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Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS

Single-domain antibodies (sdAbs) offer great features such as increased stability but are hampered by a limited serum half-life. Many strategies have been developed to improve the sdAb half-life, such as protein engineering and controlled release systems (CRS). In our study, we designed a new produc...

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Detalles Bibliográficos
Autores principales: Nicolas, Alexandre, Dejoux, Alice, Poirier, Cécile, Aubrey, Nicolas, Péan, Jean-Manuel, Velge-Roussel, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601711/
https://www.ncbi.nlm.nih.gov/pubmed/32993086
http://dx.doi.org/10.3390/pharmaceutics12100921
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author Nicolas, Alexandre
Dejoux, Alice
Poirier, Cécile
Aubrey, Nicolas
Péan, Jean-Manuel
Velge-Roussel, Florence
author_facet Nicolas, Alexandre
Dejoux, Alice
Poirier, Cécile
Aubrey, Nicolas
Péan, Jean-Manuel
Velge-Roussel, Florence
author_sort Nicolas, Alexandre
collection PubMed
description Single-domain antibodies (sdAbs) offer great features such as increased stability but are hampered by a limited serum half-life. Many strategies have been developed to improve the sdAb half-life, such as protein engineering and controlled release systems (CRS). In our study, we designed a new product that combined a hydrogel with a 3D-printed implant. The results demonstrate the implant’s ability to sustain sdAb release up to 13 days through a reduced initial burst release followed by a continuous release. Furthermore, formulation screening helped to identify the best sdAb formulation conditions and improved our understanding of our CRS. Through the screening step, we gained knowledge about the influence of the choice of polymer and about potential interactions between the sdAb and the polymer. To conclude, this feasibility study confirmed the ability of our CRS to extend sdAb release and established the fundamental role of formulation screening for maximizing knowledge about our CRS.
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spelling pubmed-76017112020-11-01 Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS Nicolas, Alexandre Dejoux, Alice Poirier, Cécile Aubrey, Nicolas Péan, Jean-Manuel Velge-Roussel, Florence Pharmaceutics Article Single-domain antibodies (sdAbs) offer great features such as increased stability but are hampered by a limited serum half-life. Many strategies have been developed to improve the sdAb half-life, such as protein engineering and controlled release systems (CRS). In our study, we designed a new product that combined a hydrogel with a 3D-printed implant. The results demonstrate the implant’s ability to sustain sdAb release up to 13 days through a reduced initial burst release followed by a continuous release. Furthermore, formulation screening helped to identify the best sdAb formulation conditions and improved our understanding of our CRS. Through the screening step, we gained knowledge about the influence of the choice of polymer and about potential interactions between the sdAb and the polymer. To conclude, this feasibility study confirmed the ability of our CRS to extend sdAb release and established the fundamental role of formulation screening for maximizing knowledge about our CRS. MDPI 2020-09-26 /pmc/articles/PMC7601711/ /pubmed/32993086 http://dx.doi.org/10.3390/pharmaceutics12100921 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
Nicolas, Alexandre
Dejoux, Alice
Poirier, Cécile
Aubrey, Nicolas
Péan, Jean-Manuel
Velge-Roussel, Florence
Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title_full Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title_fullStr Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title_full_unstemmed Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title_short Contribution of Intrinsic Fluorescence to the Design of a New 3D-Printed Implant for Releasing SDABS
title_sort contribution of intrinsic fluorescence to the design of a new 3d-printed implant for releasing sdabs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601711/
https://www.ncbi.nlm.nih.gov/pubmed/32993086
http://dx.doi.org/10.3390/pharmaceutics12100921
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