Pereira, Sarah A. P.Bobbink, Felix D.Dyson, Paul J.Saraiva, M. Lucia M. F. S.2021-05-082021-05-082021-05-082021-05-0110.1016/j.jinorgbio.2021.111399https://infoscience.epfl.ch/handle/20.500.14299/177904WOS:000637641400005An automatic methodology based on micro sequential injection analysis coupled to a lab-on-valve system (termed ?SIA-LOV) was developed and used to determine the ability of metal-based anticancer compounds to inhibit cyclooxygenase 2 (COX-2) activity. COX-2 may be involved in pathogenesis of cancer and it is overexpressed in several types of solid tumors. Since platinum-based compounds are extensively used in the treatment of cancer, and ruthenium compounds are considered as promising candidates for next generation of non-targeted anticancer drugs, it is interesting to establish whether COX-2 inhibition is relevant to their mode of action. The ?SIA-LOV system was optimized and the IC50 values of each compound were calculated. All the results present RSD values less than 2.5%. IC50 values of 9.7 ? 0.6 ?M to 207 ? 3 ?M were obtained, with the most active inhibitor for COX-2 being rofecoxib with the metal compounds exhibiting IC50 values in the range 13.7 ? 1.6 to 207 ? 3. The results obtained in this work provide significant information about the mechanism of the studied compounds, mostly ruthenium-based compounds, and the role of COX-2 in their mode of action. Moreover, this work confirmed the potential of the ?SIA-LOV system as a simple, versatile, robust, and rapid analytical tool for automating the determination of IC50 values of metal-based compounds.Biochemistry & Molecular BiologyChemistry, Inorganic & NuclearBiochemistry & Molecular BiologyChemistrycyclooxygenase 2enzyme activitymetal-based drugsinhibition assayslab-on-valveautomationtext::journal::journal article::research article