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In vivo pharmacokinetics of Glycyrrhiza uralensis polysaccharides.

Authors :
Wubuli A
Chai J
Liu H
Nijat D
Li J
Xia G
Cao Q
Zhang S
Huang W
Aipire A
Li J
Source :
Frontiers in pharmacology [Front Pharmacol] 2024 Jul 19; Vol. 15, pp. 1431221. Date of Electronic Publication: 2024 Jul 19 (Print Publication: 2024).
Publication Year :
2024

Abstract

Glycyrrhiza uralensis polysaccharides (GUPS) are widely applied in biomedicine and functional food due to their multiple pharmacological activities and low toxicity. Despite their widespread use, the in vivo metabolic profile of GUPS remains poorly understood. To address this gap, we developed a quantitative analysis method that involves labeling GUPS with visible fluorescein (5-DTAF) and near-infrared (NIR) fluorescein (Cy7), resulting in stable conjugates with substitution degrees of 0.81% for 5-DTAF and 0.39% for Cy7. The pharmacokinetic studies showed a biphasic elimination pattern in the blood concentration-time curve following both intravenous and oral administration, consistent with a two-compartment model. Using fluorescence quantification and NIR imaging, we observed that GUPS was distributed to various tissues, exhibiting higher concentrations particularly in liver, kidney and lung. Excretion studies indicated that feces were the major excretion pathway of GUPS after oral administration (60.98%), whereas urine was the main pathway after intravenous administration (31.16%). Notably, GUPS could be absorbed rapidly by gut (T <subscript>max</subscript> 1 ± 0.61 h) and showed a biological half-time t <subscript>1/2</subscript> 26.4 ± 7.72 h after oral administration. Furthermore, the Caco-2 cells uptake studies illustrated that macropinocytosis and clathrin-mediated endocytosis were participated in the transport of GUPS in intestine epithelium. This comprehensive analysis of the in vivo pharmacokinetics of GUPS not only enhances our understanding of its metabolic pathways but also establishes a foundational basis for its clinical application, optimizing its therapeutic potential and safety profile.<br />Competing Interests: Author JC was employed by Urumqi Xinze Ziqi Biotechnology Company, Limited. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.<br /> (Copyright © 2024 Wubuli, Chai, Liu, Nijat, Li, Xia, Cao, Zhang, Huang, Aipire and Li.)

Details

Language :
English
ISSN :
1663-9812
Volume :
15
Database :
MEDLINE
Journal :
Frontiers in pharmacology
Publication Type :
Academic Journal
Accession number :
39101144
Full Text :
https://doi.org/10.3389/fphar.2024.1431221