Department of Excellence of Biomedical Sciences and Public Health, University "Politecnica delle Marche" of Ancona, Ancona, Italy.
Comedical s.r.l., Trento, Italy.
Drug Test Anal. 2021 Aug;13(8):1552-1560. doi: 10.1002/dta.3055. Epub 2021 Jul 16.
A new, rapid, sensitive, and comprehensive ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) method for quantifying diuretics (acetazolamide, brinzolamide, dorzolamide, and their metabolites) in human urine and hair was developed and fully validated. Twenty-five milligrams of hair were incubated with 500-μl M3® buffer reagent at 100°C for 1 h for complete digestion. After cooling, 1-μl supernatant was injected onto chromatography system. Urine samples were simply diluted before injection. The chromatographic run time was short (8 min) through a column with a mobile phase gradient. The method was linear (determination coefficients always higher than 0.99) from limit of quantification (LOQ) to 500 ng/ml in urine and from LOQ to 10 ng/mg in hair. LOQs ranged from 0.07 to 1.16 ng/ml in urine and from 0.02 to 0.15 ng/mg in hair. No significant ion suppression due to matrix effect was observed, and process efficiency was always higher than 80%. Intra- and inter-assay precision was lower than 15%. The suitability of the methods was tested with six urine and hair specimens from patients treated with acetazolamide, dorzolamide, or brinzolamide for ocular diseases or systemic hypertension. Average urine concentrations were 266.32 ng/ml for dorzolamide and 47.61 ng/ml for N-deethyl-dorzolamide (n = 3), 109.27 ng/ml for brinzolamide and 1.02 ng/ml for O-desmethyl-brinzolamide (n = 2), and finally, 12.63 ng/ml for acetazolamide. Average hair concentrations were 5.94 ng/mg for dorzolamide and 0.048 ng/mg for N-deethyl-dorzolamide (n = 3), 3.26 ng/mg for brinzolamide (n = 2), and 2.3 ng/mg for acetazolamide (n = 1). The developed method was simple and fast both in the extraction procedures making it eligible in high-throughput analysis for clinical forensic and doping purposes.
建立并充分验证了一种新的、快速、灵敏、全面的超高效液相色谱串联质谱(UHPLC-MS/MS)法,用于定量人尿液和头发中的利尿剂(乙酰唑胺、布林佐胺、多佐胺及其代谢物)。将 25 毫克头发与 500μl M3®缓冲试剂在 100°C 孵育 1 小时以完全消化。冷却后,取 1μl 上清液注入色谱系统。尿液样品在注射前简单稀释。通过具有流动相梯度的色谱柱,色谱运行时间短(8 分钟)。该方法在尿液中从定量下限(LOQ)到 500ng/ml,在头发中从 LOQ 到 10ng/mg 呈线性(决定系数始终高于 0.99)。尿液中的 LOQ 范围为 0.07 至 1.16ng/ml,头发中的 LOQ 范围为 0.02 至 0.15ng/mg。未观察到由于基质效应引起的显著离子抑制,且过程效率始终高于 80%。内标和间标精密度均低于 15%。用来自接受乙酰唑胺、多佐胺或布林佐胺治疗眼部疾病或系统性高血压的患者的 6 份尿液和头发样本对方法的适用性进行了测试。多佐胺的平均尿液浓度为 266.32ng/ml,N-去乙基多佐胺为 47.61ng/ml(n=3),布林佐胺为 109.27ng/ml,O-去甲基布林佐胺为 1.02ng/ml(n=2),最后,乙酰唑胺为 12.63ng/ml。多佐胺的平均头发浓度为 5.94ng/mg,N-去乙基多佐胺为 0.048ng/mg(n=3),布林佐胺为 3.26ng/mg(n=2),乙酰唑胺为 2.3ng/mg(n=1)。所建立的方法在提取程序上既简单又快速,适用于临床法医和兴奋剂目的的高通量分析。