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Design, synthesis and evaluation of RGD peptidomimetic - Gold nanostar conjugates as M21 cell adhesion inhibitors

Academic Article
Publication Date:
2022
abstract:
Effective targeting of alpha vS3 integrin is of high relevance in cancer research as this protein is overexpressed on several types of tumor cells, making such receptor ideal for the development of therapeutics and of diagnostic imaging agents. In this paper, the synthesis of a novel functionalized triazole-based RGD peptidomimetic and its covalent conjugation on pegylated gold nanostars is reported. These highly stable nanoconstructs showed a multivalent effect in binding alpha vS3 integrin receptors and proved to inhibit M21 cell adhesion at 25 pM concentration. Thanks to their peculiar surface plasmon resonance in the "NIR transparent window", targeted gold nanostars may represent a promising agent for anticancer multi-modality treatments. 2009 Elsevier Ltd. All rights reserved.
Iris type:
01.01 Articolo in rivista
Keywords:
Integrin; Bioconjugate chemistry; Drug delivery; Targeted therapy; Cancer
List of contributors:
Pavone, FRANCESCO SAVERIO; Credi, Caterina
Authors of the University:
CREDI CATERINA
Handle:
https://iris.cnr.it/handle/20.500.14243/414088
Published in:
BIOORGANIC CHEMISTRY (ONLINE)
Journal
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URL

https://www.sciencedirect.com/science/article/pii/S0045206822002784
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