diethoxy-(1-phenyl-1-3-butanedionato)titanium-(iv) and Body-Weight

Bis-beta-diketonato complexes of titanium, zirconium, and hafnium were tested against autochthonous colorectal tumors in rats. The model was found to reflect the clinical situation most closely. Of the compounds tested, budotitane was the most effective in terms of decrease in tumor weight and number and in increasing the lifespan of the treated animals. The therapeutic efficiency was superior to that of 5-fluorouracil, which so far has been the drug with the best activity in patients suffering from colon cancer.

Topics: Animals; Body Weight; Carcinogens; Colonic Neoplasms; Dimethylnitrosamine; Hafnium; Male; Metals; Organometallic Compounds; Rats; Rats, Inbred Strains; Titanium; Zirconium

The antitumor-active bis-beta-diketonato metal complexes dichlorobis(1-phenylbutane-1,3-dionato)titanium (IV) and diethoxybis(1-phenylbutane-1,3-dionato)titanium (IV) (prop. INN: budotitane) are active against several transplantable tumors. Activity was demonstrated by treating the intramusculary, subcutaneously and intraperitoneally transplanted sarcoma 180 tumor and against the Walker 256 Carcinosarcoma as well. In these models an increase in survival time up to T/C-values of 200 to 300% (T/C = (median survival time of treated animals to that of controls) X 100) and reduction of tumor weight to 30 or 0%, compared with the untreated control animals, was demonstrated. The therapy of the leukemias P 388 and L 1210 turned out to be statistically significant but only marginal in terms of increase in survival time (T/C approximately 130%). The toxicological experiments demonstrate single doses up to 40 mg/kg, given intravenously in female SD-rats, as to be well tolerable. The dose 80 mg/kg caused lethality in the range between 14 and 50% in 3 independent experiments. The spontaneously dying animals showed haemorrhagic pleural effusions and haemorrhagic oedematous areas of the lung. Histopathologically hyperemia and multiple focal necroses of the liver were found. The described lung toxicity was found only in high, single and lethal doses. Chronic doses of 10 to 20 mg/kg caused only mild liver toxicity. The laboratory parameters were increased in the values of the enzymes GOT, GPT and LDH. No evidence of myelosuppression was found in the peripheral blood.(ABSTRACT TRUNCATED AT 250 WORDS)

Topics: Animals; Antineoplastic Agents; Body Weight; Carcinoma 256, Walker; Chemistry, Pharmaceutical; Cisplatin; Columbidae; Drug Evaluation, Preclinical; Leukemia L1210; Leukemia P388; Male; Mice; Mice, Inbred Strains; Neoplasm Transplantation; Organometallic Compounds; Rats; Sarcoma 180; Titanium

The antitumour activity of diethoxy-(1-phenyl-1,3-butanedionato)titanium (IV) (DBT) in comparison to cis-dichlorodiammine platinum (cisplatin, cis-DDP) and cyclophosphamide (CTX) against human breast, colo-rectal and lung tumour lines growing as xenografts in nude mice was investigated. The antitumour activities and toxicities of DBT and cis-DDP are comparable whereas CTX was the most effective agent.

Topics: Animals; Antineoplastic Agents; Body Weight; Cisplatin; Cyclophosphamide; Drug Evaluation; Humans; Mice; Mice, Nude; Neoplasm Transplantation; Neoplasms; Organometallic Compounds; Titanium; Transplantation, Heterologous