Publications by authors named "G Villaverde"

The nanoparticle's synthesis had its tipping point at the beginning of the 21st century, opening up the possibility of manufacturing nanoparticles with almost every imaginable shape and size [...

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Article Synopsis
  • Superparamagnetic iron nanoparticles (SPIONs) are enhanced with a silica (SiO) shell and carboxyl groups, creating a new hybrid system called SPION@SiO-COOH that's useful in nanomedicine.* -
  • Novel compounds, N-alkylamino- and N-alkylamido-terminated derivatives of tetrahydroisoquinolines (THIQs) and tetrahydrobenzazepines (THBs), are synthesized and integrated into this hybrid system to explore their potential dopaminergic activity.* -
  • Characterization techniques confirm the successful incorporation of THIQs and THBs, and the hybrid systems show promising efficacy towards D receptors, suggesting possible applications for treating central
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AgS nanoparticles are near-infrared (NIR) probes providing emission in a specific spectral range (~1200 nm), and superparamagnetic iron oxide nanoparticles (SPION) are colloidal systems able to respond to an external magnetic field. A disadvantage of AgS NPs is the attenuated luminescent properties are reduced in aqueous media and human fluids. Concerning SPION, the main drawback is the generation of undesirable clusters that reduce particle stability.

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AgS semiconductor nanoparticles (NPs) are near-infrared luminescent probes with outstanding properties (good biocompatibility, optimum spectral operation range, and easy biofunctionalization) that make them ideal probes for in vivo imaging. AgS NPs have, indeed, made possible amazing challenges including in vivo brain imaging and advanced diagnosis of the cardiovascular system. Despite the continuous redesign of synthesis routes, the emission quantum yield (QY) of AgS NPs is typically below 0.

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The poor delivery of nanoparticles to target cancer cells hinders their success in the clinical setting. In this work, an alternative target readily available for circulating nanoparticles has been selected to eliminate the need for nanoparticle penetration in the tissue: the tumor blood vessels. A tumor endothelium-targeted nanoparticle (employing an RGD-containing peptide) capable of co-delivering two anti-vascular drugs (one anti-angiogenic drug and one vascular disruption agent) is here presented.

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