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Yu, S.Y., Lee, I.S., Jung, S.H., Lee, Y.M., Lee, Y.R., Kim, J.H., Sun, H. and Kim, J.S. (2013) Caffeoylated Phenylpropanoid Glycosides from Brandisia hancei Inhibit Advanced Glycation End Product Formation and Aldose Reductase in Vitro and Vessel Dilation in Larval Zebrafish in Vivo. Planta Medica, 79, 1705-1709.
http://dx.doi.org/10.1055/s-0033-1351101
has been cited by the following article:
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TITLE:
Validated UPLC/Q-TOF-MS Method for Determination of Poliumoside in Rat Plasma and Its Application to Pharmacokinetic Study
AUTHORS:
Hao Qian, Danyi Lu, Wan Li, Xiaotong Zhou, Baojian Wu, Zhiguo Ma
KEYWORDS:
Poliumoside, UPLC/Q-TOF-MS, Rat Plasma, Pharmacokinetics
JOURNAL NAME:
American Journal of Analytical Chemistry,
Vol.7 No.3,
March
15,
2016
ABSTRACT: Poliumoside is the
main active constituent of Callicarpa
kwangtungensis Chun (CK), a traditional Chinese medicine for management of
hemostasis. In this study, a rapid and selective ultra-performance liquid chromatography coupled with
quadrupole time-of-flight mass spectrometry (UPLC/ Q-TOF-MS) method was
developed and validated to quantify poliumoside in rat plasma. The targeted
analytes in rat plasma were prepared through protein-precipitation method using
10% trichloroacetic acid (TCA). The chromatographic separation was performed on a Waters BEH C18 column (2.1 × 100 mm, 1.7 μm) by acetonitrile-water containing 0.1% formic
acid. The calibration curve was linear over the range of 50 - 10,000 ng/mL (r2 > 0.99). The intra-day or inter-day precision was less than 7.97% and
accuracy was within ?7.00% - 3.36%. The developed method was successfully
applied to pharmacokinetic study of poliumoside in rat plasma. Although being
rapidly absorbed (Tmax ≤ 30 min), poliumoside was poorly bioavailable
after oral administration (the absolute bioavailability was only 0.69%).