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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of bisphenol AF (BPAF) in tissues, serum, urine and feces of orally dosed rats by ultra-high-pressure liquid chromatography-electrospray tandem mass spectrometry
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Determination of bisphenol AF (BPAF) in tissues, serum, urine and feces of orally dosed rats by ultra-high-pressure liquid chromatography-electrospray tandem mass spectrometry

机译:超高压液相色谱-电喷雾串联质谱法测定口服给药大鼠组织,血清,尿液和粪便中的双酚AF(BPAF)

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摘要

As a homologue of bisphenol A (BPA), there is concern about the potential reproductive and developmental toxicity of bisphenol AF (BPAF) based on in vitro tests. In this study, a simple and universal analytical method was developed for the determination of trace BPAF in various tissues and excreta of rats after they were orally dosed. The samples were hydrolyzed with glucuronidase/arylsulfatase followed by ultrasonic extraction with acetonitrile. The crude extract was purified with a mixed-mode anion exchange (Oasis MAX) solid-phase extraction (SPE) cartridge. Separation and quantification was then conducted by ultra-high-pressure liquid chromatography/electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) in negative ionization mode. The recoveries at three fortification levels in different biological samples were from 71.0% to 102.3% with relative standard deviations no more than 13.2% (n=6). The quantification limits of the method were from 0.5μg/kg to 3μg/kg depending on the matrix. This method was successfully applied to the determination of BPAF in tissues, serum, urine and feces of orally dosed rats.
机译:作为双酚A(BPA)的同系物,基于体外试验,人们对双酚AF(BPAF)的潜在生殖和发育毒性感到担忧。在这项研究中,开发了一种简单通用的分析方法,用于口服给药后测定大鼠各种组织和排泄物中的痕量BPAF。样品用葡糖醛酸糖苷酶/芳基硫酸酯酶水解,然后用乙腈超声提取。粗提取物用混合模式阴离子交换(Oasis MAX)固相萃取(SPE)柱纯化。然后通过超高压液相色谱/电喷雾电离串联质谱法(LC-ESI-MS / MS)在负电离模式下进行分离和定量。不同生物样品在三个设防水平下的回收率从71.0%至102.3%,相对标准偏差不超过13.2%(n = 6)。该方法的定量限为0.5μg/ kg至3μg/ kg,具体取决于基质。该方法已成功应用于口服给药大鼠组织,血清,尿液和粪便中BPAF的测定。

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