Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks
Effective integration of molecular self‐assembly and additive manufacturing would provide a technological leap in bioprinting. This article reports on a biofabrication system based on the hydrodynamically guided co‐assembly of peptide amphiphiles (PAs) with naturally occurring biomolecules and prote...
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sg-ntu-dr.10356-862112020-06-01T10:13:43Z Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks Hedegaard, Clara L. Collin, Estelle C. Redondo-Gómez, Carlos Nguyen, Luong T. H. Ng, Kee Woei Castrejón-Pita, Alfonso A. Castrejón-Pita, J. Rafael Mata, Alvaro School of Materials Science & Engineering Bioinks Bioprinting Engineering::Materials Effective integration of molecular self‐assembly and additive manufacturing would provide a technological leap in bioprinting. This article reports on a biofabrication system based on the hydrodynamically guided co‐assembly of peptide amphiphiles (PAs) with naturally occurring biomolecules and proteins to generate hierarchical constructs with tuneable molecular composition and structural control. The system takes advantage of droplet‐on‐demand inkjet printing to exploit interfacial fluid forces and guide molecular self‐assembly into aligned or disordered nanofibers, hydrogel structures of different geometries and sizes, surface topographies, and higher‐ordered constructs bound by molecular diffusion. PAs are designed to co‐assemble during printing in cell diluent conditions with a range of extracellular matrix (ECM) proteins and biomolecules including fibronectin, collagen, keratin, elastin‐like proteins, and hyaluronic acid. Using combinations of these molecules, NIH‐3T3 and adipose derived stem cells are bioprinted within complex structures while exhibiting high cell viability (>88%). By integrating self‐assembly with 3D‐bioprinting, the study introduces a novel biofabrication platform capable of encapsulating and spatially distributing multiple cell types within tuneable pericellular environments. In this way, the work demonstrates the potential of the approach to generate complex bioactive scaffolds for applications such as tissue engineering, in vitro models, and drug screening. 2019-07-10T07:27:59Z 2019-12-06T16:18:08Z 2019-07-10T07:27:59Z 2019-12-06T16:18:08Z 2018 Journal Article Hedegaard, C. L., Collin, E. C., Redondo-Gómez, C., Nguyen, L. T. H., Ng, K. W., Castrejón-Pita, A. A., . . . Mata, A. (2018). Hydrodynamically Guided Hierarchical Self-Assembly of Peptide-Protein Bioinks. Advanced Functional Materials, 28(16), 1703716-. doi:10.1002/adfm.201703716 1616-301X https://hdl.handle.net/10356/86211 http://hdl.handle.net/10220/49256 10.1002/adfm.201703716 en Advanced Functional Materials © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. |
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Bioinks Bioprinting Engineering::Materials Hedegaard, Clara L. Collin, Estelle C. Redondo-Gómez, Carlos Nguyen, Luong T. H. Ng, Kee Woei Castrejón-Pita, Alfonso A. Castrejón-Pita, J. Rafael Mata, Alvaro Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
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Effective integration of molecular self‐assembly and additive manufacturing would provide a technological leap in bioprinting. This article reports on a biofabrication system based on the hydrodynamically guided co‐assembly of peptide amphiphiles (PAs) with naturally occurring biomolecules and proteins to generate hierarchical constructs with tuneable molecular composition and structural control. The system takes advantage of droplet‐on‐demand inkjet printing to exploit interfacial fluid forces and guide molecular self‐assembly into aligned or disordered nanofibers, hydrogel structures of different geometries and sizes, surface topographies, and higher‐ordered constructs bound by molecular diffusion. PAs are designed to co‐assemble during printing in cell diluent conditions with a range of extracellular matrix (ECM) proteins and biomolecules including fibronectin, collagen, keratin, elastin‐like proteins, and hyaluronic acid. Using combinations of these molecules, NIH‐3T3 and adipose derived stem cells are bioprinted within complex structures while exhibiting high cell viability (>88%). By integrating self‐assembly with 3D‐bioprinting, the study introduces a novel biofabrication platform capable of encapsulating and spatially distributing multiple cell types within tuneable pericellular environments. In this way, the work demonstrates the potential of the approach to generate complex bioactive scaffolds for applications such as tissue engineering, in vitro models, and drug screening. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Hedegaard, Clara L. Collin, Estelle C. Redondo-Gómez, Carlos Nguyen, Luong T. H. Ng, Kee Woei Castrejón-Pita, Alfonso A. Castrejón-Pita, J. Rafael Mata, Alvaro |
format |
Article |
author |
Hedegaard, Clara L. Collin, Estelle C. Redondo-Gómez, Carlos Nguyen, Luong T. H. Ng, Kee Woei Castrejón-Pita, Alfonso A. Castrejón-Pita, J. Rafael Mata, Alvaro |
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Hedegaard, Clara L. |
title |
Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
title_short |
Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
title_full |
Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
title_fullStr |
Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
title_full_unstemmed |
Hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
title_sort |
hydrodynamically guided hierarchical self-assembly of peptide-protein bioinks |
publishDate |
2019 |
url |
https://hdl.handle.net/10356/86211 http://hdl.handle.net/10220/49256 |
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1681056918377857024 |