Searcharxiv⌕ Search

arXiv subjects

Soojung Claire Hur

Publications and source records attributed to Soojung Claire Hur.

4 recordsLinked to original sources

Biocompatible Microscale DNA Hydrogels with Programmable Swelling and Sequence-Specific Dissolution

Stimulus-responsive DNA-hydrogels with swelling capabilities are a promising class of materials for biomedical applications such as drug delivery and biosensing. However, translation of these systems to microscale applications requires fabrication methods that are both biocompatible and material-efficient, while enabling precise control over stimulus-induced swelling and its impact on molecular transport. Here, we present a biocompatible fabrication and characterization platform for micron-scale DNA-hydrogels (microSDs) with tunable isotropic swelling and dissolving properties. Our approach includes a biocompatible, material-efficient fabrication workflow that conserves valuable DNA reagents by minimizing dead volume and process loss. We then demonstrated modular control over isotropic swelling in microSDs, achieving up to a two-fold size increase through programmable DNA design parameters. We further established a quantitative workflow to extract effective diffusivity and characterize swelling-induced modulation of molecular transport in spherical microSDs using YOYO-1. Finally, we demonstrate the dissolution of microSDs using a DNA strand and find that dissolution kinetics are governed by the rates of coupled strand-displacement reactions and diffusive transport. This platform enables programmable swelling and structural disassembly in microSDs. Swelling-induced network expansion further allows predictable modulation of molecular transport, thereby expanding the potential of microSDs for applications such as triggered drug delivery, multiplexed biosensing, and single-cell assays.

cond-mat.soft↗

Integrated vortex-assisted electroporation platform with enhanced throughput for genetic delivery to primary cells

Primary human cells offer the most faithful representation of native human physiology, yet their practical utility is constrained by the difficulty of introducing exogenous genetic material. Electroporation provides a promising non-viral gene delivery approach; however, conventional bulk systems lack the uniformity and integration required for heterogeneous primary cell samples. Here, we present a vortex-assisted electroporation platform integrating size-selective cell trapping with enhanced throughput, parameter optimization across buffer and electrical conditions, and robust delivery of plasmid DNA and in vitro-transcribed mRNA in primary human cells. This integrated platform provides a unified workflow that addresses sample heterogeneity, throughput demands, and delivery efficiency, enabling broader implementation of non-viral gene delivery into primary cells for research and translational applications.

physics.app-ph↗

Triaxial Asymmetry Driven Rotational Dynamics and Lateral Equilibrium Position in Inertial Flow

The growing use of triaxial particles in microfluidic, microrobotic, and biological systems makes it essential to understand how their rotational dynamics couples with lateral migration in microscale flows. Our experiments in inertial Poiseuille flow reveal that geometric asymmetry in triaxial, multifaceted disks governs their orientation, migration, and rotational period, distinguishing them from classical axisymmetric objects. We identified a Reynolds- and geometry-dependent shift in preferred rotational orientation, arising from the Dzhanibekov effect, with transition modes determined by the particle's principal-axis configuration. We quantified a scalar offset from Jeffery's orbit prediction and introduced a fitting parameter that generalizes the Jeffery equation to include moment-of-inertia effects on rotational dynamics. Finally, we report the diameter of gyration as a predictor of the lateral equilibrium position of inertially focused triaxial particles. Our results link particle asymmetry to migration and rotation in flow, expanding our understanding of particle dynamics.

physics.flu-dyn↗

Lateral migration of living cells in inertial microfluidic systems explored by fully three-dimensional numerical simulation

The effects of cell size and deformability on the lateral migration and deformation of living cells flowing through a rectangular microchannel has been numerically investigated and compared with the inertial-microfluidics data on detection and separation of cells. The results of this work indicate that the cells move closer to the centerline if they are bigger and/or more deformable and that their equilibrium position is largely determined by the solvent (cytosol) viscosity, which is much less than the polymer (cytoskeleton) viscosity measured in most rheological systems. Simulations also suggest that decreasing channel dimensions leads to larger differences in equilibrium position for particles of different viscoelastic properties, giving design guidance for the next generation of microfluidic cell separation chips.

physics.flu-dyn↗