Padhiyar Shantilal, Jivani Kamlesh M, Upadhyay Jagat, Patel Tejas, Suhagia Bhanubhai
Faculty of Pharmacy, Dharmsinh Desai University, College Rd, Nadiad, Gujarat 387001, India.
J Chromatogr Sci. 2023 Dec 13;61(10):943-952. doi: 10.1093/chromsci/bmac092.
A simple, specific, accurate and stability-indicating reversed-phase high-performance liquid chromatographic method was developed for the determination of lacosamide, using C18 column and a mobile phase composed of phosphate buffer (pH 4.0):acetonitrile (40:60 v/v). The retention time of lacosamide was found to be 2.7 min. Linearity was established for lacosamide in the range of 10-50 μg/mL. The percentage recovery of lacosamide was found to be in the range of 97.37-99.20%. The drug was subjected to acid, alkali, oxidation, dry heat and photolytic degradation. The degradation studies indicated condition was well resolved from the pure drug with significant differences in their retention time values. This method can be successfully employed for quantitative analysis of lacosamide in bulk drug and formulation.
建立了一种简单、特异、准确且具有稳定性指示作用的反相高效液相色谱法,用于测定拉科酰胺,采用C18柱,流动相由磷酸盐缓冲液(pH 4.0):乙腈(40:60 v/v)组成。发现拉科酰胺的保留时间为2.7分钟。拉科酰胺在10 - 50μg/mL范围内建立了线性关系。拉科酰胺的回收率在97.37 - 99.20%范围内。该药物进行了酸、碱、氧化、干热和光解降解试验。降解研究表明,降解产物与纯药物在保留时间值上有显著差异,能够很好地分离。该方法可成功用于原料药和制剂中拉科酰胺的定量分析。