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Improved liquid-liquid extraction by modified magnetic nanoparticles for the detection of eight drugs in human blood by HPLC-MS.


ABSTRACT: Magnetic nanoparticles modified with porous titanium dioxide were used as clean-up nanospheres for the detection of eight drug poisons in human blood by high-performance liquid chromatography-mass spectrometry. The magnetic clean-up nanospheres (Fe3O4@mTiO2) with a mesoporous structure were successfully synthesized and characterized by scanning electron microscopy/energy dispersive spectroscopy, transmission electron microscopy, X-ray diffractometry, vibrating sample magnetometry, infrared spectroscopy, and Brunauer-Emmett-Teller techniques. Lipid co-extractives, such as phosphatidic acid and fatty acids, which are major interferences in HPLC-MS analysis causing ion suppression in the MS spectra of blood, could be efficiently removed by Fe3O4@mTiO2 based on the Lewis acid-Lewis base interactions. Following the optimization of the quantities of Fe3O4@mTiO2, the method was applied to the determination of eight drugs in spiked blood. The analytical ranges typically extended from 2 to 500 ng mL-1, and the recoveries ranged from 79.5-99.9% at different concentrations of blood. The limits of quantitation for drug poisons were 0.14-1.03 ng mL-1, which makes the method a viable tool for drug poison monitoring in blood.

SUBMITTER: Yang F 

PROVIDER: S-EPMC9033689 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

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Improved liquid-liquid extraction by modified magnetic nanoparticles for the detection of eight drugs in human blood by HPLC-MS.

Yang Feiyu F   Ma Ke K   Cao Yu Y   Ni Chunfang C  

RSC advances 20210501 32


Magnetic nanoparticles modified with porous titanium dioxide were used as clean-up nanospheres for the detection of eight drug poisons in human blood by high-performance liquid chromatography-mass spectrometry. The magnetic clean-up nanospheres (Fe<sub>3</sub>O<sub>4</sub>@mTiO<sub>2</sub>) with a mesoporous structure were successfully synthesized and characterized by scanning electron microscopy/energy dispersive spectroscopy, transmission electron microscopy, X-ray diffractometry, vibrating sa  ...[more]

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