首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Identification and control of impurities in streptomycin sulfate by high-performance liquid chromatography coupled with mass detection and corona charged-aerosol detection.
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Identification and control of impurities in streptomycin sulfate by high-performance liquid chromatography coupled with mass detection and corona charged-aerosol detection.

机译:高效液相色谱结合质量检测和电晕带电气溶胶检测技术鉴定和控制硫酸链霉素中的杂质。

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摘要

For the control of impurities in streptomycin sulfate a reversed phase ion-pair high performance liquid chromatography (HPLC) method using charged aerosol detection (CAD) was developed. With this method, 21 impurities could be separated and tentatively identified using a combination of exact mass measurement by TOF-MS and MS/MS experiments with a triple quadrupole MS. For three impurities the suggested structures could be confirmed by in situ formation. The CAD detector response was found to be linear over 2 orders of magnitude allowing a straightforward quantification of all impurities. A limit of quantification of 0.09% for streptomycin sulfate and of 0.008% for streptidine sulfate (referred to the concentration of the 5mg/ml test solution) could be achieved. The HPLC method was applied to the purity testing of 12 samples of commercially available streptomycin sulfate from different manufacturers. Impurity levels between 4.6% and 16.0% were found. The current European Pharmacopoeia monograph for streptomycin sulfate only limits streptomycin B by a TLC test to 3.0%. Therefore, the results of this study underline the importance of introducing a state-of-the-art test for the control of impurities in the monograph. The new HPLC-CAD method is considered suitable for this purpose.
机译:为了控制硫酸链霉素中的杂质,开发了使用带电气溶胶检测(CAD)的反相离子对高效液相色谱(HPLC)方法。使用此方法,可以通过TOF-MS的精确质量测量和三重四极杆MS的MS / MS实验的组合来分离和初步鉴定21种杂质。对于三种杂质,建议的结构可以通过原位形成得到确认。发现CAD检测器的响应在2个数量级上呈线性,从而可以直接量化所有杂质。硫酸链霉素的定量限为0.09%,硫酸链霉素的定量限为0.008%(指5mg / ml测试溶液的浓度)。 HPLC方法用于不同厂商的12种市售硫酸链霉素样品的纯度测试。发现杂质水平在4.6%至16.0%之间。目前欧洲药典对硫酸链霉素的专论仅通过TLC试验将链霉素B限制为3.0%。因此,这项研究的结果强调了引入最新测试来控制专着中杂质的重要性。新的HPLC-CAD方法被认为适用于此目的。

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