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采用超高效液相色谱-串联质谱法同时测定大鼠血浆中 7 种蒽醌类成分,并研究口服决明子提取物后的药代动力学。

Simultaneous determination of seven anthraquinones in rat plasma by Ultra High Performance Liquid Chromatography-tandem Mass Spectrometry and pharmacokinetic study after oral administration of Semen Cassiae extract.

机构信息

College of Pharmacy, Harbin Medical University, 157 Baojian Road, Nangang Distrct., Harbin 150081, PR China.

College of Pharmacy, Harbin Medical University, 157 Baojian Road, Nangang Distrct., Harbin 150081, PR China.

出版信息

J Ethnopharmacol. 2015 Jul 1;169:305-13. doi: 10.1016/j.jep.2015.04.008. Epub 2015 Apr 20.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Semen Cassiae, called Juemingzi in China, is the seed of the annual Cassia obtusifolia L., of the leguminosae family. It has been used as healthy drinks to alleviate constipation and improve eyesight for many years in China.

AIM OF THE STUDY

A simple sensitive UHPLC-MS/MS method has been developed and validated for the simultaneous determination and pharmacokinetic study of chrysophanol, emodin, aloe-emodin, rhein, physcion, obtusifolin and aurantio-obtusin in rat plasma.

MATERIALS AND METHODS

Chromatographic separation was accomplished on a C18 column with a 5min gradient elution. A tandem mass spectrometric detection was conducted using multiple reaction monitoring (MRM) via an electrospray ionization (ESI) source and operating in the negative ionization mode. The samples were prepared by LLE with ethyl acetate after being spiked with an internal standard (butylparaben).

RESULTS

The current UHPLC-MS/MS assay was validated for linearity, intra-day and inter-day precisions, accuracy, extraction recovery and stability. The method was linear for all analytes over investigated range with all correlation coefficients greater than 0.9900. The lower limit of quantification (LLOQ) of each analyte was lower than 5ng/mL. Intra-day and inter-day precisions were less than 14.99%. The relative errors of accuracies were in the range of -14.60% to 5.11%. The mean recoveries and matrix effects of anthraquinones were higher than 65.54% and 93.26%, respectively. After oral administration 1.25g/kg of Semen Cassiae extract, the maximum plasma concentration (Cmax) was 1189.25±333.40ng/mL for chrysophanol, 38.48±3.15ng/mL for emodin, 79.20±34.76ng/mL for aloe-emodin, 152.70±23.91ng/mL for rhein, 461.85±266.77ng/mL for physcion, 243.59±22.71ng/mL for obtusifolin and 1950.44±638.86ng/mL for aurantio-obtusin, respectively. The time to reach the maximum plasma concentration (Tmax) was 0.333±0.071h for chrysophanol, 0.333±0.059h for emodin, 0.333±0.009h for aloe-emodin, 0.333±0.09h for rhein, 0.167±0.002h for physcion, 0.5±0.074h for obtusifolin and 0.333±0.06h for aurantio-obtusin, respectively.

CONCLUSION

The proposed method was further applied to investigate the pharmacokinetics of seven anthraquinones after oral administration of Semen Cassia extract to rats.

摘要

民族药理学相关性

决明子,在中国被称为决明子,是豆科决明属植物的种子。多年来,它在中国一直被用作健康饮品来缓解便秘和改善视力。

研究目的

本研究建立并验证了一种简单灵敏的 UHPLC-MS/MS 法,用于同时测定和研究大鼠血浆中大黄酚、大黄素、芦荟大黄素、大黄酸、大黄素、钝叶决明素和橙黄决明素的药代动力学。

材料与方法

采用 C18 柱,5min 梯度洗脱进行色谱分离。采用电喷雾电离(ESI)源和多反应监测(MRM)进行串联质谱检测,以负电离模式运行。样品经乙酸乙酯提取后,采用内标(对羟基苯甲酸丁酯)进行液液萃取。

结果

本 UHPLC-MS/MS 分析方法的线性、日内和日间精密度、准确度、提取回收率和稳定性均得到验证。所有分析物的线性范围均在考察范围内,所有相关系数均大于 0.9900。各分析物的定量下限(LLOQ)均低于 5ng/mL。日内和日间精密度均小于 14.99%。准确度的相对误差在-14.60%至 5.11%之间。蒽醌类化合物的平均回收率和基质效应均高于 65.54%和 93.26%。口服 1.25g/kg 决明子提取物后,大黄酚的最大血药浓度(Cmax)为 1189.25±333.40ng/mL,大黄素为 38.48±3.15ng/mL,芦荟大黄素为 79.20±34.76ng/mL,大黄酸为 152.70±23.91ng/mL,大黄素为 461.85±266.77ng/mL,钝叶决明素为 243.59±22.71ng/mL,橙黄决明素为 1950.44±638.86ng/mL。达到最大血药浓度(Tmax)的时间分别为大黄酚 0.333±0.071h,大黄素 0.333±0.059h,芦荟大黄素 0.333±0.009h,大黄酸 0.333±0.09h,大黄素 0.167±0.002h,钝叶决明素 0.5±0.074h,橙黄决明素 0.333±0.06h。

结论

该方法进一步应用于研究大鼠口服决明子提取物后 7 种蒽醌类化合物的药代动力学。

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