Simultaneous Determination of Paracetamol, Aceclofenac and Chlorzoxazone in Pharmaceutical Dosage Form by UHPLC Method

P. Kb, Murugan, Ezhilarasan, Joseph
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引用次数: 2

Abstract

Aim: UHPLC method was developed and validated for the determination of Paracetamol, Aceclofenac and Chlorzoxazone in pharmaceutical dosage form. Methods: Separation was performed in Agilent technologies 1220 infinity LC system equipped with open lab CDS Chemstation software using Eclipse plus C18 (50 × 4.6 mm id, 1.8 μm) column with mobile phase containing 0.05% orthophosphoric acid, adjusted to pH 6.0 with triethylamine and acetonitrile in the ratio of 70:30 v/v with a flow rate of 0.5 mL/min and detection wavelength 270 nm. Results: The method was found to be linear in the concentration range of 161.59-484.77 μg/mL for paracetamol, 49.69-149.09 μg/mL for aceclofenac and 124.81-374.43 μg/mL for chlorzoxazone with correlation coefficient of 0.999 for all the three drugs respectively. The %RSD of 0.57, 0.45 and 0.60 for intra-day and 0.96, 0.88 and 0.84 for inter-day precision, respectively for of Paracetamol, Aceclofenac and Chlorzoxazone suggest the precision of the method as all these values are less than 2%. The method has shown good, consistent recoveries for of Paracetamol (99.90-99.95%), Aceclofenac (99.83-99.92%) and Chlorzoxazone (99.39-99.59%) which are close to 100%. Conclusion: The method was found to be accurate, precise, specific, robust and linear for the determination of Paracetamol, Aceclofenac and Chlorzoxazone in pharmaceutical dosage form.
UHPLC法同时测定药品剂型中扑热息痛、乙酰氯芬酸和氯唑唑酮的含量
目的:建立超高效液相色谱法测定药品剂型中扑热息痛、乙酰氯芬酸和氯唑唑酮的含量。方法:采用Agilent technologies 1220 infinity LC系统,安装开放实验室CDS Chemstation软件,采用Eclipse + C18 (50 × 4.6 mm id, 1.8 μm)柱,流动相为0.05%正磷酸,以三乙胺和乙腈为流动相,以70:30 v/v的比例调节pH 6.0,流速0.5 mL/min,检测波长270 nm。结果:该方法在对乙酰氨基酚161.59 ~ 484.77 μg/mL、醋氯芬酸49.69 ~ 149.09 μg/mL、氯唑唑酮124.81 ~ 374.43 μg/mL的浓度范围内线性良好,相关系数分别为0.999。对乙酰氨基酚、醋氯芬酸和氯唑唑酮的日内精密度RSD分别为0.57、0.45和0.60,日内精密度RSD分别为0.96、0.88和0.84,均小于2%,表明该方法精密度较高。对乙酰氨基酚(99.90 ~ 99.95%)、醋氯芬酸(99.83 ~ 99.92%)和氯唑唑酮(99.39 ~ 99.59%)的加样回收率接近100%。结论:该方法准确、精密度高、专精性好、稳健性好,可用于药品剂型中扑热息痛、乙酰氯芬酸和氯唑唑酮的含量测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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