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SPECTROPHOTOMETRIC DETERMINATION OF MEFENAMIC ACID IN PHARMACEUTICAL PREPARATIONS

机译:分光光度法测定药物制剂中的速溶酸。

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The present paper describes an effective and low-cost spectrophotometric method for the determination of mefenamic acid in its pure form and pharmaceutical preparations. The method is based on the charge-transfer complexation between mefenamic acid asan n-electron donor and chloranil as psi-acceptor to form a violet chromogen measured at 540 nm. Under the optimum conditions, a linear relationship with good correlation coefficient (0.9996) was found between the absorbance and concentration of the studied drug in the range of 10-60 mu g/mL. The optimal reaction conditions such as reagent concentration, healing time and stability of the reaction product were determined. The limit of detection (LOD) was 2.16 mu g/mL and the limit of quantification (LOQ) was 7.15 mu g/mL. The method was successfully applied to the determination of mefenamic acid in pharmaceutical preparations with out any interference from common excipients.
机译:本论文描述了一种有效且低成本的分光光度法,用于测定纯形式的甲芬那酸和药物制剂。该方法是基于作为正电子供体的甲芬那酸与作为psi受体的苯甲酰氯之间的电荷转移络合形成的,在540 nm处测得紫罗兰色原。在最佳条件下,所研究药物的吸光度与浓度之间的线性关系具有良好的相关系数(0.9996),范围为10-60μg / mL。确定了最佳反应条件,例如试剂浓度,修复时间和反应产物的稳定性。检测限(LOD)为2.16μg / mL,定量限(LOQ)为7.15μg / mL。该方法已成功地用于药物制剂中甲芬那酸的测定,而不受普通赋形剂的干扰。

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