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Research: Assessment of ceftiofur residues in cow milk using commercial screening test kits

机译:研究:使用商业筛选测试试剂盒评估牛奶中的头孢噻呋残留

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摘要

Ceftiofur, a third-generation cephalosporin, is one of the most used antibiotics in dairy industry. Intramuscular injection of 1 mg/kgBW ceftiofur hydrochloride (HCl) generally results in 0 hour withdrawal time for the milk in dairy cows. Nevertheless, farmers and dairy processors occasionally complain about ceftiofur-based products in case of positive result to a commercial rapid screening test for the presence of violative residues of antimicrobials (inhibitors) in the bulk milk tank. Six lactating cows were injected with a 50 mg/ml ceftiofur HCl-based product at the dosage regimen of 1 mg/kg, intramuscularly, once a day, for five consecutive days, as per label. Milk samples were then collected just before the very last injection (T0) and then at 12, 24, 36, 48, 60, 72, 84 and 96 hours after the last injection. Individual milk samples were tested using three commercial screening test kits for inhibitor residues: DelvotestSP NT, SNAP Beta-Lactam ST Plus and ROSA MRL Beta-Lactam Test. Since bulk tank is screened in real operating conditions, samples were also diluted to 1:4, 1:10 and tested again. For the Delvotest SP NT, which lowest detected concentration is close the MRL of the ceftiofur (100 µg/kg), all results were negative. For the ROSA MRL Beta-Lactam Test and the SNAP Beta-Lactam ST Plus, several samples yielded positive and doubtful results at T0 and T12. However, after dilution to 1:10, all results were negative. Consequently, when used as officially instructed, the tested 50 mg/ml ceftiofur HCl-based injectable veterinary products are safe, and milk should be free of violative residues of ceftiofur. With consideration to the low specificity and the low positive predictive value of commercial screening tests, positive reactions of the bulk milk should be interpreted as false positive or another risky usage of β-lactam-based medicines in the farm must be investigated.
机译:头孢噻呋是第三代头孢菌素,是乳业最常用的抗生素之一。肌注1µg / kgBW盐酸头孢噻呋(HCl)通常会使奶牛的牛奶停药时间为0小时。但是,如果散装奶罐中存在抗菌素(抑制剂)的违法残留物的商业快速筛查测试呈阳性结果,农民和乳制品加工商偶尔会抱怨基于头孢噻呋的产品。根据标签,六只泌乳母牛每天肌肉注射一次50 mg / ml盐酸头孢噻呋HCl的产品,剂量为1 mg / kg,连续五天。然后在最后一次注射(T0)之前收集牛奶样品,然后在最后一次注射后的12、24、36、48、60、72、84和96小时收集牛奶样品。使用三种商业化的筛查试剂盒对单个牛奶样品进行了抑制剂残留检测:DelvotestSP NT,SNAP Beta-Lactam ST Plus和ROSA MRL Beta-Lactam Test。由于在实际操作条件下对散装储罐进行了筛选,因此样品也应分别稀释至1:4、1:10并再次测试。对于Delvotest SP NT,其最低检测浓度接近头孢噻呋的最大残留限量(100μg/ kg),所有结果均为阴性。对于ROSA MRL Beta-Lactam测试和SNAP Beta-Lactam ST Plus,一些样品在T0和T12处产生了阳性和可疑的结果。但是,稀释至1:10后,所有结果均为阴性。因此,按照官方指示使用时,经测试的50μmg/ ml盐酸头孢噻呋酯类可注射兽药是安全的,牛奶中应不含违规的头孢噻呋残留物。考虑到商业筛查测试的低特异性和低阳性预测值,应将散装牛奶的阳性反应解释为假阳性,否则必须对农场中基于β-内酰胺类药物的另一种危险用法进行调查。

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