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Preclinical Study of Pharmacological Properties of Doxorubicin-NPh

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Preclinical study of therapeutic properties of an innovative drug Doxorubicin-NPh (doxorubicin in the form of ultrafine suspension of phospholipid liposomes) in comparison with free doxorubicin (Doxorubicin-Teva) and protected doxorubicin (Caelyx) was performed on transplanted murine tumor models. All these drugs were efficient in Ca755 breast carcinoma model (tumor growth inhibition ≈100%, increase in lifespan 90.6-114.3%). In P388 lymphocytic leukemia and LLC lung carcinoma, advantages of the protected doxorubicin by the benefit/risk ratio (width of therapeutic interval) were demonstrated: Caelyx>Doxorubicin-NPh>Doxorubicin-Teva. Doxorubicin-NPh and Caelyx exhibited similar therapeutic activity in the LLC model, especially when administered 3 times with 3-day intervals; for Doxorubicin-Teva, the optimal interval between the injections was 7 days.

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Correspondence to E. R. Nemtsova.

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Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 169, No. 6, pp. 720-726, June, 2020

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Nemtsova, E.R., Tikhonova, E.G., Bezborodova, O.A. et al. Preclinical Study of Pharmacological Properties of Doxorubicin-NPh. Bull Exp Biol Med 169, 778–782 (2020). https://doi.org/10.1007/s10517-020-04977-5

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  • DOI: https://doi.org/10.1007/s10517-020-04977-5

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