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Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices
Polymeric micelles with a controlled size in the range between 41 and 80 nm were prepared by injecting the organic phase through a microengineered nickel membrane or a tapered-end glass capillary into an aqueous phase. The organic phase was composed of 1 mg·mL(−1) of PEG-b-PCL diblock copolymers wit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931524/ https://www.ncbi.nlm.nih.gov/pubmed/27231945 http://dx.doi.org/10.3390/membranes6020029 |
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author | Lu, Yu Chowdhury, Danial Vladisavljević, Goran T. Koutroumanis, Konstantinos Georgiadou, Stella |
author_facet | Lu, Yu Chowdhury, Danial Vladisavljević, Goran T. Koutroumanis, Konstantinos Georgiadou, Stella |
author_sort | Lu, Yu |
collection | PubMed |
description | Polymeric micelles with a controlled size in the range between 41 and 80 nm were prepared by injecting the organic phase through a microengineered nickel membrane or a tapered-end glass capillary into an aqueous phase. The organic phase was composed of 1 mg·mL(−1) of PEG-b-PCL diblock copolymers with variable molecular weights, dissolved in tetrahydrofuran (THF) or acetone. The pore size of the membrane was 20 μm and the aqueous/organic phase volumetric flow rate ratio ranged from 1.5 to 10. Block copolymers were successfully synthesized with M(n) ranging from ~9700 to 16,000 g·mol(−1) and polymeric micelles were successfully produced from both devices. Micelles produced from the membrane device were smaller than those produced from the microfluidic device, due to the much smaller pore size compared with the orifice size in a co-flow device. The micelles were found to be relatively stable in terms of their size with an initial decrease in size attributed to evaporation of residual solvent rather than their structural disintegration. Fluconazole was loaded into the cores of micelles by injecting the organic phase composed of 0.5–2.5 mg·mL(−1) fluconazole and 1.5 mg·mL(−1) copolymer. The size of the drug-loaded micelles was found to be significantly larger than the size of empty micelles. |
format | Online Article Text |
id | pubmed-4931524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-49315242016-07-08 Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices Lu, Yu Chowdhury, Danial Vladisavljević, Goran T. Koutroumanis, Konstantinos Georgiadou, Stella Membranes (Basel) Article Polymeric micelles with a controlled size in the range between 41 and 80 nm were prepared by injecting the organic phase through a microengineered nickel membrane or a tapered-end glass capillary into an aqueous phase. The organic phase was composed of 1 mg·mL(−1) of PEG-b-PCL diblock copolymers with variable molecular weights, dissolved in tetrahydrofuran (THF) or acetone. The pore size of the membrane was 20 μm and the aqueous/organic phase volumetric flow rate ratio ranged from 1.5 to 10. Block copolymers were successfully synthesized with M(n) ranging from ~9700 to 16,000 g·mol(−1) and polymeric micelles were successfully produced from both devices. Micelles produced from the membrane device were smaller than those produced from the microfluidic device, due to the much smaller pore size compared with the orifice size in a co-flow device. The micelles were found to be relatively stable in terms of their size with an initial decrease in size attributed to evaporation of residual solvent rather than their structural disintegration. Fluconazole was loaded into the cores of micelles by injecting the organic phase composed of 0.5–2.5 mg·mL(−1) fluconazole and 1.5 mg·mL(−1) copolymer. The size of the drug-loaded micelles was found to be significantly larger than the size of empty micelles. MDPI 2016-05-25 /pmc/articles/PMC4931524/ /pubmed/27231945 http://dx.doi.org/10.3390/membranes6020029 Text en © 2016 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 Lu, Yu Chowdhury, Danial Vladisavljević, Goran T. Koutroumanis, Konstantinos Georgiadou, Stella Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title | Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title_full | Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title_fullStr | Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title_full_unstemmed | Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title_short | Production of Fluconazole-Loaded Polymeric Micelles Using Membrane and Microfluidic Dispersion Devices |
title_sort | production of fluconazole-loaded polymeric micelles using membrane and microfluidic dispersion devices |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931524/ https://www.ncbi.nlm.nih.gov/pubmed/27231945 http://dx.doi.org/10.3390/membranes6020029 |
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