Effect of organic co-solvents in the evaluation of the hydroxyl radical scavenging activity by the 2-deoxyribose degradation assay: The paradigmatic case of ?-lipoic acid

The 2-deoxyribose degradation assay (2-DR assay) is an in vitro method broadly used for evaluating the scavenging activity against the hydroxyl radical (HOo). One of the major drawbacks of the assay, however, is that only water soluble compounds can be tested for their radical-scavenging activity. Lipoic acid (LA) is an excellent scavenger of HOo but it exhibits a low solubility in the aqueous milieu of the 2-DR assay and a high tendency to polymerize under a variety of conditions. We used LA as a paradigmatic substrate to evaluate the effect of several organic co-solvents in increasing its solubility. Most of these solvents, however, demonstrated to be potent scavengers of HOo making their use in the 2-DR assay mproper. On the other hand, acetonitrile showed a remarkably low reactivity toward HOo (rate constant ~8.7 × 106 M-1 s-1) which allowed us to use it as a co-solvent in the preparation of stock solutions of LA ~5 mM. We therefore evaluated the radical-scavenging activity of LA bythe 2-DR assay in a relatively large range of concentrations, 1-200 ?M. We found that the rate constant for LA + HOo is diffusion-controlled (~1 × 1010 M-1 s-1 in water at 25 °C) and uninfluenced by the presence of small quantities of acetonitrile. Therefore, the use of acetonitrile in the 2-DR assay does not interfere with the test and may increase the solubility of the radical scavengers.