Pharmacokinetics of a New Neuroprotector — Indenoquinoxalinone Derivative after Intravenous Administration in Rabbits and Rats; Bulletin of Experimental Biology and Medicine; Vol. 175, iss. 6
| Parent link: | Bulletin of Experimental Biology and Medicine.— .— New York: Springer Science+Business Media LLC. Vol. 175, iss. 6.— 2023.— P. 770-773 |
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| Erakunde egilea: | Томский политехнический университет |
| Beste egile batzuk: | Yanovskaya E. A. Elena Anatoljevna, Frelikh G. A. Galina Andreevna, Lakeev A. P. Aleksandr Pavlovich, Chernysheva G. A. Galina Anatoljevna, Smolyakova V. I. Vera Ivanovna, Kovrizhina A. R. Anastasia Ruslanovna |
| Gaia: | Title screen The specific JNK inhibitor and NO donor 11H-indeno[1,2-b]quinoxalin-11-one oxime (IQ-1) demonstrated pronounced neuroprotective properties in an in vivo model of ischemic stroke in rats. The pharmacokinetic behavior of IQ-1 was studied in two animal species (rats, rabbits) after intravenous administration in a dose of 1 mg/kg. IQ-1 concentrations in venous blood plasma were measured by the liquid chromatography—tandem mass spectrometry method. The pharmacokinetics of IQ-1 was adequately described by the two-compartmental model. The calculated C0 for IQ-1 in rabbit and rat plasma were 2239.83±1229.55 and 1552.50±182.23 ng/ml, respectively. Two animal species are characterized by extensive tissue distribution of IQ-1 (Vss exceeded the total body water in rabbits and rats by 3.6 and 5.6 times, respectively) and high clearance values (88-94% of hepatic blood flow) AM_Agreement |
| Hizkuntza: | ingelesa |
| Argitaratua: |
2023
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| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.1007/s10517-023-05943-7 |
| Formatua: | Baliabide elektronikoa Liburu kapitulua |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=672278 |
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