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Gurminder K. Paink

Publications and source records attributed to Gurminder K. Paink.

3 recordsLinked to original sources

Fabrication framework for three-dimensional colloidal particles with decoupled geometry and material composition

Shape-programmable particles offer significant opportunities for microrobotic systems at the individual level and for hierarchical materials with emergent functionalities arising from collective particle behavior. However, fabricating shape-changing stimuli-responsive particles with complex three-dimensional geometries at colloidal length scales remains a major challenge. Here, we introduce a general fabrication framework that decouples particle geometry from material composition to produce free-standing three-dimensional colloidal particles with complex architectures. Our approach combines soft lithography, swelling-assisted extraction, and sacrificial adhesive transfer to fabricate particles with high geometric fidelity. We establish a predictive framework that defines the accessible design space for increasingly complex particle geometries. We further extend our framework to fabricate high-aspect-ratio pillar arrays with intricate three-dimensional architectures at colloidal length scales. To demonstrate material versatility, we fabricate particles from both liquid crystal elastomers and hydrogels. We show reversible shape-changing behavior of liquid crystal elastomer particles with cylindrical and chiral shapes under thermal and optical stimuli. In suspension, these particles display collective optical dynamic behavior arising from coupling between changes in the programmed liquid crystal organization within the particles and stimulus-induced geometric reconfiguration of the particles. Collectively, this work establishes a versatile platform for geometry-programmable colloidal particles with emergent collective functionalities, providing a route toward materials and fluids with dynamically programmable properties.

cond-mat.mtrl-sci↗

Rotational 3D printing of active-passive filaments and lattices with programmable shape morphing

Natural filaments, such as proteins, plant tendrils, octopus tentacles, and elephant trunks, can transform into arbitrary three-dimensional shapes that carry out vital functions. Their shape-morphing behavior arises from intricate patterning of active and passive regions, which are difficult to replicate in synthetic matter. Here, we introduce a filament-centric strategy for programmable shape morphing in which intrinsic curvature and twist are directly encoded within multimaterial elastomeric filaments during fabrication. By harnessing rotational multimaterial 3D printing (RM-3DP), we directly prescribe the filament's natural curvature--twist field $\mathbf{k}(s)$ through controlled material distribution and helical liquid crystal mesogen alignment. When heated above their nematic-to-isotropic transition temperature ($T_\mathrm{NI}$), the helically aligned LCE regions contract along their local director field, while passive regions remain essentially unchanged. This approach enables independent control of bending and torsion at every cross-section along the filament centerline: the principal natural curvatures of the filament along two orthogonal axes as well as the local twist. Next, we printed architected lattices composed of unit cells formed by sinusoidal filaments that either reversibly contract, expand, or exhibit out-of-plane deformations. Discrete elastic rod simulations of Janus filaments with different natural curvatures and twist, which are interconnected within the printed lattices, allow accurate prediction of their observed shape-morphing behavior. By integrating active-passive elastomers, additive manufacturing, and computational modeling, we have created shape-morphing matter with complex programmable responses for applications that rely on adaptive, robotic, or deployable architectures.

cond-mat.soft↗

Cargo Delivery to Cells Using Laser-Irradiated Carbon-Black-Loaded PDMS

Effective intracellular delivery is essential for successful gene editing of cells. Spatially selective delivery to cells that is simultaneously precise, consistent, and non-destructive remains challenging using conventional state-of-the-art techniques. Here, we introduce a carrier-free method for spatiotemporal delivery of fluorescently labeled cargo into both adherent and suspension cells using carbon-black-embedded polydimethylsiloxane (PDMS) substrates irradiated by nanosecond laser pulses. This low-cost, biocompatible material, coupled with an optical approach, enables scalable, spatially selective, and sequential delivery of multiple cargo molecules, including FITC-dextran and siRNA, to a broad range of cells. Notably, we achieved siRNA delivery into the cytoplasm of hard-to-transfect K562 cells with 45% efficiency, while maintaining nearly 100% cell viability.

cond-mat.mtrl-sci↗