Click chemistry reactions have become an important tool for synthesizing user-defined hydrogels consisting of poly(ethylene glycol) (PEG) and bioactive peptides for tissue engineering. However, because click crosslinking proceeds via a step-growth mechanism, multi-arm telechelic precursors are required, which has some disadvantages. Here, we report for the first time that this requirement can be circumvented to create PEG–peptide hydrogels solely from linear precursors through the use of two orthogonal click reactions, the thiol–maleimide Michael addition and thiol–norbornene click reaction. The rapid kinetics of both click reactions allowed for quick formation of norbornene-functionalized PEG–peptide block copolymers via Michael addition, which were subsequently photocrosslinked into hydrogels with a dithiol linker. Characterization and in vitro testing demonstrated that the hydrogels have highly tunable physicochemical properties and excellent cytocompatibility. In addition, stoichiometric control over the crosslinking reaction can be leveraged to leave unreacted norbornene groups in the hydrogel for subsequent hydrogel functionalization via bioorthogonal inverse-electron demand Diels–Alder click reactions with s -tetrazines. After selectively capping norbornene groups in a user-defined region with cysteine, this feature was leveraged for protein patterning. Collectively, these results demonstrate that our novel chemical strategy is a simple and versatile approach to the development of hydrogels for tissue engineering that could be useful for a variety of applications.
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Waterborne functionalization of cellulose nanofibrils with norbornenes and subsequent thiol-norbornene gelation to create robust hydrogels
Cellulose nanofibrils (CNFs) produced through processes involving oxidation (e.g. TEMPO
oxidation) present reactive groups that allow for straightforward modification in aqueous suspension. CNFs fabricated through mechanical refinement alone can be challenging to modify for subsequent reactions due to only having hydroxyl groups present on the
surface. To address these issues, CNFs with only hydroxyl groups present were functionalized with norbornene groups in their native aqueous suspension to achieve up to 10% functionalization per anhydroglucose unit. Since quantification of surface functionalizationof CNFs is challenging through most methods, a degradation and subsequent nuclear magnetic resonance analysis method was developed to quantify norbornene functionalization. The norbornene functionalized CNFs (nCNFs) were crosslinked through UV and thermally initiated thiol-eneclick reactions to create robust CNF hydrogels. By varying the reaction conditions, hydrogels made from nCNFs and a dithiol cross-linker could achieve compression modulus values up to 25 kPa. The materials were stable in aqueous suspensions and the cross-linked hydrogels still exhibited shear thinning behavior with high recovery, which demonstrated that
even though effective cross-links were formed, a complete network was not. Through this study, thiolnorbornene crosslinking of CNFs could create robust hydrogels and improve aqueous stability that could have applications in sustainable materials and biomaterials.
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- Award ID(s):
- 1757529
- NSF-PAR ID:
- 10314380
- Date Published:
- Journal Name:
- Cellulose
- Volume:
- 28
- Issue:
- 3
- ISSN:
- 0969-0239
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Cellulose nanomaterial (CNM) and polyethylenimine (PEI) composites have attracted growing attention due to their multifunctional characteristics, which have been applied in different fields. In this work, soybean hulls were valorized into carboxyl cellulose nanofibrils (COOH-CNFs), and composited into hydrogels with PEI by combining them with cationic chelating and physical adsorption strategies. Cellulose nanofibrils (CNFs) were produced from soybean hulls prior to oxidation by a TEMPO mediated reaction to obtain COOH–CNFs; then drops of zinc chloride were added to 1.5% aqueous COOH–CNF dispersions, which were left for 24 h to form COOH-CNF hydrogels. Finally, the hydrogels were functionalized using different concentration of PEI solutions over a range of pH values. Elemental analysis results showed that 20% aq. PEI at pH 11.6 is the optimum condition to synthesize the COOH–CNF/PEI hydrogels. Additionally, the adsorption efficiency for the removal of anionic methyl blue dyes and Cu(II) ions from water was tested, reaching 82.6% and 69.8%, respectively, after 24 h. These results demonstrate the great potential of COOH–CNF/PEI hydrogels as adsorbent materials for water remediation.
Graphical abstract -
Directing polymer self-assembly through noncovalent interactions is a powerful way to control the structure and function of nanoengineered materials. Dynamic hydrogen bonds are particularly useful for materials with structures that change over time or in response to specific stimuli. In the present work, we use the supramolecular association of urea moieties to manipulate the morphology, thermal response, and mechanical properties of soft polymeric hydrogels. Urea-terminated poly(isopropyl glycidyl ether)- b -poly(ethylene oxide)- b -poly(isopropyl glycidyl ether) ABA triblock copolymers were synthesized using controlled, anionic ring-opening polymerization and subsequent chain-end functionalization. Triblock copolymers with hydroxy end-groups were incapable of hydrogelation, while polymers terminated with meta -bis-urea motifs formed robust gels at room temperature. Rheometric analysis of the bulk gels, variable-temperature infrared spectroscopy (VT-IR), differential scanning calorimetry (DSC), and small-angle X-ray scattering (SAXS) confirmed the formation of structured hydrogels via association of the meta -bis-urea end-groups. Monourea end-groups did not result in the same regular structure as the meta -bis-urea. In future, the reported hydrogels could be useful for elastomeric, shape-morphing 3D-printed constructs, or as biomimetic scaffolds with precisely tailored porosity and mechanical properties.more » « less
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1007/s10570-020-03582-z
