首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Molecularly imprinted solid-phase extraction and high-performance liquid chromatography with ultraviolet detection for the determination of urinary trans, trans-muconic acid: a comparison with ionic exchange extraction
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Molecularly imprinted solid-phase extraction and high-performance liquid chromatography with ultraviolet detection for the determination of urinary trans, trans-muconic acid: a comparison with ionic exchange extraction

机译:分子印迹固相萃取和带紫外检测的高效液相色谱法测定尿中反式,反式粘康酸的含量:与离子交换萃取的比较

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摘要

A new molecularly imprinted polymer (MIP) has been synthesized for the selective extraction of trans, trans-muconic acid (ttMA) from urine samples, followed by high-performance liquid chromatography analysis with ultraviolet detection. The synthesis was based on non-covalent interactions, and 4-vinylpyridine was used as a functional monomer. The analytical calibration curve was prepared using a pool of five urine samples of non-smokers spiked with ttMA standards with concentrations that ranged from 0.3 to 10 mg L~(?1) (r~2 = 0.999). The limit of quantification was 0.3 mg L~(?1) (lower than the biological exposure limits suggested by the ACGIH). The within-day and between-day precision and accuracy presented relative standard deviations and relative errors of less than 15%. The analytical frequency was 4 h~(?1) (considering extraction and separation/quantification steps), and the same MIP cartridge was efficiently used for approximately 100 cycles. All figures of merit were similar or better than those obtained by the procedure based on ionic exchange extraction. The proposed method could be an interesting alternative for the routine analysis of ttMA in urine for biological monitoring procedures of human exposure to benzene.
机译:合成了一种新的分子印迹聚合物(MIP),用于从尿液样本中选择性提取反式,反式粘康酸(ttMA),然后进行具有紫外检测的高效液相色谱分析。合成基于非共价相互作用,并且4-乙烯基吡啶用作功能单体。使用五种非吸烟者的尿液样品池(浓度为0.3到10 mg L〜(?1)(r〜2 = 0.999))加标以ttMA标准液来制备分析校准曲线。定量限为0.3 mg L〜(?1)(低于ACGIH建议的生物暴露限)。日内和日间精度和准确度表示相对标准偏差和相对误差小于15%。分析频率为4 h〜(?1)(考虑萃取和分离/量化步骤),相同的MIP柱可有效使用约100个循环。所有品质因数均与通过基于离子交换萃取的方法获得的相近或更好。拟议的方法可能是有趣的替代方法,用于尿液中ttMA的常规分析,以进行人类接触苯的生物监测程序。

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