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Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution

Individualized long-term management of chronic pathologies remains an elusive goal despite recent progress in drug formulation and implantable devices. The lack of advanced systems for therapeutic administration that can be controlled and tailored based on patient needs precludes optimal management...

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Autores principales: Di Trani, Nicola, Silvestri, Antonia, Wang, Yu, Demarchi, Danilo, Liu, Xuewu, Grattoni, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407659/
https://www.ncbi.nlm.nih.gov/pubmed/32707665
http://dx.doi.org/10.3390/pharmaceutics12070679
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author Di Trani, Nicola
Silvestri, Antonia
Wang, Yu
Demarchi, Danilo
Liu, Xuewu
Grattoni, Alessandro
author_facet Di Trani, Nicola
Silvestri, Antonia
Wang, Yu
Demarchi, Danilo
Liu, Xuewu
Grattoni, Alessandro
author_sort Di Trani, Nicola
collection PubMed
description Individualized long-term management of chronic pathologies remains an elusive goal despite recent progress in drug formulation and implantable devices. The lack of advanced systems for therapeutic administration that can be controlled and tailored based on patient needs precludes optimal management of pathologies, such as diabetes, hypertension, rheumatoid arthritis. Several triggered systems for drug delivery have been demonstrated. However, they mostly rely on continuous external stimuli, which hinder their application for long-term treatments. In this work, we investigated a silicon nanofluidic technology that incorporates a gate electrode and examined its ability to achieve reproducible control of drug release. Silicon carbide (SiC) was used to coat the membrane surface, including nanochannels, ensuring biocompatibility and chemical inertness for long-term stability for in vivo deployment. With the application of a small voltage (≤ 3 V DC) to the buried polysilicon electrode, we showed in vitro repeatable modulation of membrane permeability of two model analytes—methotrexate and quantum dots. Methotrexate is a first-line therapeutic approach for rheumatoid arthritis; quantum dots represent multi-functional nanoparticles with broad applicability from bio-labeling to targeted drug delivery. Importantly, SiC coating demonstrated optimal properties as a gate dielectric, which rendered our membrane relevant for multiple applications beyond drug delivery, such as lab on a chip and micro total analysis systems (µTAS).
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spelling pubmed-74076592020-08-12 Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution Di Trani, Nicola Silvestri, Antonia Wang, Yu Demarchi, Danilo Liu, Xuewu Grattoni, Alessandro Pharmaceutics Article Individualized long-term management of chronic pathologies remains an elusive goal despite recent progress in drug formulation and implantable devices. The lack of advanced systems for therapeutic administration that can be controlled and tailored based on patient needs precludes optimal management of pathologies, such as diabetes, hypertension, rheumatoid arthritis. Several triggered systems for drug delivery have been demonstrated. However, they mostly rely on continuous external stimuli, which hinder their application for long-term treatments. In this work, we investigated a silicon nanofluidic technology that incorporates a gate electrode and examined its ability to achieve reproducible control of drug release. Silicon carbide (SiC) was used to coat the membrane surface, including nanochannels, ensuring biocompatibility and chemical inertness for long-term stability for in vivo deployment. With the application of a small voltage (≤ 3 V DC) to the buried polysilicon electrode, we showed in vitro repeatable modulation of membrane permeability of two model analytes—methotrexate and quantum dots. Methotrexate is a first-line therapeutic approach for rheumatoid arthritis; quantum dots represent multi-functional nanoparticles with broad applicability from bio-labeling to targeted drug delivery. Importantly, SiC coating demonstrated optimal properties as a gate dielectric, which rendered our membrane relevant for multiple applications beyond drug delivery, such as lab on a chip and micro total analysis systems (µTAS). MDPI 2020-07-19 /pmc/articles/PMC7407659/ /pubmed/32707665 http://dx.doi.org/10.3390/pharmaceutics12070679 Text en © 2020 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
Di Trani, Nicola
Silvestri, Antonia
Wang, Yu
Demarchi, Danilo
Liu, Xuewu
Grattoni, Alessandro
Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title_full Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title_fullStr Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title_full_unstemmed Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title_short Silicon Nanofluidic Membrane for Electrostatic Control of Drugs and Analytes Elution
title_sort silicon nanofluidic membrane for electrostatic control of drugs and analytes elution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407659/
https://www.ncbi.nlm.nih.gov/pubmed/32707665
http://dx.doi.org/10.3390/pharmaceutics12070679
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