首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of cinnamaldehyde, cinnamic acid, and 2-methoxy cinnamic acid in rat whole blood after oral administration of volatile oil of Cinnamoni Ramulus by UHPLC-MS/MS: An application for a pharmacokinetic study
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Simultaneous determination of cinnamaldehyde, cinnamic acid, and 2-methoxy cinnamic acid in rat whole blood after oral administration of volatile oil of Cinnamoni Ramulus by UHPLC-MS/MS: An application for a pharmacokinetic study

机译:UHPLC-MS / MS口服肉桂肉桂挥发油后大鼠全血中肉桂醛,肉桂酸和2-甲氧基肉桂酸的同时测定:在药代动力学研究中的应用

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A simple and rapid ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method was developed for the simultaneous determination of cinnamaldehyde, cinnamic acid, and 2-methoxy cinnamic acid in rat whole blood. It was the first time to study the pharmacokinetics of 2-methoxy cinnamic acid in rat whole blood. Samples were processed by a one-step protein precipitation with acetonitrile-37% formaldehyde (90:10, v:v). Chromatographic separation was performed on a Thermo Scientific C18 column (2.1 mm x 50 mm, 1.9 mu m) at room temperature. The total run time was 4 min. The detection was accomplished by using positive and negative ion electrospray ionization in multiple reaction monitoring mode. The method was linear for all of the analytes over 1000 times concentration range with correlation coefficients greater than 0.99. The lower limits of quantification (LLOQ) were 0.1 ng/mL for cinnamaldehyde, 5.8 ng/mL for cinnamic acid, and 10 ng/mL for 2-methoxy cinnamic acid, respectively. To our knowledge, this was the first time that the LLOQ for cinnamaldehyde in validated methods for biological samples was as low as 0.1 ng/mL. Intra- and inter-day precision and accuracy were within +/-9% for all of the analytes during the assay validation. Assay recoveries were higher than 80% and the matrix effects were minimal. The half-life were 8.7 +/- 0.7 h for cinnamaldehyde, 1.0 +/- 0.5 h for cinnamic acid, and 1.4 +/- 0.4h for 2-methoxy cinnamic acid, respectively. The validated assay was firstly applied to the simultaneous quantification of cinnamaldehyde, cinnamic acid, and 2-methoxy cinnamic acid, especially for 2-methoxy cinnamic acid in rat whole blood after oral administration of 15 mg/kg essential oil of Cinnamoni Ramulus. It was observed that the Cmax and AUC of 2-methoxy cinnamic acid.(0.01% in essential oil of Cinnamoni Ramulus) were greater than those of cinnamaldehyde (83.49% in essential oil of Cinnamoni Ramulus), which implied that 2-methoxy cinnamic acid might be the major bioactive constitutes in essential oil of Cinnamoni Ramulus. (C) 2015 Elsevier B.V. All rights reserved.
机译:建立了一种简便,快速的超高效液相色谱-串联质谱(UHPLC-MS / MS)方法,用于同时测定大鼠全血中的肉桂醛,肉桂酸和2-甲氧基肉桂酸。这是首次研究2-甲氧基肉桂酸在大鼠全血中的药代动力学。样品用乙腈-37%甲醛(90:10,v:v)进行一步蛋白沉淀处理。在室温下在Thermo Scientific C18柱(2.1mm×50mm,1.9μm)上进行色谱分离。总运行时间为4分钟。通过在多个反应监控模式下使用正负离子电喷雾电离来完成检测。对于1000倍浓度范围内的所有分析物,该方法都是线性的,相关系数大于0.99。肉桂醛的定量下限(LLOQ)分别为0.1 ng / mL,肉桂酸为5.8 ng / mL和2-甲氧基肉桂酸为10 ng / mL。据我们所知,这是经过验证的生物样品方法中肉桂醛的LLOQ首次低至0.1 ng / mL。在分析验证期间,所有分析物的日内和日间精度和准确度均在+/- 9%以内。测定回收率高于80%,基质影响最小。肉桂醛的半衰期分别为8.7 +/- 0.7 h,肉桂酸的半衰期为1.0 +/- 0.5 h,2-甲氧基肉桂酸的半衰期分别为1.4 +/- 0.4h。经验证的测定方法首先用于口服定量15 mg / kg肉桂肉桂精油后大鼠全血中肉桂醛,肉桂酸和2-甲氧基肉桂酸的定量,尤其是2-甲氧基肉桂酸的定量。观察到2-甲氧基肉桂酸的Cmax和AUC(肉桂肉桂精油中的0.01%)大于肉桂醛(肉桂​​肉桂精油中的83.49%),这表明2-甲氧基肉桂酸可能是肉桂肉桂精油中的主要生物活性成分。 (C)2015 Elsevier B.V.保留所有权利。

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