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Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation

[Image: see text] Oxidative stress represents a common issue in most neurological diseases, causing severe impairments of neuronal cell physiological activity that ultimately lead to neuron loss of function and cellular death. In this work, lipid-coated polydopamine nanoparticles (L-PDNPs) are propo...

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Autores principales: Battaglini, Matteo, Marino, Attilio, Carmignani, Alessio, Tapeinos, Christos, Cauda, Valentina, Ancona, Andrea, Garino, Nadia, Vighetto, Veronica, La Rosa, Gabriele, Sinibaldi, Edoardo, Ciofani, Gianni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009471/
https://www.ncbi.nlm.nih.gov/pubmed/32693584
http://dx.doi.org/10.1021/acsami.0c05497
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author Battaglini, Matteo
Marino, Attilio
Carmignani, Alessio
Tapeinos, Christos
Cauda, Valentina
Ancona, Andrea
Garino, Nadia
Vighetto, Veronica
La Rosa, Gabriele
Sinibaldi, Edoardo
Ciofani, Gianni
author_facet Battaglini, Matteo
Marino, Attilio
Carmignani, Alessio
Tapeinos, Christos
Cauda, Valentina
Ancona, Andrea
Garino, Nadia
Vighetto, Veronica
La Rosa, Gabriele
Sinibaldi, Edoardo
Ciofani, Gianni
author_sort Battaglini, Matteo
collection PubMed
description [Image: see text] Oxidative stress represents a common issue in most neurological diseases, causing severe impairments of neuronal cell physiological activity that ultimately lead to neuron loss of function and cellular death. In this work, lipid-coated polydopamine nanoparticles (L-PDNPs) are proposed both as antioxidant and neuroprotective agents, and as a photothermal conversion platform able to stimulate neuronal activity. L-PDNPs showed the ability to counteract reactive oxygen species (ROS) accumulation in differentiated SH-SY5Y, prevented mitochondrial ROS-induced dysfunctions and stimulated neurite outgrowth. Moreover, for the first time in the literature, the photothermal conversion capacity of L-PDNPs was used to increase the intracellular temperature of neuron-like cells through near-infrared (NIR) laser stimulation, and this phenomenon was thoroughly investigated using a fluorescent temperature-sensitive dye and modeled from a mathematical point of view. It was also demonstrated that the increment in temperature caused by the NIR stimulation of L-PDNPs was able to produce a Ca(2+) influx in differentiated SH-SY5Y, being, to the best of our knowledge, the first example of organic nanostructures used in such an approach. This work could pave the way to new and exciting applications of polydopamine-based and of other NIR-responsive antioxidant nanomaterials in neuronal research.
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spelling pubmed-80094712021-03-31 Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation Battaglini, Matteo Marino, Attilio Carmignani, Alessio Tapeinos, Christos Cauda, Valentina Ancona, Andrea Garino, Nadia Vighetto, Veronica La Rosa, Gabriele Sinibaldi, Edoardo Ciofani, Gianni ACS Appl Mater Interfaces [Image: see text] Oxidative stress represents a common issue in most neurological diseases, causing severe impairments of neuronal cell physiological activity that ultimately lead to neuron loss of function and cellular death. In this work, lipid-coated polydopamine nanoparticles (L-PDNPs) are proposed both as antioxidant and neuroprotective agents, and as a photothermal conversion platform able to stimulate neuronal activity. L-PDNPs showed the ability to counteract reactive oxygen species (ROS) accumulation in differentiated SH-SY5Y, prevented mitochondrial ROS-induced dysfunctions and stimulated neurite outgrowth. Moreover, for the first time in the literature, the photothermal conversion capacity of L-PDNPs was used to increase the intracellular temperature of neuron-like cells through near-infrared (NIR) laser stimulation, and this phenomenon was thoroughly investigated using a fluorescent temperature-sensitive dye and modeled from a mathematical point of view. It was also demonstrated that the increment in temperature caused by the NIR stimulation of L-PDNPs was able to produce a Ca(2+) influx in differentiated SH-SY5Y, being, to the best of our knowledge, the first example of organic nanostructures used in such an approach. This work could pave the way to new and exciting applications of polydopamine-based and of other NIR-responsive antioxidant nanomaterials in neuronal research. American Chemical Society 2020-07-22 2020-08-12 /pmc/articles/PMC8009471/ /pubmed/32693584 http://dx.doi.org/10.1021/acsami.0c05497 Text en Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Battaglini, Matteo
Marino, Attilio
Carmignani, Alessio
Tapeinos, Christos
Cauda, Valentina
Ancona, Andrea
Garino, Nadia
Vighetto, Veronica
La Rosa, Gabriele
Sinibaldi, Edoardo
Ciofani, Gianni
Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title_full Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title_fullStr Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title_full_unstemmed Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title_short Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
title_sort polydopamine nanoparticles as an organic and biodegradable multitasking tool for neuroprotection and remote neuronal stimulation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009471/
https://www.ncbi.nlm.nih.gov/pubmed/32693584
http://dx.doi.org/10.1021/acsami.0c05497
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