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用于定量和鉴定甲硝唑剂型及人尿中甲硝唑的直接纳米电喷雾电离串联质谱法

Direct nano-electrospray ionization tandem mass spectrometry for the quantification and identification of metronidazole in its dosage form and human urine.

作者信息

Amer Sara, Zarad Walaa, El-Gendy Heba, Abdel-Salam Randa, Hadad Ghada, Masujima Tsutomu, Emara Samy

机构信息

Faculty of Pharmacy, Misr International University, Km 28 Ismailia Road, Cairo 11865, Egypt.

Quantitative Biology Center (QBiC), RIKEN, 6-2-3 Furuedai, Suita, Osaka 565-0874, Japan.

出版信息

R Soc Open Sci. 2019 Nov 6;6(11):191336. doi: 10.1098/rsos.191336. eCollection 2019 Nov.

Abstract

A rapid, sensitive and direct nano-electrospray ionization-tandem mass spectrometry (NS-ESI-MS/MS) method, using an offline nanospray (NS) capillary, has been developed and validated for the analysis of metronidazole (MTZ). A mixture of 2 µl MTZ sample solution prepared in an ionization solvent consisting of methanol : water : formic acid in a ratio of 80 : 20 : 0.3, together with 2 µl of an internal standard (IS), 1,3,6-polytyrosine, is loaded into the back of the NS capillary. The NS capillary was fitted into the ion source at a distance of 3 mm between the NS tip and MS orifice. The sample is then analysed and acquired a sustainable signal that allowed for data compilation across various data points for MTZ identification and quantification. The quantification relied on the ratio of the [M + H] peaks of MTZ and IS with values of 172.0717 and 182.0812, respectively, while the identification relied on the MS/MS of the precursor ions [M + H] of both compounds and their fragments at 128.05 for MTZ and 165.1 and 136.07 for the IS. The NS-ESI-MS/MS method was accurate and precise for the quantification of MTZ over the concentration range from 2.5 to 25 000 ng ml. The applicability of the method was confirmed by MTZ analysis in its pharmaceutical dosage form and detection of the analyte in clinical human urine samples without any sample treatment procedure.

摘要

一种使用离线纳米喷雾(NS)毛细管的快速、灵敏且直接的纳米电喷雾电离串联质谱(NS-ESI-MS/MS)方法已被开发并验证用于甲硝唑(MTZ)的分析。将2 μl在由甲醇:水:甲酸按80:20:0.3比例组成的电离溶剂中制备的MTZ样品溶液与2 μl内标(IS)1,3,6-聚酪氨酸混合,加载到NS毛细管的后端。NS毛细管安装在离子源中,NS尖端与质谱仪孔之间的距离为3 mm。然后对样品进行分析并获得可持续信号,以便在各个数据点进行数据汇编以鉴定和定量MTZ。定量依赖于MTZ和IS的[M + H]峰的比率,其值分别为172.0717和182.0812,而鉴定则依赖于两种化合物的前体离子[M + H]及其碎片的MS/MS,MTZ的碎片在128.05,IS的碎片在165.1和136.07。NS-ESI-MS/MS方法在2.5至25000 ng/ml的浓度范围内对MTZ的定量准确且精确。通过对其药物剂型中的MTZ进行分析以及在未经任何样品处理程序的临床人尿液样品中检测分析物,证实了该方法的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbfb/6894584/1626206c938a/rsos191336-g1.jpg

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