- P-ISSN 1225-0163
- E-ISSN 2288-8985
- 권한신청
- P-ISSN1225-0163
- E-ISSN2288-8985
- SCOPUS, ESCI, KCI
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Liquid chromatography-tandem mass spectrometric analysis of oleracone D and its application to pharmacokinetic study in mice
분석과학 / Analytical Science and Technology, (P)1225-0163; (E)2288-8985
2021, v.34 no.5, pp.193-201
https://doi.org/10.5806/AST.2021.34.5.193
(College of Pharmacy, Dankook University)
(College of Pharmacy, Dankook University)
(Kyungpook National University)
(Kyungpook National University)
(College of Pharmacy, Dankook University)
(College of Pharmacy, Dankook University)
(College of Pharmacy, Dankook University)
(Kyungpook National University)
(Kyungpook National University)
(College of Pharmacy, Dankook University)
(College of Pharmacy, Dankook University)
Dong,
Y.
L.
,
Tae,
Y.
L.
,
Jaehyeok,
L.
,
Im-Sook,
S.
,
Young,
T.
H.
,
&
Min-Koo,
C.
(2021). . 분석과학, 34(5), 193-201, https://doi.org/10.5806/AST.2021.34.5.193
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Abstract
We have demonstrated a sensitive analytical method of measuring oleracone D in mouse plasma using a liquid chromatography-tandem mass spectrometry (LC-MS/MS). Oleracone D and oleracone F (internal standard) in mouse plasma samples were processed using a liquid-liquid extraction method with methyl tertbutyl ether, resulting in high and reproducible extraction recovery (80.19-82.49 %). No interfering peaks around the peak elution time of oleracone D and oleracone F were observed. The standard calibration curves for oleracone D ranged from 0.5 to 100 ng/mL and were linear with r2 of 0.992. The inter- and intra-day accuracy and precision and the stability fell within the acceptance criteria. The pharmacokinetics of oleracone D following intravenous and oral administration of oleracone D at doses of 5 mg/kg and 30 mg/kg, respectively, were investigated. When oleracone D was intravenously injected, it had first-order elimination kinetics with high clearance and volume of distribution values. The absolute oral bioavailability of this compound was calculated as 0.95 %, with multi-exponential kinetics. The low aqueous solubility and a high oral dose of oleracone D may explain the different elimination kinetics of oleracone D between intravenous and oral administration. Collectively, this newly developed sensitive LC-MS/MS method of oleracone D could be successfully utilized for investigating the pharmacokinetic properties of this compound and could be used in future studies for the lead optimization and biopharmaceutic investigation of oleracone D.
- keywords
- oleracone D, LC-MS/MS, pharmacokinetics, plasma stability, protein binding
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