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使用不同物理化学介质降解产物的筛选方法对磺胺嘧啶银中特定杂质进行鉴定。

Identification of the specified impurities of silver sulfadiazine using a screening of degradation products in different stress physico-chemical media.

机构信息

Department of Drug Analysis, University of Medicine and Pharmacy "Gr.T. Popa" Iasi, Universitatii Street No. 16, Iasi, Romania.

出版信息

Talanta. 2013 Nov 15;116:653-62. doi: 10.1016/j.talanta.2013.07.029. Epub 2013 Jul 29.

DOI:10.1016/j.talanta.2013.07.029
PMID:24148458
Abstract

Determination of silver sulfadiazine degradation products in several stress media was carried out by high pressure liquid chromatography (HPLC) with diode array detector (DAD) and hybrid mass spectrometer triple quadrupole-linear trap. The optimal chromatographic method used a Hypercarb column with a stationary phase 100% carbon, a mobile phase composed by a mixture 45:55 formic acid 1% solution and acetonitrile and detection at 275 nm. Structure elucidation was carried out on the mass spectrometry system using same chromatographic conditions and based on MS/MS techniques. Under these conditions up to 9 possible impurities were demonstrated to be degradation products respecting silver sulfadiazine evolution under different stress conditions: temperature, acid, basic, oxidation, reduction and catalyzed photodegradation. Sulfacetamide, sulfanilic acid (4-aminobenzenesulfonic acid), aniline, pyrimidin-2-amine, 4-aminobenzenesulfonamide, 4-methylidenesulfanilaniline, 4-aminophenol, 4-amino-n-methyl benzenesulfonamide and benzenesulfonic acid were identified by mass spectrometry in order to cover the possible degradation paths of silver sulfadiazine. Kinetics were also evaluated to obtain the prediction of shelf life of the substance. The linearity domain for the method was between 0.0005 mg/ml and 0.25mg/ml for each compound. Recovery factors in accuracy determination were between 95 and 105% relative to target concentrations of silver sulfadiazine and the quantitation limit was 0.00025 mg/ml.

摘要

采用二极管阵列检测器(DAD)和混合质谱三重四极杆-线性阱对几种应激介质中的磺胺嘧啶银降解产物进行了高效液相色谱(HPLC)测定。最优的色谱方法采用 Hypercarb 柱,固定相为 100%碳,流动相由 45:55 甲酸 1%溶液和乙腈组成,检测波长为 275nm。在相同的色谱条件下,通过质谱系统进行结构解析,并基于 MS/MS 技术。在这些条件下,证明了多达 9 种可能的杂质是在不同的应激条件下(温度、酸、碱、氧化、还原和光催化降解)磺胺嘧啶银降解的产物。通过质谱法鉴定了磺胺醋酰、磺胺酸(4-氨基苯磺酸)、苯胺、嘧啶-2-胺、4-氨基苯磺酰胺、4-亚甲基磺酰苯胺、4-氨基酚、4-氨基-N-甲基苯磺酰胺和苯磺酸,以涵盖磺胺嘧啶银可能的降解途径。还对动力学进行了评估,以获得物质保质期的预测。该方法的线性范围为 0.0005mg/ml 至 0.25mg/ml 之间,每个化合物的回收率在准确度测定中在 95%至 105%之间,定量限为 0.00025mg/ml。

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