换一批Development and validation of a reversed-phase HPLC method for simultaneous analysis of butylhydroxyanisol, simvastatin and its impurities in tablet dosage forms.
第一作者：
M,El Karbane
第一单位：
Research team of pharmaceutical and toxicological analysis, laboratory of pharmacology and toxicology, faculty of medicine and pharmacy, Mohammed V university, Soussi, Rabat, Morocco; Physicochemical service, drugs quality control laboratory, division of drugs and pharmacy, Ministry of Health, Rabat, Morocco.
作者：
医学主题词
丁羟茴香醚(Butylated Hydroxyanisole);色谱法, 高压液相(Chromatography, High Pressure Liquid);药物污染(Drug Contamination);药物稳定性(Drug Stability);羟甲基戊二酰基CoA还原酶抑制剂(Hydroxymethylglutaryl-CoA Reductase Inhibitors);检测限(Limit of Detection);质量控制(Quality Control);参考标准(Reference Standards);结果可重复性(Reproducibility of Results);斯伐他汀(Simvastatin);分光光度法, 紫外线(Spectrophotometry, Ultraviolet);片剂(Tablets)
DOI
10.1016/j.pharma.2014.03.002
PMID
24997886
发布时间
2019-12-10
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