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牛肾、肝、血浆、尿液和口腔液中磺胺二甲氧嘧啶耗竭的组织/液相关性研究

Tissue/fluid correlation study for the depletion of sulfadimethoxine in bovine kidney, liver, plasma, urine, and oral fluid.

作者信息

Chiesa O A, Li H, Kijak P J, Li J X, Lancaster V, Smith M L, Heller D N, Thomas M H, Von Bredow J

机构信息

Food and Drug Administration, Center for Veterinary Medicine, Office of Research, Division of Applied Veterinary Research, Laurel, MD 20708, USA.

出版信息

J Vet Pharmacol Ther. 2012 Jun;35(3):249-58. doi: 10.1111/j.1365-2885.2011.01327.x. Epub 2011 Aug 11.

Abstract

Sulfonamides are among the oldest, but still effective, antimicrobial veterinary medicines. In steers and dairy cows, the sulfonamides are effective in the treatment of respiratory disease and general infections. Sulfadimethoxine (SDM) has been approved by US Food and Drug Administration (FDA) for use in steers and dairy cows with a tolerance of 100 ng/g (ppb) in edible tissues and 10 ppb in milk. The detection of SDM residue above tolerance in the animal slaughtered for food process will result in the whole carcass being discarded. This report describes a comprehensive depletion study of SDM (and its main metabolite) in plasma, urine, oral fluid, kidney, and liver. In this study, nine steers were injected intravenously with the approved dose of SDM; the loading dose was 55 mg/kg, followed by 27.5 mg/kg dose at 24 h and again at 48 h. Fluids (blood, urine, and saliva) and tissue (liver and kidney) samples were collected at intervals after the last dose of SMD. The combination of laparoscopic serial sampling technique with the liquid chromatography/mass spectrometry method provided the data to establish the tissue/fluid correlation in the depletion of SMD. A strong correlation and linearity of the log-scale concentration over time in the depletion stage has been confirmed for kidney, liver, and plasma.

摘要

磺胺类药物是最古老但仍然有效的抗微生物兽用药物之一。在公牛和奶牛中,磺胺类药物对治疗呼吸道疾病和全身感染有效。磺胺二甲氧嘧啶(SDM)已获美国食品药品监督管理局(FDA)批准用于公牛和奶牛,其在可食用组织中的耐受量为100纳克/克(ppb),在牛奶中的耐受量为10 ppb。在用于食品加工的屠宰动物中检测到超过耐受量的SDM残留将导致整个胴体被丢弃。本报告描述了SDM(及其主要代谢物)在血浆、尿液、口腔液、肾脏和肝脏中的全面消除研究。在本研究中,对9头公牛静脉注射批准剂量的SDM;负荷剂量为55毫克/千克,随后在24小时和48小时分别给予27.5毫克/千克剂量。在最后一剂SMD后,定期采集液体(血液、尿液和唾液)和组织(肝脏和肾脏)样本。腹腔镜连续采样技术与液相色谱/质谱法相结合,为建立SMD消除过程中的组织/液体相关性提供了数据。在消除阶段,已证实肾脏、肝脏和血浆中对数浓度随时间具有很强的相关性和线性关系。

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