Jinmyoung Joo

Gated Luminescence Imaging of Silicon Nanoparticles

The luminescence lifetime of nanocrystalline silicon is typically on the order of microseconds, significantly longer than the nanosecond lifetimes exhibited by fluorescent molecules naturally present in cells and tissues. Time-gated imaging, where the image is acquired at a time after termination of an excitation pulse, allows discrimination of a silicon nanoparticle probe from these endogenous signals. Because of the microsecond time scale for silicon emission, time-gated imaging is relatively simple to implement for this biocompatible and nontoxic probe. Here a time-gated system with ∼10 ns resolution is described, using an intensified CCD camera and pulsed LED or laser excitation sources. The method is demonstrated by tracking the fate of mesoporous silicon nanoparticles containing the tumor-targeting peptide iRGD, administered by retro-orbital injection into live mice. Imaging of such systemically administered nanoparticles in vivo is particularly challenging because of the low concentration of probe in the targeted tissues and relatively high background signals from tissue autofluorescence. Contrast improvements of >100-fold (relative to steady-state imaging) is demonstrated in the targeted tissues.

Highly sensitive diagnostic assay for the detection of protein biomarkers using microresonators and multifunctional nanoparticles.

We developed a novel gravimetric immunoassay for sensitive detection of multiple protein biomarkers using silicon microcantilever arrays and multifunctional hybrid nanoparticles. Magnetic-photocatalytic hybrid nanoparticles with a highly crystalline TiO(2) shell were synthesized using a solvothermal reaction without a calcination process. After functionalizing the hybrid nanoparticles and silicon cantilevers with antibodies, the nanoparticles were used to magnetically separate target biomarkers from human serum. Frequency changes of the microcantilevers due to the binding of the nanoparticles were measured using a dip-and-dry method. Frequency changes were further amplified using a photocatalytic silver reduction reaction. Several biomarkers, including interleukin-6, interferon-γ, and alpha-fetoprotein, were selectively detected using arrays of eight silicon microcantilevers. The detection limit of this assay was ∼0.1 pg/mL, which is superior to the clinical threshold of the biomarkers.

A facile and sensitive immunoassay for the detection of alpha-fetoprotein using gold-coated magnetic nanoparticle clusters and dynamic light scattering

A facile and sensitive immunoassay protocol for the detection of alpha-fetoprotein (AFP) was developed using gold-coated iron oxide magnetic nanoclusters and dynamic light scattering (DLS) methods. The increase in the average particle size due to AFP-mediated aggregation was measured using DLS, and the detection limit was better than 0.01 ng mL(-1).

The fabrication of highly uniform ZnO/CdS core/shell structures using a spin-coating-based successive ion layer adsorption and reaction method.

We developed a successive ion layer adsorption and reaction method based on spin-coating (spin-SILAR) and applied the method to the fabrication of highly uniform ZnO/CdS core/shell nanowire arrays. Because the adsorption, reaction, and rinsing steps occur simultaneously during spin-coating, the spin-SILAR method does not require rinsing steps between the alternating ion adsorption steps, making the growth process simpler and faster than conventional SILAR methods based on dip-coating (dip-SILAR). The ZnO/CdS core/shell nanowire arrays prepared by spin-SILAR had a denser and more uniform structure than those prepared by dip-SILAR, resulting in the higher power efficiency for use in photoelectrochemical cells.

Facile and Sensitive Method for Detecting Cardiac Markers using Ubiquitous pH Meters

A sensitive and easy method was developed for the detection of the cardiac marker troponin I using magnetic immunoassay and ubiquitous pH meters. Monoclonal antibody-functionalized Fe3O4 magnetic nanoparticle clusters (MNCs) were synthesized to capture troponin in human serum, and MNC-troponin complexes were magnetically isolated using a permanent magnet. These complexes were subsequently conjugated to polyclonal antibody-functionalized acetylcholinesterase (AchE) and dispersed in acetylcholine (Ach) solution. As the Ach was hydrolyzed to choline and acetic acid, the pH of the solution decreased, and the resulting pH change was measured in real time using a pH meter. The sensitivity of detection of this assay was found to be 10 pg/mL of troponin in human serum after 10 min of the hydrolysis reaction. Further, the pH change could be determined with the naked eye from the color change of a pH indicator strip.

