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Therapeutic Methods and Therapies TCIM
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1.
Drugs Exp Clin Res ; 22(3-5): 207-11, 1996.
Article in English | MEDLINE | ID: mdl-8899333

ABSTRACT

Ukrain, a semi-synthetic preparation obtained from Chelidonium majus L, is used in the treatment of cancer diseases. It has been observed to exert a protective influence in mice infected by influenza viruses. Recently, the influence of the preparation on the survival of mice infected by lethal doses of E. coli and S. aureus has been estimated. This preparation was administered to Balb/c mice subcutaneously in doses of 0.04, 0.4 and 4.0 mg/kg of body weight. Ukrain was given every second day during 20 days, or a short-term before-and-after method at 48, 24 and 2 h before the infection and or 2, 24 and 48 h after the infection of mice. The mice were infected intraperitoneally with E. coli or S. aureus in doses equivalent to 2LD50. Increased survival of mice, depending on the dose of the preparation and the kind of infecting bacterium was observed. The highest survival (50%) occurred in mice infected with E. coli and receiving the amount of the preparation corresponding to 0.4 mg/kg. The lowest survival was observed in mice infected by S. aureus and receiving the preparation in the amount of 4.0 mg/kg. Higher protective effectiveness of the Ukrain preparation was observed in mice when the preparation had been administered during 20 days as compared to the short-term before-and-after regime.


Subject(s)
Alkaloids/therapeutic use , Anti-Bacterial Agents/therapeutic use , Escherichia coli Infections/prevention & control , Staphylococcal Infections/prevention & control , Animals , Berberine Alkaloids , Mice , Mice, Inbred BALB C , Phenanthridines , Time Factors
2.
Pneumonol Alergol Pol ; 60(1-2): 28-35, 1992.
Article in Polish | MEDLINE | ID: mdl-1290976

ABSTRACT

The effect of TFX-Polfa administered alone or with three antibiotics on the survival time in mice infected with E.coli and S.aureus was estimated. TFX has been administered 48, 24, 2 hours before and 24, 48 and 72 hours after infection, in doses of 10 mg/kg of body weight. Ciprobay has been administered 2 hours after infection, and every 24 hours during the experiment in dose of 15, 7.5 and 3.75 mg/kg of body weight. Amikin has been used in doses of 7.5, 3.75 and 1.87 mg/kg of body weight, Cefobid in doses of 30, 15 and 7.5 mg/kg of body weight. The antibiotics have been administered 2 hours after infection and every 12 hours to the end of experiment. Animals have been observed 10 days after infection. The positive effect of TFX on the survival time in mice infected with E.coli has been observed, but this preparation has given a little effect on the tested parameter in mice infected with S.aureus. Best antibacterial effect of Ciprobay and Amikin has been observed after administration of clinical doses. However, simultaneous therapy with TFX and tested antibiotics resulted in various (positive and negative) effects on the survival time during 10 days of observation.


Subject(s)
Amikacin/administration & dosage , Cefoperazone/administration & dosage , Ciprofloxacin/administration & dosage , Disease Models, Animal , Escherichia coli Infections/drug therapy , Staphylococcal Infections/drug therapy , Staphylococcus aureus , Thymus Extracts/administration & dosage , Animals , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Drug Interactions , Drug Therapy, Combination , Escherichia coli Infections/mortality , Female , Male , Mice , Mice, Inbred BALB C , Staphylococcal Infections/mortality
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