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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 >The development of a sensitive and specific enzyme immunoassay for FK480, a novel cholecystokinin type-A receptor antagonist, in human plasma.
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The development of a sensitive and specific enzyme immunoassay for FK480, a novel cholecystokinin type-A receptor antagonist, in human plasma.

机译:FK480,一种新型的A型胆囊收缩素受体拮抗剂,在人血浆中的灵敏和特异性酶免疫测定方法的开发。

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A sensitive and specific enzyme immunoassay for FK480, a novel cholecystokinin type-A (CCK-A) receptor antagonist, was developed to study the pharmacokinetics of the drug at low-dose administration using a specific monoclonal antibody. The high performance liquid chromatography (HPLC) method had been used for studying toxicokinetics, but its determination limit (2.5 ng ml-1) was too high for use in clinical studies. Subsequently we developed an enzyme immunoassay (EIA) using rabbit anti-FK480 serum (polyclonal antibody). It had higher sensitivity (0.1 ng ml-1) when 0.5 ml of plasma was used but its specificity was low because of the cross-reactivity of the metabolites of FK480. Therefore we produced several monoclonal antibodies for FK480 by cell fusion, and selected the antibody which was least cross-reactive for the isolated metabolites of FK480. Finally we developed a sensitive and specific EIA using this monoclonal antibody. The lower limit of quantification of this method was 0.2 ng ml-1 when 0.2 ml of human plasma was used. The coefficient of variation over the calibration range (0.2-10 ng ml-1) was less than 15%. We used this method for clinical studies, and it showed a good correlation to the HPLC method when plasma concentration was 2.5 ng ml-1 or more.
机译:开发了一种针对FK480(一种新型的A型胆囊收缩素(CCK-A)受体拮抗剂)的灵敏且特异性的酶免疫分析方法,以研究使用特定的单克隆抗体低剂量给药时该药物的药代动力学。高效液相色谱(HPLC)方法已用于研究毒物动力学,但其测定限(2.5 ng ml-1)太高,无法用于临床研究。随后,我们使用兔抗FK480血清(多克隆抗体)开发了一种酶免疫法(EIA)。当使用0.5 ml血浆时,它具有较高的灵敏度(0.1 ng ml-1),但由于FK480代谢物的交叉反应性,其特异性较低。因此,我们通过细胞融合产生了几种针对FK480的单克隆抗体,并选择了对FK480分离的代谢产物交叉反应最小的抗体。最后,我们使用该单克隆抗体开发了灵敏且特异的EIA。当使用0.2 ml人血浆时,该方法的定量下限为0.2 ng ml-1。在校准范围(0.2-10 ng ml-1)内的变异系数小于15%。我们将该方法用于临床研究,当血浆浓度为2.5 ng ml-1或更高时,它与HPLC方法显示出良好的相关性。

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