Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2483475 | Journal of Drug Delivery Science and Technology | 2013 | 4 Pages |
Abstract
The binding and uptake of arabinogalactan and asialofetuin in HepG2 cells was kinetically characterized using I25I-labeled ligands. The number of binding sites (n) and the association constant (K) of arabinogalactan was 1.9 × 105 ± 1.2 × 105 sites/cell and 5.0 × 106 ± 3.9 × 106 M− 1, respectively, whereas the n and Ka of asialofetuin was 2.7 × 105 ± 1.1 × 105 sites/cell and 1.1 × 107 ± 0.7 × 107 M− 1, respectively. These results suggest that the binding capacity of HepG2 cells for arabinogalactan is lower than that for asialofetuin. Moreover, the amount of arabinogalactan uptake by HepG2 cells was lower than that of asialofetuin. Thus, asialofetuin was preferentially bound and internalized by hepatoma cells compared to arabinogalactan.
Related Topics
Health Sciences
Pharmacology, Toxicology and Pharmaceutical Science
Drug Discovery