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Tailor-Made Fluorinated Ionic Liquids for Protein Delivery

Nowadays, pharmaceutical companies are facing several challenges with the development and approval of new biological products. The unique properties of several fluorinated ionic liquids (FILs), such as their high surfactant power in aqueous solutions, their chemical and biological stability, and low...

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Detalles Bibliográficos
Autores principales: Vieira, N. S. M., Castro, P. J., Marques, D. F., Araújo, J. M. M., Pereiro, A. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466544/
https://www.ncbi.nlm.nih.gov/pubmed/32823882
http://dx.doi.org/10.3390/nano10081594
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author Vieira, N. S. M.
Castro, P. J.
Marques, D. F.
Araújo, J. M. M.
Pereiro, A. B.
author_facet Vieira, N. S. M.
Castro, P. J.
Marques, D. F.
Araújo, J. M. M.
Pereiro, A. B.
author_sort Vieira, N. S. M.
collection PubMed
description Nowadays, pharmaceutical companies are facing several challenges with the development and approval of new biological products. The unique properties of several fluorinated ionic liquids (FILs), such as their high surfactant power in aqueous solutions, their chemical and biological stability, and low toxicity, favor their application in the pharmaceutical industry. Furthermore, the numerous combinations between cations and anions, in the FILs design, enlarge the possibilities to construct a successful delivery system. Several FILs also proved to not affect the activity, stability, and secondary structure of the therapeutic protein lysozyme. This work aims to study the aggregation behavior of distinct FILs in the protein suitable medium, in the presence or absence of lysozyme. Besides, different incubation conditions were tested to guarantee the optimal enzymatic activity of the protein at more stable delivery systems. Following the optimization of the incubation conditions, the quantification of the encapsulated lysozyme was performed to evaluate the encapsulation efficiency of each FIL-based system. The release of the protein was tested applying variables such as time, temperature, and ultrasound frequency. The experimental results suggest that the aggregation behavior of FILs is not significantly influenced by the protein and/or protein buffer and supports their application for the design of delivery systems with high encapsulation efficiencies, maintaining the biological activity of either encapsulated and released protein.
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spelling pubmed-74665442020-09-14 Tailor-Made Fluorinated Ionic Liquids for Protein Delivery Vieira, N. S. M. Castro, P. J. Marques, D. F. Araújo, J. M. M. Pereiro, A. B. Nanomaterials (Basel) Article Nowadays, pharmaceutical companies are facing several challenges with the development and approval of new biological products. The unique properties of several fluorinated ionic liquids (FILs), such as their high surfactant power in aqueous solutions, their chemical and biological stability, and low toxicity, favor their application in the pharmaceutical industry. Furthermore, the numerous combinations between cations and anions, in the FILs design, enlarge the possibilities to construct a successful delivery system. Several FILs also proved to not affect the activity, stability, and secondary structure of the therapeutic protein lysozyme. This work aims to study the aggregation behavior of distinct FILs in the protein suitable medium, in the presence or absence of lysozyme. Besides, different incubation conditions were tested to guarantee the optimal enzymatic activity of the protein at more stable delivery systems. Following the optimization of the incubation conditions, the quantification of the encapsulated lysozyme was performed to evaluate the encapsulation efficiency of each FIL-based system. The release of the protein was tested applying variables such as time, temperature, and ultrasound frequency. The experimental results suggest that the aggregation behavior of FILs is not significantly influenced by the protein and/or protein buffer and supports their application for the design of delivery systems with high encapsulation efficiencies, maintaining the biological activity of either encapsulated and released protein. MDPI 2020-08-14 /pmc/articles/PMC7466544/ /pubmed/32823882 http://dx.doi.org/10.3390/nano10081594 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
Vieira, N. S. M.
Castro, P. J.
Marques, D. F.
Araújo, J. M. M.
Pereiro, A. B.
Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title_full Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title_fullStr Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title_full_unstemmed Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title_short Tailor-Made Fluorinated Ionic Liquids for Protein Delivery
title_sort tailor-made fluorinated ionic liquids for protein delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466544/
https://www.ncbi.nlm.nih.gov/pubmed/32823882
http://dx.doi.org/10.3390/nano10081594
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