Spectrophotometric, septrofluorimetric and LC determination of lisinopril

被引:46
作者
El-Gindy, A [1 ]
Ashour, A
Abdel-Fattah, L
Shabana, MM
机构
[1] Suez Canal Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Ismailia 41522, Egypt
[2] Ain Shams Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Cairo, Egypt
[3] Cairo Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Cairo 11562, Egypt
[4] Cairo Univ, Fac Pharm, Dept Pharmacognosy, Cairo 11562, Egypt
关键词
HPLC; lisinopril; spectrofluorometry; spectrophotometry;
D O I
10.1016/S0731-7085(01)00376-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Three methods are described for the determination of lisinopril in the pharmaceutical tablets. The spectrophotometric method depends on the reaction of the lisinopril with sodium hypochlorite and phenyl hydrazine to form a condensation product measured at 362 nm. The spectrophotometric method was extended to develop a stability indicating method. The spectrophotometric method depends on reaction of the lisinopril with o-phthalaldehyde in the presence of 2-mercaptoethanol in berate buffer pH 9.5. The fluorescence of the reaction product was measured upon excitation at a maximum of 340 nm with emission wavelength at 455 nm. The HPLC method depends on using Hypersil silica column with a mobile phase consisting of methanol-water-triethylamine (50:50:0.1 v/v) and the pH was adjusted to 1.6 with 0.1 N perchloric acid. Quantitation was achieved with UV detection at 210 nm based on peak area. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:913 / 922
页数:10
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