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Analytical Study for the Charge-Transfer Complexes of Rosuvastatin Calcium with π-Acceptors

机译:罗苏伐他汀钙与π受体的电荷转移配合物的分析研究

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Studies were carried out to investigate the charge-transfer (CT) reaction of ROS-Ca, as a n-electron donor with various π-acceptors: tetracyanoethylene, p-chloranilic acid, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, 2,3,5,6-tetrabromo-1,4-benzoquinone, 1,3,5- trinitrobenzene, 2,3,5,6-tetrachloro-1,4-benzoquinone, 7,7,8,8-tetracyano-quinodimethane, and 2,4,7-trinitro-9-fluorenone. Different colored CT complexes were obtained. The reaction mechanism and site of interaction were determined by ultraviolet-visible spectrophotometric techniques and computational molecular modeling. The formation of the colored complexes was utilized in the development of simple, rapid and accurate spectrophotometric methods for the determination of ROS-Ca. Under the optimum reaction conditions, linear relationships with good correlation coefficients (0.9984–0.9995) were found between the absorbances and the concentrations of ROS-Ca in the range of 2–200 μg mL~(?1). The limits of detection ranged from 0.41 to 12.24 μg mL~(?1). No interference could be observed from the additives commonly present in the tablets or from the drugs that are co-formulated with ROS-Ca in its combined formulations. The methods were successfully applied to the analysis of tablets with good accuracy and precision; the recovery percentages ranged from 99.54–100.46 ± 1.58–1.82%. The results were compared favorably with the reported method. The proposed methods are practical and valuable for routine application in quality control laboratories for determination of ROS-Ca in its bulk form and tablets.
机译:进行了研究以研究作为正电子供体的ROS-Ca与各种π-受体的电荷转移(CT)反应:四氰基乙烯,对氯苯甲酸,2,3-二氯-5,6-二氰基- 1,4-苯醌,2,3,5,6-四溴-1,4-苯醌,1,3,5-三硝基苯,2,3,5,6-四氯-1,4-苯醌,7,7, 8,8-四氰基-醌二甲烷和2,4,7-三硝基-9-芴酮。获得了不同颜色的CT复合物。通过紫外可见分光光度法和分子计算模型确定了反应的机理和相互作用的部位。有色络合物的形成被用于开发简单,快速和准确的分光光度法测定ROS-Ca的方法。在最佳反应条件下,吸光度与ROS-Ca浓度在2-200μgmL〜(?1)范围内,线性关系良好(0.9984-0.9995)。检测限为0.41至12.24μgmL〜(?1)。片剂中常见的添加剂或与ROS-Ca联合配制的药物均未发现干扰。该方法已成功应用于片剂的分析,具有较高的准确度和精密度。回收率范围为99.54–100.46±1.58–1.82%。将结果与报道的方法进行了比较。所提出的方法对于质量控制实验室中用于测定散装形式和片剂中的ROS-Ca的常规应用是实用且有价值的。

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