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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Main Authors: Antonella Piscioneri, Sabrina Morelli, Enrico Drioli, Loredana De Bartolo
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Membranes
Subjects:
Online Access:https://www.mdpi.com/2077-0375/11/2/112
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spelling doaj-f38c1cd971ac42299df0ae364450e8312021-02-06T00:06:11ZengMDPI AGMembranes2077-03752021-02-011111211210.3390/membranes11020112PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic CompoundsAntonella Piscioneri0Sabrina Morelli1Enrico Drioli2Loredana De Bartolo3Institute on Membrane Technology (CNR-ITM), Via P. Bucci, Cubo 17/C, 87036 Rende (CS), ItalyInstitute on Membrane Technology (CNR-ITM), Via P. Bucci, Cubo 17/C, 87036 Rende (CS), ItalyInstitute on Membrane Technology (CNR-ITM), Via P. Bucci, Cubo 17/C, 87036 Rende (CS), ItalyInstitute on Membrane Technology (CNR-ITM), Via P. Bucci, Cubo 17/C, 87036 Rende (CS), ItalyA 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<sub>1–42</sub> 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.https://www.mdpi.com/2077-0375/11/2/112disease modellingtrans-crocetin neuroprotectionPLGA membranemembrane systems
collection DOAJ
language English
format Article
sources DOAJ
author Antonella Piscioneri
Sabrina Morelli
Enrico Drioli
Loredana De Bartolo
spellingShingle Antonella Piscioneri
Sabrina Morelli
Enrico Drioli
Loredana De Bartolo
PLGA Multiplex Membrane Platform for Disease Modelling and Testing of Therapeutic Compounds
Membranes
disease modelling
trans-crocetin neuroprotection
PLGA membrane
membrane systems
author_facet Antonella Piscioneri
Sabrina Morelli
Enrico Drioli
Loredana De Bartolo
author_sort Antonella Piscioneri
title 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_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_sort plga multiplex membrane platform for disease modelling and testing of therapeutic compounds
publisher MDPI AG
series Membranes
issn 2077-0375
publishDate 2021-02-01
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<sub>1–42</sub> 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.
topic disease modelling
trans-crocetin neuroprotection
PLGA membrane
membrane systems
url https://www.mdpi.com/2077-0375/11/2/112
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