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Razvoj nove metode disperzivne mikroekstrakcije tekuće-tekuće za istovremenu analizu šest antitumorskih lijekova u ljudskoj plazmi (CROSBI ID 711637)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Turković, Lu ; Koraj, Natan ; Silovski, Tajana ; Ščavničar, Andrijana ; Lovrić, Mila ; Nigović, Biljana ; Sertić, Miranda Razvoj nove metode disperzivne mikroekstrakcije tekuće-tekuće za istovremenu analizu šest antitumorskih lijekova u ljudskoj plazmi // 27th Croatian Meeting of Chemists and Chemical Engineers, Book of Abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel et al. (ur.). Zagreb: Hrvatsko kemijsko društvo, 2021. str. 224-224

Podaci o odgovornosti

Turković, Lu ; Koraj, Natan ; Silovski, Tajana ; Ščavničar, Andrijana ; Lovrić, Mila ; Nigović, Biljana ; Sertić, Miranda

engleski

Razvoj nove metode disperzivne mikroekstrakcije tekuće-tekuće za istovremenu analizu šest antitumorskih lijekova u ljudskoj plazmi

Palbociclib, ribociclib and abemaciclib are novel anticancer agents used in combination with anastrozole, letrozole or fulvestrant in breast cancer treatment. They significantly improve therapeutic outcomes, but still exhibit an array of side-effects and a potential for inter- individual variabilities, so therapeutic drug monitoring (TDM) could prove beneficial [1]. A suitable bioanalytical method therefore needs to be developed, encompassing both the sample preparation procedure and the analytical system parameters. Optimal sample preparation ensures maximal analyte extraction recoveries, while minimizing matrix effect and prolonging the instrument lifetime [2]. Dispersive liquid-liquid microextraction is a technique in which a mixture of an organic extractant and disperser solvents is quickly injected into an aqueous solution, forming an emulsion that facilitates fast and efficient extraction. In biological sample preparation, protein precipitation (PPT) usually precedes the extraction. Since acetonitrile is commonly used as both a PPT agent and a disperser solvent, the supernatant after PPT can immediately be mixed with an extractant solvent and injected into an aqueous solution [3]. In this work, various conditions affecting analytes’ extraction recoveries were investigated: type and volume of the extractant and disperser solvent, aqueous phase pH, addition of salt, and ultrasonication. In optimal conditions, for 50 µL of plasma sample, 200 µL of acetonitrile is added for PPT. 200 µL of the supernatant is withdrawn, mixed with 400 µL of chloroform and injected into 100 µL of 5 % w/V aqueous sodium citrate solution. The organic layer is evaporated to dryness, reconstituted in 40 µL 65 % V/V methanol and analysed by liquid chromatography. The proposed method is fast, simple, with low sample and solvent consumption, and offers very high extraction yields (87.2 to 97.8 %) with significantly less matrix interferences compared to PPT alone.

oncology ; bioanalysis ; microextraction ; therapeutic drug monitoring

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Podaci o prilogu

224-224.

2021.

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objavljeno

Podaci o matičnoj publikaciji

27th Croatian Meeting of Chemists and Chemical Engineers, Book of Abstracts

Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna

Zagreb: Hrvatsko kemijsko društvo

Podaci o skupu

27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI)

poster

05.10.2021-08.10.2021

Veli Lošinj, Hrvatska

Povezanost rada

Farmacija, Kemija