化学
高效液相色谱法
美托洛尔
色谱法
医学
心脏病学
作者
Naveenarani Dharuman,Karunanidhi Santhana Lakshmi,Manikandan Krishnan
出处
期刊:Analytical Chemistry Letters
日期:2024-05-03
卷期号:14 (3): 426-445
被引量:3
标识
DOI:10.1080/22297928.2024.2357151
摘要
AbstractThe analytical community prioritizes adopting green techniques due to concerns over the environmental impact of chemical research. This study employs an integrated experimental strategy, combining the concept of design of experiment (DOE) and green analytical chemistry (GAC), to establish a robust, green RP-HPLC approach for the simultaneous estimation Cilnidipine (CIL) and Metoprolol succinate (MET). For method optimization, a central composite design (CCD) was implemented. Separation utilized Inertsil ODS 3 column (250 mm x 4.6 mm, 5 μm), with gradient mobile phase (ethanol: 17.65% at 0 min, 75.5% at 3 min) and phosphate buffer, flowing at 1 ml/ min. Detection wavelength at 230 nm. Column temperature (35±1°C), and injection volume 5 μL. Retention times: MET (4.672 min), CIL (7.457 min). The linearity was established over the range of 7-13 μg/ml for CIL and 35-65 μg/ml for MET. The values obtained for LOD and LOQ are 0.819 and 2.482 μg/ml (CIL) respectively, 3.875 and 11.743 μg/ml (MET). As per ICH Q14, the technique has been validated. Finally the green nature was examined by GAPI, AES and AGREE. Method found to be ecofriendly, simple and robust for simultaneous CIL and MET estimation in pharmaceutical formulations, easily adaptable for routine analysis.GRAPHICAL ABSTRACTDisplay full sizeKeywords: CilnidipineCentral composite designGreenness profileMetoprolol succinateStability indicating
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