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膦甲酸钠在人类免疫缺陷病毒患者静脉注射和口服给药后的药代动力学及吸收情况。

Pharmacokinetics and absorption of foscarnet after intravenous and oral administration to patients with human immunodeficiency virus.

作者信息

Sjövall J, Karlsson A, Ogenstad S, Sandström E, Saarimäki M

机构信息

Department of Clinical Pharmacology, Astra Alab AB, Södertälje, Sweden.

出版信息

Clin Pharmacol Ther. 1988 Jul;44(1):65-73. doi: 10.1038/clpt.1988.114.

Abstract

Six patients with human immunodeficiency virus were given foscarnet in oral solution, 4000 mg every 6 hours for 3 days, followed by a washout period for 2 days and continuous intravenous infusion of 16,000 mg/24 hr over 72 hours. After oral foscarnet, plasma concentrations were less than 33 mumol/L in four patients; two had occasional concentrations of 35 to 50 mumol/L. The extent of absorption varied between 12% and 22%. During intravenous infusion, plasma concentrations ranged between 75 and 265 mumol/L. The disposition of foscarnet was triphasic, with mean half-lives of 0.45, 3.3, and 18 hours. Excretion data suggested elimination was by tubular secretion and glomerular filtration. Renal clearance was 176 ml/min 1.73 m2. The apparent nonrenal clearance, 40 ml/min 1.73 m2, probably reflects sequestration of foscarnet into bone. Ten percent to 28% of the cumulative dose may have been deposited in bone 2 days after infusion. A slight increase in serum calcium levels and changes in serum phosphate values may reflect the uptake of foscarnet in bone. Five patients had diarrhea (oral) and two had thrombophlebitis (intravenous).

摘要

6例人类免疫缺陷病毒患者接受了口服膦甲酸钠治疗,每6小时4000毫克,共3天,随后有2天的洗脱期,然后在72小时内持续静脉输注16000毫克/24小时。口服膦甲酸钠后,4例患者的血浆浓度低于33微摩尔/升;2例患者偶尔有35至50微摩尔/升的浓度。吸收程度在12%至22%之间变化。静脉输注期间,血浆浓度在75至265微摩尔/升之间。膦甲酸钠的处置呈三相,平均半衰期分别为0.45小时、3.3小时和18小时。排泄数据表明其通过肾小管分泌和肾小球滤过清除。肾脏清除率为176毫升/分钟/1.73平方米。表观非肾脏清除率为40毫升/分钟/1.73平方米,可能反映了膦甲酸钠在骨骼中的螯合。输注后2天,累积剂量的10%至28%可能已沉积在骨骼中。血清钙水平略有升高和血清磷酸盐值的变化可能反映了膦甲酸钠在骨骼中的摄取。5例患者出现腹泻(口服),2例出现血栓性静脉炎(静脉注射)。

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