Article (Scientific journals)
Protein encapsulation in mesoporous silica: influence of the mesostructured and pore wall properties
Tilkin, Rémi; Mahy, Julien; Monteiro, Ana et al.
2022In Colloids and Surfaces A: Physicochemical and Engineering Aspects, 642, p. 128629
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Keywords :
biomaterials; bone reconstruction; protein encapsulation; silica gel; sol-gel process; structured silica; ordered mesoporous silica; SBA-15
Abstract :
[en] The goal of this work is to study the influence of the structured mesoporous silica (SMS), used as scaffolds for tissue engineering, on the encapsulation and on the release of a model bone morphogenetic proteins (BMP), i.e. Soybean Trypsin Inhibitor (STI). First, SBA-15 silica samples were synthesized using tetraethyl orthosilicate (TEOS) as silica precursor in the presence of P123 as the surfactant in an acidic medium. Three homemade high-pressure stainless steel reactors (with smaller Teflon reactors inside), each equipped with a temperature probe, were used for the syntheses. In addition, a swelling agent was added to increase the pore size. Indeed, the common pore size for those mesostructured materials lies between 6 nm and 8 nm, while the STI has an average radius of 4 nm. The reagent addition sequence was also investigated, by playing on the time of addition of the swelling agent. It was observed that when the swelling agent was added with TEOS, an ordered mesoporous silica was produced. On the contrary, if the swelling agent was added during the surfactant dissolution step, it resulted in an unstructured yet still mesoporous silica. Because of the high affinity of STI for hydrophobic surfaces, SMS were also produced using silica precursors containing phenylene bridging groups (1,4-bis(triethoxysilyl)benzene, BTEB). The BTEB samples exhibited two 2D-hexagonal structures with different wall thicknesses. Synthesized materials were further characterized by infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), nitrogen sorption at 77 K, transmission electron microscopy (TEM), and small-angle X-ray scattering (SAXS). The influence of both the silica composition and structure on STI encapsulation/release was studied. For samples synthesized with TEOS, the unstructured sample showed a higher protein loading and a higher protein release, which could be explained by a difference in the pore interconnectivity within the sample. In fact, a fast release of STI was observed during the first 24 h. Afterwards, the STI release slowed down and seemed to reach a plateau. On the opposite, the structured sample showed a steady release over time. Finally, the sample synthesized with BTEB did not show a significant release over the same period of time. This led us to the conclusion that the hydrophobicity of the silica surface plays a major role on the protein encapsulation and its release rate.
Disciplines :
Materials science & engineering
Chemical engineering
Author, co-author :
Tilkin, Rémi  ;  Université de Liège - ULiège > Department of Chemical Engineering > Nanomaterials, Catalysis, Electrochemistry
Mahy, Julien  ;  Université de Liège - ULiège > Department of Chemical Engineering > Nanomaterials, Catalysis, Electrochemistry
Monteiro, Ana ;  Université de Liège - ULiège > Unités de recherche interfacultaires > Centre interfacultaire des biomatériaux (CEIB)
Belet, Artium ;  Université de Liège - ULiège > Chemical engineering
Feijóo, Julio
Laird, Mathilde
Carcel, Carole
Regibeau, Nicolas ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biochimie et physiologie générales, et biochimie humaine
Goderis, Bart
Grandfils, Christian ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques
Man, Michel Wong Chi
Lambert, Stéphanie  ;  Université de Liège - ULiège > Department of Chemical Engineering > Nanomaterials, Catalysis, Electrochemistry
Language :
English
Title :
Protein encapsulation in mesoporous silica: influence of the mesostructured and pore wall properties
Publication date :
March 2022
Journal title :
Colloids and Surfaces A: Physicochemical and Engineering Aspects
ISSN :
0927-7757
eISSN :
1873-4359
Publisher :
Elsevier BV
Volume :
642
Pages :
128629
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 25 February 2022

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