Laboratorio Antidoping, Federazione Medico Sportiva Italiana, Rome, Italy.
REDs - Research and Expertise in Anti-Doping sciences, ISSUL - Institute of Sport Sciences, University of Lausanne, Lausanne, Switzerland.
Drug Test Anal. 2022 Nov;14(11-12):2007-2016. doi: 10.1002/dta.3352. Epub 2022 Aug 12.
The rectal administration of glucocorticoids, as well as any injectable, and oral ones, is currently prohibited by the World Anti-Doping Agency when occurs "in competition." A reporting level of 100 ng/ml for prednisolone and 300 ng/ml for prednisone was established to discriminate the allowed and the prohibited administration. Here, the urinary excretion profiles of prednisone and prednisolone were evaluated in five volunteers in therapy with glucocorticoid-based rectal formulations containing prednisone or prednisolone caproate. The urinary levels of the excreted target compounds were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS) following the procedure validated and currently in use in our laboratory to detect and quantitate glucocorticoids in urine. Predictably, the excretion trend of the analytes of interest were generally comparable with those obtained after oral administration, even if the excretion profile showed a broad interindividual variability, with the absorption rate and the systemic bioavailability after rectal administration being strongly influenced by the type of formulations (suppository or rectal cream, in our case) as well as the physiological conditions of the absorption area. Results showed that the target compounds were detectable for at least 30 h after drug administration. After suppository administration, prednisolone levels reached the maximum after 3 h from drug administration and then dropped below the reporting level after 15-21 h; prednisone reached the maximum after 3 h from drug administration, and then dropped below the reporting level after 12-15 h. After cream administration, both prednisone and prednisolone levels remained in a concentration below the reporting level throughout the entire monitored period.
目前,世界反兴奋剂机构禁止在“比赛中”通过直肠给予糖皮质激素,包括任何注射剂和口服制剂。为了区分允许和禁止的给药方式,建立了泼尼松龙和泼尼松的检测水平分别为 100ng/ml 和 300ng/ml。在此,评估了五名志愿者在接受含有醋酸泼尼松龙或醋酸泼尼松龙酯的直肠用糖皮质激素制剂治疗时,泼尼松龙和泼尼松的尿液排泄特征。采用经我们实验室验证并正在使用的液相色谱-串联质谱法(LC-MS/MS)测定尿液中排泄的目标化合物的水平,以检测和定量尿液中的糖皮质激素。可以预见的是,感兴趣的分析物的排泄趋势通常与口服给药后获得的趋势相当,即使排泄模式显示出广泛的个体间变异性,直肠给药的吸收速率和全身生物利用度强烈受到制剂类型(栓剂或直肠乳膏,在我们的案例中)以及吸收区域的生理状况的影响。结果表明,目标化合物在给药后至少 30 小时内可被检测到。栓剂给药后,泼尼松龙在给药后 3 小时达到最大值,然后在 15-21 小时后降至检测水平以下;泼尼松在给药后 3 小时达到最大值,然后在 12-15 小时后降至检测水平以下。乳膏给药后,泼尼松和泼尼松龙的水平在整个监测期间均保持在检测水平以下。