Galaon, TomaTomaGalaonCruceru, LilianaLilianaCruceruPetre, JanaJanaPetrePascu, Luoana FlorentinaLuoana FlorentinaPascuIancu, VasileVasileIancuNiculescu, MarcelaMarcelaNiculescu2017-03-242017-03-2420161311-5065http://hdl.handle.net/123456789/495Journal of Environmental Protection and Ecology Volume 17 Issue 1"A new sensitive, selective and accurate LC-MS/MS method with positive electrospray ionization was developed to detect eight nitrosamines from drinking water. The method separates all nitrosamines using a Zorbax Eclipse Plus C18 column (100 × 2.1 mm, 3.5 µm) kept at 15°C and a mobile phase consisting of aq. 0.005% formic acid and acetonitrile in the ratio 90/10 (v/v). A strong gradient applied in 8 min up to 90% ACN allowed analyte separation. A low mobile phase flw-rate of 0.2 ml/min was used to enhance ESI ionisation. Collision energy, fragmentor and capillary voltages were optimised to enhance analyte S/N ratio. Optimisation of LC-MS parameters generated low instrumental LOQ values between 0.05–1.84 µg/l. Detector response was linear in the range 1–100 µg/l (R2 > 0.99) for all nitrosamines. SPE using activated charcoal cartridges was used to concentrate nitrosamines from drinking water. Overall method LOQs were situated in the range 1.23–4.12 ng/l. LC-MS/MS method was fully validated with respect to specificity, linearity, precision, accuracy and LOQ, and provided good results. The method was tested on six tap water samples collected from different regions of Bucharest and the determined nitrosamine total content ranged between 2.8 and 14.8 ng/l."en-USLC-MS/MSNitrosaminesDrinking waterSolid-phase extractionElectrosprayNew LC-MS/MS method for the determination of eight nitrosamines in drinking waterArticle