Abstract
A new high-performance liquid chromatographic method with ultraviolet detection has been used to determine the levels of the new cardiotropic drug protecor in the blood of animals (chincilla rabbits, 2.2 ± 0.2 kg; and beagle dogs, 10 ± 0.5 kg). The parameters of protecor pharmacokinetics and bioavailability upon peroral administration of protecor tablets have been determined. Rabbits showed effective absorption of the drug uupon peroral administration in a single dose (100 mg/kg) with a peak concentration in the plasma (C max= 41 µg/mL) reached within T max= 3 h followed by rapid removal of the drug from the organism with a half-elimination time T /12β=1.71 h. Peroral administration of protecor in a single dose (50 mg/kg) in beagle dogs was characterized by C max= 34.6 µg/mL, T max = 3 h, and T /12β=0.75 h. The bioavailability of protecor upon peroral administration was estimated at 90% (rabbits) and 80.7% (beagle dogs).
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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 41, No. 12, pp. 3–6, December, 2007.
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Ptitsina, S.N., Bobrov, V.I., Sernov, L.N. et al. Pharmacokinetics and bioavailability of the new drug protecor upon peroral administration in rabbits and beagle dogs. Pharm Chem J 41, 625–628 (2007). https://doi.org/10.1007/s11094-008-0034-9
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DOI: https://doi.org/10.1007/s11094-008-0034-9