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Study of 4.Quinolone Antibiotics in Biological Samples by Short-Column Liquid Chromatography Coupled with Electrospray Ionization Tandem Mass Spectrometry

机译:短柱液相色谱-电喷雾串联质谱法研究生物样品中4.喹诺酮类抗生素

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Simultaneous detection and confirmation of 15 quinolone antibiotics was accomplished by fast short-column liquid chromatography coupled with electrospray ionization tandem mass spectrometry (LC/MS/MS). Several physicochemical parameters such as hydrophobicity and aqueous dissociation constants were calculated from the structural formulas of the quinolone drugs, and their impact on both chromatographic and mass spectrometric behavior was studied. Additionally, a possible influence of bulk solution pH on electrospray detection sensitivity of 4-quinolones was investigated and compared to predictions based on solution-phase equilibria. A signal intensity comparison of the MH+ ions at different pH values for all 15 compounds did not reveal ally pH effect, despite variations by several orders of magnitude in equilibrium concentrations in bulk solution. To demonstrate the potential of the LC/MS/MS method, its application to trace analysis in several biological matrices such as milk, salmon, and human urine was investigated. The method was shown to be sensitive with detection limits down to 1 ppb in both milk and salmon tissue. The versatility of the method was also exhibited by utilizing it for rapid identification of urinary metabolites of ciprofloxacin. Finally, a new, complementary approach is described for confirmatory analyses of 4-quinolones by means of a quasi-MS/ MS/MS technique involving in-source collision-induced dissociation. It is shown that LC/quasi-MS/MS/MS can significantly enhance structural information and, thus, the specificity of analysis for the investigated 4-quinolones.
机译:通过快速短柱液相色谱结合电喷雾电离串联质谱法(LC / MS / MS),可以同时检测和确认15种喹诺酮类抗生素。从喹诺酮类药物的结构式计算了几个理化参数,如疏水性和水离解常数,并研究了它们对色谱和质谱行为的影响。此外,研究了本体溶液pH对4-喹诺酮类化合物电喷雾检测灵敏度的可能影响,并将其与基于溶液相平衡的预测进行了比较。尽管在本体溶液中平衡浓度变化了几个数量级,但所有15种化合物在不同pH值下MH +离子的信号强度比较均未显示出同质pH效应。为了证明LC / MS / MS方法的潜力,研究了它在痕量分析中在牛奶,鲑鱼和人尿等几种生物基质中的应用。牛奶和鲑鱼组织中的检测限低至1 ppb,显示该方法灵敏。通过将其用于快速鉴定环丙沙星的尿代谢物,还显示了该方法的多功能性。最后,描述了一种新的补充方法,用于通过涉及源内碰撞诱导的解离的准MS / MS / MS技术对4-喹诺酮进行确认性分析。结果表明,LC /准MS / MS / MS可以显着增强结构信息,从而增强所研究的4-喹诺酮类药物的分析特异性。

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