Study on the Absorption of Silymarin Enteric Coated-PLGA Nanoparticles in Rat in situ Intestine Perfu-sion Model and Caco-2 Cell Model
10.6039/j.issn.1001-0408.2017.01.12
- VernacularTitle:水飞蓟素肠溶聚乳酸-羟基乙酸共聚物纳米粒在大鼠在体肠灌流模型及Caco-2细胞模型中的吸收研究
- Author:
Jing HE
;
Yanchuan QIU
;
Yanyin YANG
;
Fengyun LIN
;
Songqing LIU
;
Shangfei JIANG
;
Zhaojing ZHU
- Keywords:
Silymarin;
Enteric coated-PLGA nanoparticle;
in situ intestine perfusion model;
Colonic adenoma Caco-2 cell;
Ab-sorption
- From:
China Pharmacy
2017;28(1):46-49
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To study the absorption features of Silymarin enteric coated-polyllactic-co-glycolic acid (PLGA) nanoparticles in rat in situ intestine perfusion model and colonic adenoma Caco-2 cell model. METHODS:HPLC method was used to determine the content of silymarin. The absorption rate constant(Ka)and apparent absorption coefficient(Kapp)of Silymarin sus-pension,Silymarin PLGA nanoparticles and Silymarin enteric coated-PLGA nanoparticles were investigated in duodenum,jejunum, ileum and colon of rat in situ intestine perfusion model;the apparent permeability coefficient (Papp) of those drugs containing low-concentration,medium-concentration and high-concentration(20,40,60 μg/mL)of silymarin in Caco-2 cell model were also investigated. RESULTS:Compared with Silymarin suspension,Ka and Kapp of Silymarin PLGA nanoparticles and Silymarin enteric coated-PLGA nanoparticles were all increased in duodenum,jejunum,ileum and colon(P<0.05);compared with the correspond-ing concentration Silymarin suspension,two-way Papp of Silymarin PLGA nanoparticles and Silymarin enteric coated-PLGA nanopar-ticles containing low-concentration,medium-concentration and high-concentration of silymarin were all increased in Caco-2 cell model (P<0.05);there was no statistical significance between Silymarin PLGA nanoparticles and Silymarin enteric coated-PLGA nanoparticles (P>0.05). CONCLUSIONS:Silymarin enteric coated-PLGA nanoparticles can effectively increase the intestinal ab-sorption,cellular uptake and transmembrane transport rate of silymarin.