A UPLC-MS/MS Method for Simultaneous Determination of Free and Total Forms of a Phenolic Acid and Two Flavonoids in Rat Plasma and Its Application to Comparative Pharmacokinetic Studies of Polygonum capitatum Extract in Rats

被引:20
|
作者
Huang, Yong [1 ,2 ,3 ]
Sun, Hui-Yuan [2 ]
Qin, Xiao-Li [2 ]
Li, Yong-Jun [2 ,4 ]
Liao, Shang-Gao [1 ,2 ]
Gong, Zi-Peng [1 ,2 ]
Lu, Yuan [1 ,2 ,3 ]
Wang, Yong-Lin [1 ,2 ]
Wang, Ai-Min [2 ,4 ]
Lan, Yan-Yu [2 ,4 ]
Zheng, Lin [1 ,2 ]
机构
[1] Guizhou Med Univ, Prov Key Lab Pharmaceut Guizhou Prov, 4 Beijing Rd, Guiyang 550004, Peoples R China
[2] Guizhou Med Univ, Sch Pharm, 4 Beijing Rd, Guiyang 550004, Peoples R China
[3] Natl Engn Res Ctr Miaos Med, 4 Beijing Rd, Guiyang 550004, Peoples R China
[4] Guizhou Med Univ, Engn Res Ctr Dev & Applicat Ethn Med & TCM, Minist Educ, 4 Beijing Rd, Guiyang 550004, Peoples R China
来源
MOLECULES | 2017年 / 22卷 / 03期
基金
中国国家自然科学基金;
关键词
Polygonum capitatum extract; phenolic acids; flavonoids; UPLC-ESI-MS/MS; pharmacokinetics; hydrolysis; GALLIC ACID; QUERCETIN; IDENTIFICATION; BIOAVAILABILITY; METABOLITES; ABSORPTION; QUERCITRIN; GLYCOSIDES; MS;
D O I
10.3390/molecules22030353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The principal active constituents of Polygonum capitatum are phenolic acids and flavonoids, such as gallic acid, quercitrin, and quercetin. The aim of this study was to develop and validate a method to determine the three constituents and the corresponding conjugated metabolites of Polygonum capitatum in vivo and to conduct pharmacokinetic studies on the herb, a well-known Miao medicinal plant in China. Gallic acid, quercitrin, and quercetin were analysed by ultra-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS). Protein precipitation in plasma samples was performed using methanol. For the determination of total forms of analytes, an additional process of hydrolysis was conducted using -glucuronidase and sulphatase. The analytes were separated on a BEH C-18 column (50 mm x 2.1 mm; i.d., 1.7 m) and quantified by multiple reaction monitoring (MRM) mode. The linear regression showed high linearity over a 729-fold dynamic range for the three analytes. The relative standard deviations of intra- and inter-day measurements were less than 9.5%, and the method was accurate to within -11.1% to 12.5%. The extraction recoveries for gallic acid, quercitrin, and quercetin were 94.3%-98.8%, 88.9%-98.8%, and 95.7%-98.5%, respectively. All samples were stable under short- and long-term storage conditions. The validated method was successfully applied to a comparative pharmacokinetic study of gallic acid, quercitrin, and quercetin in their free and total forms in rat plasma. The study revealed significantly higher exposure of the constituents in total forms for gallic acid and quercetin, while quercitrin was detected mainly in its corresponding free form in vivo. The established method was rapid and sensitive for the simultaneous quantification of free and total forms of multiple constituents of Polygonum capitatum extract in plasma.
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页数:13
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