首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >UV-VIS SPECTROPHOTOMETRIC STUDY FOR DETERMINATION OF CEFIXIME IN PURE FORM AND IN PHARMACEUTICALS THROUGH COMPLEXATION WITH Cu(II) USING ACETATE–NaOH BUFFERIN WATER:METHANOL
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UV-VIS SPECTROPHOTOMETRIC STUDY FOR DETERMINATION OF CEFIXIME IN PURE FORM AND IN PHARMACEUTICALS THROUGH COMPLEXATION WITH Cu(II) USING ACETATE–NaOH BUFFERIN WATER:METHANOL

机译:乙酸-氢氧化钠-丁三醇水:甲醇与铜(II)络合通过紫外-可见分光光度法测定纯形式和药物中的头孢克辛

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UV-Vis spectroscopic method for the analysis of cefixime (CEFI)in pure form and pharmaceutical formations through complexation with Cu(II) using acetate-NaOH buffer in mixture water: methanol has been developed. Optimal temperature and time for coupling were established at 25±5oC with time ranging from 0 to10 min. The formation complex, CEFI: Cu(II ) gives maximum absorbance of the yellow color occurred at λ= 410 nm and the molar absorptivity is 5.12 x 103L.mol- 1.cm-1. The reaction between CEFI and Cu(II) occurred at a stoichiometric ratio of 1:1. All reaction conditions have been optimized to obtain the complex. Under optimum conditio ns Beer's law was obeyed at concentrations ranging from 0.2267 to 22.671μg.mL-1with correlation coefficients≥0.9995 in all cases with RSD generally less than 4.0%. The limit of detection (LOD) and limit of quantification (LOQ) was found to be 0.030μg.mL-1and 0.091μg.mL- 1, respectively. The proposed method was simple, economic, accurate and successfully applied to the determination of CEFI in pharmaceuticals with average recovery of 98.00 to 103.00%, the results obtained agree well with the contents stated on the labels
机译:紫外可见分光光度法通过使用乙酸-NaOH缓冲液在混合水:甲醇中与铜(II)络合,分析纯净形式和药物形成中的头孢克肟(CEFI)。最佳的偶联温度和时间建立在25±5oC,时间为0至10分钟。形成配合物CEFI:Cu(II)给出了最大的黄色吸收度,发生在λ= 410 nm处,摩尔吸光度为5.12 x 103L.mol-1.cm-1。 CEFI和Cu(II)之间的化学计量比为1:1。已优化所有反应条件以获得配合物。在最佳条件下,在所有情况下RSD通常小于4.0%,在0.2267至22.671μg.mL-1的浓度范围内遵守比尔定律,相关系数≥0.9995。检出限(LOD)和定量限(LOQ)分别为0.030μg.mL-1和0.091μg.mL-1。该方法简便,经济,准确,已成功用于药物中CEFI的测定,平均回收率为98.00〜103.00%,结果与标签上的内容吻合良好。

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