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

被引:13
作者
Gasparetto, Joao C. [1 ]
Guimaraes de Francisco, Thais M. [1 ]
Campos, Francinete R. [1 ]
Pontarolo, Roberto [1 ]
机构
[1] Univ Fed Parana, Ctr Biopharm, Dept Pharm, BR-80210170 Curitiba, Parana, Brazil
关键词
1,2-Benzopyrone; Dihydrocoumarin; Guaco; HPLC-MS/MS; Kaurenoic acid; o-Coumaric acid; Syringaldehyde; BIP. EX BAKER; MIKANIA-LAEVIGATA; COPAIFERA-LANGSDORFFII; IN-VITRO; DITERPENE;
D O I
10.1002/jssc.201000792
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 x 2.1-mm (5-mu m particle size) column maintained at 25 degrees 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.
引用
收藏
页码:740 / 748
页数:9
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