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McCorkle, E.

Publications and source records attributed to McCorkle, E..

2 recordsLinked to original sources

A robust and user-agnostic step-emulsion platform for scalable microgel fabrication

Over the past decade, the integration of microgel-based granular hydrogels in biomedical technologies has experienced substantial growth due to the numerous benefits microgels offer. However, the inability to easily adopt uniform microgel fabrication workflows at scale constitutes a major bottleneck, or in some cases, a barrier-to-entry that stunts further growth of the field. The gold-standard technique for emulsion-based microgel production is through microfluidic droplet-generating devices that produce liquid gel precursor droplets that gel post-production. However, traditional microfluidic workflows often require multiple independent flows and controlled pressure sources, along with a steep learning curve in using microfluidics to achieve uniform droplet sizes reproducibly and repeatedly. This difficulty in adopting microgel fabrication is further compounded by low throughput and the extensive flow rate calibration required when switching to new formulations (e.g., material type, droplet size). In this work, we present a step-emulsion system that bridges the gap by providing a robust and simple setup. We experimentally characterize and evaluate how flow and outlet channel dimension contribute to the generation of uniform droplet populations at specific sizes. With our large dataset consisting of various outlet channel dimensions, we evaluated outlet channel geometrical impacts (height, width, cross-sectional area, aspect-ratio, etc.) on gel precursor droplet size and generation throughput. We demonstrate robust, highly compatible, and repeatably uniform droplet generation from various gel precursor polymer backbones, users with varying microfluidics experience, and a wide viscosity range, including alginate solutions with 650 times the viscosity of water. Furthermore, we confirmed consistent gel precursor droplet generation outcomes driven by a constant flow source (syringe pump) and by direct manual injection as a simple and highly adoptable option for the generation of gel precursor droplets. This platform is ideal for researchers seeking rapid and easy microgel fabrication, regardless of microfluidics experience.

bioengineering↗

Membrane Geometric Confinement Reshapes the Lateral Electric Field Distribution and Intracellular Cargo Transport in Nanopore Electroporation

Nanopore electroporation (NanoEP) is an emerging transfection method that enables efficient and safe intracellular delivery and removal of biomolecular cargo for applications in disease modeling, tissue engineering, and therapeutic biologics manufacturing. Conventional device designs assume uniform vertical cargo flux across nanoporous membranes; however, we demonstrate that the lateral electric field distributions introduce a pronounced edge effect, with enhanced cargo delivery and depletion along the membrane perimeters. We identify and characterize the presence of this edge effect in NanoEP systems, and develop a modified Nernst-Planck model to guide the design of membrane geometries that either promote delivery uniformity or create prescribed spatial gradients within cell monolayers. By varying the internal angles formed by the membrane edges (60{degrees}C, 90{degrees}C, 120{degrees}C), we create predictable intracellular cargo gradients, while concave "serpentine" geometries with high perimeter-to-area ratios amplify delivery efficiency and minimize spatial heterogeneity compared to circular membranes. These findings establish membrane geometry as a tunable design parameter in NanoEP, enabling control over both uniform and patterned intracellular payload delivery or depletion. This geometric design principle offers a scalable strategy for next-generation transfection platforms and synthetic tissue constructs.

bioengineering↗