| Literature DB >> 28107701 |
Yumi Tsuruoka1, Takayuki Nakajima2, Maki Kanda2, Hiroshi Hayashi2, Yoko Matsushima2, Souichi Yoshikawa2, Marie Nagata2, Hiroshi Koike2, Chieko Nagano2, Kotaro Sekimura2, Tsuneo Hashimoto2, Ichiro Takano2, Tetsuya Shindo2.
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 (RSDr) ranged from 1.2% to 3.6% and the relative standard deviation of within-laboratory reproducibility (RSDWR) 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.Entities:
Keywords: Amantadine; External solvent calibration curve; LC–MS/MS; Memantine; Processed products; Rimantadine
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Year: 2017 PMID: 28107701 DOI: 10.1016/j.jchromb.2017.01.014
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205