Saleh G A, Askal H F, Radwan M F, Omar M A
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt.
Talanta. 2001 Jul 6;54(6):1205-15. doi: 10.1016/s0039-9140(01)00409-x.
Three simple, rapid and sensitive spectrophotometric procedures were developed for the analysis of cephapirin sodium (1), cefazoline sodium (2), cephalexin monohydrate (3), cefadroxil monohydrate (4), cefotaxime sodium (5), cefoperazone sodium (6) and ceftazidime pentahydrate (7) in pure form as well as in their pharmaceutical formulations. The methods are based on the reaction of these drugs as n-electron donors with the sigma-acceptor iodine, and the pi-acceptors: 2,3-dichloro-5,6-dicyano-p-benzo-quinone (DDQ) and 7,7,8,8-tetracyanoquinodimethane (TCNQ). Depending on the solvent polarity, different coloured charge-transfer complexes and radicals were developed. Different variables and parameters affecting the reactions were studied and optimized. The obtained charge-transfer complexes were measured at 364 nm for iodine (in 1,2-dichloroethane), 460 nm for DDQ (in methanol) and 843 nm for TCNQ (in acetonitrile). Ultraviolet-visible, infrared and (1)H-nuclear magnetic resonance techniques were used to study the formed complexes. Due to the rapid development of colours at ambient temperature, the obtained results were used on thin-layer chromatograms for the detection of the investigated drugs. Beer's plots were obeyed in a general concentration range of 6-50, 40-300 and 4-24 mug ml(-1) with iodine, DDQ and TCNQ, respectively, with correlation coefficients not less than 0.9989. The proposed procedures could be applied successfully to the determination of the investigated drugs in vials, capsules, tablets and suspensions with good recovery; percent ranged from 96.47 (+/-1.14) to 98.72 (+/-1.02) in the iodine method, 96.35 (+/-1.62) to 98.51 (+/-1.30) in the DDQ method, and 95.98 (+/-0.78) to 98.40 (+/-0.87) in the TCNQ method. The association constants and standard free energy changes using Benesi-Hildebrand plots were studied. The binding of cephalosporins to proteins in relation to their molar absorptivities was studied.
开发了三种简单、快速且灵敏的分光光度法,用于分析头孢匹林钠(1)、头孢唑林钠(2)、头孢氨苄一水合物(3)、头孢羟氨苄一水合物(4)、头孢噻肟钠(5)、头孢哌酮钠(6)和头孢他啶五水合物(7)的纯品及其药物制剂。这些方法基于这些药物作为n电子供体与σ受体碘以及π受体:2,3 - 二氯 - 5,6 - 二氰基 - 对苯醌(DDQ)和7,7,8,8 - 四氰基对苯二醌二甲烷(TCNQ)的反应。根据溶剂极性,形成了不同颜色的电荷转移络合物和自由基。研究并优化了影响反应的不同变量和参数。所得到的电荷转移络合物在碘(于1,2 - 二氯乙烷中)的364 nm处、DDQ(于甲醇中)的460 nm处以及TCNQ(于乙腈中)的843 nm处进行测定。采用紫外 - 可见、红外和(1)H - 核磁共振技术研究形成的络合物。由于在室温下颜色快速形成,所得结果用于薄层色谱图上以检测所研究的药物。碘、DDQ和TCNQ分别在6 - 50、40 - 300和4 - 24 μg ml⁻¹的一般浓度范围内符合比尔定律,相关系数不小于0.9989。所提出的方法可成功应用于小瓶、胶囊、片剂和混悬剂中所研究药物的测定,回收率良好;碘法的回收率范围为96.47(±1.14)%至98.72(±1.02)%,DDQ法为96.35(±1.62)%至98.51(±1.30)%,TCNQ法为95.98(±0.78)%至98.40(±0.87)%。使用贝内西 - 希尔德布兰德图研究了缔合常数和标准自由能变化。研究了头孢菌素与蛋白质的结合与其摩尔吸光率的关系。