T. R. Gaborski

This study examines how clinically relevant antibiotics affect extracellular vesicle release from E. coli, finding that beta-lactams increase release while quinolones and aminoglycosides decrease it.

This study examines how oxygen plasma treatment affects the biocompatibility of Parylene C and Parylene N membranes by analyzing cell behavior and surface properties.

The paper introduces a reconfigurable microfluidic platform that integrates microfluidic capabilities with conventional open-well systems for studying barrier tissues under flow.

The paper demonstrates that local extensional flows align collagen fibers in 3D hydrogels, enabling long-range fiber alignment and multi-layered matrix fabrication.

The paper shows that disrupted porous membrane surfaces reduce YAP nuclear localization and promote adipogenesis in ADSCs by altering cell morphology and substrate interactions.

This study evaluates hemolysis in microfluidic ECMO devices using computational models and empirical testing, finding that some models predict hemolysis more accurately than others depending on shear conditions.

This paper introduces a microfluidic method to create 3D collagen landscapes with tunable anisotropy and directionality, showing cells align with these structural cues.

This paper presents a bilayer graphene oxide membrane with high permeability and selectivity for hemodialysis, showing improved performance over existing membranes.

This paper develops gradient thickness porous membranes for in vitro modeling of physiological barriers, showing improved cell attachment and mechanical properties.

The paper presents a method using nanospheres to create nanopatterned Au:Cu films with thermoresponsive SAMs, validated by chemical and mechanical characterization.

This paper develops a nanoporous membrane platform using nanospheres to isolate and study small extracellular vesicles with a size cutoff of 300 nm.

This study shows that PKH26 labeling increases exosome size, potentially affecting their biodistribution and cellular uptake, and suggests protein binding dyes are more reliable.