Macroporous click-elastin-like hydrogels for tissue engineering applications
Creators
- 1. Department of Biohybrid & Medical Textiles (BioTex) at AME-Institute of Applied Medical Engineering, Helmholtz Institute-CBMS, RWTH Aachen University, Forckenbeckstr. 55, 52074 Aachen (Germany)
- 2. Electron Microscopy Facility, Uniklinik RWTH Aachen, Pauwelsstrasse, 30, D-52074 Aachen (Germany)
- 3. AMIBM-Aachen-Maastricht-Institute for Biobased Materials, Maastricht University, Urmonderbaan 22, 6167 RD, Geleen (Netherlands)
- 4. Bioforge Lab, University of Valladolid, CIBER-BBN, Paseo de Belen 11, 47011 Valladolid (Spain)
Description
Highlights: • Strategy to apply salt-leaching/gas foaming to click-elastin-like hydrogels • The resulting hydrogels featured controlled and interconnected porosity • Their mechanical properties compared well with those of many biological tissues. • The hydrogels were supportive of cell-ingrowth and extracellular matrix synthesis. • Applicable to click chemistry systems in general - Abstract: Elastin is a key extracellular matrix (ECM) protein that imparts functional elasticity to tissues and therefore an attractive candidate for bioengineering materials. Genetically engineered elastin-like recombinamers (ELRs) maintain inherent properties of the natural elastin (e.g. elastic behavior, bioactivity, low thrombogenicity, inverse temperature transition) while featuring precisely controlled composition, the possibility for biofunctionalization and non-animal origin. Recently the chemical modification of ELRs to enable their crosslinking via a catalyst-free click chemistry reaction, has further widened their applicability for tissue engineering. Despite these outstanding properties, the generation of macroporous click-ELR scaffolds with controlled, interconnected porosity has remained elusive so far. This significantly limits the potential of these materials as the porosity has a crucial role on cell infiltration, proliferation and ECM formation. In this study we propose a strategy to overcome this issue by adapting the salt leaching/gas foaming technique to click-ELRs. As result, macroporous hydrogels with tuned pore size and mechanical properties in the range of many native tissues were reproducibly obtained as demonstrated by rheological measurements and quantitative analysis of fluorescence, scanning electron and two-photon microscopy images. Additionally, the appropriate size and interconnectivity of the pores enabled smooth muscle cells to migrate into the click-ELR scaffolds and deposit extracellular matrix. The macroporous structure together with the elastic performance and bioactive character of ELRs, the specificity and non-toxic character of the catalyst-free click-chemistry reaction, make these scaffolds promising candidates for applications in tissue regeneration. This work expands the potential use of ELRs and click chemistry systems in general in different biomedical fields.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msec.2018.03.013Additional details
Identifiers
- DOI
- 10.1016/j.msec.2018.03.013;
- PII
- S0928493117335282;
Publishing Information
- Journal Title
- Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
- Journal Volume
- 88
- Journal Page Range
- p. 140-147
- ISSN
- 0928-4931
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 50038488
- Subject category
- S36: MATERIALS SCIENCE; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL TISSUES; CATALYSTS; CELL PROLIFERATION; CHEMISTRY; CROSS-LINKING; DEPOSITS; FLUORESCENCE; FOAMS; GENETIC ENGINEERING; HYDROGELS; LEACHING; MUSCLES; POROSITY; PROTEINS; SCANNING ELECTRON MICROSCOPY; SYNTHESIS; TRANSITION TEMPERATURE
- Descriptors DEC
- BIOTECHNOLOGY; BODY; CHEMICAL REACTIONS; COLLOIDS; DISPERSIONS; DISSOLUTION; ELECTRON MICROSCOPY; EMISSION; GELS; LUMINESCENCE; MICROSCOPY; ORGANIC COMPOUNDS; PHOTON EMISSION; PHYSICAL PROPERTIES; POLYMERIZATION; SEPARATION PROCESSES; THERMODYNAMIC PROPERTIES
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.