Pharmaceutical Chemistry Department, Faculty of Pharmacy, Deraya University, New Minia, Egypt.
Analytical Chemistry Department, Faculty of Pharmacy, Minia University, Minia, Egypt.
Luminescence. 2021 Nov;36(7):1572-1583. doi: 10.1002/bio.4057. Epub 2021 Jul 30.
Approved, basic, effective and successful spectroscopic strategies (spectrophotometric and spectrofluorimetric) were created to measure seven cephalosporins: cefpiramide (I), cefuroxime (II), cefoxitin (III), ceftazidime (IV), cefpirome (V), ceftobiprole (VI), and ceftriaxone (VII). These strategies used a two-fold complex arrangement response for the drug amino groups with Eosin Y (EY). The examined drugs were determined spectrophotometrically at 542-550 nm in acetic acid derivative buffer. The examined drugs were determined spectrofluorimetrically by measuring their quenching effect on EY local fluorescence at 545 nm after excitation at 305 nm. The absorbance-intensity plots were rectilinear over the ranges 20-100, 10-130, 20-220, 30-230, 10-210, 20-180 and 10-130 μg ml for I, II, III, IV, V, VI, and VII samples, respectively. The fluorescence-intensity plots were rectilinear over the ranges 0.5-1.5, 0.1-0.9, 0.3-1.5, 0.5-2.5, 0.1-0.9, 0.5-2.5 and 0.1-1.0 μg ml for I, II, III, IV, V, VI, and VII samples, respectively. The recommended materials were certified as adhering to International Council for Harmonisation (ICH) guidelines and were used to examine the tested drugs in different dosage forms and in human plasma tests. The approved materials matched the reference materials.
已批准的基本、有效且成功的光谱策略(分光光度法和荧光分光光度法)已被创建,用于测量七种头孢菌素:头孢匹罗(I)、头孢呋辛(II)、头孢西丁(III)、头孢他啶(IV)、头孢吡肟(V)、头孢妥仑匹酯(VI)和头孢曲松(VII)。这些策略利用 Eosin Y(EY)与药物氨基的双重络合反应。在醋酸衍生物缓冲液中,使用分光光度法在 542-550nm 处测定这些药物。通过在 305nm 激发后测量药物对 EY 局部荧光的猝灭效应,使用荧光分光光度法测定这些药物。在 20-100、10-130、20-220、30-230、10-210、20-180 和 10-130μg/ml 范围内,吸光度-强度曲线对 I、II、III、IV、V、VI 和 VII 样品均呈线性;在 0.5-1.5、0.1-0.9、0.3-1.5、0.5-2.5、0.1-0.9、0.5-2.5 和 0.1-1.0μg/ml 范围内,荧光强度曲线对 I、II、III、IV、V、VI 和 VII 样品均呈线性。所推荐的材料被证明符合国际协调理事会(ICH)的指导原则,并用于在不同剂型和人血浆试验中检查测试药物。所批准的材料与参考材料相匹配。