高效液相色谱-紫外分光光度法定量塞克硝唑片的含量

Jéssica Gonçalves Souza Lima, A. Kogawa, H. R. Salgado
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引用次数: 7

摘要

建立了一种简便、快速、经济、绿色的塞克硝唑片含量测定方法。其目的是促进绿色分析化学,因为它具有低使用的有机溶剂和低生产的有毒废物。HPLC-UV法的流动相为纯净水+ 0.7%醋酸和乙醇(78:22,v/v)的混合物,在CN Phenomenex Luna柱(250 × 4.60 mm, 5 μm粒径)上流速为1.3 mL min-1,进样量为20 μL,紫外检测波长为318 nm,保留时间为4.26 min。该方法在5 ~ 100 μ mL-1的浓度范围内呈线性关系(r = 0.9998),检测限和定量限分别为0.533和1.615 μ mL-1。方法精密度RSD < 2%。测定的平均加样回收率为99.58%。以氧化、酸性、碱性、中性、光解降解为应激条件,考察了该方法的稳定性。该方法安全可靠,可作为塞克硝唑片的常规质量控制分析的替代方法。
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GREEN ANALYTICAL METHOD FOR QUANTIFICATION OF SECNIDAZOLE IN TABLETS BY HPLC-UV
A simple, rapid, economic and green analytical method was validated for the determination of secnidazole in tablets. The aim was to contribute to the green analytical chemistry since it has low use of organic solvent and low production of toxic waste. For the HPLC-UV method, the mobile phase was a mixture of purified water + 0.7 % acetic acid and ethanol (78:22, v/v), flow rate was 1.3 mL min-1 on column CN Phenomenex Luna (250 x 4.60 mm, 5 μm particle size), injection volume was 20 μL with UV detection at 318 nm and retention time of 4.26 minutes. The method was linear over the concentration range of 5-100 μg mL-1 (r = 0.9998) with limits of detection and quantitation of 0.533 e 1.615 μg mL-1, respectively. The precision of the method showed RSD less than 2 %. The accuracy determined by the average recoveries was 99.58 %. The secnidazole tablets were subjected to oxidation, acid, alkaline, neutral and photolysis degradation as stress conditions and the method was considered as indicative of stability. The method is adequate and safe to be a great alternative method in routine quality control analyzes for determination and quantification of secnidazole tablets.
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