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采用双水相溶剂的泡腾辅助液相微萃取-高效液相色谱-二极管阵列检测法测定唾液中的皮质醇和睾酮

Effervescent-assisted Liquid-phase Microextraction Employing Switchable Hydrophilicity Solvent for the Determination of Cortisol and Testosterone in Oral Fluid by High-Performance Liquid Chromatography-Diode Array Detection.

机构信息

Programa de Pós-Graduação em Biociências, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.

Departamento de Farmacociências, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.

出版信息

J Sep Sci. 2024 Nov;47(21):e70022. doi: 10.1002/jssc.70022.

Abstract

Cortisol and testosterone are important biomarkers for diagnosing complex disorders, including polycystic ovary syndrome and Cushing's syndrome, where symptomatology usually overlaps with other prevalent disorders. This work proposes, for the first time, an analytical method based on a switchable hydrophilicity solvent as an extraction phase for the determination of cortisol and testosterone in oral fluid (OF) by high-performance liquid chromatography with diode-array detection. The optimized extraction conditions consisted of 1000 µL of OF, 100 µL of decanoic acid solution (65 mg/mL), 170 µL of NaCO, 900 µL of HSO and 150 µL of acetonitrile for dilution. The method was validated, and coefficients of determination higher than 0.9926, the limit of detection of 4.55 ng/mL and the limit of quantification of 15.00 ng/mL were obtained. Intra-day precision varied from 5.6% to 11.9%, inter-day precision ranged from 6.1% to 13.5%, and relative recoveries ranged from 98.9% to 104.6% for cortisol, and 89.1% to 103.9% for testosterone. This methodology was successfully applied to five OF samples from volunteers. Moreover, the greenness of this methodology was evaluated based on the sample preparation metric of sustainability achieving a global score of 7.37 which can be considered sustainable.

摘要

皮质醇和睾酮是诊断多囊卵巢综合征和库欣综合征等复杂疾病的重要生物标志物,这些疾病的症状通常与其他常见疾病重叠。本工作首次提出了一种基于可切换亲水性溶剂的分析方法,作为高效液相色谱-二极管阵列检测法中用于测定唾液中皮质醇和睾酮的萃取相。优化的萃取条件包括 1000µL 唾液、100µL 癸酸溶液(65mg/mL)、170µL NaCO、900µL HSO 和 150µL 乙腈用于稀释。该方法经过验证,得到的决定系数均高于 0.9926,检测限为 4.55ng/mL,定量限为 15.00ng/mL。日内精密度变化范围为 5.6%至 11.9%,日间精密度变化范围为 6.1%至 13.5%,皮质醇的相对回收率范围为 98.9%至 104.6%,睾酮的相对回收率范围为 89.1%至 103.9%。该方法成功应用于 5 名志愿者的 5 份唾液样本。此外,基于可持续性的样品制备指标对该方法的绿色度进行了评估,其全球评分为 7.37,可被视为可持续的。

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