Capillary electrokinetic chromatography for studying interactions between β-blockers and Intralipid emulsion

0573930 - ÚOCHB 2024 RIV NL eng J - Článek v odborném periodiku
Ravald, H. - Jaikishan, S. - Samuelsson, J. - Sukhova, A. - Šolínová, Veronika - Fornstedt, T. - Kašička, Václav - Wiedmer, S. K.
Capillary electrokinetic chromatography for studying interactions between β-blockers and Intralipid emulsion.
Journal of Pharmaceutical and Biomedical Analysis. Roč. 234, September (2023), č. článku 115554. ISSN 0731-7085. E-ISSN 1873-264X
Institucionální podpora: RVO:61388963
Klíčová slova: adsorption isotherm * β-blockers * capillary electrokinetic chromatography * distribution constant * drug toxicities * Intralipid emulsion
Obor OECD: Analytical chemistry
Impakt faktor: 3.4, rok: 2022
Způsob publikování: Open access
https://doi.org/10.1016/j.jpba.2023.115554

Toxicity of β-blockers is one of the most common causes of poison-induced cardiogenic shock throughout the world. Therefore, methodologies for in vivo removal of the drugs from the body have been under investigation. Intralipid emulsion (ILE) is a common commercial lipid emulsion used for parenteral nutrition, but it has also been administered to patients suffering from drug toxicities. In this work, a set of β-blockers of different hydrophobicity's (log KD values ranging from 0.16 to 3.8) were investigated. The relative strength of the interactions between these compounds and the ILE was quantitatively assessed by means of binding constants and adsorption constants of the formed β-blocker-ILE complexes. The binding constants were determined by capillary electrokinetic chromatography and the adsorption constants were calculated based on different adsorption isotherms. Expectedly, the binding constants were strongly related to the log KD values of the β-blockers. The binding and adsorption constants also show that less hydrophobic β-blockers interact with ILE, suggesting that this emulsion could be useful for capturing such compounds in cases of their overdoses. Thus, the use of ILE for treatment of toxicities caused by a larger range of β-blockers is worth further investigation.
Trvalý link: https://hdl.handle.net/11104/0344318