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首页> 外文期刊>Der Pharmacia Lettre >Development and validation of UV spectrophotometric method for simultaneous estimationof Tramadol hydrochloride and Quercetin in niosomes formulation
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Development and validation of UV spectrophotometric method for simultaneous estimationof Tramadol hydrochloride and Quercetin in niosomes formulation

机译:紫外分光光度法同时估测脂质体中盐酸曲马多和槲皮素的开发与验证

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Simultaneous estimation of Tramadol HCl and Quercetin (Dihydrate) using a specific, rapid and simple UV spectrophotometric method with good sensitivity in niosome formulation has been developed. From the optical characteristics of the proposed methods, it was found that the λ max of Tramadol HCl and Quercetin(Dihydrate) was found to 271 nm and 372 nm respectively. Tramadol HCl and Quercetin (Dihydrate) obey linearity within the concentration range of 0 – 20 μg/ml and 2-20 μg/ml. Recovery study was performed to confirm the accuracy of the method. According to ICH guidelines Method development and validation has been adopted for routine estimation of Tramadol HCL and Quercetin (Dihydrate) niosome formulation.
机译:已经开发出了一种特异,快速,简单的紫外分光光度法,同时可以很好地检测纳米脂质体中的曲马多盐酸盐和槲皮素(二水合物)。从所提出方法的光学特性,发现曲马多盐酸盐和槲皮素(二水合物)的λmax分别为271nm和372nm。盐酸曲马多和槲皮素(二水合物)在0 – 20μg/ ml和2-20μg/ ml的浓度范围内呈线性关系。进行恢复研究以确认该方法的准确性。根据ICH指南,曲马多盐酸盐和槲皮素(二水合物)脂质体制剂的常规估算已采用方法开发和验证。

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