Askar H, Fathy M E, Tolba M M, Aly Fatma A, Metwally Mohammed E-S
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.
R Soc Open Sci. 2024 Jul 24;11(7):240268. doi: 10.1098/rsos.240268. eCollection 2024 Jul.
A sensitive, rapid and green synchronous spectrofluorimetric method was developed to simultaneously analyze a binary mixture of diosmin (DSM) and hesperidin (HSP). The RSFI of both medications was measured in methanol at Δ of 100 nm. The results indicated that specific experimental factors had an impact on these intensities. The optimization and thorough examination of these parameters were conducted. The plots of synchronous fluorescence intensity-concentration for DSM and HSP were found to be linear within the concentration ranges of 0.5-5.0 µg ml and 0.2-3.0 µg ml, respectively. The detection limits for DSM and HSP were 0.107 µg ml and 0.048 µg ml, respectively. The limits of quantification were 0.323 µg ml and 0.144 µg ml for DSM and HSP, respectively. The method outlined in this study was successfully used to determine the quantities of both drugs present in commercially available mixed tablets. The results obtained using this method were subsequently compared to those of a comparison method. Greenness assessment of the suggested procedure was accomplished by applying the GAPI method. Consequently, the recommended method can be used in the routine quality control analysis of the two cited drugs with minimum harmful effect on the environment as well as the individuals.
建立了一种灵敏、快速且绿色的同步荧光光谱法,用于同时分析地奥司明(DSM)和橙皮苷(HSP)的二元混合物。在甲醇中以100 nm的波长差测量两种药物的相对同步荧光强度(RSFI)。结果表明,特定的实验因素会对这些强度产生影响。对这些参数进行了优化和全面考察。发现DSM和HSP的同步荧光强度-浓度曲线在浓度范围分别为0.5 - 5.0 μg/ml和0.2 - 3.0 μg/ml内呈线性。DSM和HSP的检测限分别为0.107 μg/ml和0.048 μg/ml。DSM和HSP的定量限分别为0.323 μg/ml和0.144 μg/ml。本研究中概述的方法成功用于测定市售混合片剂中两种药物的含量。随后将使用该方法获得的结果与对照方法的结果进行比较。通过应用绿色分析程序指数(GAPI)方法完成了对所建议方法的绿色度评估。因此,所推荐的方法可用于这两种药物的常规质量控制分析,对环境和个人的有害影响最小。