a Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry , University of Alexandria , Alexandria , Egypt.
b Faculty of Pharmacy and Drug Manufacturing, Department of Pharmaceutical Chemistry , Pharos University in Alexandria , Alexandria , Egypt.
Drug Dev Ind Pharm. 2019 Feb;45(2):265-272. doi: 10.1080/03639045.2018.1535603. Epub 2018 Oct 26.
Objective and Significance: Methocarbamol (MET) and aspirin (ASP) are widely used as a muscle relaxant combination. The USP reports guaifenesin (GUA) and salicylic acid (SAL) as related substances and hydrolytic products of MET and ASP, respectively. This work aimed at developing and validating a simple and sensitive RP-HPLC method for the determination of both drugs as well as their related substances (at their pharmacopeial limits) in their bulk powders, laboratory prepared mixtures, and MET-ASP combined tablets. Methods and Results: Chromatographic separation was achieved in less than 9 min with the required resolution, peak symmetry, and accuracy on C column using isocratic elution system of diluted acetic acid (pH 3.2): acetonitrile at the ratio of 79: 21, v/v, at a flow rate of 1 mL/min. Detection was achieved with photodiode array at 233 nm for MET, GUA, and SAL and at 273 nm for ASP. The developed method has been validated as per ICH guidelines and the calibration plots were linear over the concentration ranges of 2-150, 0.4-30, 25-450, and 0.2-27 μg/mL for MET, GUA, ASP, and SAL, respectively. Conclusion: The optimized method proved to be specific, robust and precise for the quality control of the studied drugs in pharmaceutical preparations to ascertain that their related substances are not exceeding the permitted pharmacopeial limits.
美索巴莫(MET)和阿司匹林(ASP)被广泛用作肌肉松弛剂组合。USP 报告说,愈创甘油醚(GUA)和水杨酸(SAL)分别是 MET 和 ASP 的有关物质和水解产物。本工作旨在开发和验证一种简单灵敏的反相高效液相色谱法,用于测定两种药物及其在原料药、实验室制备混合物和 MET-ASP 复方片剂中的有关物质(在其药典限度内)。
使用 C 柱在等度洗脱系统中,用稀释乙酸(pH 3.2):乙腈以 79:21,v/v 的比例,以 1 mL/min 的流速,在不到 9 分钟内实现了色谱分离,具有所需的分辨率、峰对称性和准确性。MET、GUA 和 SAL 采用 233nm 光电二极管阵列检测,ASP 采用 273nm 检测。所开发的方法已按照 ICH 指南进行验证,MET、GUA、ASP 和 SAL 的校准曲线在 2-150、0.4-30、25-450 和 0.2-27μg/mL 的浓度范围内呈线性。
优化后的方法被证明具有特异性、稳健性和精密度,可用于药物制剂中研究药物的质量控制,以确保其有关物质不超过允许的药典限度。