期刊
MICROCHEMICAL JOURNAL
卷 146, 期 -, 页码 798-806出版社
ELSEVIER
DOI: 10.1016/j.microc.2019.02.007
关键词
Stir bar sorptive extraction; MOP-derived magnetic porous carbons; Pluorouracil; Biological samples; Liquid desorption; Phenobarbital; Experimental design
资金
- University of Kashan
- University of Mazandaran
- Iran National Science Foundation (INSF) [95008040]
A simple and cost-effective method was developed to determine fluorouracil (5-FU) and phenobarbital (PHB) in human body fluids. A coating based on a zeolitic imidazole framework-67 (ZIF-67) template cobalt nanoporous carbon (Co-NPC) was synthesized by one-step carbonization of ZIF-67 without using any other carbon precursors in the present study. The prepared Co-NPC was then fabricated on the surface of a prepared stir bar to be used as stir bar sorptive extraction (SBSE) method. The extracted analytes were then analyzed via high performance liquid chromatography-ultraviolet detection (HPLC-UV). Plackett-Burman design was employed for screening the experimental factors. The effective factors were then optimized using Central Composite Design (CCD). Under the optimum conditions, limits of detections (LODs) of 5-FU were 0.36, 0.41 and 1.2 mu g L-1 in water, urine and plasma samples, respectively. Limits of quantifications (LOQs) were also 1.2, 1.3 and 4.5 mu g L-1 in water, urine and plasma samples, respectively. Relative standard deviations (RSDs) at a spiked concentration of 10 mu g L-1 were 8.1, 7.9 and 8.6% (as intra-day RSD) in water, urine and plasma samples, respectively. The linear dynamic ranges (LDRs) were in the range of 1-200 mu g L-1. Moreover, LODs of PHB were 0.21, 0.32 and 1.4 mu g L-1 in water, urine and plasma samples, respectively. LOQs were also 0.9, 1.1 and 4.6 mu g L-1 in water, urine and plasma samples, respectively. Relative standard deviations (RSDs) at a spiked concentration of 10 mu g L-1 were 6.3, 6.5 and 6.9% (as intra-day RSD) in water, urine and plasma samples, respectively. The linear dynamic ranges (LDRs) were in the range of 1-500 mu g L-1. The applicability of the method was investigated by the extraction and determination of the target analytes in different biological fluids including urine and plasma samples.
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