A new spectrofluorimetric method for the determination of lisinopril in tablets

Aktas, Esra; Ersoy, Lale; Sağırlı, Olcay

doi:10.1016/s0014-827x(02)00013-7

Cited by 37 publications

(23 citation statements)

References 13 publications

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“…These include titrimetric [3], spectrophotometric [4][5][6][7][8][9], spectrofluorimetric [4,6,10], high performance liquid chromatographic (HPLC) followed by spectrophotometric detection [4,11,12] and gas chromatographic (GC) [13] techniques. Although some of these methods are sensitive, not all of them can be directly applied to the assay of lisinopril in biological samples, due to the interferences of endogenous substances.…”

Section: Introductionmentioning

confidence: 99%

An HPLC method for the determination of lisinopril in human plasma and urine with fluorescence detection

Sağırlı

Ersoy

2004

Journal of Chromatography B

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Section: Introductionmentioning

confidence: 99%

An HPLC method for the determination of lisinopril in human plasma and urine with fluorescence detection

Sağırlı

Ersoy

2004

Journal of Chromatography B

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“…Numerous analytical methods have been developed for the determination of lisinopril in tablets. These include spectrophotometry,2–4 spectrofluorimetry,2, 4, 5 and high‐performance liquid chromatography (HPLC) with spectrophotometric detection 2. Although some of these methods are sensitive, not all of them can be directly applied to the assay of lisinopril in biological samples, due to interferences from endogenous substances.…”

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confidence: 99%

Development of a liquid chromatography/tandem mass spectrometry assay for the quantification of lisinopril in human plasma

Huang

Liu

et al. 2005

Rapid Comm Mass Spectrometry

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A simple and sensitive liquid chromatography/tandem mass spectrometry method employing electrospray ionization, to quantify lisinopril in human plasma using pseudoephedrine hydrochloride as the internal standard (IS), has been developed and validated. A mixture of methanol and 0.1% formic acid in water (50:50, v/v) was used as the isocratic mobile phase. A simple liquid-liquid extraction procedure was used as sample preparation method. The method validation demonstrated the specificity, lower limit of quantification, accuracy, and precision of measurements. Selected reaction monitoring was specific for lisinopril and pseudoephedrine hydrochloride; no endogenous materials from blank plasma interfered with the analysis of lisinopril or the IS. The assay was linear over the concentration range 0.78-100 ng/mL. The correlation coefficients for the calibration curves ranged from 0.9984-0.9998. The intra- and inter-day precision, determined for quality control samples, were less than 4.18%. The method was employed in a pharmacokinetic study after oral administration of 10 mg lisinopril to 20 healthy volunteers.

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“…Enalapril maleate has been simultaneously determined with hydrochlorothiazide and furosemide commonly used diuretics [23], commonly used NSAIDs [24], anti diabetic drugs [25], cholesterol lowering agent statins [26] and with metformin, glibenclamide and glimepride [27] in bulk material, pharmaceutical formulations and human serum using RP-HPLC. Spectrophotometric methods after derivatization of lisinopril and other techniques has been describe previously [3,6,[28][29][30][31][32][33].…”

Section: Reported Methods Of Analysismentioning

confidence: 99%

Analytical Determination of Lisinopril Using UV Spectrophotometer and HPLC: An Overview

Sattar¹

2014

Mod Chem Appl

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Present review article determine the analytical methods for the quantitative determinations of lisinopril (ACE Inhibitor) by UV spectrophotometery and High-Performance Liquid chromatography. Pharmaceutical analysis of lisinopril requires effective analytical procedures for QC quality control analysis in Pharmaceuticals dosage formulations and human serum. An extensive survey for determination of LSP compiled from the research articles published in various pharmaceutical and analytical chemistry Journals. This appraisal illustrate that majority of the HPLC methods reviewed are based on the quantitative analysis of drug in Active Pharmaceutical ingredients (API), formulations, biological fluids such as serum and plasma and they are appropriate for therapeutic monitoring of drug, for pharmacokinetic purpose.

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A new spectrofluorimetric method for the determination of lisinopril in tablets

Cited by 37 publications

References 13 publications

An HPLC method for the determination of lisinopril in human plasma and urine with fluorescence detection

An HPLC method for the determination of lisinopril in human plasma and urine with fluorescence detection

Development of a liquid chromatography/tandem mass spectrometry assay for the quantification of lisinopril in human plasma

Analytical Determination of Lisinopril Using UV Spectrophotometer and HPLC: An Overview

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