基于UHPLC-MS/MS测定3种α-二羰基化合物唾液干斑的新方法——在糖尿病患者唾液中的应用

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Guangyi Zhang , Chengqiang Han , Yuxuan Li, Xi-Ling Li, Hongmei Jin, Jun Zhe Min
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引用次数: 0

摘要

人唾液中的α-二羰基化合物(α-DCs)与糖尿病密切相关,但其固有的不稳定性给样品运输和检测带来了挑战。本研究提出了一种利用4,5-二甲基-1,2-苯二胺(DMPD)衍生结合UHPLC-MS/MS同时检测干燥唾液斑点中3种α- dcs - 3-脱氧葡萄糖苷(3-DG)、乙二醛(GO)和甲基乙二醛(MG)的新方法。选择直径5.0 mm的双圆定性滤纸作为干燥唾液的底物,最佳提取条件为两次提取,提取时间为3分钟。色谱分离采用CSH™C18色谱柱(2.1 × 50 mm, 1.7 μm)梯度洗脱,流动相为0.1 %甲酸水溶液和0.1 %甲酸乙腈水溶液。整个分离过程在5.0 min的时间框架内完成。3-DG和GO在0.10 ~ 12.5 μM、MG在0.24 ~ 31.25 μM范围内呈线性关系。(r2≥0.9994)。日内、日间精密度RSD值为0.59 % ~ 5.78 %,平均加样回收率为99.78 % ~ 108.50 %。检出限为0.85 ~ 12.85 fmol。将该方法应用于分析44名健康志愿者(HVs)和46名糖尿病患者(dp)的干燥唾液样本,发现HVs和dp之间3-DG、GO和MG的浓度存在显著差异(p <; 0.001)。该研究结果验证了干燥唾液样品中α- dc作为糖尿病潜在生物标志物候选物的实用性,同时为其在临床环境中的应用引入了一种创新的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel method for the determination of dried saliva spots (DSS) based on UHPLC-MS/MS for three α-dicarbonyl compounds: An application in the saliva of diabetes patients
α-Dicarbonyl compounds (α-DCs) in human saliva are closely associated with diabetes, but their inherent instability presents challenges for sample transportation and detection. This study introduces a novel approach for the simultaneous detection of three α-DCs—3-deoxyglucoside (3-DG), glyoxal (GO), and methylglyoxal (MG)—in dried saliva spots using 4,5-dimethyl-1,2-phenylenediamine (DMPD) derivatization combined with UHPLC-MS/MS. 5.0 mm diameter double-circle qualitative filter paper was selected as the substrate for dried saliva, with optimal extraction conditions involving two 3-minute extractions. Chromatographic separation was performed on a CSH™ C18 column (2.1 × 50 mm, 1.7 μm) via gradient elution, utilizing a mobile phase consisting of 0.1 % formic acid in water and 0.1 % formic acid in acetonitrile. The entire separation process was completed within a 5.0 min timeframe. The linearity of 3-DG and GO in the concentration range of 0.10–12.5 μM, and MG in the range of 0.24–31.25 μM. (R2 ≥ 0.9994). Intra- and inter-day precision yielded RSD values ranging from 0.59 % to 5.78 %, with average recoveries between 99.78 % and 108.50 %. The detection limits were 0.85–12.85 fmol. This method was applied to analyze dried saliva samples from 44 healthy volunteers (HVs) and 46 diabetic patients (DPs), revealing significant differences (p < 0.001) in the concentrations of 3-DG, GO, and MG between HVs and DPs. The research outcomes validate the practicality of α-DCs in dried saliva samples as prospective biomarker candidates for diabetes, while introducing an innovative methodology for their utilization in clinical settings.
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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