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Spectrophotometric methods for determination of enalapril and timolol in bulk and in drug formulations

机译:分光光度法测定散装和药物制剂中依那普利和噻吗洛尔的含量

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Two simple and accurate spectrophotometric methods for determination of timolol and enalapril maleate are described. The first method is based on chelate formation with palladium(II) chloride in buffered medium. The second method is based on the formation of the colored complex between palladium(II), eosin, and the two cited drugs using methylcellulose as surfactant to increase the solubility and intensity of the formed complexes. Under optimum conditions the complexes showed maximum absorption at 369.4 nm and 362.8 nm for timolol and enalapril maleate, respectively, in the first method and 552.2 and 550.6 nm for the second method. Apparent molar absorptivities were 1.8 * 10~3 and 1.3 * 10~3 and Sandell's sensitivities were 5.9 * 10~(-4) and 2.7 * 10~(-4) for timolol and enalapril maleate in the first method; in the second method molar absorptivities were 2.8 * 10~4 and 1.1 * 10~4 while Sandell's constants were 9.1 * 10~(-3) and 2.3 * 10~(-3) for timolol and enalapril maleate. The solutions of the complexes obeyed Beer's law in the concentration ranges 20-200 μg mL~(-1) and 50-300 μg mL~(-1) for timolol and enalapril maleate, respectively. In the second method, because the reaction was more sensitive the ranges were reduced to 1.6-16 μg mL~(-1) for timolol 8-56 μg mL~(-1) for enalapril maleate. The proposed methods were applied to the determination of the two drugs in their pharmaceutical formulation.
机译:描述了两种简单而准确的分光光度法测定噻吗洛尔和马来酸依那普利。第一种方法是基于在缓冲介质中与氯化钯(II)形成螯合物。第二种方法基于使用甲基纤维素作为表面活性剂在钯(II),曙红和两种引用药物之间形成有色络合物,以增加形成的络合物的溶解度和强度。在最佳条件下,第一种方法中的噻吗洛尔和马来酸依那普利复合物分别在369.4 nm和362.8 nm处显示最大吸收,第二种方法显示552.2和550.6 nm。在第一种方法中,对噻吗洛尔和马来酸依那普利的表观摩尔吸收率为1.8 * 10〜3和1.3 * 10〜3,Sandell的敏感性为5.9 * 10〜(-4)和2.7 * 10〜(-4)。在第二种方法中,噻吗洛尔和马来酸依那普利的摩尔吸收率分别为2.8 * 10〜4和1.1 * 10〜4,而Sandell常数为9.1 * 10〜(-3)和2.3 * 10〜(-3)。替莫洛尔和马来酸依那普利的复合物溶液的浓度分别在20-200μgmL〜(-1)和50-300μgmL〜(-1)范围内符合比尔定律。在第二种方法中,由于反应更加灵敏,因此将噻吗洛尔的范围降至1.6-16μgmL〜(-1),而马来酸依那普利的范围降至8-56μgmL〜(-1)。所提出的方法用于确定两种药物在其药物制剂中的含量。

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