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Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations

[Image: see text] We present an approach for the rational development of stimuli-responsive ionogels which can be formulated for precise control of multiple unique ionogel features and fill niche pharmaceutical applications. Ionogels are captivating materials, exhibiting self-healing characteristics...

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Autores principales: Shmool, Talia A., Martin, Laura K., Jirkas, Andreas, Matthews, Richard P., Constantinou, Anna P., Vadukul, Devkee M., Georgiou, Theoni K., Aprile, Francesco A., Hallett, Jason P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413859/
https://www.ncbi.nlm.nih.gov/pubmed/37576585
http://dx.doi.org/10.1021/acs.chemmater.3c00303
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author Shmool, Talia A.
Martin, Laura K.
Jirkas, Andreas
Matthews, Richard P.
Constantinou, Anna P.
Vadukul, Devkee M.
Georgiou, Theoni K.
Aprile, Francesco A.
Hallett, Jason P.
author_facet Shmool, Talia A.
Martin, Laura K.
Jirkas, Andreas
Matthews, Richard P.
Constantinou, Anna P.
Vadukul, Devkee M.
Georgiou, Theoni K.
Aprile, Francesco A.
Hallett, Jason P.
author_sort Shmool, Talia A.
collection PubMed
description [Image: see text] We present an approach for the rational development of stimuli-responsive ionogels which can be formulated for precise control of multiple unique ionogel features and fill niche pharmaceutical applications. Ionogels are captivating materials, exhibiting self-healing characteristics, tunable mechanical and structural properties, high thermal stability, and electroconductivity. However, the majority of ionogels developed require complex chemistry, exhibit high viscosity, poor biocompatibility, and low biodegradability. In our work, we overcome these limitations. We employ a facile production process and strategically integrate silk fibroin, the biocompatible ionic liquids (ILs) choline acetate ([Cho][OAc]), choline dihydrogen phosphate ([Cho][DHP]), and choline chloride ([Cho][Cl]), traditional pharmaceutical excipients, and the model antiepileptic drug phenobarbital. In the absence of ILs, we failed to observe gel formation; yet in the presence of ILs, thermoresponsive ionogels formed. Systems were assessed via visual tests, transmission electron microscopy, confocal reflection microscopy, dynamic light scattering, zeta potential and rheology measurements. We formed diverse ionogels of strengths ranging between 18 and 642 Pa. Under 25 °C storage, formulations containing polyvinylpyrrolidone (PVP) showed an ionogel formation period ranging over 14 days, increasing in the order of [Cho][DHP], [Cho][OAc], and [Cho][Cl]. Formulations lacking PVP showed an ionogel formation period ranging over 32 days, increasing in the order of [Cho][OAc], [Cho][DHP] and [Cho][Cl]. By heating from 25 to 60 °C, immediately following preparation, thermoresponsive ionogels formed below 41 °C in the absence of PVP. Based on our experimental results and density functional theory calculations, we attribute ionogel formation to macromolecular crowding and confinement effects, further enhanced upon PVP inclusion. Holistically, applying our rational development strategy enables the production of ionogels of tunable physicochemical and rheological properties, enhanced drug solubility, and structural and energetic stability. We believe our rational development approach will advance the design of biomaterials and smart platforms for diverse drug delivery applications.
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spelling pubmed-104138592023-08-11 Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations Shmool, Talia A. Martin, Laura K. Jirkas, Andreas Matthews, Richard P. Constantinou, Anna P. Vadukul, Devkee M. Georgiou, Theoni K. Aprile, Francesco A. Hallett, Jason P. Chem Mater [Image: see text] We present an approach for the rational development of stimuli-responsive ionogels which can be formulated for precise control of multiple unique ionogel features and fill niche pharmaceutical applications. Ionogels are captivating materials, exhibiting self-healing characteristics, tunable mechanical and structural properties, high thermal stability, and electroconductivity. However, the majority of ionogels developed require complex chemistry, exhibit high viscosity, poor biocompatibility, and low biodegradability. In our work, we overcome these limitations. We employ a facile production process and strategically integrate silk fibroin, the biocompatible ionic liquids (ILs) choline acetate ([Cho][OAc]), choline dihydrogen phosphate ([Cho][DHP]), and choline chloride ([Cho][Cl]), traditional pharmaceutical excipients, and the model antiepileptic drug phenobarbital. In the absence of ILs, we failed to observe gel formation; yet in the presence of ILs, thermoresponsive ionogels formed. Systems were assessed via visual tests, transmission electron microscopy, confocal reflection microscopy, dynamic light scattering, zeta potential and rheology measurements. We formed diverse ionogels of strengths ranging between 18 and 642 Pa. Under 25 °C storage, formulations containing polyvinylpyrrolidone (PVP) showed an ionogel formation period ranging over 14 days, increasing in the order of [Cho][DHP], [Cho][OAc], and [Cho][Cl]. Formulations lacking PVP showed an ionogel formation period ranging over 32 days, increasing in the order of [Cho][OAc], [Cho][DHP] and [Cho][Cl]. By heating from 25 to 60 °C, immediately following preparation, thermoresponsive ionogels formed below 41 °C in the absence of PVP. Based on our experimental results and density functional theory calculations, we attribute ionogel formation to macromolecular crowding and confinement effects, further enhanced upon PVP inclusion. Holistically, applying our rational development strategy enables the production of ionogels of tunable physicochemical and rheological properties, enhanced drug solubility, and structural and energetic stability. We believe our rational development approach will advance the design of biomaterials and smart platforms for diverse drug delivery applications. American Chemical Society 2023-07-20 /pmc/articles/PMC10413859/ /pubmed/37576585 http://dx.doi.org/10.1021/acs.chemmater.3c00303 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Shmool, Talia A.
Martin, Laura K.
Jirkas, Andreas
Matthews, Richard P.
Constantinou, Anna P.
Vadukul, Devkee M.
Georgiou, Theoni K.
Aprile, Francesco A.
Hallett, Jason P.
Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title_full Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title_fullStr Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title_full_unstemmed Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title_short Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations
title_sort unveiling the rational development of stimuli-responsive silk fibroin-based ionogel formulations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413859/
https://www.ncbi.nlm.nih.gov/pubmed/37576585
http://dx.doi.org/10.1021/acs.chemmater.3c00303
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