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Zusammenfassung
After the administration of cis-Pt (gly-gly-OEt)2Cl2 complex [60426-60-0] (80 mg/kg and 0.8 mg/kg) to tumor-bearing rats, instrumental neutron activation anal. showed selective uptake of Pt by the ascitic carcinosarcoma cells and significant retention of Pt by the kidney. These findings confirm the drug's usefulness as an antitumor agent and suggest the possibility of nephrotoxicity.
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