Rapid quantification of 14 saponins of Maesa lanceolata by UPLC-MS/MS

Saponins are high molecular weight glycosides which are known for their broad range of biological activities. In case of Maesa lanceolata, a tree growing in African countries, the maesasaponins showed virucidal. haemolytic, molluscicidal and anti-angiogenic activity Since the different activities are dependent on the structure of the saponins. a method was developed and validated for the analysis of the individual saponins in this plant Since the saponins were only present in small amounts, it was necessary to develop a very sensitive analytical method For the fast and sensitive analysis of the extracted and purified plant samples ultra-performance liquid chromatography was coupled to a triple quadrupole mass spectrometer for MS/MS detection. A method in positive ESI mode, using sodium acetate in the mobile phase, was developed The sodium adduct ion was selected as the precursor ion since it provided better sensitivity and a better, more stable fragmentation compared to the deprotonated and protonated ions The intensity of the signal obtained by fragmentation of the sodium adducts of the saponins, was optimized by the addition of different concentrations of sodium acetate to the mobile phase Reference standards were not available for all 14 saponins Therefore, a relative MS/UV response was calculated allowing the estimation of the saponins in real samples alpha-Hederin was used as external standard The method was linear over the investigated concentration range with a good correlation coefficient (>0.99) The intra- and inter-clay precisions were below 15% for most maesasaponins with the exception of maesasaponin II, which showed a precision within 20% The recoveries of the spiked pure compounds maesasaponin IV I and VII.1 were 96 6% and 85 5%. respectively The validated method can be applied in the investigation of the content of 14 saponins in transgenic and non-transgenic plant material of M lanceolata (C) 2010 Elsevier B V. All rights reserved.