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Development and validation of a HPLC method for the determination of benzo(a)pyrene in human breast milk

机译:测定人母乳中苯并(a)a的HPLC方法的建立与验证

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摘要

A simple analytical procedure was developed for the quantitation of benzo(a)pyrene in human breast milk using solid phase extraction (SPE) combined with high performance liquid chromatography. Before the chromatographic process, SPE, including C18 functional groups in silicagel cartridges, was conducted for sample preparation. A C18 column (100×4.6 mm id, 3 μm particle size) was used with acetonitrile:water (80:20) as the mobile phase at a flow rate 1mL/min at 30°C. Fluorimetric detection was performed for excitation and emission at 290 and 406 nm, respectively. It was observed that the calibration curve was linear over the range of 0.5–80 ng/mL. The limit of detection and limit of quantitation were found to be 0.5 and 1.07 ng/mL, respectively. Intraday and interday relative standard deviation values were less than 5.15%. Moreover, the newly developed method provides a fast, simple, cost effective, and sensitive assay to detect an important carcinogen substance, benzo(a)pyrene, in human breast milk.
机译:使用固相萃取(SPE)和高效液相色谱法,开发了一种简单的分析程序,用于定量母乳中的苯并(a)re。在色谱过程之前,进行了固相萃取,包括硅胶柱中的C18官能团,用于样品制备。使用C18色谱柱(内径100×4.6 mm,粒径3μm),以乙腈:水(80:20)作为流动相,在30°C下的流速为1mL / min。分别对290和406 nm处的激发和发射进行荧光检测。据观察,校准曲线在0.5–80 ng / mL范围内呈线性。检出限和定量限分别为0.5和1.07 ng / mL。日内和日间相对标准偏差值小于5.15%。此外,新开发的方法提供了一种快速,简单,经济高效且灵敏的检测方法,可检测母乳中一种重要的致癌物质苯并(a)py。

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