Document Detail

Investigation of the mechanisms of improved oral bioavailability of bergenin using bergenin-phospholipid complex.
MedLine Citation:
PMID:  23317338     Owner:  NLM     Status:  Publisher    
Abstract Aim: The purpose of this study was to investigate the detailed mechanisms of oral absorption enhancement of bergenin (BN) using BN-phospholipid complex (BPC). Methods: Multiple models such as ex vivo everted rat gut sac model and in vitro Caco-2 cell model were used. Meanwhile, the effect of chitosan on the enhancement of the permeability of BPC was evaluated. Results: The limited absorption of BN was significantly improved in both ex vivo everted rat gut sac model and in vitro Caco-2 cell model when combined with phospholipid. The transport of BPC was uppermost 5.19-fold higher than that of BN. The results of ex vivo everted rat gut sac model showed that small intestine was a more suitable site for the absorption of BN and BPC than colon. Passive diffusion was the only way employed in the transport of BN, while BPC could transport across enterocytes by both passive diffusion and active transport which was found to be the clathrine-dependent receptor-mediated endocytosis. The absorption of BN was barely improved by the physical mixture of BN and phospholipid due to lack of stable intermolecular interactions. Moreover, the addition of chitosan could open the tight junctions of intestinal epithelial cells, thus significantly increasing the transport of BPC via paracellular route. Conclusions: Totally different mechanisms, which led to the enhanced oral bioavailability, were utilized in the uptake and transport process of BPC compared with BN. These results would be of significance for the future development of oral delivery systems of BN.
Shan Guan; Xuan Qin; Zhou Zhou; Qiang Zhang; Yuan Huang
Related Documents :
22744878 - Regression calibration with more surrogates than mismeasured variables.
23964998 - Wholecellviz: data visualization for whole-cell models.
22505268 - Implementing an x-ray validation pipeline for the protein data bank.
22797228 - Prioritization of rehabilitation interventions for urban water assets using multiple cr...
16472218 - Systematic analysis of large screening sets in drug discovery.
24352528 - Carbon-14 dynamics in rice: an extension of the oryza2000 model.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-1-15
Journal Detail:
Title:  Drug development and industrial pharmacy     Volume:  -     ISSN:  1520-5762     ISO Abbreviation:  Drug Dev Ind Pharm     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-1-15     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7802620     Medline TA:  Drug Dev Ind Pharm     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Key Laboratory of Drug Targeting and Drug Delivery System, Ministry of Education, West China School of Pharmacy, Sichuan University , Chengdu , PR China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  To enhance the efficiency of nefopam transdermal iontophoresis by using a novel method based on ion-...
Next Document:  Thermal sintering: a novel technique used in the design, optimization and biopharmaceutical evaluati...