Publications by authors named "Park Bum Jun"

Article Synopsis
  • * Many particles remain in unstable positions, possibly because of "contact line pinning," which prevents them from moving freely.
  • * Our findings suggest that moving particles up and down (vertical motion) helps them reach a stable state more effectively than rotating them, highlighting the need for further research on how surface tension and roughness affect these behaviors.
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This study presents a simple approach for fabricating low-density drug-polymer amorphous solid dispersions (ASDs) using a piezoelectric inkjet method, demonstrating potential applications for floating drug delivery systems (FDDS). By adjusting the ratio of two polymers, polylactic acid, and Eudragit RLPO, the floatability and drug release rate of the drug-polymer ASD particles can be easily manipulated. Kinetic model analyses have been conducted to interpret the drug release mechanism.

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We report on the use of a microfluidic antisolvent crystallization method to investigate the effect of solution volume on the chiral symmetry breaking (CSB) phenomena of enantiomeric sodium chlorate crystals. The utilization of a microfluidic device is capable of periodically producing emulsion droplets of uniform size and facilitates the quantitative analysis and visualization of crystallization phenomena occurring within the individual emulsions immersed in an oil continuous medium (, dodecane). To promote nucleation and crystallization, a small amount of an antisolvent (, ethanol) is introduced into the continuous phase.

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Monitoring mechanical stresses in microchannels is challenging. Herein, we report the development of a mechanofluorescence sensor system featuring a fluorogenic single polydiacetylene (PDA) particle, fabricated using a co-flow microfluidic method. We construct a stenotic vessel-mimicking capillary channel, in which the hydrodynamically captured PDA particle is subjected to controlled fluid flows.

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Article Synopsis
  • * The technique effectively produces spherical composite particles that dissolve better in water compared to traditional crystalline drugs, offering potential improvements in how medications work in the body.
  • * Despite some challenges like needing a continuous water supply and managing solvent solubility, this method stands out for its flexibility and ability to create uniform particles, marking a significant step forward in drug formulation and delivery.
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Understanding deracemization is crucial for progress in chiral chemistry, especially for improving separation techniques. Here, we first report the phenomenon of chiral flipping (or reverse deracemization) in a chiral material (i.e.

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The attention to materials with hot exciton channel and triplet-triplet fusion (TTF) mediated high-lying reverse intersystem crossing (hRISC) has been raised for their ability to convert non-emissive 'dark' triplets into radiative singlet excitons. This spin conversion process results in high exciton utilization efficiency (EUE) that exceeds the theoretical limits. Notably, it is known that such spin conversion processes from the high-lying excited triplet to the singlet state are facilitated by the orthogonal orbital transition effect governed by the El-Sayed's rule.

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Colloids often behave in a manner similar to their counterparts in molecular space and are used as model systems to understand molecular behavior. Here, we study like-charged colloidal attractions between a permanent dipole on an interfacial particle and its induced dipole on a water-immersed particle caused by diffuse layer polarization. We find that the scaling behavior of the measured dipole-induced dipole (D‒I) interaction via optical laser tweezers is in good agreement with that predicted from the molecular Debye interaction.

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This study investigates the effects of interparticle interactions and wettability on the particle attachment efficacy to the oil‒water interface. Three types of PS particles with different surface functional groups were examined at varying salt concentrations and the number of particles injected into the interface. Based on the microfluidic method and the surface coverage measurement, we found that the two contributing factors significantly influenced particle attachment efficiency to the interface, while the wettability factor has a major contribution.

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Non-spherical polymer nanoparticles (NPs) have gained attention in various fields, but their fabrication remains challenging. In this study, we present a simple protocol for synthesizing partially etched polystyrene (PS) nanoparticles through emulsion polymerization and chemical etching. By adjusting the degree of crosslinking, we selectively dissolve the weakly crosslinked portions of the particles, resulting in partially etched PS NPs with increased surface area.

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We report spontaneous chiral symmetry breaking in the evaporative crystallization of sodium chlorate by controlling the solution volume. We determine the critical volume, below which complete chiral symmetry breaking spontaneously occurs. This can be explained with regard to the rare probability of the simultaneous formation of multiple nuclei in a small volume, depletion attributed to the rapid consumption of surrounding sodium chlorate molecules upon crystal growth, and secondary nucleation.

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Interactions among colloidal particles govern the hierarchical microstructure and its physical properties. Here, optical laser tweezers and Monte Carlo simulations are used to evaluate the effects of azimuthal rotation of Janus particles at the oil-water interface on interparticle interactions. We find that the capillary-induced attractive force between two Janus particles at the interface can be relaxed by azimuthal rotation around the critical separation region, at which the capillary force is ∼0.

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Hypothesis: A solvent evaporation-induced phase separation method, which is based on the preferential partitioning of two or more immiscible materials after solvent evaporation on providing heat, has been one of the main strategies for synthesis of Janus particles (JPs). Considering this approach, it should be possible to synthesize surfactant free-JPs in continuous flow by the ultrasonic nebulizer spray method.

Experiments: Two polymers, polystyrene and polymethylmethacrylate, were dissolved in dichloromethane, and droplets of a precursor solution generated by an ultrasonic nebulizer were then conveyed through a borosilicate glass cylinder with two heating zones.

