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采用液相色谱-高分辨质谱法(LC-HRMS)测定速溶咖啡预混料中的磷酸二酯酶 5(PDE5)抑制剂。

Determination of phosphodiesterase 5 (PDE5) inhibitors in instant coffee premixes using liquid chromatography-high-resolution mass spectrometry (LC-HRMS).

机构信息

Centre for Forensic Science, University of Technology Sydney, Ultimo, NSW, 2007, Australia; Pharmacy Enforcement Division, Ministry of Health, Petaling Jaya, Selangor, 46200, Malaysia.

Centre for Forensic Science, University of Technology Sydney, Ultimo, NSW, 2007, Australia.

出版信息

Talanta. 2019 Nov 1;204:36-43. doi: 10.1016/j.talanta.2019.05.078. Epub 2019 May 21.

Abstract

As a widely consumed beverage, coffee tends to be a target for intentional adulteration. This study describes the application of modified quick, easy, cheap, effective, rugged, and safe (QuEChERS) coupled to liquid chromatography-high-resolution mass spectrometry (LC-HRMS) for simultaneous screening, identification, and quantification of undeclared phosphodiesterase 5 (PDE5) inhibitors in instant coffee premixes (ICPs). The mass spectrometer was operated in auto MS/MS acquisition for simultaneous MS and MS/MS experiments. Qualitative establishments from the suspected-target screening and targeted identification processes led to an unambiguous analyte assignment from the protonated molecule ([M+H]) precursor ion which is subsequently used for quantification of 23 targeted PDE5 inhibitors. The analytical method validation covered specificity, linearity, range, accuracy, limit of detection (LOD), limit of quantification (LOQ), precisions, matrix effect (ME), and extraction recovery (RE). The specificity was established using the optimised chromatographic separation as well as the distinguishable [M+H] precursor ion. The linearity of each target analyte was demonstrated with a coefficient of determination (r) of >0.9960 over the expected range of sample concentrations. The accuracy ranged from 88.1%-119.3% with LOD and LOQ of <70 ng/mL and 80 ng/mL, respectively. Excellent precisions were established within 0.4%-9.1% of the relative standard deviation. An insignificant ME within -5.2% to +8.7% was achieved using three different strategies of chromatography, sample extraction, and sample dilution. The RE was good for all target analytes within 84.7%-123.5% except for N-desethylacetildenafil at low (53.8%) and medium (65.1%) quality control levels. The method was successfully applied to 25 samples of ICPs where 17 of them were found to be adulterated with PDE5 inhibitors and their analogues. Further quantification revealed the total amount of these adulterants ranged from 2.77 to 121.64 mg per sachet.

摘要

作为一种广泛消费的饮料,咖啡往往是故意掺假的目标。本研究描述了改良的快速、简便、廉价、有效、耐用和安全(QuEChERS)与液相色谱-高分辨率质谱(LC-HRMS)相结合,用于同时筛选、鉴定和定量即溶咖啡预混料(ICPs)中的未申报磷酸二酯酶 5(PDE5)抑制剂。质谱仪在自动 MS/MS 采集模式下进行同时的 MS 和 MS/MS 实验。可疑目标筛选和靶向鉴定过程中的定性建立导致了从质子化分子([M+H]+)前体离子进行明确的分析物分配,随后用于定量 23 种靶向 PDE5 抑制剂。分析方法验证涵盖了特异性、线性、范围、准确性、检测限(LOD)、定量限(LOQ)、精密度、基质效应(ME)和提取回收率(RE)。特异性是通过优化的色谱分离以及可区分的[M+H]+前体离子来建立的。每个目标分析物的线性通过预期样品浓度范围内的相关系数(r)>0.9960 来证明。准确度范围为 88.1%-119.3%,LOD 和 LOQ 分别<70ng/mL 和 80ng/mL。在相对标准偏差的 0.4%-9.1%内建立了良好的精密度。使用三种不同的色谱、样品提取和样品稀释策略,实现了-5.2%至+8.7%的无显著 ME。除了低(53.8%)和中(65.1%)质控水平的 N-去乙基西地那非外,所有目标分析物的回收率均良好,范围为 84.7%-123.5%。该方法成功应用于 25 份 ICP 样品,其中 17 份被发现掺有 PDE5 抑制剂及其类似物。进一步的定量分析显示,这些掺杂物的总量每个小袋为 2.77 至 121.64 毫克。

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