Soft, precision engineered porous, hydrogel scaffolds mechanically tailored toward applications in the central nervous system

Diseases and traumatic injuries to the central nervous system (CNS) demand the development of new biomaterials to improve healing and treatment options. Matching material mechanical properties to specific tissues and optimizing material porous structures are central goals for improving biomaterials. However, biomaterials with both precision-controlled porous structures and brain-matched mechanical properties (low modulus) are still lacking. In this study, we developed soft hydrogel scaffolds with mechanical properties similar to that of CNS tissues, and a uniform 40 µm porous structure—40 µm pores have been shown to be optimal for healing in many tissues. The two characteristics were achieved by a new fabrication process combining phase separation and sphere templating. The resulting scaffolds are non-cytotoxic according to the ISO 10993-5 standard. In addition, the three-dimensional culture of microglial cells within the scaffolds demonstrates cell attachment and maintenance of a rounded, quiescent morphology, potentially due to spatial confinement. These results justify further in vivo studies and suggest broad potential in CNS applications, such as brain-computer interfaces, neural regeneration, and basic neurobiology. Subject classification codes: Neural Interfaces, soft hydrogel, synthetic biomaterials

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Publication Details

Journal
Journal of Bioactive and Compatible Polymers
Published
2024-11-01
DOI
https://doi.org/10.1177/08839115241287215
Citations
2
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
0.37

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article

Soft, precision engineered porous, hydrogel scaffolds mechanically tailored toward applications in the central nervous system

Lars Crawford, Ningjing Chen, Manjari Anant, Le Zhen et al.
2 citations
Journal of Bioactive and Compatible Polymers
3D Printing in Biomedical Research
0.37
article

Soft, precision engineered porous, hydrogel scaffolds mechanically tailored toward applications in the central nervous system

Lars Crawford, Ningjing Chen, Manjari Anant, Le Zhen, Ian Dryg, Buddy D. Ratner, Lahari Gorantla, Robert D. Darrow, Chaoyang Tang
article en
2 citations

Abstract

Diseases and traumatic injuries to the central nervous system (CNS) demand the development of new biomaterials to improve healing and treatment options. Matching material mechanical properties to specific tissues and optimizing material porous structures are central goals for improving biomaterials. However, biomaterials with both precision-controlled porous structures and brain-matched mechanical properties (low modulus) are still lacking. In this study, we developed soft hydrogel scaffolds with mechanical properties similar to that of CNS tissues, and a uniform 40 µm porous structure—40 µm pores have been shown to be optimal for healing in many tissues. The two characteristics were achieved by a new fabrication process combining phase separation and sphere templating. The resulting scaffolds are non-cytotoxic according to the ISO 10993-5 standard. In addition, the three-dimensional culture of microglial cells within the scaffolds demonstrates cell attachment and maintenance of a rounded, quiescent morphology, potentially due to spatial confinement. These results justify further in vivo studies and suggest broad potential in CNS applications, such as brain-computer interfaces, neural regeneration, and basic neurobiology. Subject classification codes: Neural Interfaces, soft hydrogel, synthetic biomaterials

Journal of Bioactive and Compatible PolymersVol. 39(6)
University of Washington (US)
Institute of Translational Health Sciences, University of Washington
Good health and well-being
Openalex Percentile: Top 42%
3D Printing in Biomedical Research
0.37
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Soft, precision engineered porous, hydrogel scaffolds mechanically tailored toward applications in the central nervous system — Lars Crawford, Ningjing Chen, et al. · Journal of Bioactive and Compatible Polymers (2024) | TGRS Research Map | TGRS