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采用特异性放射免疫分析法研究硫代秋水仙苷在人体内的药代动力学。

Pharmacokinetics of thiocolchicoside in humans using a specific radioimmunoassay.

作者信息

Sandouk P, Chappey O, d'Yvoire M B, Scherrmann J M

机构信息

INSERM U.26, Hôpital F. Widal, Paris, France.

出版信息

Ther Drug Monit. 1995 Oct;17(5):544-8. doi: 10.1097/00007691-199510000-00018.

Abstract

The myorelaxant thiocolchicoside (TC), an analogue of colchicine (COL), was assayed in plasma and urine by a radioimmunoassay (RIA) using a cross-reacting COL-specific polyclonal antibody. Cross-reactivity was 56% for TC, giving a limit of quantification of 0.5 ng/ml and a linear response from 0.5 to 100 ng/ml. Specificity was checked by cross-reactivity studies with COL analogues and by using liquid chromatography and RIA in tandem on urine samples. Two immunoreactive peaks were detected, but the nonspecific peak represented < 2% of the total urine concentration of TC. Pharmacokinetics of TC following infusion of 4 mg in two subjects revealed a moderate distribution (Vss from 31 to 35 L) and mainly extrarenal elimination (75% of the total body clearance). Terminal half-lives ranged from 2.4 to 2.7 h in plasma and from 3.2 to 3.7 h in urine.

摘要

使用与秋水仙碱(COL)交叉反应的特异性多克隆抗体,通过放射免疫分析法(RIA)对肌松剂硫代秋水仙碱(TC)进行血浆和尿液检测,TC是COL的类似物。TC的交叉反应率为56%,定量限为0.5 ng/ml,线性响应范围为0.5至100 ng/ml。通过与COL类似物的交叉反应研究以及对尿液样本串联使用液相色谱和RIA来检查特异性。检测到两个免疫反应峰,但非特异性峰占TC总尿液浓度的比例不到2%。两名受试者输注4 mg TC后的药代动力学显示分布适中(稳态分布容积为31至35 L),主要经肾外消除(占全身清除率的75%)。血浆中终末半衰期为2.4至2.7小时,尿液中为3.2至3.7小时。

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