| Literature DB >> 16165165 |
Bin Ji1, Jun Maeda, Makoto Higuchi, Kaori Inoue, Hidetaka Akita, Hideyoshi Harashima, Tetsuya Suhara.
Abstract
Lactoferrin (Lf) is an iron-binding glycoprotein belonging to the transferrin (Tf) family. Lf was reported to cross the blood brain barrier (BBB) via receptor-mediated transcytosis in an in vitro model of the BBB. In the present study, we compared the in vivo brain uptake of Lf with that of OX26, an anti-Tf receptor antibody, and Tf. These three proteins were radiolabeled with 125I and administered to rats by i.v. injection. We found that Lf was more rapidly eliminated from the blood compared with OX26 and Tf (The half-life of Lf was approximately 8 and 6 times shorter than that of OX26 and Tf, respectively; the area under the blood concentration-time curve of Lf was approximately 15 and 17 times smaller than that of OX26 and Tf, respectively), and mainly accumulated in the liver, spleen, and kidney. Markedly high brain uptake was observed for Lf relative to Tf and OX26. Lf might be useful as a ligand for facilitating drug delivery into the brain.Entities:
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Year: 2005 PMID: 16165165 DOI: 10.1016/j.lfs.2005.05.085
Source DB: PubMed Journal: Life Sci ISSN: 0024-3205 Impact factor: 5.037