scholarly journals Electrochemical Determination of Lacidipine

1999 ◽  
Vol 82 (5) ◽  
pp. 1077-1082 ◽  
Author(s):  
Juan A Squella ◽  
Anny E Iribarren ◽  
Juan C Sturm ◽  
Luis J Núñez-Vergara

Abstract Lacidipine is an antihypertensive drug that is oxidizable at the glassy carbon electrode. The voltammetric oxidation of lacidipine in aqueous-alcoholic solutions (70 + 30) produces a well-defined voltammetric peak when subjected to a differential pulse voltammetric experiment. This peak is due to oxidation of the dihydropyridine ring to a pyridine derivative. This voltammetric response result is irreversible, pH dependent, and diffusion controlled. The best resolution for the peak was obtained at pH 6 in Britton-Robinson buffer-ethanol (70 + 30). The peak potential at pH 6 was 800 mV against an Ag-AgCI reference electrode. A linear relationship between peak current and lacidipine concentration was obtained. For analytical purposes, a calibration curve for lacidipine that covered concentrations between 5 x 10-6 and 2 x 10-6 was used. Detection and quantitation limits were 3.52 x 10-6 and 3.78 x 10-6M, respectively. The repeatability of the measurement was 2%. On the basis of the voltammetric response, we also developed high-performance liquid chromatographic methods with electrochemical detection. For comparative purposes, we also developed a spectrophotometric method.

2020 ◽  
Vol 16 (8) ◽  
pp. 1059-1067
Author(s):  
Jéssica Maurício Batista ◽  
Christian Fernandes

Background: Linezolid is a synthetic broad-spectrum antibacterial belonging to the class of oxazolidinones. Linezolid for intravenous infusion is isotonized with dextrose. In acidic environment, the dehydration of dextrose produces furan derivatives, 5-hydroxymethylfurfural (5-HMF) being the main one. The determination of this degradation product is of fundamental importance, since there is evidence it is cytotoxic, genotoxic, mutagenic and carcinogenic. However, there is no official method for the determination of 5-HMF in drug products. Objective: The aim of this study was to develop and validate a high performance liquid chromatographic method to quantify 5-HMF in injection of linezolid. Methods: The chromatographic separation, after optimization, was performed on C18 (150 x 4.6 mm, 5 μm) column. Mobile phase was composed of 14 mM potassium phosphate buffer pH 3.0 ([H+] = 1.0 x 10-3) and methanol in gradient elution at 1.0 mL min-1. The injection volume was 10 μL and detection was performed at 285 nm. Results: The method was optimized and validated, showing selectivity, linearity in the range from 0.075 to 9.0 μg mL-1, precision (RSD ≤ 2.0%), accuracy (mean recovery of 100.07%) and robustness for temperature and pH variation. Conclusion: The method was shown to be adequate to determine 5-HMF in injection containing linezolid in routine analysis.


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