Ng L L
Merck Sharp and Dohme, Research Laboratories, West Point, PA 19486.
J Assoc Off Anal Chem. 1988 May-Jun;71(3):534-8.
A reverse-phase liquid chromatographic method for determination of dexamethasone acetate and of cortisone acetate was subjected to an interlaboratory study by 8 collaborators for each steroid acetate. Bulk drug substance, suspensions, and tablets were assayed. Bulk drug or dosage form is dissolved in an acetonitrile-buffer mixture and analyzed by an external standard method. The steroid acetate is resolved from extraneous components by reverse-phase chromatography and detected at 254 nm. The sample solutions are stable for at least 72 h. For dexamethasone acetate, coefficients of variation were 0.9 and less than or equal to 3.1% for the bulk drug substance and the suspensions, respectively. For cortisone acetate, coefficients of variation were 0.7% for bulk material, less than or equal to 2.0% for suspensions, and less than or equal to 2.5% for tablets. All dosage forms were commercial formulations. The 2 methods have been adopted official first action.
一种用于测定醋酸地塞米松和醋酸可的松的反相液相色谱法,由8位合作者对每种醋酸甾体进行了实验室间研究。对原料药、混悬剂和片剂进行了分析。将原料药或剂型溶解在乙腈-缓冲液混合物中,采用外标法进行分析。通过反相色谱法将醋酸甾体与杂质成分分离,并在254nm处进行检测。样品溶液至少72小时内稳定。对于醋酸地塞米松,原料药和混悬剂的变异系数分别为0.9%和小于或等于3.1%。对于醋酸可的松,原料药的变异系数为0.7%,混悬剂小于或等于2.0%,片剂小于或等于2.5%。所有剂型均为市售制剂。这两种方法已被官方首次采用。