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Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods

Silk fibroin nanoprecipitation by organic desolvation in semi-batch and microfluidic formats provides promising bottom-up routes for manufacturing narrow polydispersity, spherical silk nanoparticles. The translation of silk nanoparticle production to pilot, clinical, and industrial scales can be aid...

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Detalles Bibliográficos
Autores principales: Matthew, Saphia A. L., Rezwan, Refaya, Perrie, Yvonne, Seib, F. Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000471/
https://www.ncbi.nlm.nih.gov/pubmed/35408763
http://dx.doi.org/10.3390/molecules27072368
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author Matthew, Saphia A. L.
Rezwan, Refaya
Perrie, Yvonne
Seib, F. Philipp
author_facet Matthew, Saphia A. L.
Rezwan, Refaya
Perrie, Yvonne
Seib, F. Philipp
author_sort Matthew, Saphia A. L.
collection PubMed
description Silk fibroin nanoprecipitation by organic desolvation in semi-batch and microfluidic formats provides promising bottom-up routes for manufacturing narrow polydispersity, spherical silk nanoparticles. The translation of silk nanoparticle production to pilot, clinical, and industrial scales can be aided through insight into the property drifts incited by nanoprecipitation scale-up and the identification of critical process parameters to maintain throughout scaling. Here, we report the reproducibility of silk nanoprecipitation on volumetric scale-up in low-shear, semi-batch systems and estimate the reproducibility of chip parallelization for volumetric scale-up in a high shear, staggered herringbone micromixer. We showed that silk precursor feeds processed in an unstirred semi-batch system (mixing time > 120 s) displayed significant changes in the nanoparticle physicochemical and crystalline properties following a 12-fold increase in volumetric scale between 1.8 and 21.9 mL while the physicochemical properties stayed constant following a further 6-fold increase in scale to 138 mL. The nanoparticle physicochemical properties showed greater reproducibility after a 6-fold volumetric scale-up when using lower mixing times of greater similarity (8.4 s and 29.4 s) with active stirring at 400 rpm, indicating that the bulk mixing time and average shear rate should be maintained during volumetric scale-up. Conversely, microfluidic manufacture showed high between-batch repeatability and between-chip reproducibility across four participants and microfluidic chips, thereby strengthening chip parallelization as a production strategy for silk nanoparticles at pilot, clinical, and industrial scales.
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spelling pubmed-90004712022-04-12 Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods Matthew, Saphia A. L. Rezwan, Refaya Perrie, Yvonne Seib, F. Philipp Molecules Article Silk fibroin nanoprecipitation by organic desolvation in semi-batch and microfluidic formats provides promising bottom-up routes for manufacturing narrow polydispersity, spherical silk nanoparticles. The translation of silk nanoparticle production to pilot, clinical, and industrial scales can be aided through insight into the property drifts incited by nanoprecipitation scale-up and the identification of critical process parameters to maintain throughout scaling. Here, we report the reproducibility of silk nanoprecipitation on volumetric scale-up in low-shear, semi-batch systems and estimate the reproducibility of chip parallelization for volumetric scale-up in a high shear, staggered herringbone micromixer. We showed that silk precursor feeds processed in an unstirred semi-batch system (mixing time > 120 s) displayed significant changes in the nanoparticle physicochemical and crystalline properties following a 12-fold increase in volumetric scale between 1.8 and 21.9 mL while the physicochemical properties stayed constant following a further 6-fold increase in scale to 138 mL. The nanoparticle physicochemical properties showed greater reproducibility after a 6-fold volumetric scale-up when using lower mixing times of greater similarity (8.4 s and 29.4 s) with active stirring at 400 rpm, indicating that the bulk mixing time and average shear rate should be maintained during volumetric scale-up. Conversely, microfluidic manufacture showed high between-batch repeatability and between-chip reproducibility across four participants and microfluidic chips, thereby strengthening chip parallelization as a production strategy for silk nanoparticles at pilot, clinical, and industrial scales. MDPI 2022-04-06 /pmc/articles/PMC9000471/ /pubmed/35408763 http://dx.doi.org/10.3390/molecules27072368 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
Matthew, Saphia A. L.
Rezwan, Refaya
Perrie, Yvonne
Seib, F. Philipp
Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title_full Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title_fullStr Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title_full_unstemmed Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title_short Volumetric Scalability of Microfluidic and Semi-Batch Silk Nanoprecipitation Methods
title_sort volumetric scalability of microfluidic and semi-batch silk nanoprecipitation methods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000471/
https://www.ncbi.nlm.nih.gov/pubmed/35408763
http://dx.doi.org/10.3390/molecules27072368
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