Beniamin Mariam Wasim, Kessiba Amira Mohamed, Hegazy Maha Abdelmonem, El Gendy Ahmed Emad, Kormod Lubna Ahmed
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Misr International University, KM 28, Cairo, Egypt.
Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, 11562, Egypt.
BMC Chem. 2025 May 23;19(1):141. doi: 10.1186/s13065-025-01507-0.
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 C 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 C of both drugs with a correlation coefficient (r) 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).
已开发并验证了一种采用荧光检测(FD)的环保、灵敏、选择性好、精确且准确的高效液相色谱法,用于同时测定两种降压药物非洛地平和美托洛尔在其纯样品、复方药物剂型以及加标人血浆中的含量。分离在Inertsil C柱(150 mm×4.6 ID;粒径5 µm)上进行,流动相由乙醇和30 mM磷酸二氢钾缓冲液组成,用正磷酸调节至pH 2.5(40:60,v/v)。采用环境温度下1.0 mL/min的恒定流速。根据ICH Q2 R2进行方法验证,并根据FDA指南进行生物分析方法验证,以同时测定生物基质中的两种药物。该方法在0.01 - 1.00 µg/mL和0.003 - 1.00 µg/mL的浓度范围内显示出优异的线性,这是根据两种药物的C值选择的,非洛地平和美托洛尔在人血浆中的相关系数(r)分别为0.9998和0.9999。其纯品形式和加标人血浆中的日内和日间精密度≤2%,两种药物纯品形式的准确度在标称浓度的±2%以内,人血浆中的准确度在标称浓度的±10%以内。对所提出的方法与已报道的方法进行了统计比较;结果表明,两种方法在准确度和精密度方面均无显著差异。所提出的方法经三种绿色评估工具(AGREE计算器、MoGAPI、RGBfast研究)证明是环保的。