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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >A double antibody radioimmunoassay for the determination of XV459, the active hydrolysis metabolite of roxifiban, in human plasma.
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A double antibody radioimmunoassay for the determination of XV459, the active hydrolysis metabolite of roxifiban, in human plasma.

机译:一种双抗体放射免疫测定法,用于测定人血浆中的roxifiban的活性水解代谢产物XV459。

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摘要

A radioimmunoassay (RIA) was developed for the determination of XV459, the active hydrolysis metabolite of the oral prodrug roxifiban (DMP 754), in human plasma. XV459 is a potent antagonist of the glycoprotein IIb/IIIa receptor. The method utilizes a competitive double antibody format employing an 125I-labeled XV459 analogue tracer which competes with XV459 for antibody binding sites and a second antibody precipitation step to separate antibody bound analyte from free analyte. The method has a validated lower quantification limit of 0.35 ng/ml (0.81 nM) using 12.5 microl of plasma and with dilution can accommodate clinical plasma samples ranging up to 48.0 ng/ml (110.7 nM). Cross-validation to an existing quantitative liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) method showed good correlation (r(2)=0.98). The RIA has been successfully used to assay over 10000 clinical samples with sensitivity and specificity comparable to the LC-MS/MS method, but with faster turn around time and at greatly reduced costs.
机译:开发了一种放射免疫测定(RIA),用于测定人血浆中口服前药roxifiban(DMP 754)的活性水解代谢产物XV459。 XV459是糖蛋白IIb / IIIa受体的有效拮抗剂。该方法利用竞争性双抗体形式,该形式采用125 I标记的XV459类似物示踪剂,该示踪剂与XV459竞争抗体结合位点,并进行第二次抗体沉淀步骤以将抗体结合的分析物与游离的分析物分开。该方法使用12.5微升血浆的经验证的较低定量下限为0.35 ng / ml(0.81 nM),稀释后可容纳高达48.0 ng / ml(110.7 nM)的临床血浆样品。对现有的定量液相色谱-质谱/质谱(LC-MS / MS)方法进行交叉验证显示出良好的相关性(r(2)= 0.98)。 RIA已成功用于测定10000多个临床样品,其灵敏度和特异性与LC-MS / MS方法相当,但具有更快的周转时间和大大降低的成本。

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