Surfactant-enhanced spectrofluorimetric detection after magnetic nanoparticles-based micro-solid-phase extraction coupled with dispersive liquid-liquid micro-extraction for determination of ciprofloxacin in human plasma

被引:3
作者
Rastegar, Hossein [1 ]
Dadgarnejad, Manouchehr [1 ]
Zolfaghari, Fatemeh [1 ]
Taherimaslak, Zohreh [1 ]
Amoli-Diva, Mitra [2 ]
机构
[1] MOHE, Food & Drug Adm, Food & Drug Res Inst, Cosmet Prod Res Ctr, Tehran, Iran
[2] Kharazmi Tarbiat Moalem Univ, Fac Chem, Tehran, Iran
关键词
nanoparticles; spectrochemical analysis; organic compounds; calibration; superparamagnetism; surfactants; drugs; magnetic particles; hydrophobicity; adsorption; iron compounds; nanomedicine; colloids; nanosensors; Fe3O4; surfactant-enhanced spectrofluorimetric detection; DLLME; micelle enhanced spectrofluorimetric detection; human plasma samples; disperser; 1-octanol; -SPE step; extraction solvent; dispersive liquid-liquid microextraction; magnetic nanoparticle-based microsolid-phase extraction; ciprofloxacin antibiotics; methanol; oleic acid-modified nanoparticles; hydrophobic adsorbents; surface area; signal enhancement; analyte recovery; calibration curve; calibration equation; interday precisions; intraday precisions; relative standard deviation; ULTRASOUND-ASSISTED EMULSIFICATION; CAPILLARY-ELECTROPHORESIS; WATER SAMPLES; MICROEXTRACTION; FLUORESCENCE; FLUOROQUINOLONE; CHROMATOGRAPHY; URINE; ANTIBACTERIALS; ENROFLOXACIN;
D O I
10.1049/mnl.2018.5101
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A sensitive and fast micro-solid-phase extraction (-SPE) coupled with dispersive liquid-liquid micro-extraction (DLLME) was reported before micelle enhanced spectrofluorimetric detection for determination of ciprofloxacin antibiotic in human plasma samples. The DLLME was performed using methanol as disperser and 1-octanol as extracting solvent. Oleic acid-modified Fe3O4 nanoparticles (as hydrophobic adsorbents) were applied in -SPE step to extract the analyte from DLLME procedure. The method uses the advantageous of high surface area and strong superparamagnetism of these nanoparticles to many avoid labourhood column/cartridge-passing processes of traditional SPE. The major parameters affecting signal enhancement and analyte recovery were evaluated and optimised. Under the optimal conditions, the calibration curve (with calibration equation of I-f = 2.5826 C + 10.273) was linear in the range 0.5-600 g L-1 (R-2 = 0.997) with low limit of detection of 0.21 mu g L-1 and limit of quantification of 0.63 mu g L-1. The intra-day and inter-day precisions (as relative standard deviation) were in the range of 1.01-1.67% and high recoveries in the range of 93.5-102.4% were obtained. The results demonstrated that the proposed method is easy, low cost, and accurate. In addition, it confirms that choosing extraction solvent was not restricted to the high-density solvents which can extent the versatility of DLLME.
引用
收藏
页码:1564 / 1569
页数:6
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