Cargando…
In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes
Nanotechnology applications have emerged as one of the most actively researched areas in recent years. As a result, substantial study into nanoparticulate lipidic systems and liposomes (LPs) has been conducted. Regardless of the advantages, various challenges involving traditional manufacturing proc...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699034/ https://www.ncbi.nlm.nih.gov/pubmed/36432675 http://dx.doi.org/10.3390/pharmaceutics14112484 |
_version_ | 1784838969259720704 |
---|---|
author | Sommonte, Federica Weaver, Edward Mathew, Essyrose Denora, Nunzio Lamprou, Dimitrios A. |
author_facet | Sommonte, Federica Weaver, Edward Mathew, Essyrose Denora, Nunzio Lamprou, Dimitrios A. |
author_sort | Sommonte, Federica |
collection | PubMed |
description | Nanotechnology applications have emerged as one of the most actively researched areas in recent years. As a result, substantial study into nanoparticulate lipidic systems and liposomes (LPs) has been conducted. Regardless of the advantages, various challenges involving traditional manufacturing processes have hampered their expansion. Here, the combination of microfluidic technology (MF) and 3D printing (3DP) digital light processing (DLP) was fruitfully investigated in the creation of novel, previously unexplored “diamond shaped” devices suitable for the production of LPs carrying lysozyme as model drug. Computer-aided design (CAD) software was used designing several MF devices with significantly multiple and diverse geometries. These were printed using a high-performance DLP 3DP, resulting in extremely high-resolution chips that were tested to optimize the experimental condition of MF-based LPs. Monodisperse narrow-sized lysozyme-loaded PEGylated LPs were produced using in-house devices. The developed formulations succumbed to stability tests to determine their consistency, and then an encapsulation efficacy (EE) study was performed, yielding good findings. The in vitro release study indicated that lysozyme-loaded LPs could release up to 93% of the encapsulated cargo within 72 h. Therefore, the proficiency of the association between MF and 3DP was demonstrated, revealing a potential growing synergy. |
format | Online Article Text |
id | pubmed-9699034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96990342022-11-26 In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes Sommonte, Federica Weaver, Edward Mathew, Essyrose Denora, Nunzio Lamprou, Dimitrios A. Pharmaceutics Article Nanotechnology applications have emerged as one of the most actively researched areas in recent years. As a result, substantial study into nanoparticulate lipidic systems and liposomes (LPs) has been conducted. Regardless of the advantages, various challenges involving traditional manufacturing processes have hampered their expansion. Here, the combination of microfluidic technology (MF) and 3D printing (3DP) digital light processing (DLP) was fruitfully investigated in the creation of novel, previously unexplored “diamond shaped” devices suitable for the production of LPs carrying lysozyme as model drug. Computer-aided design (CAD) software was used designing several MF devices with significantly multiple and diverse geometries. These were printed using a high-performance DLP 3DP, resulting in extremely high-resolution chips that were tested to optimize the experimental condition of MF-based LPs. Monodisperse narrow-sized lysozyme-loaded PEGylated LPs were produced using in-house devices. The developed formulations succumbed to stability tests to determine their consistency, and then an encapsulation efficacy (EE) study was performed, yielding good findings. The in vitro release study indicated that lysozyme-loaded LPs could release up to 93% of the encapsulated cargo within 72 h. Therefore, the proficiency of the association between MF and 3DP was demonstrated, revealing a potential growing synergy. MDPI 2022-11-16 /pmc/articles/PMC9699034/ /pubmed/36432675 http://dx.doi.org/10.3390/pharmaceutics14112484 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sommonte, Federica Weaver, Edward Mathew, Essyrose Denora, Nunzio Lamprou, Dimitrios A. In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title | In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title_full | In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title_fullStr | In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title_full_unstemmed | In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title_short | In-House Innovative “Diamond Shaped” 3D Printed Microfluidic Devices for Lysozyme-Loaded Liposomes |
title_sort | in-house innovative “diamond shaped” 3d printed microfluidic devices for lysozyme-loaded liposomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699034/ https://www.ncbi.nlm.nih.gov/pubmed/36432675 http://dx.doi.org/10.3390/pharmaceutics14112484 |
work_keys_str_mv | AT sommontefederica inhouseinnovativediamondshaped3dprintedmicrofluidicdevicesforlysozymeloadedliposomes AT weaveredward inhouseinnovativediamondshaped3dprintedmicrofluidicdevicesforlysozymeloadedliposomes AT mathewessyrose inhouseinnovativediamondshaped3dprintedmicrofluidicdevicesforlysozymeloadedliposomes AT denoranunzio inhouseinnovativediamondshaped3dprintedmicrofluidicdevicesforlysozymeloadedliposomes AT lamproudimitriosa inhouseinnovativediamondshaped3dprintedmicrofluidicdevicesforlysozymeloadedliposomes |