Simultaneous Determination of Hydrochlorothiazide and Benazepril Hydrochloride or Amiloride Hydrochloride in Presence of Hydrochlorothiazide Impurities: Chlorothiazide and Salamide by HPTLC Method

被引:10
|
作者
Naguib, Ibrahim A. [1 ]
Abdelaleem, Eglal A. [1 ]
Zaazaa, Hala E. [2 ]
Draz, Mohammed E. [3 ]
机构
[1] Beni Suef Univ, Dept Analyt Chem, Fac Pharm, Bani Suwayf 62111, Egypt
[2] Cairo Univ, Dept Analyt Chem, Fac Pharm, Cairo 11562, Egypt
[3] Nahda Univ, Dept Analyt Chem, Fac Pharm, Bani Suwayf, Egypt
关键词
PERFORMANCE LIQUID-CHROMATOGRAPHY; SPECTROPHOTOMETRIC DETERMINATION; DERIVATIVE SPECTROPHOTOMETRY; PHARMACEUTICAL FORMULATIONS; RATIO SPECTRA; TABLETS; VALIDATION; LC;
D O I
10.1093/chromsci/bmu016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Simple, selective and sensitive high-performance thin layer chromatographic (HPTLC) method has been developed and validated for the simultaneous determination of hydrochlorothiazide (HCZ) in the presence of its impurities (chlorothiazide (CT) and salamide (DSA)), in two quaternary mixtures with benazepril hydrochloride (BZ) or amiloride hydrochloride (AM). The separation was carried out on HPTLC silica gel 60 F-254 using ethyl acetate-methanol-glacial acetic acid (85: 2: 0.3 v/v/v) followed by densitometric measurement of bands at 240 nm for the first mixture containing HCZ, CT, DSA, BZ and by using ethyl acetate-methanol-water-ammonia (90: 10: 5: 3 v/v/v) followed by densitometric measurement at 278 nm for the second mixture containing HCZ, CT, DSA, AM. Calibration curves were constructed in the range of (0.2-1.8 mg/band) and (0.4-2.2 mg/band) with good accuracy for HCZ and BZ, respectively, for the first mixture and in the range of (0.6-1.8 mu g/band) and (0.4-2.4 mu g/band) with good accuracy for HCZ and AM, respectively, for the second mixture. The developed method was validated according to ICH guidelines and demonstrated good accuracy and precision. Moreover, the methods were successfully applied for the determination of HCZ and BZ and AM in pure form and pharmaceutical dosage forms. The results were statically compared with the reported methods with no significant difference, indicating the ability of the proposed method to be used for routine analysis of drug product.
引用
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页码:183 / 188
页数:6
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