Lee A R, Hu T M
School of Pharmacy, National Defense Medical Center, Taipei, Taiwan, Republic of China.
J Pharm Biomed Anal. 1994 Jun;12(6):747-52. doi: 10.1016/0731-7085(93)e0025-i.
Rapid, simple and direct assay procedures based on selective first (D1)- and second (D2)-derivative spectrophotometry, using a zero-crossing technique of measurement at 279.2 and 280.0 nm, respectively, have been developed for the specific determination of guaiphenesin in the presence of dextromethorphan, drugs with closely overlapping absorption spectra, in synthetic admixtures and in pharmaceutical dosage forms (tablets and syrups). The methods do not require extraction with organic solvents and are easier to perform than their conventional counterparts. Calibration graphs were linear (r = 0.99999 for D1 and 0.99969 for D2, respectively). Good selectivity, accuracy and precision were found. However, the performance of the analysis of guaiphenesin by the second-derivative mode deteriorated when the ratio of dextromethorphan to guaiphenesin was greater than one. Thus, the first-derivative spectrophotometry is the method of choice for the assay of tablets and syrups containing the two drugs.
基于选择性一阶(D1)和二阶(D2)导数分光光度法,分别采用在279.2和280.0 nm处的零交叉测量技术,已开发出快速、简单且直接的测定程序,用于在右美沙芬(吸收光谱紧密重叠的药物)存在的情况下,在合成混合物以及药物剂型(片剂和糖浆剂)中特异性测定愈创甘油醚。这些方法不需要用有机溶剂萃取,并且比传统方法更容易操作。校准曲线呈线性(D1的r分别为0.99999,D2的r为0.99969)。发现具有良好的选择性、准确度和精密度。然而,当右美沙芬与愈创甘油醚的比例大于1时,二阶导数模式下愈创甘油醚分析的性能会变差。因此,一阶导数分光光度法是测定含有这两种药物的片剂和糖浆剂的首选方法。