2009
DOI: 10.1002/jssc.200900415
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Simultaneous determination of five tetracycline and macrolide antibiotics in feeds using HPCE

Abstract: This work demonstrates the potential of HPCE in the analysis of antibiotics in a complex matrix such as feedstuffs. Using 20 mM citric acid-40 mM Na 2 HPO 4 buffer (pH 2.65), the five antibiotics, tetracycline, oxytetracycline, doxycycline, tilmicosin, and tylosin were successfully separated at 30 kV in a 64.5 cm  75 mm id capillary. Good repeatability, stability, and reliability of the method were supported by o10% CV with mean recoveries of 470%, and the limit of detection of the five analytes was 0.5-1 mg/… Show more

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Cited by 48 publications
(23 citation statements)
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“…However, recoveries were low, due to the tendency of tetracyclines to form chelation complexes with different cations. Therefore, initial extraction with McIlvaine/EDTA buffer was employed and gave satisfactory results, as in previously reported methods [7, 21, 28, 29]. Tetracyclines dissolved in the McIlvaine/EDTA solution were then extracted with ethyl acetate, as these two solutions are immiscible, and separation could be easily conducted as the organic phase stays on the top layer.…”
Section: Resultsmentioning
confidence: 82%
“…However, recoveries were low, due to the tendency of tetracyclines to form chelation complexes with different cations. Therefore, initial extraction with McIlvaine/EDTA buffer was employed and gave satisfactory results, as in previously reported methods [7, 21, 28, 29]. Tetracyclines dissolved in the McIlvaine/EDTA solution were then extracted with ethyl acetate, as these two solutions are immiscible, and separation could be easily conducted as the organic phase stays on the top layer.…”
Section: Resultsmentioning
confidence: 82%
“…Zhang et al determined tilmicosin in feeds by high performance liquid chromatography (HPLC) with ultraviolet detection, where the limit of detection was 2 mg kg −1 [3]. Determination of tilmicosin in feeds by capillary electrophoresis has been described, where the limit of detection was 5 mg kg −1 [4]. Because of the variation in components of feeds, it is difficult to find a suitable cleanup procedure in some cases.…”
Section: Introductionmentioning
confidence: 99%
“…At present, the methods for multi-residue analysis of macrolide antibiotics mainly include high-performance liquid chromatography (HPLC) (Clark, Dowling, & Boison, 2009;De La Huebra, Vincent, Bordin, & Rodriguez, 2005;Edder, Coppex, Cominoli, & Corvi, 2002;Lagan a, 2009;Bogialli, Di Corcia, Lagan a, Mastrantoni, & Sergi, 2007;Dickson, 2014;Dickson, O'Byrne, & Chan, 2012;Granja et al, 2009;Horie, Takegami, Toya, & Nakazawa, 2003;Jacobsen, Halling-Sørensen, Ingerslev, & Hansen, 2004;Thompson, Noot, Calvert, & Pernal, 2005;Wang & Leung, 2009;Yang & Carlson, 2004), and capillary electrophoresis (CE) (Deng, Kang, Li, & Xu, 2007a;Deng, Kang, Li, & Xu, 2007b;Liu, Shi, Liu, & Tian, 2010;Tong, Rao, Zhu, Jiang, & Ding, 2009). Compared to HPLC and LC-MS, CE has the virtue of rapid separation and low reagent consumption.…”
Section: Introductionmentioning
confidence: 99%