Pharmacokinetics of a new drug based on polysaccharide from acorus calamus in an experiment on laboratory animals
Introduction. α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane is a water-soluble heteropolysaccharide isolated from the rhizomes of calamus marsh ( Acorus calamus L.) and has antitumor, antimetastatic, immunomodulatory and hepatoprotective effects, protective effect on hematopoiesis suppressed during cytostatic treatment. Aim. Validation of the bioanalytical method for the determination of α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane Acorus calamus L. and the study of the pharmacokinetic parameters of a new drug based on it after a single administration of 120 mg/kg to rats and 24, 30, 42 mg/kg to rabbits. Materials and methods. In the study, 8 male rats (average weight – 300 g) were used as the main animals. 6 male rabbits (average body weight – 2.5 kg) were used as an additional animal species. The dose assessment experiment was carried out on 24 rabbits (body weight – 2.3–2.5 kg). The quantitative determination of α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane Acorus calamus L. in the blood plasma of animals was carried out by HPLC-MS/MS, the analytical form was galacturonic acid. The method of sample preparation of biological samples included the stage of enzymatic hydrolysis of α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane Acorus calamus L. with a solution of pectinase for the formation of galacturonic acid. Results and discussions. The pharmacokinetics of the new drug α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane Acorus calamus L. was studied after a single dose of 120 mg/kg to rats and 24, 30, 42 mg/kg to rabbits. The average residence time of the drug in the rabbit's body was 1.0 ± 0.21 hours, the half-life was 0.7 ± 0.15 hours. The average residence time of the drug in the rat body was 1.16 hours, the half-life T 1/2 was 0.80 hours. After a single intravenous administration to rabbits of 24, 30 and 42 mg/kg, the maximum concentration in the systemic bloodstream is reached 5 minutes after administration and averages 133.95 ± 27.04, 145.86 ± 40.90 and 226.13 ± 41.27 µg/ml, respectively, the half-life ranged from 0.22 to 0.26 h, the half-life from 3.52 to 3.96 hours. Conclusion. The pharmacokinetic parameters of α(1,2)-L-rhamno-α(1,4)-D-galactopyranosyluronane Acorus calamus L. were evaluated in animals based on the use of the method of quantitative determination of galacturonic acid by HPLC-MS/MS.
Authors
- Yu. G. Zyuz’kova
- O. S. Bryushinina
- Е. А. Yanovskaya (ORCID: https://orcid.org/0000-0002-4635-8046)
- М. В. Белоусов (ORCID: https://orcid.org/0000-0002-2153-7945)
- В. В. Удут
- С. В. Кривощеков (ORCID: https://orcid.org/0000-0001-5505-7141)
- Д. А. Исаков (ORCID: https://orcid.org/0009-0005-9919-7353)
- A. V. Zykova (ORCID: https://orcid.org/0009-0008-9365-800X)
- A. M. Guryev
- R. V. Gurto
Institutions
- Russian Academy of Sciences (RU)
- Siberian State Medical University (RU)
- Tomsk National Research Medical Center (RU)
- Research Institute of Pharmacology and Regenerative Medicine named ED Goldberg (RU)
Publication Details
- Journal
- Drug development & registration
- Published
- 2024-09-13
- DOI
- https://doi.org/10.33380/2305-2066-2024-13-4-1795
- Citations
- 2
- Primary Topic
- Flavonoids in Medical Research
- Type
- article
- Field-Weighted Citation Impact
- 0.90