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[生物体液中一种新型β受体阻滞剂阿替洛尔的荧光分光光度法测定及其在药代动力学研究中的应用(作者译)]

[Spectrofluorimetric estimation in biological fluids of a new beta-blockader: atenolol. Application to its pharmacokinetic study (author's transl)].

作者信息

Flouvat B, Bazin M, Lucsko M, Roux A, Guedon J

出版信息

Ann Biol Clin (Paris). 1978;36(4):339-46.

PMID:32816
Abstract

The authors describe a simple method of fluorimetric estimation of atenolol, applicable to blood and urine, sufficiently sensitive to permit a pharmacokinetic study. After administration of a dose of 200 mg by the oral route to hypertensive subjects, one may observe a maximal plasma concentration 3 hours after the dose average value 3.91 +/- 0.71 mumol/l (1.04 +/- 0.19 mg/l). The apparent half life of elimination of phase beta is 14.1 +/- 4.9 h, values comparable with those calculated from urinary data 14.6 +/- 2.0 h. The renal clearance was 140 +/- 32 ml/min; 54 +/- 14% of the administered dose are excreted in the urine. After administration by the venous route, urinary excretion represents 96% of the dose administered.

摘要

作者描述了一种简单的阿替洛尔荧光测定法,适用于血液和尿液,灵敏度足以进行药代动力学研究。给高血压受试者口服200毫克剂量后,给药后3小时可观察到最大血浆浓度,平均值为3.91±0.71微摩尔/升(1.04±0.19毫克/升)。β相消除的表观半衰期为14.1±4.9小时,与根据尿液数据计算的14.6±2.0小时的值相当。肾清除率为140±32毫升/分钟;给药剂量的54±14%经尿液排泄。静脉给药后,尿液排泄占给药剂量的96%。

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