Spruss T, Schertl S, Schneider M R, Gust R, Bauer K, Schönenberger H
Institut für Pharmazie, Universität Regensburg, Germany.
J Cancer Res Clin Oncol. 1993;119(12):707-16. doi: 10.1007/BF01195341.
The platinum complex [meso-1,2-bis(2,6-dichloro-4-hydroxyphenyl)- ethylenediamine]dichloroplatinum(II),K, was tested for its antitumor activity on hormone-sensitive tumor models under peroral administration. The resorption from the gastrointestinal tract was proved by determining the estrogenic effect of K in a dose/activity study using the immature-mouse uterine weight test. In comparison to the subcutaneous injection, a tenfold peroral dose was administered to achieve identical effects. By peroral treatment of the hormone-sensitive MXT(M3.2) mammary carcinoma of the mouse with K an almost complete inhibition of the tumor growth was obtained. This effect was superior to that of subcutaneously applied cisplatin and significantly better than that obtained by perorally administered ligand L at an equimolar dose, indicating that the antitumor effect is caused by the intact complex K and not by the liberated ligand L. The strong antitumor activity of perorally applied K was also demonstrated on the hormone-sensitive Noble Nb-R prostatic carcinoma of the rat. Histological examinations showed that the platinum complex K did not cause cisplatin-like kidney damage or irritations of gastric or intestinal mucosa when given perorally.
对铂配合物[内消旋-1,2-双(2,6-二氯-4-羟基苯基)-乙二胺]二氯铂(II),即K,进行了口服给药时对激素敏感肿瘤模型的抗肿瘤活性测试。通过使用未成熟小鼠子宫重量试验在剂量/活性研究中测定K的雌激素效应,证明了其从胃肠道的吸收情况。与皮下注射相比,口服剂量需增加10倍才能达到相同效果。通过用K口服治疗小鼠的激素敏感型MXT(M3.2)乳腺癌,几乎完全抑制了肿瘤生长。这种效果优于皮下应用顺铂,并且在等摩尔剂量下明显优于口服配体L所获得的效果,表明抗肿瘤作用是由完整的配合物K引起的,而不是由游离的配体L引起的。口服K对大鼠激素敏感型诺布尔Nb-R前列腺癌也显示出很强的抗肿瘤活性。组织学检查表明,口服铂配合物K不会引起类似顺铂的肾脏损伤或胃或肠黏膜刺激。