Dispersive solid phase extraction of apixaban from human plasma samples prior to capillary electrophoresis determination using zirconium-based metal organic frameworks prepared by different modulator and solvent

被引:1
作者
Abbasalizadeh, Aysa [1 ,2 ]
Mogaddam, Mohammad Reza Afshar [3 ,4 ]
Farajzadeh, Mir Ali [1 ,5 ]
Nemati, Mahboob [3 ]
Sorouraddin, Saeed Mohammad [1 ]
机构
[1] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[2] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[4] Khazar Univ, Chem & Chem Engn Dept, 41 Mehseti St, AZ-1096 Baku, Azerbaijan
[5] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkiye
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2025年 / 1251卷
关键词
Dispersive solid phase extraction; Apixaban; Metal-organic framework; Plasma; Capillary electrophoresis; SIMULTANEOUS QUANTIFICATION; LIQUID-CHROMATOGRAPHY; MS/MS METHOD; RIVAROXABAN; DABIGATRAN; MANAGEMENT; ADSORPTION;
D O I
10.1016/j.jchromb.2024.124417
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here, a zirconium-based metal organic framework-dispersive solid phase extraction method was established as an efficient, robust, and accurate approach for quantifying apixaban in human plasma samples prior to capillary electrophoresis with diode array detection. Various types of metal organic frameworks based on UiO-66-NH2 were synthesized by altering modulators and solvents and applied as sorbents in the extraction procedure. Among the tested sorbents, UiO-66-NH2 prepared in dimethylformamide in the presence of acetic acid was found to be the best sorbent in this method for the extraction of apixaban with high extraction efficiency comparable to other types of UiO-66-NH2 metal organic frameworks. The extraction and preconcentration of apixaban were carried out by adding 5 mg of synthesized sorbent to a 5 mL sample solution, followed by vortexing for 3 min. After discarding the supernatant, the adsorbed analyte was eluted from the sorbent surface using 60 mu L acetonitrile under vortexing for 2 min. The effective parameters of the offered method were optimized and validated using a one-parameter-at-a- time strategy. The detection and quantification limits of the method were 9.9 and 32 ng mL- 1 in plasma and 1.5 and 4.9 ng mL- 1 in deionized water, respectively. The method was linear ranging from 4.9 to 1000 ng mL- 1 in deionized water and from 32 to 500 ng mL- 1 in plasma, respectively. The enrichment factor and extraction recovery values were 44 % and 53 %, respectively. The relative standard deviations were <= 6.2 % for intra- and inter-day precisions. Finally, the proposed method was successfully employed to quantify apixaban in human plasma samples.
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页数:9
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