Suppr超能文献

通过液相色谱-串联质谱法对土霉素及其杂质进行定量分析。

Quantitative analysis of oxytetracycline and its impurities by LC-MS-MS.

作者信息

Lykkeberg Anne Kruse, Halling-Sørensen Bent, Cornett Claus, Tjørnelund Jette, Honoré Hansen Steen

机构信息

Department of Analytical Chemistry, The Danish University of Pharmaceutical Sciences, Universitetsparken 2, DK-2100 Copenhagen, Denmark.

出版信息

J Pharm Biomed Anal. 2004 Feb 4;34(2):325-32. doi: 10.1016/S0731-7085(03)00500-4.

Abstract

A liquid chromatographic-tandem mass spectrometric method using an Xterra MS C(18) chromatographic column ( 100 mm x 2.1 mm i.d., 3.5microm) that allows complete separation of oxytetracycline (OTC) and the impurities: 4-epi-oxytetracycline (EOTC), tetracycline (TC), 4-epi-tetracycline (ETC), 2-acetyl-2-decarboxamido-oxytetracycline (ADOTC), alpha-apo-oxytetracycline (alpha-AOTC) and beta-apo-oxytetracycline (beta-AOTC) was developed. Gradient elution was used and calibration curves were obtained using the scan mode selected reaction monitoring (SRM). Acceptable correlations were obtained for OTC, TC, EOTC and ADOTC whereas the correlations of alpha-AOTC and beta-AOTC were less accurate resulting in higher limits of quantification (LOQ) and limits of detection (LOD) relative to the other compounds. The intraday and interday accuracy varied for all the compounds from 90 to 112% and the intraday and interday precision were lower than 7.1%. The method was applied for analysis of commercial available ointments containing OTC resulting in an acceptable quantification of OTC and the impurities in the drug preparations. The advantage of this method compared to the other separation methods is an empty separation window right after the large peak corresponding to OTC in the chromatogram, which facilitates an accurate determination of ADOTC and the other impurities.

摘要

开发了一种液相色谱 - 串联质谱法,该方法使用Xterra MS C(18)色谱柱(100 mm×2.1 mm内径,3.5微米),可实现土霉素(OTC)及其杂质:4 - 表土霉素(EOTC)、四环素(TC)、4 - 表四环素(ETC)、2 - 乙酰基 - 2 - 脱羧酰胺基土霉素(ADOTC)、α - 去甲土霉素(α - AOTC)和β - 去甲土霉素(β - AOTC)的完全分离。采用梯度洗脱,并使用扫描模式选择反应监测(SRM)获得校准曲线。OTC、TC、EOTC和ADOTC获得了可接受的相关性,而α - AOTC和β - AOTC的相关性不太准确,导致相对于其他化合物具有更高的定量限(LOQ)和检测限(LOD)。所有化合物的日内和日间准确度在90%至112%之间变化,日内和日间精密度低于7.1%。该方法用于分析市售含OTC的软膏剂,结果药物制剂中OTC及其杂质的定量结果可接受。与其他分离方法相比,该方法的优势在于色谱图中对应OTC的大峰之后有一个空的分离窗口,这便于准确测定ADOTC和其他杂质。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验