An eco-friendly bioanalytical RP-HPLC method coupled with fluorescence detection for simultaneous estimation of felodipine and metoprolol

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mariam Wasim Beniamin, Amira Mohamed Kessiba, Maha Abdelmonem Hegazy, Ahmed Emad El Gendy, Lubna Ahmed Kormod
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引用次数: 0

Abstract

An ecofriendly, sensitive, selective, precise, and accurate HPLC method with fluorescence detection (FD) has been developed and validated for simultaneous determination of two hypertensive drugs, felodipine and metoprolol in their pure samples, combined pharmaceutical dosage form and in spiked human plasma. Separation was carried out on Inertsil C18 column (150 mm × 4.6 ID; Particle size 5 µm) and a mobile phase composed of ethanol and 30mM potassium dihydrogen phosphate buffer, adjusted to pH 2.5 using ortho-phosphoric acid (40:60, v/v) was used. A constant flow rate of 1.0 mL/min at an ambient temperature was adopted. Method validation was performed according to the ICH Q2 R2 and bioanalytical method validation was done according to FDA guidelines for determination of both drugs simultaneously in biological matrices. The method demonstrated excellent linearity over the concentration range of 0.01–1.00 µg/mL and 0.003–1.00 µg/mL that were selected with accordance to the Cmax of both drugs with a correlation coefficient (r2) of 0.9998 and 0.9999 for felodipine and metoprolol, respectively in human plasma. The intra-day and inter-day precision were ≤ 2% in their pure forms and in spiked human plasma, and the accuracy was within ± 2% of the nominal concentration for both drugs in their pure forms and within ± 10% of the nominal concentration in human plasma. A statistical comparison was conducted between the proposed method and the reported method; it showed no significant difference between both methods regarding both accuracy and precision. The proposed method proved to be eco-friendly with three green assessment tools (AGREE calculator, MoGAPI, RGBfast study).

Graphical Abstract

采用反相高效液相色谱-荧光检测法同时测定非洛地平和美托洛尔的含量
建立了一种环保、灵敏、选择性、精确、准确的高效液相色谱荧光检测(FD)方法,用于同时检测高血压药物非洛地平和美托洛尔的纯样品、复方剂型和加标血浆。色谱柱为Inertsil C18 (150 mm × 4.6 ID;粒径为5µm),流动相为乙醇和30mM磷酸二氢钾缓冲液,用正磷酸(40:60,v/v)调节pH为2.5。在室温下,流速为1.0 mL/min。方法验证按照ICH Q2 R2进行,生物分析方法验证按照FDA指南在生物基质中同时测定两种药物进行。该方法在0.01 ~ 1.00µg/mL和0.003 ~ 1.00µg/mL的浓度范围内呈良好的线性关系,对人血浆中非洛地平和美托洛尔的Cmax的相关系数(r2)分别为0.9998和0.9999。纯形式和加标人血浆的日内和日内精密度≤2%,纯形式和加标人血浆的准确度在标称浓度的±2%以内,人血浆中标称浓度的±10%以内。将提出的方法与报道的方法进行统计比较;两种方法的准确度和精密度均无显著差异。该方法通过三种绿色评估工具(AGREE计算器、MoGAPI、RGBfast研究)证明是生态友好的。图形抽象
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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