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首页> 外文期刊>Journal of Analytical Toxicology >Elimination of cocaine and metabolites in plasma, saliva, and urine following repeated oral administration to human volunteers.
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Elimination of cocaine and metabolites in plasma, saliva, and urine following repeated oral administration to human volunteers.

机译:反复向人类志愿者口服后,消除血浆,唾液和尿液中的可卡因和代谢产物。

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Chronic administration of lipophilic drugs can result in accumulation and prolonged elimination during abstinence. It has been suggested that cocaine and/or metabolites can be detected in saliva and urine for an extended period following long-term, high-dose administration. The effects of chronic oral cocaine administration in healthy volunteer subjects with a history of cocaine abuse were investigated. Subjects were housed on a closed clinical ward and were administered oral cocaine in up to 16 daily sessions. In each session, volunteers received five equal doses of oral cocaine with 1 h between doses. Across sessions, cocaine was administered in ascending doses from an initial dose of 100 mg (500 mg/day) up to 400 mg (2 g/day), increasing by 25 mg/dose/session (125 mg/session). Participation in the study was terminated if cardiovascular safety parameters were exceeded. Plasma and saliva specimens were collected periodically during the dosing sessions and during the one-week withdrawal phase at the end of the study. All urine specimens were collected throughout the entire study. Specimens were analyzed for cocaine and metabolites by solid-phase extraction followed by gas chromatographic-mass spectrometric analysis in the SIM mode. The limit of detection for each analyte was approximately 1 ng/mL. The analytes measured included benzoylecgonine (BZE), ecgonine methyl ester, cocaine, benzoylnorecgonine, norcocaine, m- and p-hydroxycocaine, and m- and p-hydroxybenzoylecgonine. Noncompartmental analysis was employed for the determination of plasma and saliva pharmacokinetic parameters. Urinary elimination half-lives for cocaine and metabolites were determined by constructing ARE (amount remaining to be excreted) plots. Two phases of urinary elimination of cocaine and metabolites were observed. An initial elimination phase was observed during withdrawal that was similar to the elimination pattern observed after acute dosing. The mean (N = 6) plasma, saliva, and urine cocaine elimination half-lives were 1.5 +/- 0.1 h, 1.2 +/- 0.2 h, and 4.1 +/- 0.9 h, respectively. For three subjects, the mean cocaine urinary elimination half-life for the terminal phase was 19.0 +/- 4.2 h. There was some difficulty in determining if a terminal elimination phase for cocaine was present for the remaining three subjects because of interference by high concentrations of BZE. A terminal elimination phase was also observed for cocaine metabolites with half-life estimates ranging from 14.6 to 52.4 h. These terminal elimination half-lives greatly exceeded previous estimates from studies of acute cocaine administration. These data suggest that cocaine accumulates in the body with chronic use resulting in a prolonged terminal elimination phase for cocaine and metabolites.
机译:长期施用亲脂性药物可导致禁欲期间的蓄积和长期消除。有人提出,长期,大剂量给药后,可在唾液和尿液中检测到可卡因和/或代谢产物很长时间。调查了长期服用可卡因对有可卡因滥用历史的健康志愿者的影响。将受试者安置在封闭的临床病房中,并在每天最多16次疗程中口服可卡因。在每个疗程中,志愿者接受五次相等剂量的口服可卡因,每次给药之间间隔1小时。在整个疗程中,可卡因以从最初的100毫克(500毫克/天)到400毫克(2克/天)的递增剂量递增给药,以25毫克/剂量/疗程(125毫克/疗程)增加。如果超过心血管安全参数,则终止参与研究。在给药期间和研究结束后的为期一周的戒断阶段中定期收集血浆和唾液标本。在整个研究过程中收集所有尿液标本。通过固相萃取,然后在SIM模式下进行气相色谱-质谱法分析样品中的可卡因和代谢物。每种分析物的检出限约为1 ng / mL。测得的分析物包括苯甲酰基芽子碱(BZE),芽子碱甲酯,可卡因,苯甲酰基正芽子碱,降丁卡因,间羟基和对羟基可卡因以及间羟基和对羟基苯甲酰基芽子碱。非房室分析用于确定血浆和唾液的药代动力学参数。可卡因和代谢产物的排尿半衰期是通过构建ARE(待排泄量)图来确定的。观察到尿液中可卡因和代谢物的清除分为两个阶段。在撤药期间观察到初始消除阶段,类似于急性给药后观察到的消除模式。血浆,唾液和尿液中可卡因消除的平均(N = 6)半衰期分别为1.5 +/- 0.1小时,1.2 +/- 0.2小时和4.1 +/- 0.9小时。对于三名受试者,末期的平均可卡因排尿半衰期为19.0 +/- 4.2 h。由于高浓度BZE的干扰,在确定其余三个受试者是否存在可卡因的终末消除阶段方面存在一些困难。可卡因代谢物也观察到了最终消除阶段,其半衰期估计范围为14.6至52.4小时。这些终末消除半衰期大大超过了先前从急性可卡因给药研究中得出的估计值。这些数据表明,长期使用可卡因会在体内蓄积,导致可卡因和代谢产物的最终消除期延长。

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