Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2017 Feb 25;22(3):353.
doi: 10.3390/molecules22030353.

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

Affiliations
Comparative Study

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

Yong Huang et al. Molecules. .

Abstract

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 β-glucuronidase and sulphatase. The analytes were separated on a BEH C18 column (50 mm × 2.1 mm; i.d., 1.7 μm) 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.

Keywords: Polygonum capitatum extract; UPLC-ESI-MS/MS; flavonoids; hydrolysis; pharmacokinetics; phenolic acids.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Chemical structures of (a) gallic acid; (b) quercitrin; (c) quercetin; and (d) puerarin (I.S.).
Figure 2
Figure 2
Chromatograms of the analytes and puerarin (I.S.) in rat plasma. Blank plasma sample (a); a plasma sample spiked with gallic acid, quercitrin, and quercetin, or puerarin (I.S.), respectively (b); and a plasma sample obtained from a rat 60 min after oral administration of P. capitatum extract (c).
Figure 3
Figure 3
Mean plasma concentration-time curves of (a) gallic acid; (b) quercitrin; and (c) quercetin after oral administration of P. capitatum extract (equivalent to 21.35 mg/kg of gallic acid, 2.17 mg/kg of quercitrin, and 0.39 mg/kg of quercetin, respectively) to rats (n = 6).
Figure 4
Figure 4
MS/MS spectra of (a) gallic acid; (b) quercitrin; (c) quercetin; and (d) I.S.
Figure 4
Figure 4
MS/MS spectra of (a) gallic acid; (b) quercitrin; (c) quercetin; and (d) I.S.

Similar articles

Cited by

References

    1. Liao S.-G., Zhang L.-J., Sun F., Zhang J.-J., Chen A.Y., Lan Y.-Y., Li Y.-J., Wang A.-M., He X., Xiong Y., et al. Antibacterial and anti-inflammatory effects of extracts and fractions from polygonum capitatum. J. Ethnopharmacol. 2011;134:1006–1009. doi: 10.1016/j.jep.2011.01.050. - DOI - PubMed
    1. Editorial Committee of Chinese Materia Medica, State Administration of TCM . Miao’s Material Medica, Chinese Materia Medica (Zhonghua Bencao) Publishier of Guizhou Science and Technology; Guiyang, China: 2005. pp. 223–224.
    1. Editorial Committee of Chinese Pharmacopoeia . Chinese Pharmacopoeia. China Medical Science and Technology Press; Beijing, China: 2010. p. 992.
    1. Li Y.-M., Gong Y. The research progress on the chemical component and the pharmacology of polygotum capitatum ham ex d. Don. J. Guizhou Univ. (Nat. Sci.) 2007;24:205–207.
    1. Liu M., Luo C.-L., Zhang Y.-P., Qiu D.-W. Analgesic, anti-inflammatory, and diuretic effects of polygonum capitatum and toddalia asiatica. Guizhou Med. J. 2007;31:370–371.

Publication types

LinkOut - more resources