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Herein, we represent a novel ecofriendly bilayer-amine group incorporated microcrystalline cellulose (MCC)/chitosan (CS) hydrogel, fabricated via integrating polydopamine (PDA) and polyethyleneimine (PEI) for reliable and effective extraction of copper (Cu), zinc (Zn), and nickel (Ni) ions from effluents. Owing to abundant adsorptive sites, the MCC-PDA-PEI/CS-PDA-PEI hydrogel showed excellent Cu, Zn, and Ni adsorbabilities of ~434.8, ~277.

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A micro-capillary electrophoresis (μCE) system is one of the widely adopted techniques in the molecular diagnostics and DNA sequencing due to the benefits of high resolution, rapid analysis, and low reagent consumption, but due to the requirements of bulky high-power suppliers and an expensive laser-induced fluorescence detector module, the conventional set-up of μCE system is not adequate for point-of-care (POC) molecular diagnostics. In this study, we constructed a miniaturized and integrated μCE system which can be manipulated by a smartphone. The smartphone not only powers two boost converters and an excited laser, but also controls the relay for the power switch.

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A platform is introduced for bilayered coacervation of oppositely charged nanoplatelets (NPLs) at the oil-water interface. To this end, we synthesized two types of zirconium hydrogen phosphate (ZrHP) NPLs, cationically charged NPLs (CNPLs), and anionically charged NPLs (ANPLs) by conducting surface-initiated atom transfer radical polymerization. Taking advantage of the platelet geometry and controlled wettability, we demonstrated that ANPLs and CNPLs coacervate themselves to form a bilayered NPL membrane at the interface, which was directly confirmed by confocal laser scanning microscopy.

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Industrial waste discharge comprising heavy metals into potable water bodies induces many health hazards. This study investigates the role of metal-organic frameworks (MOFs) doped alginate beads (MOFs@ABs) as potential adsorbents for Cr(VI). Effects of pH, stirring rate, temperature, initial chrome concentration, and particles dosage on Cr(VI) adsorption are studied to evaluate adsorption ability of UiO-66@ABs for Cr(VI) removal from aqueous solution.

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In current work, Prussian blue (PB)- and hydroxyapatite (HAp)-embedded micro-adsorbents (PB-HAp-MAs) were rationally fabricated through an easy and flexible custom-made micronozzle system as a novel bifunctional adsorbent. The adsorption performance of the as-prepared samples was conducted based on the removal of cesium (Cs) and strontium (Sr) ions. Adsorption behaviors of the PB-HAp-MAs were also evaluated as function extrusion dimensions and adsorbate concentration.

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Hypothesis: The geometric features of charged particles at a fluid-fluid interface substantially affect their interfacial configurations and interparticle interactions (electrostatic and capillary forces). Because lenticular particles exhibit both spherical and nonspherical surface characteristics, an investigation of their interfacial phenomena can provide in-depth understanding of the relationship between the configuration and the interactions of these particles at the interface.

Experiments: Three types of lenticular particles are prepared using a seeded emulsion polymerization method.

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We introduce amphiphilic nanoplatelets (ANPLs) that not only have a nanoscale Janus platelet geometry, but can also induce complementary face-to-face interactions among Pickering emulsion droplets. We showed that the ANPLs with such high surface activity can be a promising colloid surfactant enabling smart rheology modification of complex emulsion fluids.

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Hypothesis: The charged spherical colloidal particles at the fluid-fluid interface experience considerably strong and long-ranged electrostatic and capillary interactions. The contribution of capillary force becomes more significant as the particle size increases beyond a certain limit. The relative strengths of the two competing interactions between the spherical polystyrene particles at the oil-water interface are quantified depending on their size.

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Creation of hollow, one-dimensional nanomaterials has gained great recent attention in the chemical and material sciences. In a study aimed at discovering new functional materials of this type, we observed that an amphiphilic diacetylene (DA) derivative, containing an azobenzene moiety and an oligo-ethylene group, self-assembles to form nanotubes and undergoes photopolymerization to form hollow polydiacetylene (PDA) nanotubes with a uniform wall thickness and diameter. The azobenzene-PDA nanotubes are photoresponsive in that on-and-off UV-irradiation leads to a reversible morphological change between straight and bent forms in association with E-Z photoisomerization of the azobenzene group.

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In this study, we measured the force of electrostatic interactions between poly(methyl methacrylate) (PMMA) particles dispersed in organic solvent mixtures of cyclohexyl bromide (CHB) and n-decane. Optical laser tweezers were employed to directly measure interactive forces between paired PMMA particles in a CHB medium that contained n-decane in various volume ratios. CHB, having a moderate dielectric constant, provided an environment with a high charge storage capacity.

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Uniform Ag nanocubes are reproducibly synthesized by a AgCl particle-mediated heterogeneous nucleation and disassembly process in polyol chemistry. By introducing N,N-dimethylformamide (DMF) in a conventional polyol method with HCl etchant, Ag nanocrystals (NCs) begin to be nucleated on the surface of AgCl-precipitated particles due to the promoted reduction reaction by DMF. The nucleated Ag NCs on the AgCl particles are grown to Ag nanocubes in shape by consuming Ag sources from the AgCl mother particles.

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