Motwani Sanjay K, Khar Roop K, Ahmad Farhan J, Chopra Shruti, Kohli K, Talegaonkar S
Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.
Anal Chim Acta. 2007 Jan 16;582(1):75-82. doi: 10.1016/j.aca.2006.08.053. Epub 2006 Sep 1.
A simple, sensitive, selective, precise and stability-indicating high-performance thin-layer chromatographic (HPTLC) method for densitometric determination of moxifloxacin both as a bulk drug and from pharmaceutical formulation was developed and validated as per the International Conference on Harmonization (ICH) guidelines. The method employed TLC aluminium plates pre-coated with silica gel 60F-254 as the stationary phase and the mobile phase consisted of n-propanol-ethanol-6M ammonia solution (4:1:2, v/v/v). Densitometric analysis of moxifloxacin was carried out in the absorbance mode at 298 nm. Compact spots for moxifloxacin were found at R(f) value of 0.58+/-0.02. The linear regression analysis data for the calibration plots showed good linear relationship with r=0.9925 in the working concentration range of 100-800 ng spot(-1). The method was validated for precision, accuracy, ruggedness, robustness, specificity, recovery, limit of detection (LOD) and limit of quantitation (LOQ). The LOD and LOQ were 3.90 and 11.83 ng spot(-1), respectively. Drug was subjected to acid and alkali hydrolysis, oxidation, dry heat, wet heat treatment and photodegradation. All the peaks of degradation products were well resolved from the standard drug with significantly different R(f) values. Statistical analysis proves that the developed HPTLC method is reproducible and selective. As the method could effectively separate the drug from its degradation products, it can be employed as stability-indicating one. Moreover, the proposed HPTLC method was utilized to investigate the kinetics of the acidic and alkaline degradation processes at different temperatures. Arrhenius plot was constructed and apparent pseudo-first-order rate constant, half-life and activation energy were calculated. In addition the pH-rate profile for degradation of moxifloxacin in constant ionic strength buffer solutions within the pH range 1.2-10.8 was studied.
按照国际协调会议(ICH)指南,开发并验证了一种简单、灵敏、选择性好、精确且具有稳定性指示作用的高效薄层色谱(HPTLC)方法,用于密度测定莫西沙星原料药及其制剂。该方法采用预涂硅胶60F - 254的TLC铝板作为固定相,流动相由正丙醇 - 乙醇 - 6M氨溶液(4:1:2,v/v/v)组成。在298nm波长下以吸光度模式对莫西沙星进行密度分析。发现莫西沙星的斑点致密,比移值(Rf)为0.58±0.02。校准曲线的线性回归分析数据显示,在100 - 800ng斑点-1的工作浓度范围内具有良好的线性关系,r = 0.9925。该方法在精密度、准确度、耐用性、稳健性、特异性、回收率、检测限(LOD)和定量限(LOQ)方面进行了验证。LOD和LOQ分别为3.90和11.83ng斑点-1。对药物进行了酸、碱水解、氧化、干热、湿热处理和光降解。所有降解产物峰与标准药物峰均能很好地分离,Rf值有显著差异。统计分析证明所开发的HPTLC方法具有可重复性和选择性。由于该方法能有效将药物与其降解产物分离,可作为稳定性指示方法。此外,所提出的HPTLC方法用于研究不同温度下酸性和碱性降解过程的动力学。构建了阿仑尼乌斯图,并计算了表观伪一级速率常数、半衰期和活化能。此外,还研究了莫西沙星在pH范围1.2 - 10.8的恒定离子强度缓冲溶液中的pH - 速率降解曲线。