Abstract
Scutellarin is widely used in treating various cardiovascular diseases. Few data are available regarding its metabolism and pharmacokinetics in humans. The objectives of this study were to develop methods to identify major metabolites of scutellarin in human urine and plasma and to determine simultaneously the parent drug and its major metabolites in human plasma for pharmacokinetic studies. Four metabolites were detected in urine samples by liquid chromatography coupled with electrospray multi-stage mass spectrometry (MS), but only one of them was found in plasma. Its structure was confirmed as scutellarein 6-O-β-d-glucuronide by MS, NMR, and UV absorbance spectra. The plasma concentrations of scutellarin and the major metabolite were simultaneously determined using liquid chromatography-tandem MS. After a single p.o. administration of 60 mg of scutellarin to 20 healthy subjects, the plasma concentrations of scutellarin were very low, and its plasma concentration-time curve was also anomalous. Plasma concentration of the major metabolite was comparatively high, and the peak plasma concentration was 87.0 ± 29.1 ng/ml. The Tmax was late (7.85 ± 1.62 h), and part of individual pharmacokinetic profiles showed double peaks, which indicated scutellarin could be absorbed into the intestine after hydrolysis to its aglycone by bacterial enzymes. This was followed by reconjugation in the intestinal cell and/or liver with glucuronic acid catalyzed by the phase II enzyme, which showed regioselectivity and species difference. The regioselectivity of glucuronoconjugation for scutellarin may be of importance for pharmacological activity. Plasma concentration of isoscutellarin can be used as a biomarker of scutellarin intake.
Footnotes
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This work was supported by Grant 30271525 of the National Natural Science Foundation of China.
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Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.
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doi:10.1124/dmd.106.009779.
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ABBREVIATIONS: LC/MS/MS, liquid chromatography/tandem mass spectrometry; LC/MS, liquid chromatography/mass spectrometry; LC/MSn, liquid chromatography/ion trap mass spectrometry; HPLC, high-performance liquid chromatography; ESI, electrospray ionization; QC, quality control; AUC, area under the plasma concentration-time curve.
- Received February 10, 2006.
- Accepted May 16, 2006.
- The American Society for Pharmacology and Experimental Therapeutics
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