Abstract
The kinetics of oxidation of the HMG-CoA reductase inhibitors lovastatin, simvastatin, L-157,012, and L-647,318 were studied in an aqueous surfactant solution. A thermally labile free radical initiator was used to attain measurable reaction rates at 40°C and rate constants were determined by measuring oxygen consumption using an oxygen electrode. The stability of the drugs was found to increase in the order lovastatin = simvastatin < L-157,012 < L-647,318. The addition of butylated hydroxyanisole (BHA) was found to stabilize the drugs. For the oxidation of lovastatin, the effectiveness of antioxidants increased in the order propyl gallate < BHA < alpha-tocopherol. It is concluded that the stability of oxidizable drugs can be rapidly and conveniently assessed by the techniques described herein. © 1990, Plenum Publishing Corporation. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Kaufman, M. J. (1990). Applications of Oxygen Polarography to Drug Stability Testing and Formulation Development: Solution-Phase Oxidation of Hydroxymethylglutaryl Coenzyme A (HMG-CoA) Reductase Inhibitors. Pharmaceutical Research: An Official Journal of the American Association of Pharmaceutical Scientists, 7(3), 289–292. https://doi.org/10.1023/A:1015886415210
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.