Analytical Methods for Environmental Contaminants of Emerging Concern. Группа авторов

10.1016/j.chroma.2011.12.064.

      67 67 Assis, R.C., Mageste, A.B., de Lemos, L.R., Orlando, R.M., and Rodrigues, G.D. (2020). Application of aqueous two-phase systems for the extraction of pharmaceutical compounds from water samples. J. Mol. Liq. 301: 112411. doi: 10.1016/j.molliq.2019.112411.

      68 68 Sadkowska, J., Caban, M., Chmielewski, M., Stepnowski, P., and Kumirska, J. (2019). The use of gas chromatography for determining pharmaceutical residues in clinical, cosmetic, food and environmental samples in the light of the requirements of sustainable development. Arch. Environ. Prot. 45(1): 42–49. doi: 10.24425/aep.2019.124829.

      69 69 Caban, M., Migowska, N., Stepnowski, P., Kwiatkowski, M., and Kumirska, J. (2012). Matrix effects and recovery calculations in analyses of pharmaceuticals based on the determination of β-blockers and β-agonists in environmental samples. J. Chromatogr. A 1258: 117–127. doi: 10.1016/j.chroma.2012.08.029.

      70 70 Caban, M., Czerwicka, M., Łukaszewicz, P., Migowska, N., Stepnowski, P., Kwiatkowski, M., and Kumirska, J. (2013). A new silylation reagent dimethyl(3,3,3-trifluoropropyl)silyldiethylamine for the analysis of estrogenic compounds by gas chromatography-mass spectrometry. J. Chromatogr. A 1301: 215–224. doi: 10.1016/j.chroma.2013.05.073.

      71 71 Evershed, R. (1993). Advances in silylation. In: Handbook of Derivatives for Chromatography, 2nd (ed. K. Blau and J.M. Halket), 51–108. London: Wiley.

      72 72 Kumirska, J., Plenis, A., Łukaszewicz, P., Caban, M., Migowska, N., Białk-Bielińska, A., Czerwicka, M., and Stepnowski, P. (2013). Chemometric optimization of derivatization reactions prior to gas chromatography – mass spectrometry analysis. J. Chromatogr. A 1296: 164–178. doi: 10.1016/j.chroma.2013.04.079.

      73 73 Caban, M., Stepnowski, P., Kwiatkowski, M., Migowska, N., and Kumirska, J. (2011). Determination of β-blockers and β-agonists using gas chromatography and gas chromatography – mass spectrometry – a comparative study of the derivatization step. J. Chromatogr. A 1218(44): 8110–8122. doi: 10.1016/j.chroma.2011.08.093.

      74 74 Caban, M., Mioduszewska, K., Łukaszewicz, P., Migowska, N., Stepnowski, P., Kwiatkowski, M., and Kumirska, J. (2014). A new silylating reagent – dimethyl(3,3,3-trifluoropropyl)silyldiethylamine – for the derivatisation of non-steroidal anti-inflammatory drugs prior to gas chromatography-mass spectrometry analysis. J. Chromatogr. A 1346: 107–116. doi: 10.1016/j.chroma.2014.04.054.

      75 75 Migowska, N., Stepnowski, P., Paszkiewicz, M., Gołębiowski, M., and Kumirska, J. (2010). Trimethylsilyldiazomethane (TMSD) as a new derivatization reagent for trace analysis of selected non-steroidal anti-inflammatory drugs (NSAIDs) by gas chromatography methods. Anal. Bioanal. Chem. 397(7): 3029–3034. doi: 10.1007/s00216-010-3853-y.

      76 76 Caban, M. and Stepnowski, P. (2018). Silylation of acetaminophen by trifluoroacetamide-based silylation agents. J. Pharm. Biomed. Anal. 154: 433–437. doi: 10.1016/j.jpba.2018.03.037.

      77 77 Caban, M. and Stepnowski, P. (2020). The application of isotopically labeled analogues for the determination of small organic compounds by GC/MS with selected ion monitoring. Anal. Methods 12(30): 3854–3864. doi: 10.1039/D0AY00723D.

      78 78 Evans, S.E. and Kasprzyk-Hordern, B. (2014). Applications of chiral chromatography coupled with mass spectrometry in the analysis of chiral pharmaceuticals in the environment. Trends Environ. Anal. Chem. 1: 34–51. doi: 10.1016/j.teac.2013.11.005.

      79 79 Guitart, C. and Readman, J.W. (2010). Critical evaluation of the determination of pharmaceuticals, personal care products, phenolic endocrine disrupters and faecal steroids by GC/MS and PTV-GC/MS in environmental waters. Anal. Chim. Acta 658(1): 32–40. doi: 10.1016/j.aca.2009.10.066.

      80 80 Huang, S., Zhu, F., Jiang, R., Zhou, S., Zhu, D., Liu, H., and Ouyang, G. (2015). Determination of eight pharmaceuticals in an aqueous sample using automated derivatization solid-phase microextraction combined with gas chromatography-mass spectrometry. Talanta 136: 198–203. doi: 10.1016/j.talanta.2014.11.071.

      81 81 Aspromonte, J., Wolfs, K., and Adams, E. (2019). Current application and potential use of GC × GC in the pharmaceutical and biomedical field. J. Pharm. Biomed. Anal. 176: 112817. doi: 10.1016/j.jpba.2019.112817.

      82 82 Caban, M., Białk-Bielińska, A., Stepnowski, P., and Kumirska, J. (2016). Current issues in pharmaceutical residues in drinking water. Curr. Anal. Chem. 12(3): 1–9. doi: 10.2174/1573411012666151009194401.

      83 83 Świacka, K., Szaniawska, A., and Caban, M. (2019). Evaluation of bioconcentration and metabolism of diclofenac in mussels Mytilus trossulus – laboratory study. Mar. Pollut. Bull. 141: 249–255. doi: 10.1016/j.marpolbul.2019.02.050.

      84 84 Rosal, R., Rodríguez, A., Perdigón-Melón, J.A., Petre, A., García-Calvo, E., Gómez, M.J., Agüera, A., and Fernández-Alba, A.R. (2010). Occurrence of emerging pollutants in urban wastewater and their removal through biological treatment followed by ozonation. Water Res. 44(2): 578–588. doi: 10.1016/j.watres.2009.07.004.

      85 85 Boyd, G.R., Palmeri, J.M., Zhang, S., and Grimm, D.A. (2004). Pharmaceuticals and personal care products (PPCPs) and endocrine disrupting chemicals (EDCs) in stormwater canals and Bayou St. John in New Orleans, Louisiana, USA. Sci. Total Environ. 333: 137–148. doi: 10.1016/j.scitotenv.2004.03.018.

      86 86 Kołecka, K., Gajewska, M., Stepnowski, P., and Caban, M. (2019). Spatial distribution of pharmaceuticals in conventional wastewater treatment plant with Sludge Treatment Reed Beds technology. Sci. Total Environ. 647: 149–157. doi: