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HPTLC method for analysis of sertraline in pure bulk drug and lipidic nano delivery system: A stress degradation studies

机译:HPTLC方法分析纯散装药物和脂质纳米传递系统中的舍曲林:应力降解研究

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摘要

A sensitive, selective, precise, and stability-indicating, high-performance, thin-layer chromatographic (HPTLC) method for analysis of sertraline, both as a bulk drug and in house formulation, was developed and validated. The method employed thin-layer chromatographic (TLC) aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of Toulene/Ethyl acetate/Ammonia (1:5:0.1, v/v) as a mobile phase. The densitometric analysis were carried out at 273 nm using Camag TLC scanner which generated compact spots for SRT (Rf = 0.70 ± 0.02). The linear regression data for the calibration plots showed good linear relationship with r2 = 0.998 in the concentration range of 25-2000 ng spot -1. Sertraline was subjected to acid and alkali hydrolysis, oxidation, photodegradation, and dry heat treatment. Also, the degraded products were well separated from the pure drug. The method was validated for precision, accuracy, ruggedness, and recovery. As the method could effectively separate the drug from its degradation products, it can be employed as a stability indicating one. Moreover, the proposed HPTLC method was utilized to investigate the kinetics of acid and base degradation process.
机译:开发并验证了灵敏的,选择性的,精确的和指示稳定性的高性能薄层色谱法(HPTLC),用于分析舍曲林作为大宗药物和内部制剂。该方法使用预先涂有硅胶60F-254作为固定相的薄层色谱(TLC)铝板。溶剂系统由甲苯/乙酸乙酯/氨水(1:5:0.1,v / v)组成,为流动相。使用Camag TLC扫描仪在273 nm处进行光密度分析,该扫描仪生成了SRT的致密斑点(Rf = 0.70±0.02)。在浓度范围为25-2000 ng spot -1时,校准图的线性回归数据显示出良好的线性关系,r2 = 0.998。对舍曲林进行酸和碱水解,氧化,光降解和干热处理。而且,降解产物与纯药物充分分离。该方法的准确性,准确性,坚固性和回收率均得到验证。由于该方法可以有效地从降解产物中分离出药物,因此可以用作一种指示稳定性的药物。此外,提出的HPTLC方法被用来研究酸和碱降解过程的动力学。

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