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

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(3)O(4)@mTiO(2)) with a mesoporous structure were su...

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Detalles Bibliográficos
Autores principales: Yang, Feiyu, Ma, Ke, Cao, Yu, Ni, Chunfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033689/
https://www.ncbi.nlm.nih.gov/pubmed/35479245
http://dx.doi.org/10.1039/d1ra01530c
Descripción
Sumario: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(3)O(4)@mTiO(2)) 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 Fe(3)O(4)@mTiO(2) based on the Lewis acid–Lewis base interactions. Following the optimization of the quantities of Fe(3)O(4)@mTiO(2), 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.