Lowe D R, Fuller S H, Pesko L J, Garnett W R, Karnes H T
Department of Pharmacy, Richmond, VA 23298-0581.
Am J Hosp Pharm. 1989 May;46(5):982-4.
The stability of carbamazepine in commercially available suspension that had been repackaged in various single-dose containers was studied. Carbamazepine suspension was repackaged in 2-mL and 8-mL aliquots in amber glass vials, polypropylene vials, and amber polypropylene syringes and in 2-mL aliquots in amber glass oral syringes. Containers were stored at room temperature and continuously exposed to fluorescent light for up to 12 weeks. Samples from each container type and volume were assayed for carbamazepine content by high-performance liquid chromatography at various intervals during storage. Carbamazepine concentrations in the samples were compared with the carbamazepine concentration in the original manufacturer's container. The pH of the samples was also determined, and the suspensions were inspected for color, odor, and large particles. There was no significant decrease in carbamazepine concentration of more than 10% in samples stored for up to eight weeks. After 12 weeks, significant decreases in concentration were observed in all but one container type. No changes in color, odor, or consistency were observed during the 12 weeks, and there were no significant changes in pH. In commercially available suspension repackaged in volumes corresponding to common pediatric doses, carbamazepine (20 mg/mL) is stable for at least eight weeks when stored at room temperature in the containers tested.
研究了卡马西平在已重新包装于各种单剂量容器中的市售混悬液中的稳定性。卡马西平混悬液被分装成2毫升和8毫升的等分试样,分别置于琥珀色玻璃瓶、聚丙烯瓶、琥珀色聚丙烯注射器中,以及2毫升等分试样置于琥珀色玻璃口服注射器中。容器在室温下储存,并持续暴露于荧光灯下长达12周。在储存期间的不同时间间隔,通过高效液相色谱法对每种容器类型和体积的样品进行卡马西平含量测定。将样品中的卡马西平浓度与原制造商容器中的卡马西平浓度进行比较。还测定了样品的pH值,并检查混悬液的颜色、气味和大颗粒。储存长达八周的样品中,卡马西平浓度没有显著下降超过10%。12周后,除一种容器类型外,所有容器类型中的浓度均出现显著下降。在12周内未观察到颜色、气味或稠度的变化,pH值也没有显著变化。在重新包装成相当于常见儿科剂量体积的市售混悬液中,当在测试的容器中于室温下储存时,卡马西平(20毫克/毫升)至少稳定八周。