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Pre-equilibrium In vivo Soild Phase Microextraction for Monitoring Drug Concentration Changes in Brain Tissue

机译:体内固相微萃取的预平衡以监测脑组织的药物浓度变化

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An advantage of pre-equilibrium solid phase microextraction (SPME) method has been utilized to quantitatively determine the concentrations of carbamazepine from the cortex and striatum regions of the brain of freely moving rats. The method was validated with a parallel microdialysis sampling and the results compared with conventional plasma sample analysis. A 10-min extraction was employed for SPME extractions while 30 min sampling time was required for MD. A pharmacokinetic studies of carbamazepine in both steady and dynamic states was investigated using microdialysis and SPME. Comparable results were obtained for both methods. Drug concentrations in the cortex and striatum measured with solid phase extraction method did not show any significant differences. The CV(percent) recorded for both methods were <= 15.
机译:已经利用预平衡固相微萃取(SPME)方法的优点来定量地确定来自自由移动大鼠脑的皮层和纹状体区域的群毒物的浓度。与常规等离子体样品分析相比,该方法用平行的微透析抽样和结果进行了验证。使用10分钟的萃取用于SPME提取,而MD需要30分钟的取样时间。使用微透析和SPME研究了稳态和动态状态的颅脑中的药代动力学研究。两种方法获得了可比的结果。用固相萃取方法测量的皮质和纹状体中的药物浓度没有显示出任何显着差异。为两种方法记录的CV(百分比)是<= 15。

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