| Literature DB >> 30537383 |
Gonzalo Villaverde1,2,3, Arantzazu Alfranca4,5, África Gonzalez-Murillo5,6, Gustavo J Melen5,6, Rafael R Castillo1,2,3, Manuel Ramírez5,6, Alejandro Baeza1,2,3,7, María Vallet-Regí1,2,3.
Abstract
The selective delivery of therapeutic and imaging agents to tumoral cells has been postulated as one of the most important challenges in the nanomedicine field. Meta-iodobenzilguanidine (MIBG) is widely used for the diagnosis of neuroblastoma (NB) due to its strong affinity for the norepinephrine transporter (NET), usually overexpressed on the membrane of malignant cells. Herein, a family of novel Y-shaped scaffolds has been synthesized, which have structural analogues of MIBG covalently attached at each end of the Y-structure. The cellular uptake capacity of these double-targeting ligands has been evaluated in vitro and in vivo, yielding one specific Y-shaped structure that is able to be engulfed by the malignant cells, and accumulates in the tumoral tissue, at significantly higher levels than the structure containing only one single targeting agent. This Y-shaped ligand can provide a powerful tool for the current treatment and diagnosis of this disease.Entities:
Keywords: meta-iodobenzylguanidine; molecular scaffold; nanomedicine; neuroblastoma; targeting
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Year: 2019 PMID: 30537383 PMCID: PMC6667334 DOI: 10.1002/anie.201811691
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336