Enhanced Photocatalytic Activity of Highly Crystallized and Ordered Mesoporous Titanium Oxide Measured by Silicon Resonators

Ordered mesoporous TiO(2) was synthesized using the combined assembly of soft and hard chemistries method and deposited as a film coating on a microcantilever sensor array along with two other types of TiO(2) film: one from nanoparticles and one prepared via a sol-gel reaction. After loading methylene blue molecules on the TiO(2) films, the films were exposed to ultraviolet radiation. The photocatalytic decomposition of methylene blue was monitored by measuring changes in the resonance frequency of each cantilever. The mesoporous TiO(2) film showed higher photocatalytic activity than conventional TiO(2) films fabricated from nanoparticles or via a sol-gel reaction; this difference is attributed to the purely anatase crystalline morphology of the mesoporous TiO(2) film as well as its well-organized pore structure. The three-dimensionally interconnected pore network facilitates the diffusion of methylene blue molecules to the photocatalytically active sites of the mesoporous TiO(2).

Magnetophoretic Chromatography for the Detection of Pathogenic Bacteria with the Naked Eye

A facile and sensitive analytical method that uses gold-coated magnetic nanoparticle clusters (Au/MNCs) and magnetophoretic chromatography with a precision pipet has been developed for the detection of Salmonella bacteria. Antibody-conjugated Au/MNCs are used to capture the Salmonella bacteria in milk and are then separated from the milk by applying an external magnetic field. The Salmonella-containing solution is sucked into a precision pipet tip to which a viscous polymer solution is then added. Once the magnetophoretic chromatography process has been carried out for 10 min, the presence of 100 cfu/mL Salmonella bacteria can be detected with the naked eye because the bacteria have become concentrated at the narrow pipet tip. The performance of this method was evaluated by using dynamic light scattering and light absorption spectroscopy.

Novel heterostructure of CdS nanoparticle/WO3 nanowhisker: Synthesis and photocatalytic properties

A novel heterostructure of CdS nanoparticles/WO3 nanowhiskers was synthesized using a simple two-step process; thermal evaporation and chemical bath deposition. First, WO3 nanowhiskers (NWs) were grown on a tungsten substrate by thermal evaporation of WO3 powder in a tube furnace at 1050°C. Sequentially, CdS nanoparticles (NPs) were deposited on WO3 nanowhiskers by chemical bath deposition. CdS nanoparticles modified WO3 nanowhiskers showed enhanced visible light absorption compared to bare WO3 nanowhiskers. The photocatalytic activity was studied by the photodegradation of methylene blue. CdS NP/WO3 NW heterostructures showed remarkably enhanced photodecomposition efficiencies compared to bare WO3 nanowhiskers.

Photocatalytic silver enhancement reaction for gravimetric immunosensors

A novel microgravimetric immunosensor has been developed using TiO(2) nanoparticle-modified immunoassay and silver enhancement reaction. An antibody-conjugated TiO(2) nanoparticle is bound to the AFP antigen immobilized on a quartz resonator. When the nanoparticles are exposed to UV light in a silver nitrate solution, the photocatalytic reduction of silver ions results in the formation of metallic silver onto the nanoparticles and induces a decrease in the resonance frequency. The frequency change by this photocatalytic reduction reaction is three orders of magnitude larger than the change by antigen binding alone. The efficiency of the photocatalytic reaction has been found to increase with the fraction of anatase crystallites in the nanoparticles and the concentration of the AgNO(3) solution. The results highlight the potential of the photocatalytic nanoparticles for the detection of low concentrations of target molecules using gravimetric sensors.

Precise characterization method of antibody‐conjugated magnetic nanoparticles for pathogen detection using stuffer‐free multiplex ligation‐dependent probe amplification

Antibody‐conjugated magnetic nanoparticles (Ab‐MNPs) have potential in pathogen detection because they allow target cells to be easily separated from complex sample matrices. However, the sensitivity and specificity of pathogen capture by Ab‐MNPs generally vary according to the types of MNPs, antibodies, and sample matrices, as well as preparation methods, including immobilization. Therefore, achieving a reproducible analysis utilizing Ab‐MNPs as a pathogen detection method requires accurate characterization of Ab‐MNP capture ability and standardization of all handling processes. In this study, we used high‐resolution CE‐single strand conformational polymorphism coupled with a stuffer‐free multiplex ligation‐dependent probe amplification system to characterize Ab‐MNPs. The capture ability of Ab‐MNPs targeting Salmonella enteritidis and nine pathogens, including S. enteritidis, was analyzed in phosphate buffer and milk. The effect of storage conditions on the stability of Ab‐MNPs was also assessed. The results showed that the stuffer‐free multiplex ligation‐dependent probe amplification system has the potential to serve as a standard characterization method for Ab‐MNPs. Moreover, the precise characterization of Ab‐MNPs facilitated robust pathogen detection in various applications.