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首页> 外文期刊>Die Pharmazie >Determination of lornoxicam in pharmaceutical preparations by zero and first order derivative UV spectrophotometric methods.
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Determination of lornoxicam in pharmaceutical preparations by zero and first order derivative UV spectrophotometric methods.

机译:零和一阶导数紫外分光光度法测定药物制剂中的氯诺昔康。

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Zero and first order derivative UV spectrophotometric methods were developed for the analysis of lornoxicam (LOR). The solutions of the standards and pharmaceutical samples were prepared in 0.05 N NaOH. Absorbances of LOR were measured at 376 nm for the zero order by measuring height of peak from zero and at 281 and 302 nm for the first order derivative spectrophotometric method by measuring peak to peak height. The linearity ranges were found to be 0.5-35 microg/mL for the zero order and 0.2-75 microg/mL for the first order derivative UV spectrophotometric method. The methods were validated and applied to the determination of LOR in pharmaceutical preparations (tablet and injectable, both containing 8 mg LOR). It was concluded that the methods developed were accurate, sensitive, precise, robust, rugged and useful for the quality control of LOR in pharmaceutical preparations.
机译:开发了零级和一阶导数紫外分光光度法用于氯诺昔康(LOR)的分析。在0.05 N NaOH中制备标准溶液和药物样品。通过测量从零开始的峰高,在376 nm处测量了零阶LOR的吸光度,对于一阶导数分光光度法,通过测量峰到峰的高度在281和302 nm下测量了LOR的吸光度。线性范围为零阶为0.5-35 microg / mL,一阶导数紫外分光光度法为0.2-75 microg / mL。该方法经过验证,可用于测定药物制剂(片剂和注射剂,均含8 mg LOR)中的LOR。结论是,开发的方法准确,灵敏,精确,鲁棒,坚固耐用,可用于药物制剂中LOR的质量控制。

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