Résumé
IntroductionSimalikalactone E (SkE) from Quassia amara, has been proved to be a valuable anti-malarial and anti-cancer compound. As SkE is very scarce, methods of quantitation are needed in order to optimise its isolation process and to determine pharmacokinetic data.
ObjectiveTo validate methods using liquid chromatography coupled to mass spectrometry for the quantitation of SkE in plant extracts and in biological fluids.
MethodsHigh- and ultrahigh-performance liquid chromatography (UHPLC) coupled to ion trap mass spectrometry (MS) with single ion monitoring detection and to triple quadrupole-linear ion trap tandem mass spectrometry with multiple reaction monitoring detection methods were developed. Validation procedure was realised according to the International Conference on Harmonisation guideline. Methanol extracts of dried Quassia amara leaves, and mouse-blood samples obtained after various routes of administration, were analysed for SkE.
ResultsMethods were validated and gave similar results regarding the content of SkE expressed per kilogram of dry leaves in the traditional decoction (16012mg/kg) and in the methanol extract (932mg/kg). The recovery of the analyte from mouse blood ranged from 80.7 to 119.8%. Simalikalactone E was only detected using UHPLC-MS/MS (0.2 +/- 0.03mg/L) in mouse blood after intravenous injection: none was detected following intraperitoneal or oral gavage administration of SkE.
ConclusionThe LC-MS methods were used for the quantitation of SkE in plant extracts and in mouse blood. These methods open the way for further protocol optimisation of SkE extraction and the determination of its pharmacokinetic data. Copyright (c) 2014 John Wiley & Sons, Ltd.
Simalikalactone E (SkE), a new quassinoid obtained from Quassia amara leaves, has proven to be a valuable anti-malarial and anti-cancer compound. Two liquid chromatography combined with mass spectrometry methods have been and developed validated for the quantitation of SkE in plant extracts and in mice blood after intravenous administration. These methods can be used for the optimization of the extraction and isolation process of SkE and for the determination of its pharmacokinetic data.