Analytical method development and validation of ketoprofen tablet by UV spectrophotometer

M. Shahnaz, Shivani Sharma, Anchal Sharma, D. Prasad
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引用次数: 1

Abstract

Precision: The degree of agreement among individual test results when a method is applied to multiple samplings of a homogeneous sample. It is a measure of either the degree of reproducibility (agreement under different conditions) or of repeatability (agreement under same condition) of the method. Linearity: The ability of a method to produce results that is directly or indirectly proportional to the conc. of the analyte in samples within a given range. Range: The interval between upper and lower level of analyte (including those levels) that has been shown to be determined with precision, accuracy and linearity using the method as written. Accuracy: The closeness of test results obtained by method to the true value. It is a measure of the exactness of the method. Ruggedness: The ruggedness of an analytical method is the degree of reproducibility of test results obtained by analysis of the same samples under a variety of normal test conditions. Such as different laboratories, different analyst, different instruments, different lots of reagents different elapsed assay times, differently days at normal lab. Conditions etc. Intermediate precision is normally expressed as the lack of influence on test results of operational and environmental variables of the analytical method. Ultraviolet Visible spectrometric assay developed for the quantification of Ketoprofen was performed in methanol in the concentration of 10 mcgml. Single Point Standardization method was used for the quantitative analysis of drug. The drug obeys Lambert – Beer’s law in the concentration range of 5 mcgml. The absorbance maxima occur at 256 nm. The developed method was validated as per ICH norms. Single Point Standardization method involves simple calculations. The absorbance value at 256 nm was found to be around 0.291. The results obtained on the validation parameters of developed method meets the ICH requirements. It infers that the method was found to be simple, specific, precise, accurate
酮洛芬片紫外分光光度分析方法的建立与验证
精密度:当一种方法应用于均匀样品的多个采样时,单个测试结果之间的一致程度。它是对方法的再现性(在不同条件下的一致性)或可重复性(在相同条件下的一致性)程度的度量。线性度:一种方法产生的结果直接或间接与系数成正比的能力。在给定范围内的样品中的分析物。范围:分析物的上、下水平之间的间隔(包括那些水平),已被证明可以使用所写的方法以精密度、准确度和线性来确定。准确度:通过该方法得到的测试结果与真实值的接近程度。它是对方法准确性的一种度量。牢固性:一种分析方法的牢固性是指在各种正常试验条件下对同一样品进行分析所获得的试验结果的可重复性程度。比如不同的实验室,不同的分析师,不同的仪器,不同数量的试剂不同的测定时间,在正常实验室不同的天数。条件等。中间精度通常表示为分析方法的操作变量和环境变量对测试结果没有影响。建立了酮洛芬的紫外可见分光光度法,在浓度为10 mcgml的甲醇中进行定量分析。药物定量分析采用单点标准化法。本品在5mcgml浓度范围内符合朗伯-比尔定律。吸光度最大值出现在256 nm处。所开发的方法按照ICH规范进行了验证。单点标准化方法计算简单。256 nm处的吸光度值约为0.291。所建立方法的验证参数符合ICH要求。由此可见,该方法简便、特异、精确、准确
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