首页> 外文期刊>Therapeutic Drug Monitoring >Disposition of gamma-hydroxybutyric acid in conventional and nonconventional biologic fluids after single drug administration: issues in methodology and drug monitoring.
【24h】

Disposition of gamma-hydroxybutyric acid in conventional and nonconventional biologic fluids after single drug administration: issues in methodology and drug monitoring.

机译:单一药物给药后常规和非常规生物流体中γ-羟基丁酸的处置:方法学和药物监测方面的问题。

获取原文
获取原文并翻译 | 示例
           

摘要

Little controlled drug administration data are available to aid in the interpretation of gamma-hydroxybutyric acid (GHB) distribution in conventional and nonconventional fluids and the potential correlation between the pharmacokinetics of GHB and drug effects. Single oral sodium GHB doses of 50 mg/kg were administered to five volunteers. Plasma, oral fluid, urine, and sweat were analyzed for GHB by gas chromatography-mass spectrometry. GHB stability in plasma was studied at different storage temperatures. Subjective effects were measured using a set of 13 different visual analog scales. Mean peak GHB plasma concentrations at 30 minutes were 83.1 microg/mL. After the absorption phase, concentrations declined to mean values of 0.9 microg/mL at 6 hours. GHB was found in oral fluid at peak value concentrations equivalent to one third to one fourth of those found in plasma. The oral fluid-to-plasma ratio varied two fold in the 1- to 6-hour time range but always was lower than unit. The mean half-life (t1/2)of GHB was approximately 0.7 hour in plasma and approximately 1.2 hours in oral fluid. GHB urinary excretion is less than 2% of the dose administered. GHB was also detected in sweat at low concentrations. GHB showed a mixed sedative-stimulant pattern with subjective effects peaking between 1 and 1.5 hours after drug administration and lasting for 2 hours. Oral fluid and sweat appeared not to be suitable biologic matrices for monitoring GHB consumption. GHB-mediated subjective effects are related to GHB plasma concentrations.
机译:几乎没有药物控制数据可用于解释常规和非常规液体中γ-羟基丁酸(GHB)的分布以及GHB药代动力学与药物作用之间的潜在相关性。五名志愿者服用了50 mg / kg的单次口服GHB钠剂量。通过气相色谱-质谱法分析血浆,口腔液,尿液和汗液中的GHB。在不同的储存温度下研究了血浆中GHB的稳定性。使用一组13种不同的视觉模拟量表来测量主观效果。 30分钟时的GHB血浆平均峰值浓度为83.1 microg / mL。吸收阶段之后,浓度在6小时下降至0.9微克/毫升的平均值。在口腔液中发现的GHB的峰值浓度相当于血浆中的GHB的三分之一至四分之一。口服液与血浆的比率在1至6小时的时间范围内变化了两倍,但始终低于单位。 GHB的平均半衰期(t1 / 2)在血浆中约为0.7小时,在口服液中约为1.2小时。 GHB尿液排泄量小于给药剂量的2%。在低浓度的汗液中也检测到了GHB。 GHB显示出混合的镇静-兴奋剂模式,其主观作用在给药后1至1.5小时达到峰值,并持续2小时。口服液和汗液似乎不是监测GHB摄入量的合适生物基质。 GHB介导的主观效应与GHB血浆浓度有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号