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Microdialysis sampling and high-performance liquid chromatography with chemiluminescence detection for in-vivo on-line determination and study of the pharmacokinetics of levodopa in blood

机译:微透析取样和高效液相色谱-化学发光检测用于体内在线测定和血液中左旋多巴的药代动力学研究

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摘要

A simple, reliable, and reproducible method for in-vivo on-line separation and determination of levodopa has been based on microdialysis then high-performance liquid chromatography with chemiluminescence detection. The perfusate is perfused at a flow rate of 5 mu L min(-1). The concentration of levodopa in the dialysate is determined on line with a chemiluminescence system. The dialysate sample volume is approximately 20 mu L. The response of the system is linearly related to the concentration of levodopa in the range 1 x 10(-8) to 1 x 10(-6) g mL(-1) (r(2) = 0.9995) with a detection limit (3 sigma) of 3 x 10(-9) g mL(-1) and sample throughput of 12 h(-1); RSD is 2.8% (n = 11). The method has been successfully used to study the pharmacokinetics of levodopa in vivo; the values of the pharmacokinetics parameters C-max, AUC(0) (t) and T-max were 16.60, 20.92 ng mL(-1), and 90 min, respectively.
机译:一种简单,可靠且可重现的体内在线分离和测定左旋多巴的方法,是基于微透析,然后采用化学发光检测的高效液相色谱法。以5μL min(-1)的流速灌注灌注液。通过化学发光系统在线测定透析液中左旋多巴的浓度。透析液样品量约为20μL。系统的响应与左旋多巴的浓度在1 x 10(-8)至1 x 10(-6)g mL(-1)(r( 2)= 0.9995),检测极限(3 sigma)为3 x 10(-9)g mL(-1),样品通量为12 h(-1); RSD为2.8%(n = 11)。该方法已成功用于研究左旋多巴的体内药代动力学。药代动力学参数C-max,AUC(0)(t)和T-max的值分别为16.60、20.92 ng mL(-1)和90分钟。

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