Axelsson C K, Damkjaer Nielsen M, Kappelgaard A M
Clin Chim Acta. 1982 Jun 3;121(3):309-19. doi: 10.1016/0009-8981(82)90240-6.
A solid-phase radioimmunoassay for the determination of pepsinogen I in serum has been developed. The antibody was raised in rabbits with pepsinogen I isolated from urine as previously described. Radioiodination was carried out with a chloramine-T procedure resulting in a tracer with excellent shelf life. In the standard procedure with a 24-h incubation time, followed by 2-h incubation with a second antibody coupled to a solid phase, 50 microliter serum was analyzed, standard range 1.88-60 ng PG I. An eight times more sensitive method was also developed using sequential saturation techniques. Specificity studies demonstrated 0.6% crossreactivity with PG II. The immunoreactivity of PG I purified from urine was nearly identical with the immunoreactivity of PG I purified from gastric mucosa. The levels of PG I in serum from 121 control subjects were similar to those obtained with conventional phase separation methods. It is concluded that the method is simple, precise and free from non-specific serum interference.
已开发出一种用于测定血清中胃蛋白酶原I的固相放射免疫分析方法。如前所述,用从尿液中分离出的胃蛋白酶原I对兔子进行免疫,从而产生抗体。采用氯胺-T法进行放射性碘化,得到的示踪剂保质期长。在标准程序中,先进行24小时孵育,然后与偶联到固相上的第二抗体进行2小时孵育,分析50微升血清,标准范围为1.88 - 60 ng PG I。还采用连续饱和技术开发了一种灵敏度高八倍的方法。特异性研究表明与胃蛋白酶原II的交叉反应率为0.6%。从尿液中纯化的胃蛋白酶原I的免疫反应性与从胃黏膜中纯化的胃蛋白酶原I的免疫反应性几乎相同。121名对照受试者血清中胃蛋白酶原I的水平与用传统相分离方法得到的水平相似。结论是该方法简单、精确且无血清非特异性干扰。