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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of nine flavonoids in Polygonum hydropiper L. samples using nanomagnetic powder three-phase hollow fibre-based liquid-phase microextraction combined with ultrahigh performance liquid chromatography-mass spectrometry.
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Simultaneous determination of nine flavonoids in Polygonum hydropiper L. samples using nanomagnetic powder three-phase hollow fibre-based liquid-phase microextraction combined with ultrahigh performance liquid chromatography-mass spectrometry.

机译:纳米粉末三相中空纤维基液相微萃取-超高效液相色谱-质谱法同时测定虎杖中的9种类黄酮。

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摘要

A simple, inexpensive, and efficient nanomagnetic powder three-phase hollow fibre-based liquid-phase microextraction (HF-LPME) technique combined with ultrahigh performance liquid chromatography-mass spectrometry (UPLC-MS) was developed for the simultaneous analysis of nine flavonoids in Polygonum hydropiper L. samples. The final, optimised extraction conditions were as follows: an organic solvent of ethyl acetate, a donor phase of aqueous KHPO at pH 3.0, an acceptor phase of aqueous NaHCO at pH 8.5, a stirring rate of 1000 rpm, and an extraction time of 50 min. Under these conditions, analyte calibration curves were all linear, with correlation coefficients >/= 0.9994. The relative standard deviation for all analytes in intra-day (0.8-2.2%) and inter-day (1.7-3.5%) precision tests was well within the acceptable ranges, as were the limits of quantitation (LOQ < 0.054 mug/L) and detection (LOD < 0.170 mug/L). Recoveries for all standard compounds were between 95.17% and 99.82%, with a RSD of no more than 2.3%. Correlative analyses demonstrated that the physicochemical parameters of the compounds themselves also influenced the extraction efficiency. This technology proved to be rapid, sensitive, and reliable for the quality control of P. hydropiper L. samples.
机译:结合超高效液相色谱-质谱法(UPLC-MS),开发了一种简单,廉价且高效的纳米磁性粉末基于三相空心纤维的液相微萃取(HF-LPME)技术,用于同时分析其中的9种类黄酮。 gon水pi样品。最优化的最终萃取条件如下:乙酸乙酯的有机溶剂,pH 3.0的KHPO水溶液的供体相,pH 8.5的NaHCO水溶液的受主相,1000 rpm的搅拌速度和50的萃取时间分钟在这些条件下,分析物校准曲线均为线性,相关系数> / = 0.9994。日内(0.8-2.2%)和日间(1.7-3.5%)精密度测试中所有分析物的相对标准偏差都在可接受的范围内,定量限也很好(LOQ <0.054 cup / L)和检测(LOD <0.170杯/升)。所有标准化合物的回收率在95.17%至99.82%之间,RSD不超过2.3%。相关分析表明,化合物本身的理化参数也影响萃取效率。事实证明,这项技术对水生毕赤酵母样品的质量控制是快速,灵敏和可靠的。

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