Willson V J, Preston J R, Lockley W J, Singh J, Wilkinson D
Department of Physical Chemistry, Astra Charnwood, Loughborough, Leics., UK.
J Pharm Biomed Anal. 1996 Mar;14(5):593-600. doi: 10.1016/0731-7085(95)01643-0.
A radioimmunoassay has been developed for the determination of ARL 15849XX, a cholecystokinin-8 (CCK-8) analogue, in dog plasma. The method incorporates solid-phase sample extraction and is suitable for the determination of the analyte at picogram per millilitre concentrations. The antiserum was raised in Suffolk-cross sheep following primary and booster immunisations with an immunogen prepared by conjugating ARL 16935XX, an analogue of ARL 15849KF, to bovine serum albumin. The radioligand was prepared by the no-carrier-added 125I iodination of a non-sulphated derivative, ARL 15745XX. The solid-phase extraction procedure, carried out using ion-exchange aminopropyl and octadecyl sorbents sequentially, was introduced to remove matrix interferences in the plasma and to enhance the method sensitivity. The calibration range is 20-1000 pg ml-1, using a 1 ml sample of undiluted dog plasma.
已开发出一种放射免疫分析法,用于测定犬血浆中的胆囊收缩素-8(CCK-8)类似物ARL 15849XX。该方法采用固相样品萃取,适用于测定皮克每毫升浓度的分析物。用ARL 15849KF的类似物ARL 16935XX与牛血清白蛋白偶联制备免疫原,经初次和加强免疫后,在萨福克杂交绵羊中制备抗血清。放射性配体由非硫酸化衍生物ARL 15745XX的无载体添加125I碘化制备。采用离子交换氨丙基和十八烷基吸附剂依次进行固相萃取程序,以去除血浆中的基质干扰并提高方法灵敏度。使用1毫升未稀释的犬血浆样品,校准范围为20-1000 pg ml-1。