Hanna G M, Lau-Cam C A
Pharmazie. 1984 Dec;39(12):816-8.
Direct dissolution of the bulk material, capsule, or freeze-dried solution for injection and an internal standard in chloroform-d and recording of the PMR spectra provides a simple, specific, and accurate assay method form diphenhydramine hydrochloride [2-(diphenyl-methoxy)-N,N-dimethylethanamine hydrochloride] in pharmaceutical samples. The drug content can be calculated from the integral values for the N-methyl protons of diphenhydramine at ca. 2.85 ppm and for the methyl protons of tert-butyl alcohol at ca. 1.27 ppm. The mean +/- SD% recoveries from synthetic mixtures simulating capsules and injectables were 100.0 +/- 0.2 (n = 11) and 100.1 +/- 0.4 (n = 4), respectively. The method also permits the detection of degradation of diphenhydramine such as benzhydrol, diphenylchloromethane, and 2-(dimethylamino)ethanol to a minimum of about 2% of the parent compound.
将原料药、胶囊或注射用冻干溶液与内标物直接溶解于氘代氯仿中,记录质子磁共振(PMR)谱,为药物样品中盐酸苯海拉明[2 -(二苯基甲氧基)-N,N -二甲基乙胺盐酸盐]提供了一种简单、特异且准确的测定方法。药物含量可根据苯海拉明在约2.85 ppm处N -甲基质子的积分值以及叔丁醇在约1.27 ppm处甲基质子的积分值来计算。模拟胶囊和注射剂的合成混合物的平均回收率±标准差分别为100.0±0.2(n = 11)和100.1±0.4(n = 4)。该方法还能检测到苯海拉明的降解产物,如二苯甲醇、二苯基氯甲烷和2 -(二甲氨基)乙醇,最低可检测到约为母体化合物2%的含量。