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 >A new validated SPE-HPLC method for monitoring crocetin in human plasma-Application after saffron tea consumption.
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A new validated SPE-HPLC method for monitoring crocetin in human plasma-Application after saffron tea consumption.

机译:一种新的经过验证的SPE-HPLC方法,用于监测藏红花茶饮用后血浆中的藏红花素-应用。

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摘要

Saffron (stigmas of Crocus sativus L.) is a well-known spice with many attributed therapeutic uses throughout centuries. Although studies have demonstrated that crocetin and crocins from saffron have various biological functions, issues concerning the route and way of saffron administration, the absorption and metabolism of saffron carotenoids in humans have not been answered yet. In the present study, an isocratic reversed-phase liquid chromatographic method was developed and validated for the determination of crocetin in plasma. Samples were pre-treated by solid phase extraction (recoveries >72%) and were chromatographed on a Luna C-18 column (4.6mmx250mm, 5mum) with a mobile phase consisting of methanol-water-trifluoroacetic acid (75.0:24.5:0.5, v/v/v) at a flow rate of 1.0mLmin(-1). The HPLC method developed resulted in sharp peaks at 10.7 (trans-crocetin) and 18.6min (cis-crocetin), whereas the calibration curve of total crocetin in plasma displayed a good linearity for concentrations of 0.020-20muM (R(2)=0.999). Specificity, precision, accuracy and stability were studied with spiked plasma samples and were acceptable. The developed method was applied to the determination of crocetin levels in plasma of four healthy human volunteers before and after consumption of one cup of saffron tea (200mg of saffron in 80 degrees C water for 5min). Results showed that the concentration of crocetin was high after 2h (1.24-3.67muM) and still determined after 24h (0.10-0.24). Interestingly, the percentage of the cis-isomer ranges from 25 to 50%, suggesting in vivo isomerization.
机译:藏红花(藏红花的柱头)是一种众所周知的香料,在整个世纪中都有许多可归因于治疗的用途。尽管研究表明藏红花中的藏红花素和藏红花具有多种生物学功能,但是有关藏红花给药途径和方式,藏红花类胡萝卜素在人体中的吸收和代谢的问题尚未得到解答。在本研究中,开发了等度反相液相色谱方法,并验证了血浆中藏红花素的测定。样品通过固相萃取(回收率> 72%)进行预处理,并在Luna C-18色谱柱(4.6mmx250mm,5mum)上进行色谱分离,流动相由甲醇-水-三氟乙酸(75.0:24.5:0.5, v / v / v),流速为1.0mLmin(-1)。开发的HPLC方法在10.7(反式-crocetin)和18.6min(顺式-crocetin)处出现尖峰,而血浆中总crocetin的校正曲线在0.020-20μM的浓度下显示出良好的线性(R(2)= 0.999) )。用加标血浆样品研究了特异性,精密度,准确性和稳定性,并且可以接受。所开发的方法用于测定四名健康志愿者的血浆中的藏红花素水平,这些样品在饮用一杯红花茶(200毫克藏红花在80摄氏度的水中5分钟)之前和之后。结果表明,藏红花素的浓度在2小时后较高(1.24-3.67μM),而在24小时后仍测定(0.10-0.24)。有趣的是,顺式异构体的百分比为25%至50%,表明体内异构化。

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