首页> 外文期刊>Acta Poloniae Pharmaceutica: Durg Research >DETERMINATION OF SOTALOL, OXPRENOLOL AND LABETALOL IN BINARY MIXTURES AND IN SPIKED HUMAN SERUM BY DERIVATIVE SPECTROPHOTOMETRIC METHOD
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DETERMINATION OF SOTALOL, OXPRENOLOL AND LABETALOL IN BINARY MIXTURES AND IN SPIKED HUMAN SERUM BY DERIVATIVE SPECTROPHOTOMETRIC METHOD

机译:用衍生物分光光度法测定二元混合物中的发光醇,牛产醇和樟本子醛酚

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The usefulness of derivative spectrophotometry for the determination of labetalol, sotalol and oxprenolol in binary mixtures and in human spiked serum was checked. To this aim a spectrophotometric analysis of samples in the UV range was carried out and the obtained results revealed that derivative spectrophotometry allows for the fast, accurate and precise determination of the tested substances in spite of their clear interference in the zero-order spectra. For quantitative determinations izero-crossing technique was used to establish wavelengths for zeros of specified component. In a mixture of labetalol and oxprenolol the following wavelengths were established: D1 lambda = 245.32 nm and 266.03 nm, D2 lambda = 243.30 nm and 301.09 nm. respectively. D3 derivative did not show zeros suitable for quantitative analysis. For the analysis of labetalol and sotalol mixture, D3 derivative spectrophotometry was used at the following wavelengths: lambda = 246.03 nm and lambda = 249.91 nm, respectively. In this case, the curves of D1 and D2 derivatives showed no zeros that can be used in quantitative analysis. To determine the concentration of the components in a mixture containing oxprenolol and sotalol the following wavelengths were selected: for oxprenolol D1 lambda = 245.32 nm, D2 lambda = 240.18 nm, D3 lambda = 232.05 nm and for sotalol D1 lambda = 230.56 nm, D2 lambda = 232.65 nm and D3 lambda = 238.84 nm, respectively. The developed spectrophotometric method was characterized by high sensitivity and accuracy, LOD determined for sotalol was in the range of 0.21-1.88 mu g/mL, for labetalol 1.00-3.43 mu g/mL and for oxprenolol 0.16-2.06 mu g/mL; LOQ determined for sotalol was in the range of 0.65-5.70 mu g/mL, for labetalol 3.11-10.39 mu g/mL and for oxprenolol 0.47-6.23 mu g/mL, depending on the composition of the tested mixture and the order of the derivative. The recovery of the individual components was within the range of 100 +/- 5%. The linearity range was wide and estimated for sotalol in the range of 11.00-38.50 mu g/mL, for labetalol 12.80-44.80 mu g/mL and for oxprenolol 12.60-44.10 mu g/mL with correlation coefficients in the range of 0.9977-0.9999.
机译:检查衍生分光光度法用于测定二元混合物中和人尖刺血清中的樟本子醇,发光醇和牛产酚的用途。为此目的,进行UV范围中样品的分光光度分析,得到的结果显示,衍生分光光度法允许尽管在零阶光谱中清晰干扰,但衍生物分光光度法允许快速,准确和精确地测定测试物质。对于定量确定,Izero交叉技术用于建立指定组分的零的波长。在Labetalol和Oxpronolol的混合物中建立了以下波长:D1λ= 245.32nm和266.03nm,d2λ= 243.30nm和301.09nm。分别。 D3衍生物未显示适合定量分析的零。为了分析Labetalol和Sotalol混合物,在以下波长下使用D3衍生物分光光度法:Lambda = 246.03nm和λ= 249.91nm。在这种情况下,D1和D2衍生物的曲线显示出可用于定量分析的零。为了确定含有牛产洛尔醇和发光甲醇的混合物中组分的浓度,选择以下波长:对于氧化丙醇D1λ= 245.32nm,d2λ= 240.18nm,d3λ= 232.05nm和sotalol d1 lambda = 230.56nm,d2λ = 232.65nm和d3λ= 238.84nm。发育的分光光度法的特征在于高灵敏度和精度,测定的Sotalol LOD在0.21-1.88μg/ ml的范围内,对于LABETALOL1.00-3.43μg/ mL和氧化醇0.16-2.06μg/ ml;用于Sotalol的LOQ在0.65-5.70μmg/ ml的范围内,对于Labetalol3.11-10.39μg/ ml,对于氧化醇0.47-6.23μg/ ml,取决于测试混合物的组成和阶数衍生物。各个组分的恢复在100 +/- 5%的范围内。线性范围宽,估计在11.00-38.50μmg/ ml的Sotalol,对于Labetalol12.80-44.80μmg/ ml和氧化戊洛尔12.60-44.10μmg/ ml,其相关系数在0.9977-0.9999的范围内。

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