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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >DEVELOPMENT AND VALIDATION OF DIFFERENTIAL PULSE POLAROGRAPHIC ANALYSIS OF FENOFIBRATE IN PURE AND PHARMACEUTICAL DOSAGE FORMS USING DROPPING MERCURY ELECTRODE
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DEVELOPMENT AND VALIDATION OF DIFFERENTIAL PULSE POLAROGRAPHIC ANALYSIS OF FENOFIBRATE IN PURE AND PHARMACEUTICAL DOSAGE FORMS USING DROPPING MERCURY ELECTRODE

机译:滴加汞法测定纯净和制药剂量形式中的女性纤维状粉末的微脉冲极谱分析法的建立和验证

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摘要

Objective: An easy, fast, accurate and sensitive differential pulse polarographic analysis for determination of fenofibrate (FEN) in pure and pharmaceutical dosage forms using dropping mercury electrode (DME) was applied. Methods: The method involves the electrochemical reduction of fenofibrate at DME by differential pulse polarographic analysis (DPPA). Different buffer solutions were used over a wide pH range (1.0–10.0). The best definition of the analytical signals was found in lithium perchlorate trihydrate buffer at pH 6.0 containing 24% (v/v) acetonitrile at-994 to-1025mV (versus Ag/AgCl). Results: Under optimized conditions the peak current (I p ) is linear over the range 0.0361-3.608 μg/ml. The DPPA was used successfully for the determination of FEN in pure and pharmaceutical dosage forms. The relative standard deviation did not exceed 2.1% for the concentration of FEN 0.0361 μg/ml. Regression analysis showed a good correlation coefficient (R 2 = 0.9994) between Ip and concentration at the mentioned range. The limit of detection (LOD) and the limit of quantification (LOQ) was to be 0.0025 and 0.0076 μg/ml, respectively. The proposed method was validated for linearity, precision and accuracy, repeatability, sensitivity (LOD and LOQ), robustness and specificity with an average recovery of 99.8-100.6%. Conclusion: The developed method is applicable for the determination of FEN in pure and different dosage forms with the assay of marketed formulations 99.8-104.0% and the results are in good agreement with those obtained by square-wave voltammetry (SWV) reference method. Keywords: Differential pulse polarographic analysis, Fenofibrate, Pharmaceutical formulations
机译:目的:采用滴汞电极(DME)简便,快速,准确,灵敏地测定纯药物剂型中的非诺贝特(FEN)的微分脉冲极谱法。方法:该方法涉及通过差动脉冲极谱分析(DPPA)在DME上电化学还原非诺贝特。在广泛的pH范围(1.0–10.0)中使用了不同的缓冲溶液。分析信号的最佳定义是在pH 6.0的高氯酸锂三水合物缓冲液中,该缓冲液含有-994至1025mV(相对于Ag / AgCl)的24%(​​v / v)乙腈。结果:在优化条件下,峰值电流(I p)在0.0361-3.608μg/ ml范围内呈线性。 DPPA已成功用于测定纯和药物剂型中的FEN。对于FEN 0.0361μg/ ml的浓度,相对标准偏差不超过2.1%。回归分析表明,在上述范围内,Ip与浓度之间具有良好的相关系数(R 2 = 0.9994)。检测限(LOD)和定量限(LOQ)分别为0.0025和0.0076μg/ ml。所提方法的线性,精密度和准确性,可重复性,灵敏度(LOD和LOQ),稳健性和特异性均得到验证,平均回收率为99.8-100.6%。结论:开发的方法适用于市售制剂的99.8-104.0%含量的测定,适用于纯净和不同剂型的FEN测定,结果与方波伏安法(SWV)参比方法所得结果吻合良好。关键字:微分脉冲极谱分析,非诺贝特,药物制剂

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