杨莉, 陈志良, 王新亚. 吹扫捕集-气相色谱-质谱联用测定试验犬体内全氟丙烷血药浓度J. 药学学报, 2005, 40(4): 358-360.
引用本文: 杨莉, 陈志良, 王新亚. 吹扫捕集-气相色谱-质谱联用测定试验犬体内全氟丙烷血药浓度J. 药学学报, 2005, 40(4): 358-360.
YANG Li, CHEN Zhi-liang, WANG Xin-ya. Determination of perfluoropropane in canine whole blood by purge and trap concentrator-GC-MSJ. Acta Pharmaceutica Sinica, 2005, 40(4): 358-360.
Citation: YANG Li, CHEN Zhi-liang, WANG Xin-ya. Determination of perfluoropropane in canine whole blood by purge and trap concentrator-GC-MSJ. Acta Pharmaceutica Sinica, 2005, 40(4): 358-360.

吹扫捕集-气相色谱-质谱联用测定试验犬体内全氟丙烷血药浓度

Determination of perfluoropropane in canine whole blood by purge and trap concentrator-GC-MS

  • 摘要: 目的建立对一种新型的包裹全氟丙烷气体的白蛋白微囊超声造影剂静脉给药后直接测定全氟丙烷血药浓度的方法,研究全氟丙烷在试验犬体内的药代动力学行为。方法试验犬麻醉后静脉给药,给药剂量0.6 mL·kg-1,取全血样品,直接进样。应用Tekmar 3000吹扫捕集-气相色谱质谱组合分析仪对全氟丙烷血药浓度进行定量分析,用非室模型计算药代动力学参数。结果全氟丙烷测定的线性范围为0.016 8-4.03 mg·L-1。主要药代动力学参数平均滞留时间(MRT)为(63±5) s,T1/2为(44±4) s,Tmax为30 s,Cmax为(2.20±0.20) mg·L-1,AUC0-∞为(96±11) mg·s·L-1。结论该法简便、快速、灵敏度好、精密度高。可用于包裹氟碳类气体的微囊类超声造影剂的药代动力学研究

     

    Abstract: AimTo develop a method for direct determination of perfluoropropane in canine whole blood and to study its pharmacokinetics after a suspension of perfluoropropane-containing albumin microcapsules was administered intravenously. MethodsPerfluoropropane-containing albumin microcapsule suspension was administered intravenously to anesthetized canines at the dosage of 0.6 mL·kg-1. Whole blood samples were collected and added directly into the purging glass tube in Tekmar 3000 Purge and Trap Concentrator coupled with a GC-MS for the determination of perfluoropropane. The pharmacokinetic parameters of perfluoropropane were calculated by non-compartment model statistics. ResultsThe linear range was 0.016 8-4.03 mg·L-1. The main pharmacokinetic parameters of perfluoropropane was obtained as follows: mean residence time (MRT) was (63±5) s, T1/2 was (44±4) s, Tmax was 30 s, Cmax was (2.20±0.20) mg·L-1, AUC0-∞ was (96±11) mg·s·L-1. ConclusionThe method is sensitive, specific and simple. It can be used to determine fluorocarbon contained in microcapsule ultrasound contrast agents for studying its pharmacokinetics.

     

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