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Sensitive analysis of trace caffeine in human serum by HPLC using tetraazacalix[2]arene[2]triazine-modified silica as SPE sorbent

机译:四氮杂lix [2]芳烃[2]三嗪改性二氧化硅作为SPE吸附剂的HPLC灵敏分析人血清中的咖啡因

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In this paper, a rapid and effective SPE-HPLC method, using tetraazacalix[2]arene[2]triazine modified silica gel (NCSi) as solid-phase extraction (SPE) sorbent, was established to enrich and determine caffeine in human serum. All the main influence factors of SPE including amount of NCSi sorbent, sample flow rate, and volume and composition of washing solution were investigated and evaluated in the sample pretreatment step. The limits of detection (LODs) and quantitation (LOQs) were 1 ng mL(-1) and 5 ng mL(-1), respectively, whereas the overall recoveries ranged from 90.3% to 93.5%, the relative standard deviation (RSD) of the method was less than 3.4%. In addition, the retention mechanism of caffeine on NCSi was investigated by quantum chemistry calculations. The optimized supramolecular structures showed that pi-pi and CH-pi interactions exist between NCSi and caffeine. Thermodynamic results from quantum chemistry calculation (QCC) were consistent with the retention behaviors of caffeine on NCSi. The method of non-covalent interaction (NCI) 28 index developed by Yang and co-workers was used to distinguish strong interaction, van der Waals interaction and repulsive steric interactions. The QCC results further illustrated the stronger retention of caffeine on the tetraazacalix[2]arene[2]triazine-modified silica stationary phase. All of the results implied that NCSi was a promising SPE sorbent, and can be applied to the preconcentration and determination of trace caffeine in human serum.
机译:本文建立了一种以四氮杂PE [2]芳烃[2]三嗪改性硅胶(NCSi)为固相萃取(SPE)吸附剂的快速有效的SPE-HPLC方法,以富集和测定人血清中的咖啡因。在样品预处理步骤中,研究和评估了固相萃取的所有主要影响因素,包括NCSi吸附剂的量,样品流速,洗涤液的体积和组成。检出限(LOD)和定量限(LOQ)分别为1 ng mL(-1)和5 ng mL(-1),而总回收率在90.3%至93.5%之间,相对标准偏差(RSD)该方法的小于3.4%。另外,通过量子化学计算研究了咖啡因在NCSi上的保留机理。优化的超分子结构表明,NCSi和咖啡因之间存在pi-pi和CH-pi相互作用。量子化学计算(QCC)的热力学结果与咖啡因在NCSi上的保留行为一致。由Yang和同事开发的非共价相互作用(NCI)28指数方法用于区分强相互作用,范德华相互作用和排斥性空间相互作用。 QCC结果进一步说明了咖啡因在四氮杂az [2]芳烃[2]三嗪改性的硅胶固定相上的保留力更强。所有结果都表明NCSi是一种很有前途的SPE吸附剂,可用于人血清中痕量咖啡因的预浓缩和测定。

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