| Literature DB >> 23524643 |
Nabila Brabez1, Kara Saunders, Kevin L Nguyen, Thanuja B M Jayasundera, Craig Weber, Ronald M Lynch, Gerard Chassaing, Solange Lavielle, Victor J Hruby.
Abstract
In order to develop agents for early detection and selective treatment of melanomas, high affinity and high specificity molecular tools are required. Enhanced specificity may be obtained by simultaneously binding to multiple cell surface targets via the use of multimeric analogs of naturally occurring ligands. Trimers targeting overexpressed melanocortin receptors have been found to be potential candidates for this purpose. In the present letter, we describe the synthesis and study of multimers based on a dendrimer-like scaffold. The binding affinity and activity results revealed that dendrimers promote multivalent interactions via statistical and/or cooperative effects on binding. Moreover, viability studies showed no significant toxicity at micromolar concentrations, which will allow these molecular complexes to be used in vivo. Finally, imaging studies showed effective internalization for all the molecules confirming their potential as delivery agents.Entities:
Keywords: Multivalent interactions; cancer; delivery; dendrimers; melanoma; multimers; peptides; targeted therapy
Year: 2012 PMID: 23524643 PMCID: PMC3601667 DOI: 10.1021/ml300312b
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345