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Quantitative detection of inhaled salmeterol in human urine and relevance to doping control analysis.

机译:人体尿液中吸入沙美特罗的定量检测及其与兴奋剂控制分析的相关性。

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Salmeterol is a frequently prescribed beta-agonist used for the treatment of asthma. Due to performance-enhancing effects of some beta-agonists, salmeterol appears on the prohibited list published by the World Anti-Doping Agency and its therapeutic use is allowed but restricted to inhalation. Because the data on urinary concentrations originating from therapeutic use are limited, no discrimination can be made between use and abuse when a routine sample is found to contain salmeterol. Therefore, the urinary excretion of 100 mug of inhaled salmeterol was investigated. A liquid chromatography-tandem mass spectrometry method was developed and validated for the quantification of urine samples. Sample preparation consists of an enzymatic hydrolysis of the urine samples followed by a liquid-liquid extraction at pH 9.5 with diethyl ether/isopropanol (5/1). Analysis was performed using selected reaction monitoring after electrospray ionization. The method was linear in the range of 0.5-50 ng/mL. The limits of quantification were 500 pg/mL. The inaccuracy ranged between 10.4% and -3.7%. Results show that salmeterol could be detected for 48 hours. The maximum urinary concentration detected was 1.27 ng/mL. Cumulative data showed that only 0.27% of the administered dose is excreted as parent drug within the first 12 hours. Analysis of 47 routine doping samples, declared to contain salmeterol during routine analysis, did not exhibit concentrations that could be considered originating from supratherapeutic doses.
机译:沙美特罗是用于治疗哮喘的常用处方β激动剂。由于某些β受体激动剂的性能增强作用,沙美特罗出现在世界反兴奋剂机构发布的禁止清单上,允许其治疗用途,但仅限于吸入。由于源自治疗用途的尿液浓度数据有限,因此当发现常规样本中含有沙美特罗时,不能在使用和滥用之间进行区分。因此,研究了100杯吸入沙美特罗的尿排泄情况。开发了液相色谱-串联质谱法,并验证了尿液样品的定量方法。样品制备包括尿液样品的酶水解,然后用乙醚/异丙醇(5/1)在pH 9.5下进行液-液萃取。在电喷雾电离后,使用选定的反应监控器进行分析。该方法在0.5-50 ng / mL范围内是线性的。定量限为500 pg / mL。误差范围在10.4%和-3.7%之间。结果表明,沙美特罗可检测48小时。检测到的最大尿液浓度为1.27 ng / mL。累积数据显示,最初12小时内仅将0.27%的给药剂量作为母体药物排出体外。在常规分析期间宣布含有沙美特罗的47个常规掺杂样品的分析未显示出可以认为是超治疗剂量的浓度。

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