Validated chromatographic methods for concurrent determination of atorvastatin and perindopril

IF 1.8 Q3 CHEMISTRY, ANALYTICAL
Sagar Patel, C. Patel, J. Surati, A. Akabari, K. Shah
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引用次数: 2

Abstract

: Two simple, selective, precise, and accurate chromatographic methods, namely reversed-phase high-performance liquid chromatography (RP-HPLC) method and High-performance thin-layer chromatography (HPTLC), were developed and validated for the simultaneous determination of Atorvastatin (ATO) and Perindopril (PER). The developed HPTLC method was used for the separation and quantitation of the studied drugs on silica gel 60F254 TLC plates. Dichloromethane: Methanol: Ethyl acetate: Glacial acetic acid (6:2:2:0.1, v/v/v/v) was used as a developing system and the separated bands were UV-scanned at 221 nm. Linear relationships were obtained in the range of 800 – 4800 ng/band for Atorvastatin and 200 – 1200 ng/band for Perindopril with a regression coefficient greater than 0.999. The Rf value of the drug was found to be 0.70 ± 0.02 and 0.39 ± 0.03 for Atorvastatin and Perindopril respectively. The developed RP-HPLC depended on chromatographic separation of the studied drugs on a C18 column using Acetonitrile: Methanol: Potassium dihydrogen orthophosphate (pH 3 adjusted with orthophosphoric acid) ((40:10:50), v/v/v) as a mobile phase delivered at a constant flow rate of 1 mL/min with UV detection at 240 nm. The calibration curves were linear (r2 > 0.999) over the concentration range 20-100 µg/mL for Atorvastatin and 10-50µg/mL for Perindopril. The average retention times for Atorvastatin and Perindopril were 3.42 and 8.92 min, respectively. Factors affecting the developed methods have been studied and optimized. Further, methods validation has been carried out according to ICH guidelines. The proposed methods were successfully applied for the determination of the studied drug simultaneously in bulk and synthetic mixture qualitatively and quantitatively. Statistical analysis by the F test showed no significant difference between the results obtained by the two methods. The uncertainty measurement was also carried out for the quantification of both components. The proposed HPTLC method proved to be more sensitive, while the HPLC gave more reproducible results and was time-saving.
验证了同时测定阿托伐他汀和培哚普利的色谱方法
建立了反相高效液相色谱法(RP-HPLC)和高效薄层色谱法(HPTLC)两种简便、选择性强、精密度高、准确度高的色谱方法,用于同时测定阿托伐他汀(ATO)和培哚普利(PER)。采用所建立的高效液相色谱法在硅胶60F254薄层板上对所研究药物进行分离定量。以二氯甲烷:甲醇:乙酸乙酯:冰醋酸(6:2:2:0.1,v/v/v/v)为显影体系,在221 nm处进行紫外扫描。阿托伐他汀在800 ~ 4800 ng/频带范围内与培哚普利在200 ~ 1200 ng/频带范围内呈线性关系,回归系数大于0.999。阿托伐他汀和培哚普利的Rf值分别为0.70±0.02和0.39±0.03。所建立的反相高效液相色谱是在C18色谱柱上,以乙腈:甲醇:正磷酸二氢钾(pH值为正磷酸调节)((40:10:50),v/v/v)为流动相,以1 mL/min的恒定流速进行色谱分离,紫外检测波长为240 nm。在阿托伐他汀20 ~ 100µg/mL和培哚普利10 ~ 50µg/mL的浓度范围内,校准曲线呈线性(r2 > 0.999)。阿托伐他汀和培哚普利的平均滞留时间分别为3.42 min和8.92 min。并对影响所开发方法的因素进行了研究和优化。此外,方法验证已根据ICH指南进行。所建立的方法可同时用于原料药和复方药的定性和定量测定。经F检验统计分析,两种方法所得结果无显著差异。对两组分进行了不确定度测定。结果表明,该方法灵敏度高,HPLC法重现性好,省时。
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来源期刊
Journal of Chemical Metrology
Journal of Chemical Metrology CHEMISTRY, ANALYTICAL-
CiteScore
2.30
自引率
15.40%
发文量
7
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