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A novel nonaqueous capillary electrophoresis method for effective separation and simultaneous determination of aurantio-obtusin, emodin and rhein in semen cassiae and cassia seed tea

机译:一种有效分离并同时测定精液中决明子和决明子茶中的金-Obtusin,大黄素和大黄酸的新型非水毛细管电泳方法

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摘要

Anthraquinones (aurantio-obtusin, emodin and rhein) cannot be determined simultaneously using capillary zone electrophoresis because aurantio-obtusin has a low solubility in water. Therefore, a novel nonaqueous capillary electrophoresis (NACE) method with diode-array detection was developed for effective separation and simultaneous determination of the three anthraquinones. A BGE solution of 40 mM NaAc-40 mM NH4Ac-40 mM NaOH in methanol was used for separation of the three anthraquinones. The effects of ultrasonic extraction conditions and the NACE conditions on separation were investigated in detail. Under the optimized conditions, the analytes can be effectively separated in 7 min. The standard curves of the three anthraquinones showed good linearity, with correlation coefficients of r >0.999. The limit of detection (LOD; signal to noise ratio {S/N) of 3) of aurantio-obtusin, emodin and rhein were 0.25, 0.12 and 0.19 μg mL~(-1), respectively. Their average intra- and inter-day analytical precisions (relative standard deviation) were less than 2.8% and 4.0%, respectively. The recoveries of the three spiked levels of aurantio-obtusin, emodin and rhein from semen cassiae and cassia seed tea samples were in the range of 86.6-106%. The proposed method provides the speediness, selectivity, sensitivity, linearity and accuracy as well as low reagent consumption necessary for simultaneous analysis of the test anthraquinones. The ultrasonic extraction-NACE method was used for the analysis of aurantio-obtusin, emodin and rhein in semen cassiae and cassia seed tea with satisfactory results, and could be applied for quality control of semen cassiae and cassia seed tea.
机译:蒽醌(金-obtusin,大黄素和大黄酸)不能通过毛细管区带电泳同时测定,因为金-obtusin在水中的溶解度低。因此,开发了一种具有二极管阵列检测的新型非水毛细管电泳(NACE)方法,可以有效分离和同时测定三种蒽醌。使用40 mM NaAc-40 mM NH4Ac-40 mM NaOH在甲醇中的BGE溶液分离三种蒽醌。详细研究了超声提取条件和NACE条件对分离的影响。在优化的条件下,分析物可以在7分钟内有效分离。三种蒽醌的标准曲线均具有良好的线性,相关系数r> 0.999。 ur-卵磷脂,大黄素和大黄酸的检出限(LOD;信噪比(S / N)为3)分别为0.25、0.12和0.19μgmL〜(-1)。它们的日内和日间平均分析精度(相对标准偏差)分别小于2.8%和4.0%。从精液中的决明子和决明子茶样品中,三个加标的金黄色-ob丁素,大黄素和大黄酸的回收率在86.6-106%之间。所提出的方法提供了快速,选择性,灵敏度,线性和准确性以及同时分析测试蒽醌所必需的低试剂消耗量。超声提取-NACE法分析了决明子和决明子茶中的金-ob丁素,大黄素和大黄酸,结果令人满意,可用于决明子和决明子茶的质量控制。

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