SPECIFIC INTERACTION BETWEEN GALACTOSE BRANCHED-CYCLODEXTRINS AND HEPATOCYTES IN-VITRO

Citation
T. Shinoda et al., SPECIFIC INTERACTION BETWEEN GALACTOSE BRANCHED-CYCLODEXTRINS AND HEPATOCYTES IN-VITRO, International journal of pharmaceutics, 167(1-2), 1998, pp. 147-154
Citations number
23
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
03785173
Volume
167
Issue
1-2
Year of publication
1998
Pages
147 - 154
Database
ISI
SICI code
0378-5173(1998)167:1-2<147:SIBGBA>2.0.ZU;2-W
Abstract
The purpose of this experiment was to investigate specific interaction between galactose branched-cyclodextrins (gal-CyDs) and hepatocytes i n vitro. Gal-CyDs were synthesized by an enzymatic method by using P-g alactosidase. Gal-CyDs, galactose, glucose branched-CyDs (glu-CyDs) or glucose were incubated with hepatocytes on lactosyl polystyrene polym er (PVLA, high binding to hepatocytes) coated dish. It was found that adherence of hepatocytes to PVLA was inhibited by incorporation of gal -CyDs or galactose in the incubation medium at a concentration of Ip m M, but was not inhibited by incorporation of glu-CyDs or glucose at 20 mM. Further, after incubation of hepatocyte suspension with both fluo rescein isothiocyanate-PVLA (FITC-PVLA) and gal-CyDs, gal-CyDs at 10 m M did inhibit the binding of FITC-PVLA to hepatocytes. In conclusion, it was suggested that enzymatically synthesized gal-CyDs have specific interaction with hepatocytes and may be useful as a drug targeting ca rrier to hepatocytes. (C) 1998 Elsevier Science B.V. All rights reserv ed.