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Temporal Resolution of Solid-Phase Microextraction: Measurement of Real-Time Concentrations within a Dynamic System

机译:固相微萃取的时间分辨率:动态系统中实时浓度的测量

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摘要

To address the challenge of measuring real-time analyte concentrations within dynamic systems, the temporal resolution of the solid-phase microextraction (SPME) approach has been investigated. A mass-uptake model for SPME within a dynamic system was developed and validated, with experimental factors affecting the temporal resolution (sampling time, agitation, SPME fiber dimensions, sample concentration and change rate, and instrument sensitivity) characterized. Calibration methods for time-resolved sampling in a dynamic system were compared. To demonstrate the efficacy of time-resolved SPME, this approach was successfully applied to investigate the binding kinetics between plasma proteins and pharmaceuticals, which verified a decrease in free pharmaceutical concentrations over time in the presence of bovine serum albumin. The current study provides the theoretical and logistical framework for applying SPME to the real-time measurement of dynamic systems, facilitating future SPME applications such as in vivo metabolomic studies.
机译:为了解决在动态系统中测量实时分析物浓度的挑战,已经研究了固相微萃取(SPME)方法的时间分辨率。开发并验证了动态系统中SPME的质量吸收模型,并表征了影响时间分辨率(采样时间,搅拌,SPME纤维尺寸,样品浓度和变化率以及仪器灵敏度)的实验因素。比较了动态系统中时间分辨采样的校准方法。为了证明时间分辨的SPME的功效,该方法已成功地应用于研究血浆蛋白与药物之间的结合动力学,这证实了在牛血清白蛋白存在下游离药物浓度随时间的推移而降低。当前的研究提供了将SPME应用于动态系统实时测量的理论和后勤框架,为将来SPME的应用提供了便利,例如体内代谢组学研究。

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