Rapid UHPLC–MS/MS measurement of pregnanediol 3-glucuronide in spot urine samples for detecting ovulation

IF 1.8 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Biomedical Chromatography Pub Date : 2024-08-16 DOI:10.1002/bmc.5982
Laura Leoni, Federica Rosmini, Francesca Ledda, Mirko Parasiliti-Caprino, Fabio Settanni, Antonello Nonnato, Ezio Ghigo, Paolo Moghetti, Giulio Mengozzi, Federico Ponzetto
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Abstract

Biochemical confirmation of ovulation typically involves measuring serum progesterone levels during the mid-luteal phase. Alternatively, this information could be obtained by monitoring urinary excretion of conjugated metabolites of ovarian steroids such as pregnanediol 3-glucuronide (PDG) using immunoassay techniques that have methodological limitations. The aim of the present study was to develop a mass spectrometry (MS)-based method for the rapid and accurate measurement of urinary PDG levels in spot urine samples. A “dilute and shoot” ultra-high-performance liquid cromatography tandem mass spectrometry (UHPLC-MS/MS) method was developed for measuring PDG urinary concentration with a 6-min analysis time. The method underwent validation in accordance with ISO 17025 documentation for quantitative methods, proving an efficient separation of PDG from other structurally similar glucuro-conjugated steroid metabolites and ensuring a sufficient sensitivity for detecting the target analyte at concentrations as low as 0.01 μg/mL. The validation protocol yielded satisfactory results in terms of accuracy, repeatability, intermediate precision, and combined uncertainty. Additionally, the stability of both the samples and calibration curves was also conducted. The application to real urine samples confirmed the method's capability to measure PDG levels throughout an entire menstrual cycle and detecting ovulation. The rapidity of the analytical platform would therefore enable high throughput analysis, which is advantageous for large cohort clinical studies.

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快速超高效液相色谱-质谱/质谱法测量定点尿样中的孕二醇-3-葡萄糖醛酸苷,用于检测排卵。
排卵的生化确认通常包括在黄体中期测量血清孕酮水平。另一种方法是使用免疫测定技术监测卵巢类固醇共轭代谢物(如孕烷二醇-3-葡萄糖醛酸苷(PDG))的尿排泄量,但这种方法存在方法学上的局限性。本研究旨在开发一种基于质谱(MS)的方法,用于快速、准确地测量定点尿样中的尿 PDG 水平。本研究开发了一种 "稀释和检测 "超高效液相色谱串联质谱(UHPLC-MS/MS)方法,用于测定尿液中的 PDG 浓度,分析时间为 6 分钟。该方法按照 ISO 17025 定量方法文件进行了验证,证明能有效地将 PDG 与其他结构相似的葡萄糖结合类固醇代谢物分离,并确保了足够的灵敏度,可在低至 0.01 μg/mL 的浓度下检测目标分析物。验证方案在准确度、重复性、中间精度和综合不确定性方面都取得了令人满意的结果。此外,还对样品和校准曲线进行了稳定性测试。对真实尿样的应用证实,该方法能够测量整个月经周期的 PDG 水平并检测排卵。因此,该分析平台的快速性可实现高通量分析,这对大型队列临床研究非常有利。
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来源期刊
Biomedical Chromatography
Biomedical Chromatography 生物-分析化学
CiteScore
3.60
自引率
5.60%
发文量
268
审稿时长
2.3 months
期刊介绍: Biomedical Chromatography is devoted to the publication of original papers on the applications of chromatography and allied techniques in the biological and medical sciences. Research papers and review articles cover the methods and techniques relevant to the separation, identification and determination of substances in biochemistry, biotechnology, molecular biology, cell biology, clinical chemistry, pharmacology and related disciplines. These include the analysis of body fluids, cells and tissues, purification of biologically important compounds, pharmaco-kinetics and sequencing methods using HPLC, GC, HPLC-MS, TLC, paper chromatography, affinity chromatography, gel filtration, electrophoresis and related techniques.
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