Journal
ADVANCED SCIENCE
Volume 10, Issue 13, Pages -Publisher
WILEY
DOI: 10.1002/advs.202207403
Keywords
3D writing; biopolymers; nanoscale confinement; solvent-exclusive evaporation; sub-micron resolution
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Through nanoscale confinement, evaporation, and solidification, the direct 3D printing of intact biopolymers is demonstrated, allowing precise control of molecular-scale structures and shapes. Different biopolymers can be patterned with desired size and geometry by controlling concentrations and molecular weights, and their 3D architectures are biologically active in various solvents.
Biopolymers are essential building blocks that constitute cells and tissues with well-defined molecular structures and diverse biological functions. Their three-dimensional (3D) complex architectures are used to analyze, control, and mimic various cells and their ensembles. However, the free-form and high-resolution structuring of various biopolymers remain challenging because their structural and rheological control depend critically on their polymeric types at the submicron scale. Here, direct 3D writing of intact biopolymers is demonstrated using a systemic combination of nanoscale confinement, evaporation, and solidification of a biopolymer-containing solution. A femtoliter solution is confined in an ultra-shallow liquid interface between a fine-tuned nanopipette and a chosen substrate surface to achieve directional growth of biopolymer nanowires via solvent-exclusive evaporation and concurrent solution supply. The evaporation-dependent printing is biopolymer type-independent, therefore, the 3D motor-operated precise nanopipette positioning allows in situ printing of nucleic acids, polysaccharides, and proteins with submicron resolution. By controlling concentrations and molecular weights, several different biopolymers are reproducibly patterned with desired size and geometry, and their 3D architectures are biologically active in various solvents with no structural deformation. Notably, protein-based nanowire patterns exhibit pin-point localization of spatiotemporal biofunctions, including target recognition and catalytic peroxidation, indicating their application potential in organ-on-chips and micro-tissue engineering.
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