Association of valdecoxib, a nonsteroidal anti-inflammatory drug, with human serum albumin.

Maria V Encinas, Eduardo Lissi, Claudio Vergara

Photochemistry and photobiology 2013 Nov-Dec

filter terms:

Valdecoxib addition quenches the intrinsic human serum albumin (HSA) fluorescence. This allows an evaluation of the drug-protein association. However, both the number of binding sites and their affinity for the drug depend upon the methodology employed for their evaluation and the employed protein concentration. In this work, we measured the effect of valdecoxib on HSA fluorescence yield over a wide range of experimental conditions and discuss the validity of the binding parameters derived from the different data treatments: Stern-Volmer, Scatchard, double logarithmic, quadratic equation, Benesi-Hilderand, and Encinas-Lissi. It is proposed that a combination of Encinas-Lissi and Scatchard treatments of the data renders the most reliable results. From these data, it is concluded that HSA presents three high-affinity binding sites for valdecoxib (K(as) = 4.5 × 10(4) m(-1)) and several secondary sites of smaller activity. © 2013 The American Society of Photobiology.

Citation

Maria V Encinas, Eduardo Lissi, Claudio Vergara. Association of valdecoxib, a nonsteroidal anti-inflammatory drug, with human serum albumin. Photochemistry and photobiology. 2013 Nov-Dec;89(6):1399-405