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Detection and disposition of tolmetin in the horse.

机译:马中托美汀的检测和处置。

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摘要

Non-steroidal anti-inflammatory drugs (NSAIDs) are prohibited by the International Federation of Horse Racing Authorities but are commonly used in veterinary practice. Plasma and urinary concentrations of the NSAID tolmetin were determined by a high-performance liquid chromatographic procedure with UV detection following oral administration of a dose of 1 g to six fasted untrained standard bred mares. With a limit of quantitation (LOQ) of 0.05 microg/ml tolmetin was present in plasma for 9-12 h post-administration. Maximum concentrations of 2.1+/-0.89 microg/ml were found after 0.7+/-0.25 h. The elimination half-life was 2+/-1.25 h. Plasma protein binding at concentrations of 0.25 and 2.5 microg/ml was 92+/-4.9 and 84+/-4.2%, respectively. As early as 1 h after dosage, tolmetin could be detected in unhydrolysed urine and remained detectable up to 48 h (LOQ=0.5 microg/ml). The maximum concentrations occurred 1.8+/-0.4 h after administration. The percentage of the dose excreted as unchanged tolmetin within 12 h was 58+/-7.9%. Neither conjugates nor metabolites could be detected under the experimental conditions studied. For confirmatory analysis in doping control, an LC-MS method was developed. Analysis was performed on an ion trap LC-MS system equipped with an ESI probe in positive MS(2) mode.
机译:国际赛马当局联合会禁止使用非甾体类抗炎药(NSAID),但通常在兽医实践中使用。口服1 g剂量至六只禁食的未经训练的标准繁殖母马后,通过高效液相色谱和紫外线检测,测定NSAID托美汀的血浆和尿液浓度。在给药后9-12小时血浆中存在托曼汀的定量极限(LOQ)为0.05微克/毫升。 0.7 +/- 0.25小时后发现最大浓度为2.1 +/- 0.89 microg / ml。消除半衰期为2 +/- 1.25 h。浓度为0.25和2.5微克/毫升的血浆蛋白结合分别为92 +/- 4.9和84 +/- 4.2%。最早在给药后1小时,在未水解的尿液中就可以检测到托美汀,并在48小时内仍可检测到(LOQ = 0.5 microg / ml)。给药后最大浓度为1.8 +/- 0.4小时。在12小时内作为不变的托美汀排泄的剂量百分比为58 +/- 7.9%。在研究的实验条件下都无法检测到缀合物或代谢产物。为了在掺杂控制中进行验证性分析,开发了一种LC-MS方法。在配备有正MS(2)模式的ESI探针的离子阱LC-MS系统上进行分析。

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