Black W D, Gentry R D
Can Vet J. 1984 Apr;25(4):158-61.
A single oral dose of oxytetracycline hydrochloride (50 mg/kg) produced detectable residues in the following tissues; adrenal, bile, fat, heart, kidney (cortex), kidney (medulla), liver, lung, lymph node (mesenteric), muscle, serum, spleen, thyroid and urine. The highest residue levels were observed in the urine (441 mug/mL) at three hours after administration and they were still present at 48 hours. Maximum serum levels were observed at two hours after administration. Bile samples were positive for inhibitors in all animals sampled. Drug residues were not detected in spleen, thyroid, lymph node, adrenals and heart at 48 hours.Drug levels in important edible tissues were expressed as a percentage of drug levels in two tissues with high drug concentrations - urine and kidney cortex. The percentages were highly variable when compared with urine and much less variable when compared to kidney cortex.Kidney cortex appears to be an excellent tissue for drug residue monitoring.
单次口服盐酸土霉素(50毫克/千克)后,在以下组织中可检测到残留:肾上腺、胆汁、脂肪、心脏、肾脏(皮质)、肾脏(髓质)、肝脏、肺、淋巴结(肠系膜)、肌肉、血清、脾脏、甲状腺和尿液。给药后三小时,尿液中的残留水平最高(441微克/毫升),48小时时仍有残留。给药后两小时观察到血清最高水平。所有采样动物的胆汁样本均含有抑制剂。48小时时,脾脏、甲状腺、淋巴结、肾上腺和心脏中未检测到药物残留。重要可食用组织中的药物水平以两种药物浓度较高的组织——尿液和肾皮质中的药物水平的百分比表示。与尿液相比,这些百分比变化很大,与肾皮质相比变化则小得多。肾皮质似乎是监测药物残留的优良组织。