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Determination of silodosin in biological samples using UPLC–MS/MS combined with magnetic carboxylated multiwalled carbon nanotubes

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Novel magnetic solid-phase extraction using carboxylated multiwalled carbon nanotubes was proposed with ultra high-performance liquid chromatography–tandem mass spectrometry for the determination of silodosin in biological samples. The effects of various experimental parameters including adsorbent amount, pH, adsorption time, desorption conditions, and adsorbent reusability were systematically validated. Under the optimized conditions, the calibration curve was linear within the concentration range of 1.0–800 ng mL−1 with the correlation coefficient of 0.9997 and the lower limit of detection was 0.3 ng mL−1. The extraction recoveries were over 90.0% with relative standard deviation (RSD) of less than 5.0%. All these results suggested that magnetic extraction method can be used for enrichment and quantification of silodosin in biological samples.
Rocznik
Strony
47--53
Opis fizyczny
Bibliogr. 36 poz., rys.
Twórcy
autor
  • Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, Yunnan, China
  • Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, China
  • Kunming Jida Pharmaceutical Co., Ltd., Kunming 650106, Yunnan, China
autor
  • Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, Yunnan, China
  • Research Center for Analysis and Measurement, Kunming University of Science and Technology, Kunming 650093, China
  • Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, China
autor
  • Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, China
Bibliografia
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Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2018).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d63fc0cd-756e-401b-8b54-4d8870e19343
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