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A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods

Recent years have witnessed an increased interest in the development of nanoparticles (NPs) owing to their potential use in a wide variety of biomedical applications, including drug delivery, imaging agents, gene therapy, and vaccines, where recently, lipid nanoparticle mRNA-based vaccines were deve...

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Autores principales: Agha, Abdulrahman, Waheed, Waqas, Stiharu, Ion, Nerguizian, Vahé, Destgeer, Ghulam, Abu-Nada, Eiyad, Alazzam, Anas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936499/
https://www.ncbi.nlm.nih.gov/pubmed/36800044
http://dx.doi.org/10.1186/s11671-023-03792-x
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author Agha, Abdulrahman
Waheed, Waqas
Stiharu, Ion
Nerguizian, Vahé
Destgeer, Ghulam
Abu-Nada, Eiyad
Alazzam, Anas
author_facet Agha, Abdulrahman
Waheed, Waqas
Stiharu, Ion
Nerguizian, Vahé
Destgeer, Ghulam
Abu-Nada, Eiyad
Alazzam, Anas
author_sort Agha, Abdulrahman
collection PubMed
description Recent years have witnessed an increased interest in the development of nanoparticles (NPs) owing to their potential use in a wide variety of biomedical applications, including drug delivery, imaging agents, gene therapy, and vaccines, where recently, lipid nanoparticle mRNA-based vaccines were developed to prevent SARS-CoV-2 causing COVID-19. NPs typically fall into two broad categories: organic and inorganic. Organic NPs mainly include lipid-based and polymer-based nanoparticles, such as liposomes, solid lipid nanoparticles, polymersomes, dendrimers, and polymer micelles. Gold and silver NPs, iron oxide NPs, quantum dots, and carbon and silica-based nanomaterials make up the bulk of the inorganic NPs. These NPs are prepared using a variety of top-down and bottom-up approaches. Microfluidics provide an attractive synthesis alternative and is advantageous compared to the conventional bulk methods. The microfluidic mixing-based production methods offer better control in achieving the desired size, morphology, shape, size distribution, and surface properties of the synthesized NPs. The technology also exhibits excellent process repeatability, fast handling, less sample usage, and yields greater encapsulation efficiencies. In this article, we provide a comprehensive review of the microfluidic-based passive and active mixing techniques for NP synthesis, and their latest developments. Additionally, a summary of microfluidic devices used for NP production is presented. Nonetheless, despite significant advancements in the experimental procedures, complete details of a nanoparticle-based system cannot be deduced from the experiments alone, and thus, multiscale computer simulations are utilized to perform systematic investigations. The work also details the most common multiscale simulation methods and their advancements in unveiling critical mechanisms involved in nanoparticle synthesis and the interaction of nanoparticles with other entities, especially in biomedical and therapeutic systems. Finally, an analysis is provided on the challenges in microfluidics related to nanoparticle synthesis and applications, and the future perspectives, such as large-scale NP synthesis, and hybrid formulations and devices. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-99364992023-02-17 A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods Agha, Abdulrahman Waheed, Waqas Stiharu, Ion Nerguizian, Vahé Destgeer, Ghulam Abu-Nada, Eiyad Alazzam, Anas Discov Nano Review Recent years have witnessed an increased interest in the development of nanoparticles (NPs) owing to their potential use in a wide variety of biomedical applications, including drug delivery, imaging agents, gene therapy, and vaccines, where recently, lipid nanoparticle mRNA-based vaccines were developed to prevent SARS-CoV-2 causing COVID-19. NPs typically fall into two broad categories: organic and inorganic. Organic NPs mainly include lipid-based and polymer-based nanoparticles, such as liposomes, solid lipid nanoparticles, polymersomes, dendrimers, and polymer micelles. Gold and silver NPs, iron oxide NPs, quantum dots, and carbon and silica-based nanomaterials make up the bulk of the inorganic NPs. These NPs are prepared using a variety of top-down and bottom-up approaches. Microfluidics provide an attractive synthesis alternative and is advantageous compared to the conventional bulk methods. The microfluidic mixing-based production methods offer better control in achieving the desired size, morphology, shape, size distribution, and surface properties of the synthesized NPs. The technology also exhibits excellent process repeatability, fast handling, less sample usage, and yields greater encapsulation efficiencies. In this article, we provide a comprehensive review of the microfluidic-based passive and active mixing techniques for NP synthesis, and their latest developments. Additionally, a summary of microfluidic devices used for NP production is presented. Nonetheless, despite significant advancements in the experimental procedures, complete details of a nanoparticle-based system cannot be deduced from the experiments alone, and thus, multiscale computer simulations are utilized to perform systematic investigations. The work also details the most common multiscale simulation methods and their advancements in unveiling critical mechanisms involved in nanoparticle synthesis and the interaction of nanoparticles with other entities, especially in biomedical and therapeutic systems. Finally, an analysis is provided on the challenges in microfluidics related to nanoparticle synthesis and applications, and the future perspectives, such as large-scale NP synthesis, and hybrid formulations and devices. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2023-02-17 /pmc/articles/PMC9936499/ /pubmed/36800044 http://dx.doi.org/10.1186/s11671-023-03792-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Agha, Abdulrahman
Waheed, Waqas
Stiharu, Ion
Nerguizian, Vahé
Destgeer, Ghulam
Abu-Nada, Eiyad
Alazzam, Anas
A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title_full A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title_fullStr A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title_full_unstemmed A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title_short A review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
title_sort review on microfluidic-assisted nanoparticle synthesis, and their applications using multiscale simulation methods
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936499/
https://www.ncbi.nlm.nih.gov/pubmed/36800044
http://dx.doi.org/10.1186/s11671-023-03792-x
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