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Stability indicating liquid chromatography method for the analysis of Vecuronium bromide: study of the degradation profile

机译:用于溴化维库溴铵分析的稳定性指示液相色谱方法:降解曲线的研究

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摘要

Neuromuscular blocker agent namely; Vecuronium bromide (VEC) was quantified through developing a simple reversed phase liquid chromatographic (RP-LC) method, in drug substance and in drug product. The proposed method could quantify VEC in the presence of its degradation products produced from exposing VEC to different stress conditions as recommended by the International Conference on harmonization (ICH) guidelines. Acidic (2M HCl), basic (2MNaOH) hydrolysis, oxidation (3% H O ), photolysis (UV light at 254nm), and thermal (135 °C) degradation were estimated by exposing the drug substances to different stress conditions. The separation of the drug from its degradation products was successfully conducted on Tracer Extrasil CN (150 × 4.6mm; 5μm) column using O-phosphoric acid (pH6; 0.05M)-acetonitrile (50:50v/v) as mobile phase. The detection and quantification was done with UV detection at210nm.The validation data were found to be acceptable over a concentration range10-120 μg/ml. The limit of quantification (LOQ) and detection (LOD) were 8.10 and 2.67 μg/ml, respectively. The proposed method met all criteria for validation in accordance with the International Conference on harmonization (ICH) guidelines. The presented work monitored the degradation profile for VEC under various stress conditions and provided a simple LC method for its routine analysis. The structures of the forced degradation products had been described in details using the MS data and the possible degradation pathways were outlined. Besides, the results obtained from the developed method compared statistically with that of the official method indicting high accuracy and precision.
机译:即神经肌肉阻滞剂;通过开发一种简单的反相液相色谱(RP-LC)方法,可以在原料药和药品中对溴化维库溴铵(VEC)进行定量。根据国际协调会议(ICH)指南的建议,所提出的方法可以在存在降解产物的情况下对VEC进行量化,该降解产物是通过将VEC暴露于不同的应力条件而产生的。通过将药物暴露于不同的压力条件下,可以评估到酸性(2M HCl),碱性(2MNaOH)水解,氧化(3%H O),光解(254nm的紫外线)和热降解(135°C)。使用O-磷酸(pH6; 0.05M)-乙腈(50:50v / v)作为流动相,在Tracer Extrasil CN(150×4.6mm;5μm)色谱柱上成功进行了药物与降解产物的分离。在210nm处用UV检测进行检测和定量。验证数据在10-120μg/ ml的浓度范围内是可以接受的。定量限(LOQ)和检测限(LOD)分别为8.10和2.67μg/ ml。提议的方法符合国际协调会议(ICH)指南的所有验证标准。提出的工作监测了各种应力条件下VEC的降解情况,并为其常规分析提供了一种简单的LC方法。已使用MS数据详细描述了强迫降解产物的结构,并概述了可能的降解途径。此外,从开发的方法获得的结果与官方方法的统计结果进行了比较,表明其准确性和准确性较高。

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