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一种新开发的用于可乐定的精确且灵敏的放射免疫测定法。

A newly developed precise and sensitive radioimmunoassay for clonidine.

作者信息

Arndts D, Stähle H, Struck C J

出版信息

Arzneimittelforschung. 1979;29(3):532-8.

PMID:582739
Abstract

A new precise and sensitive radioimmunoassay for clonidine has been developed. Synthesis and analysis of the hapten (4-carboxy-clonidine; St 1984) as well as antibody production in rabbits are described in detail. At a final dilution of 1:1000 the resulting immune serum binds 50% of a tritiated clonidine standard containing 1 ng of clonidine. The detection limit of the presented radioimmunoassay for clonidine is 0.1 ng/ml. The coefficient of variation did not exceed 4.3% for any of 7 standard determinations with 5 replicates. There was no relevant cross-reactivity of inactive clonidine metabolites apart from 4-OH-clonidine. To avoid any errors from cross-reaction clonidine was selectively and quantitatively extracted into diethylether from unknown plasma samples. Following concentration of the extracts even such low concentrations as 20 pg of clonidine/ml plasma were detectable. With the radioimmunoassay applied in pharmacokinetic studies a maximal clonidine concentration in blood plasma of healthy human volunteers was determined to 0.6 ng/ml 1.5 h after oral administration of 150 micrograms.

摘要

已开发出一种用于可乐定的新型精确且灵敏的放射免疫测定法。详细描述了半抗原(4-羧基可乐定;St 1984)的合成与分析以及兔体内抗体的产生。最终稀释度为1:1000时,所得免疫血清能结合含1 ng可乐定的氚标记可乐定标准品的50%。所呈现的可乐定放射免疫测定法的检测限为0.1 ng/ml。7次含5个重复的标准测定中,变异系数均未超过4.3%。除4-羟基可乐定外,无活性的可乐定代谢物无相关交叉反应。为避免交叉反应产生的任何误差,从未知血浆样本中选择性地将可乐定定量提取到二乙醚中。提取物浓缩后,即使血浆中可乐定浓度低至20 pg/ml也可检测到。将该放射免疫测定法应用于药代动力学研究,在150微克可乐定口服给药后1.5小时,测定健康人类志愿者血浆中可乐定的最大浓度为0.6 ng/ml。

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