2015
DOI: 10.1007/s12161-015-0192-9
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Development and Application of Immunoaffinity Column for the Simultaneous Determination of Norfloxacin, Pefloxacin, Lomefloxacin, and Enrofloxacin in Swine and Chicken Meat Samples

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Cited by 20 publications
(11 citation statements)
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“…To assess the prepared immunoaffinity column, pork meat obtained from local supermarket was fortified with ENR at the final concentration of 10, 25 and 50 ng/g. A total of 5 g homogenized muscle tissues were mixed with 5 mL 0.01 mol/L PBS (pH 7.4) in polypropylene centrifuge tubes followed by vortexing for 5 min (Sun et al, 2016). After centrifugation at 9000 rpm for 15 min, the supernatants were collected, and the precipitate was pre-extracted with 5 mL 0.01 mol/L PBS (pH 7.4).…”
Section: Application Of Immunoaffinity Column For Real Samples Clean-upmentioning
confidence: 99%
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“…To assess the prepared immunoaffinity column, pork meat obtained from local supermarket was fortified with ENR at the final concentration of 10, 25 and 50 ng/g. A total of 5 g homogenized muscle tissues were mixed with 5 mL 0.01 mol/L PBS (pH 7.4) in polypropylene centrifuge tubes followed by vortexing for 5 min (Sun et al, 2016). After centrifugation at 9000 rpm for 15 min, the supernatants were collected, and the precipitate was pre-extracted with 5 mL 0.01 mol/L PBS (pH 7.4).…”
Section: Application Of Immunoaffinity Column For Real Samples Clean-upmentioning
confidence: 99%
“…The selection of the most appropriate eluting conditions was made considering (1) the recovery of the analyte, (2) the volume needed for an acceptable recovery, (3) the potential damage of the IAC after several cycles of usage and (4) the compatibility with the immunochemical analytical method (Sanvicens, Moore, Guilbault, & Marco, 2006). Previous research has shown that the mixtures of organic solvents, such as methanol or acetonitrile, were suitable to remove analytes from IAC (Sun et al, 2016;Wang et al, 2011). In this study, five eluting solutions with different methanol concentrations were evaluated.…”
Section: Optimization Of Extraction Conditions For Immunoaffinity Columnmentioning
confidence: 99%
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“…Ommunoaffinity chromatography takes the advantage of specific and reversible interaction between antibody and the analyte, and enables selective extraction and enrichment of individual compounds or classes of compounds in one step (Şenyuva & Gilbert, 2010;Pichon & Combes, 2016). On the last decade, the application of immunoaffinity chromatography for a variety of samples pretreatment in mycotoxins (Longobardi et al, 2013;Marley et al, 2015;Wilcox et al, 2015;Zhang et al, 2016), veterinary drugs (Mei et al, 2014;Sun et al, 2016;Yang et al, 2016) and pesticides (Esteve-Turrillas et al, 2011;Xu et al, 2012) residues analyses have been reported.…”
Section: Introductionmentioning
confidence: 99%
“…They are effective to control a wide range of bacteria, both gram positive and negative as well as other bacteria and often used in the treatment of a range of illnesses. Due to the fact that its resistance in the environment can cause undesirable effects on aquatic ecosystems and human health, QNs have obtained growing attention [1,2]. Therefore, the analysis of the occurrence, distribution and risks of quinolone antibiotics became crucial to environment monitoring.…”
Section: Introductionmentioning
confidence: 99%