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首页> 外文期刊>Instrumentation Science & Technology >SIMULTANEOUS QUANTIFICATION OF 10 BIOACTIVE CONSTITUENTS IN MAILUONING INJECTION BY UPLC-MS/MS
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SIMULTANEOUS QUANTIFICATION OF 10 BIOACTIVE CONSTITUENTS IN MAILUONING INJECTION BY UPLC-MS/MS

机译:使用UPLC-MS / MS同时定量注射液中10种生物活性成分

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A rapid and comprehensive ultra-performance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) method was developed for simultaneous determination of 10 major bioactive constituents in Mailuoning injection. Within 15 min, chromatographic separation was achieved on an Acquity UPLC BEH C18 column (50 mm × 2.1 mm I.D.) packed with 1.7 μm particles by a linear gradient elution. The analytes were monitored in a selected-ion reaction (SIR) mode with the electrospray ionization interface by the following ions: m/z 353.4 for isomers of chlorogenic acid, m/z 515.4 for isomers of 1,3-dicaffeoylquinic acid, m/z 179.2 for caffeic acid, m/z 192.9 for ferulic acid, m/z 503.2 for ecdysterone, and m/z 147.1 for cinnamic acid, respectively. The calibration curves of all analytes revealed good linear regression (r2 ≥ 0.9983) within test ranges. This method provided excellent sensitivity with LOQ and good precision with RSDs of intra- and interday variation less than 1.26% and 2.27%, respectively. The validated method was then applied to quantify the 10 major constituents in three batches of Mailuoning injection. The results indicated that the established method could be considered as an improved tool for quality control of Mailuoning injection.View full textDownload full textKeywordsMailuoning injection, quality control, quantification, UPLC-MS/MSRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10739149.2012.704471
机译:建立了快速,全面的超高效液相色谱/串联质谱(UPLC-MS / MS)方法,用于同时测定麦罗宁注射液中的10种主要生物活性成分。在15分钟内,在Acquity UPLC BEH C 18 色谱柱(50毫米×2.1毫米内径)上用线性梯度洗脱填充了1.7 µm颗粒,实现了色谱分离。使用电喷雾电离界面通过以下离子在选择离子反应(SIR)模式下对分析物进行监测:m / z 353.4适用于绿原酸的异构体,m / z 515.4适用于1,3-二咖啡酰奎尼酸的异构体,m / z咖啡酸的z 179.2,阿魏酸的m / z 192.9,蜕皮甾酮的m / z 503.2和肉桂酸的m / z 147.1。所有分析物的校准曲线显示在测试范围内良好的线性回归(r 2 ≥0.9983)。该方法具有出色的LOQ灵敏度和良好的精度,日内和日间变化的RSD分别小于1.26%和2.27%。然后将验证的方法应用于定量三批美罗宁注射液中的10种主要成分。结果表明,所建立的方法可以作为美洛宁注射液质量控制的一种改进工具。查看全文下载全文关键词美洛宁注射液,质量控制,定量,UPLC-MS / MS相关变量var addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线” ,services_compact:“ citeulike,netvibes,twitter,technorati,美味,linkedin,facebook,stumbleupon,digg,google,更多”,发布号:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10739149.2012.704471

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