Joo-Kang Kang
Ulsan National Institute of Science and Technology · Engineering
About the Lab
Professor Joo-Kang Kang's research lab specializes in microfluidic and micromagnetic systems for biomedical applications, with a focus on the isolation and culture of circulating tumor cells and the purification of nanomaterials such as single-walled carbon nanotubes. The lab integrates advanced materials science, including organic semiconductors like pentacene, with microfabrication techniques to develop high-performance devices for diagnostics and drug testing. Key research directions include the design of functional microfluidic platforms with enhanced performance through computational modeling and innovative magnetic architectures.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Here we describe a combined microfluidic-micromagnetic cell separation device that has been developed to isolate, detect and culture circulating tumor cells (CTCs) from whole blood, and demonstrate its utility using blood from mammary cancer-bearing mice. The device was fabricated from polydimethylsiloxane and contains a microfluidic architecture with a main channel and redundant 'double collection' channel lined by two rows of dead-end side chambers for tumor cell collection. The microdevice de
Petacene is one of the most promising organic semiconductors for thin-film transistors. Transport measurements in the past have established the presence of shallow traps but their origins have remained a mystery. Here we show that shallow traps in vapor-deposited crystalline pentacene thin films are due to local defects resulting from the sliding of pentacene molecules along their long molecular axis, while two-dimensional crystalline packing is maintained. Electronic structural calculation conf
Scanning tunneling microscopy with high impedance has been used to image the growth of pentacene thin films on Au(111). Instead of the herringbone structure in bulk solid, pentacene molecules in these thin films form a cofacial, π-stacked crystalline phase with their molecular planes parallel to the surface. The growth of this crystalline phase is attributed to the formation of a close-packed, crystalline monolayer which seeds the growth of the π-stacked multilayer film.
We report an analysis of pressure-driven bubble elimination for a gas-permeable microfluidic device. In this study, we described bubble elimination in a microfluidic device employing a gas permeation model and calculated the removal efficiency of bubbles. The correction factor for the simplified model was estimated with respect to the applied pressure. Based on the established model, the required time to remove a trapped bubble with a certain area was shown to be within an error of 11.58% by com
) was robust enough to flow culture medium through the device without leakage even at a gauge pressure of above 135 kPa. For validation of its utility in drugs testing, we successfully demonstrated that human lung adenocarcinoma cells cultured in the PMMA devices show more reliable cytotoxicity results for vincristine in comparison to conventional polydimethylsiloxane (PDMS) devices due to the inherent property of PMMA of it being impervious to small molecules. Given that the current organ-on-a-
A magnetophoretic continuous purification method is presented of single-walled carbon nanotubes (SWCNTs) from the superparamagnetic iron-catalyst impurities in a microfluidic device without any influence on inherent SWCNT properties. By employing microfluidics and a magnetic-field-induced saw-tooth nickel microstructure, a highly enhanced magnetic force in adjoining microchannels is exploited. The iron impurities of SWCNTs are attracted towards areas of higher magnetic-flux density in the microc
Pentacene, as well as other polyacenes, is known to adsorb on metal surfaces in a lying-down geometry, that is, with the molecular plane parallel to the surface. Here we show using scanning tunneling microscopy that the lying-down pentacene monolayer seeds the growth of a multilayer polycrystalline film in a layer-by-layer fashion, with the molecular planes parallel to the substrate surface. Growth in the submonolayer region is characterized by a large number of ordered molecular structures as c
Magnetic nanoparticles have been employed to capture pathogens for many biological applications; however, optimal particle sizes have been determined empirically in specific capturing protocols. Here, a theoretical model that simulates capture of bacteria is described and used to calculate bacterial collision frequencies and magnetophoretic properties for a range of particle sizes. The model predicts that particles with a diameter of 460 nm should produce optimal separation of bacteria in buffer
We report an improved magnetophoretic method, isomagnetophoresis, employing the magnetic susceptibility gradient across a microfluidic channel applied by magnetic field, and we have successfully discriminated the polystyrene (PS; 14.78 ± 0.20 μm in diameter), poly(methyl methacrylate) (PMMA; 15.00 ± 0.77 μm) and borosilicate (BS; 14.01 ± 1.00 μm) microspheres, where PS and PMMA particles have similar diamagnetic susceptibility that cannot be distinguished by conventional magnetophoresis. This pl
Abstract A major challenge to scale up a microfluidic magnetic separator for extracorporeal blood cleansing applications is to overcome low magnetic drag velocity caused by viscous blood components interfering with magnetophoresis. Therefore, there is an unmet need to develop an effective method to position magnetic particles to the area of augmented magnetic flux density gradients while retaining clinically applicable throughput. Here, a magnetophoretic cell separation device, integrated with s
We report a simple method for the fabrication of a poly(dimethylsiloxane) (PDMS) membrane with through-holes by blowing a residual prepolymer away from a photoresist (PR)-patterned Si wafer. The fabrication method for the perforated polymer membrane is crucial to achieve both complicated three-dimensional microfluidic devices and polymer sieve sheets. This method has several advantages over the previous methods in that we can repeatedly make the well-defined holes on the PDMS membranes even if t
The current diagnosis of bacteremia mainly relies on blood culture, which is inadequate for the rapid and quantitative determination of most bacteria in blood. Here, a quantitative, multiplex, microfluidic fluorescence in situ hybridization method (μFISH) is developed, which enables early and rapid (3-h) diagnosis of bacteremia without the need for prior blood culture. This novel technology employs mannose-binding lectin-coated magnetic nanoparticles, which effectively opsonize a broad range of
Research Areas
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