Collste P, Garle M, Rawlins M D, Sjöqvist F
Eur J Clin Pharmacol. 1976 Feb 6;9(4):319-25. doi: 10.1007/BF00561667.
A gas chromatographic method has been employed to determine chlorthalidone in plasma and whole blood after therapeutic doses. Radioactively labelled chlorthalidone was used for in vitro studies of the uptake of chlorthalidone from plasma by red blood cells. Chlorthalidone was markedly concentrated in red cells and as a compartment they would account for at least 30% of total drug in the body after multiple doses. The ratio between the plasma and red cell concentration of chlorathidone varied between individuals. After a single oral dose of 50 mg in 6 healthy volunteers chlorthalidone was eliminated with a half-life of 51 to 89 hours. The apparent volume of distribution varied between 3 and 13 1/kg and the clearance between 53 and 145 ml/min. The mean steady-state plasma concentrations during treatment with a standard dose of 50 mg daily (n = 10) varied 5-fold between individuals. During the steady state approximately 50% of the daily dose was excreted unchanged in the urine during 24 hrs. The plasma levels observed in patients were higher than those preducted from the single oral dose studies in healthy volunteers.
已采用气相色谱法测定治疗剂量后血浆和全血中的氯噻酮。用放射性标记的氯噻酮进行体外研究,以观察红细胞从血浆中摄取氯噻酮的情况。氯噻酮在红细胞中显著浓集,作为一个隔室,多次给药后它们在体内至少占总药物的30%。氯噻酮的血浆浓度与红细胞浓度之比在个体间有所不同。6名健康志愿者单次口服50 mg后,氯噻酮的消除半衰期为51至89小时。表观分布容积在3至13 l/kg之间,清除率在53至145 ml/min之间。每日标准剂量50 mg治疗期间(n = 10),个体间平均稳态血浆浓度相差5倍。在稳态期间,约5%的每日剂量在24小时内以原形经尿液排泄。在患者中观察到的血浆水平高于在健康志愿者单次口服剂量研究中预测的水平。