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建立并验证了两种高效液相色谱-串联质谱法,用于测定番石榴叶提取物和制剂中 1,2-苯并吡喃酮、二氢香豆素、邻香豆酸、丁香醛和贝壳杉烯酸的含量。

Development and validation of two methods based on high-performance liquid chromatography-tandem mass spectrometry for determining 1,2-benzopyrone, dihydrocoumarin, o-coumaric acid, syringaldehyde and kaurenoic acid in guaco extracts and pharmaceutical preparations.

机构信息

Department of Pharmacy, Center of Biopharmacy, Federal University of Paraná, Curitiba, Paraná, Brazil.

出版信息

J Sep Sci. 2011 Apr;34(7):740-8. doi: 10.1002/jssc.201000792. Epub 2011 Mar 4.

Abstract

In this study, two HPLC-ESI-MS/MS methods were developed and validated for the determination of 1,2-benzopyrone (COU), o-coumaric acid (OCA), kaurenoic acid (KAU), syringaldehyde (SYR), and dihydrocoumarin (DIH) in guaco extracts and pharmaceutical preparations (syrup and oral solution). The chromatographic separation was achieved using a C18 XBridge 150×2.1-mm (5-μm particle size) column maintained at 25°C. The mobile phases consisted of a gradient of water and acetonitrile containing 0.05% formic acid or 5  mM ammonium formate for the positive and negative ion modes, respectively. All of the calibration curves showed excellent coefficients of correlation (r≥0.9970) over the ranges of 1.25-400  ng/mL for coumarin, 10-600  ng/mL for dihydrocoumarin, 5-250  ng/mL for KAU, and 25-500  ng/mL for o-coumaric acid and syringaldehyde. The range of recovery was 96.3-103% with an RSD% of <4.85% for intraday and interday precision. The results indicate that the developed methods are fast, efficient, and sensitive for the quantification of the guaco metabolites in extracts and pharmaceutical forms while avoiding purification and derivatization steps.

摘要

本研究建立并验证了两种高效液相色谱-电喷雾串联质谱法(HPLC-ESI-MS/MS),用于测定番泻叶提取物及制剂(糖浆和口服溶液)中 1,2-苯并吡喃酮(COU)、对香豆酸(OCA)、贝壳杉烯酸(KAU)、丁香醛(SYR)和二氢香豆素(DIH)的含量。采用 C18 XBridge 150×2.1-mm(5-μm 粒径)色谱柱,在 25°C 下进行色谱分离。正离子模式和负离子模式的流动相分别为水和乙腈梯度,其中含有 0.05%甲酸或 5mM 甲酸铵。香豆素在 1.25-400ng/mL、二氢香豆素在 10-600ng/mL、KAU 在 5-250ng/mL、对香豆酸和丁香醛在 25-500ng/mL 范围内,各校准曲线的相关系数(r≥0.9970)均良好。日内和日间精密度的 RSD%均<4.85%,回收率为 96.3-103%。结果表明,该方法快速、高效、灵敏,可用于提取物和药用形式中番泻叶代谢物的定量分析,同时避免了纯化和衍生化步骤。

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