Wood M J, Irwin W J, Scott D K
Department of Pharmaceutical Sciences, Aston University, Birmingham, U.K.
J Clin Pharm Ther. 1990 Aug;15(4):291-300. doi: 10.1111/j.1365-2710.1990.tb00387.x.
The degradation kinetics of doxorubicin, daunorubicin and epirubicin in aqueous solution under fluorescent light and sunlight were studied using high-performance liquid chromatographic (HPLC) methods. The rates of photodegradation of all three drugs were similar, they were inversely proportional to the drug concentration and were accelerated by an increase in the pH of the vehicle. Photodegradation followed first-order kinetics. At concentrations greater than or equal to 500 micrograms/ml no special precautions appeared to be necessary to protect freshly prepared solutions of these agents from light. Photolysis was very rapid, however, at concentrations in the low microgram range therefore, when these solutions are used for in-vitro work or stability studies, they should be protected from light at all times. In addition, adsorptive losses, which may also be pronounced in low concentration solutions, should be prevented by storage in polypropylene containers.
采用高效液相色谱(HPLC)法研究了阿霉素、柔红霉素和表柔比星在荧光灯和日光下于水溶液中的降解动力学。这三种药物的光降解速率相似,与药物浓度成反比,并随溶剂pH值的升高而加快。光降解遵循一级动力学。当浓度大于或等于500微克/毫升时,似乎无需采取特殊措施来保护这些药物的新配制溶液避光。然而,当浓度处于低微克范围时,光解非常迅速,因此,当这些溶液用于体外实验或稳定性研究时,应始终避光保存。此外,低浓度溶液中也可能出现明显的吸附损失,应通过储存在聚丙烯容器中来防止。