Abstract

An electroanalytical study of timolol in Britton–Robinson buffer is described. The reduction process on the hanging mercury drop electrode gives rise to two adjacent peaks above −1.0 V (versus Ag/AgCl), the latter on the background discharge, within the entire pH range studied (1.8–10.5), the polarographic p K a value obtained was 6.75. The results proved that the reduction of timolol is irreversible and the limiting current is adsorption controlled. The dependence of the peak current on concentration was studied by means of different polarographic and voltammetric techniques. Using adsorptive stripping square wave voltammetry (AdS-SWV), the height for the first peak was proportional to the concentration of timolol in two linear ranges: 1.0×10 −9 to 1.2×10 −8 M and 1.2×10 −8 to 1.1×10 −7 M, the 3 σ detection limit being 6.6×10 −10 mol l −1. For square wave polarography (SWP) the linear range and the detection limit were 4.0×10 −8 to 3.0×10 −6 M with two different slopes and 2.5×10 −8 M, respectively. A mechanism is proposed for the reduction of timolol. Two procedures, based on SWP and AdS-SWV, were developed for the determination of timolol in ophthalmologic drops.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call