首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Sample preparation strategy for the simultaneous determination of macrolide antibiotics in animal feedingstuffs by liquid chromatography with electrochemical detection (HPLC-ECD).
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Sample preparation strategy for the simultaneous determination of macrolide antibiotics in animal feedingstuffs by liquid chromatography with electrochemical detection (HPLC-ECD).

机译:液相色谱-电化学检测(HPLC-ECD)同时测定动物饲料中大环内酯类抗生素的样品制备策略。

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摘要

A novel and suitable clean-up method that allows, for the first time, the simultaneous determination of a rather large number of macrolide antibiotics (erythromycin, rosamicin, spiramycin, tylosin, kitasamycin and josamycin in feedingstuffs by high performance liquid chromatography with electrochemical detection (HPLC-ECD) is presented in this work. The effectiveness of the developed clean-up method allows the quantification of the target macrolides in poultry feed using standard calibration curves instead of matrix matched standards, which overcomes the general problem of finding representative blanks. Furthermore an additional back extraction included in the sample preparation procedure allows the determination of an additional macrolide (oleandomycin) with detection limits, expressed as apparent concentration in poultry feed, ranging from 0.04 to 0.22 mg kg(-1) and relative standard deviation values ranging from 3.6 to 10.1% depending on the target analyte. Moreover, this additional step has been proven to enlarge the scope of the method by the extension of its applicability, at the target level of concentration, to other animal feedingstuffs such as pig and cattle. The analysis of real feedingstuffs containing macrolides demonstrated the fitness for purpose of the whole analytical procedure as well as a good fitting between real and spiked samples. The proposed methods appeared therefore as a sound alternative in the frame of control (e.g. for post-screening purposes) and/or monitoring surveillance programmes at the target level of 1.0 mg kg(-1) established according to the reported lowest dosage of additive needed to lead a growth promoting effect.
机译:一种新颖且合适的净化方法,该方法首次允许通过高效液相色谱-电化学检测法同时测定饲料中相当数量的大环内酯类抗生素(红霉素,罗米霉素,螺旋霉素,泰乐菌素,基他霉素和交沙霉素)(本工作介绍了HPLC-ECD,开发的净化方法的有效性允许使用标准校准曲线代替基质匹配标准品定量家禽饲料中的目标大环内酯类药物,从而克服了寻找代表性空白的一般问题。样品制备程序中还包括额外的反萃取,因此可以测定其他大环内酯类(油霉素),其检出限为家禽饲料中的表观浓度,范围为0.04至0.22 mg kg(-1),相对标准偏差范围为取决于目标分析物3.6%至10.1%。已经证明,通过在目标浓度水平上将其适用性扩展到其他动物饲料(例如猪和牛),该步骤扩大了该方法的范围。对包含大环内酯类化合物的实际饲料的分析表明,该方法适用于整个分析过程,并且适合真实样品和加标样品之间的拟合。因此,根据报告的所需最低添加剂剂量建立的目标水平为1.0 mg kg(-1),建议的方法可作为控制框架(例如用于后筛查目的)和/或监测监控程序的合理选择。起到促进增长的作用。

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