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PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds

A proper validation of an engineered brain microenvironment requires a trade of between the complexity of a cellular construct within the in vitro platform and the simple implementation of the investigational tool. The present work aims to accomplish this challenging balance by setting up an innovat...

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Autores principales: Piscioneri, Antonella, Morelli, Sabrina, Drioli, Enrico, De Bartolo, Loredana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915411/
https://www.ncbi.nlm.nih.gov/pubmed/33562851
http://dx.doi.org/10.3390/membranes11020112
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author Piscioneri, Antonella
Morelli, Sabrina
Drioli, Enrico
De Bartolo, Loredana
author_facet Piscioneri, Antonella
Morelli, Sabrina
Drioli, Enrico
De Bartolo, Loredana
author_sort Piscioneri, Antonella
collection PubMed
description A proper validation of an engineered brain microenvironment requires a trade of between the complexity of a cellular construct within the in vitro platform and the simple implementation of the investigational tool. The present work aims to accomplish this challenging balance by setting up an innovative membrane platform that represents a good compromise between a proper mimicked brain tissue analogue combined with an easily accessible and implemented membrane system. Another key aspect of the in vitro modelling disease is the identification of a precise phenotypic onset as a definite hallmark of the pathology that needs to be recapitulated within the implemented membrane system. On the basis of these assumptions, we propose a multiplex membrane system in which the recapitulation of specific neuro-pathological onsets related to Alzheimer’s disease pathologies, namely oxidative stress and β-amyloid(1–42) toxicity, allowed us to test the neuroprotective effects of trans-crocetin on damaged neurons. The proposed multiplex membrane platform is therefore quite a versatile tool that allows the integration of neuronal pathological events in combination with the testing of new molecules. The present paper explores the use of this alternative methodology, which, relying on membrane technology approach, allows us to study the basic physiological and pathological behaviour of differentiated neuronal cells, as well as their changing behaviour, in response to new potential therapeutic treatment.
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spelling pubmed-79154112021-03-01 PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds Piscioneri, Antonella Morelli, Sabrina Drioli, Enrico De Bartolo, Loredana Membranes (Basel) Article A proper validation of an engineered brain microenvironment requires a trade of between the complexity of a cellular construct within the in vitro platform and the simple implementation of the investigational tool. The present work aims to accomplish this challenging balance by setting up an innovative membrane platform that represents a good compromise between a proper mimicked brain tissue analogue combined with an easily accessible and implemented membrane system. Another key aspect of the in vitro modelling disease is the identification of a precise phenotypic onset as a definite hallmark of the pathology that needs to be recapitulated within the implemented membrane system. On the basis of these assumptions, we propose a multiplex membrane system in which the recapitulation of specific neuro-pathological onsets related to Alzheimer’s disease pathologies, namely oxidative stress and β-amyloid(1–42) toxicity, allowed us to test the neuroprotective effects of trans-crocetin on damaged neurons. The proposed multiplex membrane platform is therefore quite a versatile tool that allows the integration of neuronal pathological events in combination with the testing of new molecules. The present paper explores the use of this alternative methodology, which, relying on membrane technology approach, allows us to study the basic physiological and pathological behaviour of differentiated neuronal cells, as well as their changing behaviour, in response to new potential therapeutic treatment. MDPI 2021-02-05 /pmc/articles/PMC7915411/ /pubmed/33562851 http://dx.doi.org/10.3390/membranes11020112 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Piscioneri, Antonella
Morelli, Sabrina
Drioli, Enrico
De Bartolo, Loredana
PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title_full PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title_fullStr PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title_full_unstemmed PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title_short PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
title_sort plga multiplex membrane platform for disease modelling and testing of therapeutic compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915411/
https://www.ncbi.nlm.nih.gov/pubmed/33562851
http://dx.doi.org/10.3390/membranes11020112
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