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两种非对映异构体地塞米松和倍他米松在兔血浆和脑脊液中的比较药代动力学

Comparative pharmacokinetics of two diastereoisomers dexamethasone and betamethasone in plasma and cerebrospinal fluid in rabbits.

作者信息

Trenque T, Lamiable D, Vistelle R, Millart H, Leperre A, Choisy H

机构信息

Laboratoire de Pharmacologie, CHU Maison Blanche, Reims, France.

出版信息

Fundam Clin Pharmacol. 1994;8(5):430-6. doi: 10.1111/j.1472-8206.1994.tb00822.x.

Abstract

The two diastereoisomers dexamethasone (DXM) and betamethasone (BTM) were infused at two different doses (2, 10 mg.kg-1) in anesthetized rabbits. Samples of plasma and cerebrospinal fluid were collected over a 180-min period. Steroid concentrations were measured by high performance liquid chromatography. The terminal half life (85.7 +/- 20.8 min and 102.2 +/- 29.6 min for DXM; 117.6 +/- 19.8 min and 118.5 +/- 15.8 min for BTM) and the mean residence time (121.4 +/- 27.7 min and 146.1 +/- 41.3 min for DXM; 168.6 +/- 28.1 min and 172.2 +/- 20.6 min for BTM) were unchanged between the doses. Dose-dependent changes in the area under the curve normalized by the dose, then volume distribution and clearance were observed. The average percentage of DXM and BTM bound to plasma proteins were 78.1 +/- 11.5% and 88.3 +/- 5.1% respectively at the lower dose, and decreased significantly with 10 mg.kg-1. DXM appeared more rapidly in the CSF, the highest concentrations of DXM were obtained within 15 min after the end of the injection. The CSF levels were lower than that of plasma unbound and the passage through the blood-brain barrier was saturable. These results will complicate pharmacokinetic and pharmacodynamic analysis.

摘要

将地塞米松(DXM)和倍他米松(BTM)这两种非对映异构体以两种不同剂量(2、10mg·kg⁻¹)注入麻醉的兔子体内。在180分钟内采集血浆和脑脊液样本。通过高效液相色谱法测量类固醇浓度。两种剂量下,终末半衰期(DXM分别为85.7±20.8分钟和102.2±29.6分钟;BTM分别为117.6±19.8分钟和118.5±15.8分钟)和平均驻留时间(DXM分别为121.4±27.7分钟和146.1±41.3分钟;BTM分别为168.6±28.1分钟和172.2±20.6分钟)没有变化。观察到剂量归一化曲线下面积、然后体积分布和清除率的剂量依赖性变化。较低剂量时,与血浆蛋白结合的DXM和BTM的平均百分比分别为78.1±11.5%和88.3±5.1%,在10mg·kg⁻¹时显著降低。DXM在脑脊液中出现得更快,注射结束后15分钟内达到DXM的最高浓度。脑脊液水平低于血浆未结合水平,通过血脑屏障的过程是可饱和的。这些结果将使药代动力学和药效学分析复杂化。

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