Study on pharmacokinetics and tissue distribution of stealth matrine liposomes in rats.
- Author:
Wenying WU
1
;
Jie HUANG
;
Shuo LIU
;
Xinghua LI
;
Yan CAI
Author Information
- Publication Type:Journal Article
- MeSH: Alkaloids; administration & dosage; blood; pharmacokinetics; Animals; Calibration; Female; Linear Models; Liposomes; Male; Quinolizines; administration & dosage; blood; pharmacokinetics; Rats; Sensitivity and Specificity; Tissue Distribution
- From: China Journal of Chinese Materia Medica 2009;34(6):751-755
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo determine the concentration of matrine in rats plasma and tissue and study the pharmacokinetics and tissues distribution of matrine solution (MS), regular matrine liposome (ML) and stealth matrine liposome (LML) after the intravenous administration at a single dose of 15 mg x kg(-1) to rats.
METHODReversed-phase HPLC was used to determine matrine concentration in rats plasma and tissues.
RESULTThe concentration-time curves of MS, ML and LML were fitted to a two-compartment model. The terminal half-life of LML was 2.7-fold higher than MS and 2-fold higher than ML. The area under the plasma concentration curve (AUC) of LML was 63-fold higher than MS and 2.3-fold higher than ML. Tissues distribution results proved that the area under the plasma concentration curve of LML was significantly different from ML and MS (P<0.05). The area under the liver and spleen curve of LML was significantly different from ML (P<0.05). The ratio between the area under the curve of plasma and the area under the curve of reticulo-endothelial system (Blood/RES) of LML was 5.4-fold higher than ML.
CONCLUSIONOur present studies demonstrate that, compared to MS and ML, LML significantly alters its pharmacokinetics in plasma and tissues targeting.