El-Saharty Yasser S, Hassan Nagiba Y, Metwally Fadia H
Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, El-Kasr, El-Aini St., ET-11562, Cairo, Egypt.
J Pharm Biomed Anal. 2002 May 15;28(3-4):569-80. doi: 10.1016/s0731-7085(01)00692-6.
A binary mixture of terbinafine hydrochloride and triamcinolone acetonide was determined by three different methods. The first one concerned with determination of both drugs using first derivative (D(1)) spectrophotometric technique at 297 and 274 nm over concentration ranges of 5-30 and 4-24 microg ml(-1), with mean percentage accuracies 99.90+/-0.67 and 100.25+/-0.49, respectively. The second method depends on ratio-spectra 1st derivative (RSD(1)) spectrophotometry at 298 and 248 nm over the same concentration ranges with mean percentage accuracies 100.22+/-0.51 and 99.93+/-0.56, respectively. The spectrodensitometric analysis provides a rapid and precise method for the separation and quantitation of both terbinafine hydrochloride and triamcinolone acetonide. The method depends on the quantitative densitometric evaluation of thin layer chromatogram of terbinafine hydrochloride and triamcinolone acetonide at 283 and 238 nm over concentration ranges of 5-25 and 2.5-22.5 microg spot(-1), with mean percentage accuracies 100.66+/-0.51 and 100.27+/-0.73, respectively. The suggested procedures were checked using laboratory prepared mixtures and were successfully applied for the analysis of their pharmaceutical preparations. The three methods retained their accuracy and precision when applying the standard addition technique. The results obtained by applying the proposed methods were statistically analysed and compared with those obtained by a reported method.
采用三种不同方法对盐酸特比萘芬和曲安奈德二元混合物进行了测定。第一种方法是利用一阶导数(D(1))分光光度法在297和274 nm处测定两种药物,浓度范围分别为5 - 30和4 - 24 μg ml(-1),平均百分准确度分别为99.90±0.67和100.25±0.49。第二种方法是在相同浓度范围内,于298和248 nm处采用比率光谱一阶导数(RSD(1))分光光度法,平均百分准确度分别为100.22±0.51和99.93±0.56。分光密度法为盐酸特比萘芬和曲安奈德的分离与定量提供了一种快速且精确的方法。该方法基于在283和238 nm处对盐酸特比萘芬和曲安奈德薄层色谱图进行定量光密度评估,浓度范围分别为5 - 25和2.5 - 22.5 μg spot(-1),平均百分准确度分别为100.66±0.51和100.27±0.73。使用实验室配制的混合物对所建议的方法进行了验证,并成功应用于其药物制剂的分析。应用标准加入技术时,这三种方法均保持了其准确度和精密度。对应用所提出方法获得的结果进行了统计分析,并与报道方法获得的结果进行了比较。