonitrile and 0.1 mol/L ethylenediamine tetraacetic acid disodium-Mcllvaine buffer (1:4, v/v) by one step sample preparation procedure. The validated method presented a broad linear range and good linearity with weighted least square method. The decision limit of the analytes ranged from 0.61 to 0.77 mg/kg for olaquindox, 0.90 to 1.2 mg/kg for oxytetracycline and 1.3 to 2.0 mg/kg for chlorotetracycline. The average recovery values found in intermediate precision conditions were ranged from 88.0 to 99.7% for olaquindox with RSD lower than 11.1%, from 84.4 to 99.0% for oxytetracycline with RSD lower than 9.6%, from 83.8 to 97.5% for chlorotetracycline with RSD lower than 10.0%. By Youden test and bottom-up method, the method was proved to be sufficiently robust and had a small uncertainty for different concentration levels. The developed method was successfully utilized for commercial feed samples to monitor complex cross contamination and residue conditions. Online synchronous derivation and separation using ultraviolet detector in series with fluorescence detector can effectively prevent false positive of chlorotetracycline in feed caused by vegetable meal. Since olaquindox, oxytetracycline and chlorotetracycline ar
机译:喹乙醇、土霉素和金霉素作为抗生素和生长促进剂广泛应用于饲料中,以提高饲料转化率和动物增重率。然而,由于担心动物的污染和耐药性,这些抗生素在饲料中的使用逐渐被禁止。在三种不同基质(复合饲料、浓缩饲料和预混料)中,开发、优化并验证了一种通过配备紫外检测器和荧光检测器(HPLC-UVD-FLD)的高效液相色谱法测定饲料中喹乙醇、土霉素和金霉素含量的定量验证方法。通过一步样品制备程序,使用乙腈和0.1 mol/L乙二胺四乙酸二钠缓冲液(1:4,v/v)的混合物进行分析物提取。验证后的方法与加权最小二乘法相比,线性范围宽,线性度好。分析物的决定限为喹乙醇0.61至0.77 mg/kg,土霉素0.90至1.2 mg/kg,金霉素1.3至2.0 mg/kg。在中等精密度条件下,喹乙醇的平均回收率为88.0%至99.7%,RSD低于11.1%;土霉素的平均回收率为84.4%至99.0%,RSD低于9.6%;金霉素的平均回收率为83.8%至97.5%,RSD低于10.0%。通过Youden试验和自底向上方法,该方法被证明具有足够的鲁棒性,并且对于不同浓度水平具有较小的不确定度。所开发的方法已成功用于商业饲料样品,以监测复杂的交叉污染和残留情况。采用紫外检测器与荧光检测器串联在线同步衍生分离,可有效防止饲料中金霉素因菜粕引起的假阳性。由于喹乙醇、土霉素和金霉素

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