Pharmaceutical Chemistry Department, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, Egypt.
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
Luminescence. 2024 Jul;39(7):e4839. doi: 10.1002/bio.4839.
A green, sensitive, and fast spectrofluorimetric technique for the simultaneous determination of atenolol (ATN) and losartan potassium (LSR) was developed. The proposed technique relied on the implementation of a first derivative synchronous fluorescence spectroscopy for the determination of the investigated drugs simultaneously without pretreatment procedures. The synchronous fluorescence of both drugs was measured in methanol at Δλ of 100 nm, and the first derivative peak amplitudes (D) were measured at 321 nm for ATN and 348 nm for LSR, each at the zero-crossing point of the other. The method was rectilinear over the concentration ranges of 100-1000 ng/mL and 50-500 ng/mL for ATN and LSR, respectively. The proposed technique was successfully applied for the determination of the studied drugs in their laboratory-prepared mixture and pharmaceutical formulations, demonstrating high mean recoveries of 100.54% for ATN and 100.62% for LSR, without interference from common excipients. The results were in good agreement with those obtained by the comparison method. Three recent greenness assessment tools, the Eco-Scale tool, the Green Analytical Procedure Index (GAPI) metric, and the Analytical GREEnness metric approach, were employed to affirm the greenness of the proposed method. The developed method was proven to be eco-friendly.
建立了一种用于同时测定阿替洛尔(ATN)和氯沙坦钾(LSR)的灵敏、快速、绿色的同步荧光分光光度法。该方法无需预处理,直接采用一阶导数同步荧光光谱法同时测定两种药物。两种药物的同步荧光在甲醇中测定,Δλ为 100nm,ATN 的一阶导数峰振幅(D)在 321nm 处,LSR 的一阶导数峰振幅(D)在 348nm 处,均在另一个药物的零交点处测量。该方法在 100-1000ng/mL 和 50-500ng/mL 范围内对 ATN 和 LSR 均呈线性关系。该方法成功应用于实验室制备的混合物和药物制剂中两种药物的测定,ATN 的平均回收率为 100.54%,LSR 的平均回收率为 100.62%,无常见赋形剂干扰。所得结果与比较法一致。采用三种最新的绿色评估工具,即生态规模工具、绿色分析程序指数(GAPI)度量和分析绿色度方法,来证实所提出方法的绿色性。所建立的方法被证明是环保的。