Article ID Journal Published Year Pages File Type
1424802 Journal of Controlled Release 2012 8 Pages PDF
Abstract

We investigated the biodistribution of arginine-rich cell-penetrating peptides (CPPs) in tumor-xenografted nude mice after intravenous injection of fluorescently labeled CPPs using in vivo imaging. The CPPs used included HIV-1 Tat (48–60), penetratin, and the l- and d-enantiomers of oligoarginines (8, 12, and 16 residues), all of which are reported to have high cell penetration. Among the tested peptides, high accumulation in tumors was observed for the D-form of octaarginine (r8), and glycosaminoglycans played a key role. Injection of an r8-doxorubicin conjugate (4 mg doxorubicin/kg) effectively suppressed tumor proliferation, with no significant decrease in mouse weight, whereas administration of doxorubicin itself (6 mg/kg), yielding a similar degree of tumor-growth suppression, resulted in significant weight loss. These results suggest the potential of r8 as a prototypic tumor-targeting vector.

Graphical abstractTumor accumulation of D-octaarginine in tumor-xenografted mouse after intravenous administration.Figure optionsDownload full-size imageDownload high-quality image (112 K)Download as PowerPoint slide

Related Topics
Physical Sciences and Engineering Materials Science Biomaterials
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