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咖啡因在人体中的血浆和唾液药代动力学。

Plasma and salivary pharmacokinetics of caffeine in man.

作者信息

Newton R, Broughton L J, Lind M J, Morrison P J, Rogers H J, Bradbrook I D

出版信息

Eur J Clin Pharmacol. 1981;21(1):45-52. doi: 10.1007/BF00609587.

Abstract

Plasma and salivary caffeine concentrations were measured by gas-liquid chromatography in 6 healthy caffeine-free volunteers following oral administration of 50, 300, 500 and 750 mg caffeine. Caffeine was also given to a single subject intravenously in doses of 300, 500 and 750 mg. Caffeine was rapidly absorbed and was completely available at all doses. The apparent first-order elimination rate constant decreased linearly with dose and was 0.163 +/- 0.081 h-1 for 50 mg and 0.098 +/- 0.027 h-1 for 750 mg. The total body clearance was unaffected by dose and was 0.98 +/- 0.38 ml/min/kg. There was a trend towards increasing apparent volume of distribution with increasing dose. A linear relationship existed between the area under the plasma concentration, time curve and dose and dose-normalised plasma concentration, time plots were superimposable. These findings suggest that caffeine obeys linear pharmacokinetics over the dose range investigated. Despite significant inter-individual differences in pharmacokinetic parameters there was good reproducibility within 5 subjects given 300 mg caffeine orally on 3 occasions. Salivary caffeine levels probably reflect the unbound plasma caffeine concentration and can be used to estimate the pharmacokinetic parameters of the drug. Overall the saliva/plasma concentration ratio was 0.74 +/- 0.08 but within subjects some time-dependence of the ratio was found with higher ratios initially (even after intravenous administration) and lower ratios at longer time intervals after the dose. Urinary elimination of caffeine was low and independent of dose: 1.83% of the dose was eliminated unchanged.

摘要

在6名健康的未摄入咖啡因的志愿者口服50、300、500和750毫克咖啡因后,通过气液色谱法测量了血浆和唾液中的咖啡因浓度。还对一名受试者静脉注射了300、500和750毫克剂量的咖啡因。咖啡因吸收迅速,在所有剂量下均可完全吸收。表观一级消除速率常数随剂量呈线性下降,50毫克时为0.163±0.081 h⁻¹,750毫克时为0.098±0.027 h⁻¹。总体清除率不受剂量影响,为0.98±0.38毫升/分钟/千克。分布容积有随剂量增加而增加的趋势。血浆浓度-时间曲线下面积与剂量之间存在线性关系,剂量归一化的血浆浓度-时间图可叠加。这些发现表明,在所研究的剂量范围内,咖啡因遵循线性药代动力学。尽管药代动力学参数存在显著的个体间差异,但5名受试者在3次口服300毫克咖啡因时,结果具有良好的重现性。唾液中的咖啡因水平可能反映了未结合的血浆咖啡因浓度,可用于估计药物的药代动力学参数。总体而言,唾液/血浆浓度比为0.74±0.08,但在个体内发现该比值存在一定的时间依赖性,最初比值较高(即使在静脉注射后),给药后较长时间间隔时比值较低。咖啡因的尿排泄量较低且与剂量无关:给药剂量的1.83%以原形排出。

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