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

被引:5
作者
Amer, Sara [1 ,2 ]
Zarad, Walaa [1 ]
El-Gindy, Heba [1 ]
Abdel-Salam, Randa [3 ]
Hadad, Ghada [3 ]
Masujima, Tsutomu [2 ]
Emara, Samy [1 ]
机构
[1] Misr Int Univ, Fac Pharm, Km 28 Ismailia Rd, Cairo 11865, Egypt
[2] RIKEN, Quantitat Biol Ctr QBic, 6-2-3 Furuedai, Suita, Osaka 5650874, Japan
[3] Univ Suez Canal, Fac Pharm, Pharmaceut Analyt Chem Dept, Ismailia 41522, Egypt
关键词
direct mass spectrometry; nanospray electrospray ionization; nanospray capillary; metronidazole; human urine; 1; 3; 6-polytyrosine; LIQUID-CHROMATOGRAPHY; HPLC METHOD; SPECTROPHOTOMETRIC DETERMINATION; ELECTROCHEMICAL REDUCTION; NITROIMIDAZOLE RESIDUES; TRICHOMONAS-VAGINALIS; HUMAN PLASMA; ION-TRAP; CELLS; SPIRAMYCIN;
D O I
10.1098/rsos.191336
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mu l 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 mu l 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 m/z 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(-1). 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.
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页数:16
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