Comparison of clonidine and cyproheptadine determination in animal-derived foods by sweeping-micellar electrokinetic chromatography and large volume sample stacking-capillary zone electrophoresis

IF 1.7 4区 化学 Q3 CHEMISTRY, ANALYTICAL Acta Chromatographica Pub Date : 2021-11-29 DOI:10.1556/1326.2021.00970
Zhihan Zheng, Li Xiaobin, Huitao Liu, Yuan Gao
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引用次数: 4

Abstract

This study establishes a method for rapid detection of clonidine and cyproheptadine in foods of animal origin. In order to obtain the best detection method, capillary zone electrophoresis (CZE), large volume sample stacking (LVSS), and sweeping-micellar electrokinetic capillary chromatography (sweeping-MEKC) were used respectively. The limits of detection (LODs) of clonidine and cyproheptadine by LVSS-CZE were 0.028 μg mL−1 and 0.034 μg mL−1, and those by sweeping-MEKC were 0.023 μg mL−1 and 0.031 μg mL−1, respectively. Compared with the CZE method, the two online pre-concentration technologies have greatly improved the detection sensitivity and achieved good enrichment results. However, compared with the sweeping-MEKC system, the LVSS system consumed a longer time and was greatly affected by the actual sample matrix. The sweeping-MEKC method was proved to be suitable for real sample analysis. Under the best sweeping-MEKC conditions, clonidine and cyproheptadine could be well separated within 8 min and good linear relationships in the range of 0.1–1.0 μg mL−1 (r 2 > 0.99) were obtained. This method was successfully applied to the determination of clonidine and cyproheptadine in animal-derived foods with the recoveries of 82.3%–90.1% and the relative standard deviations (RSDs) less than 3.11%. The sweeping-MEKC method is simple to operate and has great potential in the rapid detection of clonidine and cyproheptadine in animal-derived foods.
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扫描胶束电动色谱法和大容量堆积毛细管区带电泳法测定动物性食品中可乐定和赛庚啶的比较
建立了动物源性食品中可乐定和赛庚胺的快速检测方法。为获得最佳检测方法,分别采用毛细管区带电泳(CZE)、大体积样品堆积法(LVSS)和扫胶束电动毛细管色谱法(sweep - mekc)。LVSS-CZE法对可乐定和赛庚啶的检出限分别为0.028 μ mL - 1和0.034 μ mL - 1, sweep - mekc法对可乐定和赛庚啶的检出限分别为0.023 μ mL - 1和0.031 μ mL - 1。与CZE法相比,两种在线预富集技术均大大提高了检测灵敏度,富集效果良好。然而,与扫描- mekc系统相比,LVSS系统消耗的时间更长,并且受实际样品矩阵的影响较大。结果表明,扫描- mekc方法适用于实际样品的分析。在最佳扫描- mekc条件下,可乐定和赛庚啶可在8 min内分离,且在0.1 ~ 1.0 μg mL−1 (r 2 > 0.99)范围内具有良好的线性关系。该方法可用于动物性食品中可乐定和赛庚啶的含量测定,加样回收率为82.3% ~ 90.1%,相对标准偏差(rsd)小于3.11%。扫描- mekc方法操作简便,在动物源性食品中可乐定和赛庚胺的快速检测中具有较大的应用潜力。
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来源期刊
Acta Chromatographica
Acta Chromatographica 化学-分析化学
CiteScore
4.00
自引率
0.00%
发文量
55
审稿时长
2.3 months
期刊介绍: Acta Chromatographica Open Access Acta Chromatographica publishes peer-reviewed scientific articles on every field of chromatography, including theory of chromatography; progress in synthesis and characterization of new stationary phases; chromatography of organic, inorganic and complex compounds; enantioseparation and chromatography of chiral compounds; applications of chromatography in biology, pharmacy, medicine, and food analysis; environmental applications of chromatography; analytical and physico-chemical aspects of sample preparation for chromatography; hyphenated and combined techniques; chemometrics and its applications in separation science.
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