Pharmacokinetics of the drug Amoxyantar in pigs DOI Creative Commons
С.В. Енгашев, А. А. Комаров, A. M. Lunegov

и другие.

Legal regulation in veterinary medicine, Год журнала: 2024, Номер 3, С. 98 - 101

Опубликована: Окт. 18, 2024

The article presents the results of pharmacokinetic studies drug Amoxiyantar in pigs. obtained indicate that amoxicillin is distributed throughout tissues animals, providing therapeutic concentrations studied dosage, ensuring effective distribution organs and body pigs, also confirm bioavailability succinic acid with a high concentration blood plasma for an average two hours. Based on determining dynamics excretion residual amounts amoxicillin, it was detected only one animal kidneys at 54.9 μg/kg muscle tissue 25.2 μg/kg. In remaining samples pigs days after application drug, as well all from sixth day to 18th not detected.

Язык: Английский

Nanometerizing Taxifolin Into Selenized Liposomes to Ameliorate Its Hypoglycemic Effect by Optimizing Drug Release and Bioavailability DOI Creative Commons

Chunli Qi,

Huijie Xing,

Ning Ding

и другие.

International Journal of Nanomedicine, Год журнала: 2025, Номер Volume 20, С. 2225 - 2240

Опубликована: Фев. 1, 2025

Diabetes mellitus (DM) remains a significant health challenge, with traditional treatments often failing to provide lasting solutions. Taxifolin (Tax), potential phytomedicine antioxidant and anti-hyperglycemic properties, suffers from low water solubility poor bioavailability, necessitating advanced delivery systems. This study aims nanometerize taxifolin (Tax) into selenized liposomes (Tax-Se@LPs) for enhanced oral hypoglycemic effect. Tax-Se@LPs were fabricated through thin-film hydration/in situ reduction technique. The resulting nanomedicine was characterized in vitro release studies, pharmacokinetic pharmacodynamic evaluations, cellular uptake assays, formulation stability tests. optimized demonstrated an average particle size of 185.3 nm entrapment efficiency 95.25% after optimization. In studies revealed that exhibited slower more sustained profile compared conventional liposomes, favoring gastrointestinal drug absorption. Pharmacokinetic evaluations normal rats indicated achieved relative bioavailability 216.65%, significantly higher than Tax suspensions unmodified liposomes. Furthermore, diabetic GK rats, resulted maximal blood glucose 46.8% therapeutic duration other formulations. Cellular tests manifested selenization altered the internalization mechanisms while preserving their absorption aptness by intestinal epithelial cells. physiological also reinforced selenization. Overall, not only improve but enhance its efficacy. These findings underscore as promising strategy DM management.

Язык: Английский

Процитировано

0

Pharmacokinetics of the drug Amoxyantar in pigs DOI Creative Commons
С.В. Енгашев, А. А. Комаров, A. M. Lunegov

и другие.

Legal regulation in veterinary medicine, Год журнала: 2024, Номер 3, С. 98 - 101

Опубликована: Окт. 18, 2024

The article presents the results of pharmacokinetic studies drug Amoxiyantar in pigs. obtained indicate that amoxicillin is distributed throughout tissues animals, providing therapeutic concentrations studied dosage, ensuring effective distribution organs and body pigs, also confirm bioavailability succinic acid with a high concentration blood plasma for an average two hours. Based on determining dynamics excretion residual amounts amoxicillin, it was detected only one animal kidneys at 54.9 μg/kg muscle tissue 25.2 μg/kg. In remaining samples pigs days after application drug, as well all from sixth day to 18th not detected.

Язык: Английский

Процитировано

0