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Simultaneous determination of amantadine, rimantadine, and memantine in processed products, chicken tissues, and eggs by liquid chromatography with tandem mass spectrometry.

作者信息

Tsuruoka Yumi, Nakajima Takayuki, Kanda Maki, Hayashi Hiroshi, Matsushima Yoko, Yoshikawa Souichi, Nagata Marie, Koike Hiroshi, Nagano Chieko, Sekimura Kotaro, Hashimoto Tsuneo, Takano Ichiro, Shindo Tetsuya

机构信息

Tokyo Metropolitan Institute of Public Health, Shinjuku-ku, Tokyo 169-0073, Japan.

Tokyo Metropolitan Institute of Public Health, Shinjuku-ku, Tokyo 169-0073, Japan.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Feb 15;1044-1045:142-148. doi: 10.1016/j.jchromb.2017.01.014. Epub 2017 Jan 11.

Abstract

A simultaneous determination of amantadine, rimantadine, and memantine in processed products (deep-fried chicken, fried chicken, fried quail egg, and grilled chicken) with liquid chromatography tandem mass spectrometry (LC-MS/MS) was developed. This new method was also applicable for chicken tissue (muscle, liver, and gizzard) and eggs. The chromatographic separation was performed on a Kinetex XB-C18 core-shell technology column using a mobile phase of acetonitrile and 0.1% formic acid in a 10mmol/L ammonium formate solution, resulting in the complete separation of isomers (rimantadine and memantine) and any other obstructive peaks from the sample matrices. Sample preparation was performed by a modified QuEChERS method using acetonitrile and a 0.1% acetic acid extraction solution and cleaned using an Oasis MCX cartridge. The sample matrix had no effect on the identification of the compounds. For quantification, an external solvent calibration curve was used. This new method exhibited good accuracy ranging from 79.9% to 91.5%. The relative standard deviation of repeatability (RSD) ranged from 1.2% to 3.6% and the relative standard deviation of within-laboratory reproducibility (RSD) ranged from 1.3% to 6.0%. These standard deviations satisfied the criteria for Japanese validation guidelines. The limit of quantification (LOQ) was 1.0μg/kg for all samples. Analyte residues were not detected in 55 samples using the validated method.

摘要

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