Besch W, Woltanski K P, Knospe S, Ziegler M, Keilacker H
Acta Biol Med Ger. 1980;39(4):495-502.
A reproducible method for preparation of 125I-monoiodoinsulin with fully biological activity was developed. Monoiodoinsulin has been prepared from a heterogeneous 125I-iodination mixture by anion exchange chromatography on DEAE-Sephadex A-25 without using any gradient elution technique. The specific radioactivity of 125I-monoiodoinsulin was calculated to 14.3 +/- 0.8 TBq/g, i.e. an iodine content of 1.04 +/- 0.06 atoms per molecule of insulin. Monoiodoinsulin was indistinguishable from native insulin with respect to binding to guinea pig anti-insulin serum, and to insulin receptors of isolated rat adipocytes. The biological potency (96.5 +/- 7.5 per cent of the immunoreactive insulin activity) determined by the conversion of [14C1]-D-glucose to 14CO2 in vitro by rat fat cells was not significantly different from that of native insulin.
开发了一种制备具有完全生物活性的125I-单碘胰岛素的可重复方法。通过在DEAE-葡聚糖A-25上进行阴离子交换色谱,从异质的125I碘化混合物中制备单碘胰岛素,无需使用任何梯度洗脱技术。计算得出125I-单碘胰岛素的比放射性为14.3±0.8 TBq/g,即每分子胰岛素的碘含量为1.04±0.06个原子。在与豚鼠抗胰岛素血清结合以及与分离的大鼠脂肪细胞的胰岛素受体结合方面,单碘胰岛素与天然胰岛素没有区别。通过大鼠脂肪细胞在体外将[14C1]-D-葡萄糖转化为14CO2测定的生物活性(免疫反应性胰岛素活性的96.5±7.5%)与天然胰岛素没有显著差异。