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Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems

We describe the manufacture of low-cost microfluidic systems to produce nanoscale liposomes with highly uniform size distributions (i.e., low polydispersity indexes (PDI)) and acceptable colloidal stability. This was achieved by exploiting a Y-junction device followed by a serpentine micromixer geom...

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Detalles Bibliográficos
Autores principales: Aranguren, Andres, Torres, Carlos E., Muñoz-Camargo, Carolina, Osma, Johann F., Cruz, Juan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760644/
https://www.ncbi.nlm.nih.gov/pubmed/33260732
http://dx.doi.org/10.3390/mi11121050
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author Aranguren, Andres
Torres, Carlos E.
Muñoz-Camargo, Carolina
Osma, Johann F.
Cruz, Juan C.
author_facet Aranguren, Andres
Torres, Carlos E.
Muñoz-Camargo, Carolina
Osma, Johann F.
Cruz, Juan C.
author_sort Aranguren, Andres
collection PubMed
description We describe the manufacture of low-cost microfluidic systems to produce nanoscale liposomes with highly uniform size distributions (i.e., low polydispersity indexes (PDI)) and acceptable colloidal stability. This was achieved by exploiting a Y-junction device followed by a serpentine micromixer geometry to facilitate the diffusion between the mixing phases (i.e., continuous and dispersed) via advective processes. Two different geometries were studied. In the first one, the microchannels were engraved with a laser cutting machine on a polymethyl methacrylate (PMMA) sheet and covered with another PMMA sheet to form a two-layer device. In the second one, microchannels were not engraved but through-hole cut on a PMMA sheet and encased by a top and a bottom PMMA sheet to form a three-layer device. The devices were tested out by putting in contact lipids dissolved in alcohol as the dispersed phase and water as the continuous phase to self-assemble the liposomes. By fixing the total flow rate (TFR) and varying the flow rate ratio (FRR), we obtained most liposomes with average hydrodynamic diameters ranging from 188 ± 61 to 1312 ± 373 nm and 0.30 ± 0.09 PDI values. Such liposomes were obtained by changing the FRR from 5:1 to 2:1. Our results approached those obtained by conventional bulk synthesis methods such as a thin hydration bilayer and freeze-thaw, which produced liposomes with diameters ranging from 200 ± 38 to 250 ± 38 nm and 0.30 ± 0.05 PDI values. The produced liposomes might find several potential applications in the biomedical field, particularly in encapsulation and drug delivery.
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spelling pubmed-77606442020-12-26 Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems Aranguren, Andres Torres, Carlos E. Muñoz-Camargo, Carolina Osma, Johann F. Cruz, Juan C. Micromachines (Basel) Article We describe the manufacture of low-cost microfluidic systems to produce nanoscale liposomes with highly uniform size distributions (i.e., low polydispersity indexes (PDI)) and acceptable colloidal stability. This was achieved by exploiting a Y-junction device followed by a serpentine micromixer geometry to facilitate the diffusion between the mixing phases (i.e., continuous and dispersed) via advective processes. Two different geometries were studied. In the first one, the microchannels were engraved with a laser cutting machine on a polymethyl methacrylate (PMMA) sheet and covered with another PMMA sheet to form a two-layer device. In the second one, microchannels were not engraved but through-hole cut on a PMMA sheet and encased by a top and a bottom PMMA sheet to form a three-layer device. The devices were tested out by putting in contact lipids dissolved in alcohol as the dispersed phase and water as the continuous phase to self-assemble the liposomes. By fixing the total flow rate (TFR) and varying the flow rate ratio (FRR), we obtained most liposomes with average hydrodynamic diameters ranging from 188 ± 61 to 1312 ± 373 nm and 0.30 ± 0.09 PDI values. Such liposomes were obtained by changing the FRR from 5:1 to 2:1. Our results approached those obtained by conventional bulk synthesis methods such as a thin hydration bilayer and freeze-thaw, which produced liposomes with diameters ranging from 200 ± 38 to 250 ± 38 nm and 0.30 ± 0.05 PDI values. The produced liposomes might find several potential applications in the biomedical field, particularly in encapsulation and drug delivery. MDPI 2020-11-28 /pmc/articles/PMC7760644/ /pubmed/33260732 http://dx.doi.org/10.3390/mi11121050 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
Aranguren, Andres
Torres, Carlos E.
Muñoz-Camargo, Carolina
Osma, Johann F.
Cruz, Juan C.
Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title_full Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title_fullStr Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title_full_unstemmed Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title_short Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems
title_sort synthesis of nanoscale liposomes via low-cost microfluidic systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760644/
https://www.ncbi.nlm.nih.gov/pubmed/33260732
http://dx.doi.org/10.3390/mi11121050
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