Intestinal absorption of the effective components of Schisandra chinensis Baill by rats single-pass perfusion in situ.
- Author:
Xin-Min CHEN
1
;
Jun-Song LI
;
Wen LI
;
Lei HAN
;
Xun-Hong LIU
;
Liu-Qing DI
;
Bao-Chang CAI
Author Information
1. School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Chromatography, High Pressure Liquid;
Colon;
metabolism;
Cyclooctanes;
administration & dosage;
isolation & purification;
pharmacokinetics;
Dose-Response Relationship, Drug;
Drugs, Chinese Herbal;
administration & dosage;
isolation & purification;
pharmacokinetics;
Duodenum;
metabolism;
Fruit;
chemistry;
Ileum;
metabolism;
Intestinal Absorption;
Jejunum;
metabolism;
Lignans;
administration & dosage;
isolation & purification;
pharmacokinetics;
Male;
Perfusion;
Permeability;
Plants, Medicinal;
chemistry;
Polycyclic Compounds;
administration & dosage;
isolation & purification;
pharmacokinetics;
Rats;
Rats, Sprague-Dawley;
Schisandra;
chemistry
- From:
Acta Pharmaceutica Sinica
2010;45(5):652-658
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the study is to investigate rat intestinal absorption behavior of three main active components, schisandrol A, schisandrin A and schisandrin B in Schisandra chinensis Baill extracts in intestine of rats. With phenol red as the indicator, in situ single pass intestinal perfusion (SPIP) model was used and the concentrations of three main active components in perfusion solution of different intestinal segments (duodenum, jejunum, ileum, and colon) were determined by HPLC in combination with diode array detection. The results showed that the absorption rate constant (Ka) and effective permeability values (Peff) of three main active components in Schisandra chinensis Baill extracts had significant difference (P < 0.05) at different concentrations of perfusion solution, the Ka and Peff first increased and then decreased with the increase of drug concentration, the middle concentration was higher than those of the other two concentrations. The saturate absorption phenomena were observed, and it suggested that the transport mechanisms of three main active components in vivo were similar to active transport or facilitated diffusion. Three active components can be well absorbed in all of the intestinal segments, while duodenum is the best absorption region. The Ka and Peff of three active components in jejunum and ileum had no significant difference (P > 0.05). The absorption of the three active components displayed significant difference (P < 0.05) at different intestinal segments of rats. Schisandrin A had the best absorption in duodenum. The Ka and Peff among three active components were sequenced as follows: schisandrin A > schisandrin B > schisandrol A in other intestinal segments, and there is significant difference (P < 0.05) between them.
