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首页> 外文期刊>Journal of Chromatographic Science >Simultaneous Quantification of Related Substances of Perindopril Tert-Butylamine Using a Novel Stability Indicating Liquid Chromatographic Method
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Simultaneous Quantification of Related Substances of Perindopril Tert-Butylamine Using a Novel Stability Indicating Liquid Chromatographic Method

机译:新型稳定性指示液相色谱法同时定量测定培哚普利叔丁胺的有关物质

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摘要

A novel stability indicating gradient reverse-phased high-performance liquid chromatographic method has been developed for the quantification of impurities of perindopril tert-butylamine (PER) in pharmaceutical dosage form. Separation of the active substance and its known (Impurities B, C, D, E, F) and unknown impurities was achieved on a BDS Hypersil C18 column (250 mm x 4.6 mm, 5 mu m), thermostated at 70 degrees C, using a mobile phase comprised of aqueous solution of sodium 1-heptanesulfonate adjusted to pH 2 with perchloric acid and acetonitrile. The flow rate was maintained at 1.5 mL min(-1), injection volume of 20 mu L was utilized and detection of analytes was performed at 215 nm. The developed method was validated in accordance with current ICH Guidelines for all suggested parameters, including forced degradation studies and proved to be linear, accurate, precise and suitable for the impurity testing of PER, being subsequently applied during on-going stability studies of a newly developed generic formulation.
机译:已开发出一种新的稳定性指示梯度反相高效液相色谱方法,用于定量药物剂型中培哚普利叔丁胺(PER)的杂质。使用BDS Hypersil C18色谱柱(250 mm x 4.6 mm,5μm),将活性物质及其已知(杂质B,C,D,E,F和未知杂质)和未知杂质分离,使用流动相由1-庚烷磺酸钠水溶液组成,该溶液已用高氯酸和乙腈调节至pH 2。流速保持在1.5 mL min(-1),进样量为20μL,分析物的检测在215 nm进行。所开发的方法已根据当前的ICH指南针对所有建议的参数进行了验证,包括强制降解研究,并被证明是线性,准确,精确的,适用于PER的杂质测试,随后在新的正在进行的稳定性研究中应用开发通用配方。

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