Jin-Kyoung Yang

Single-step and rapid growth of silver nanoshells as SERS-active nanostructures for label-free detection of pesticides.

We explored a single-step approach for the rapid growth of Ag nanoshells (Ag NSs) under mild conditions. Without predeposition of seed metals, a uniform and complete layer of Ag shells was rapidly formed on silica core particles within 2 min at 25 °C via single electron transfer from octylamine to Ag(+) ions. The size and thickness of the Ag NSs were effectively tuned by adjusting the concentration of silica nanoparticles (silica NPs) with optimal concentrations of AgNO3 and octylamine. This unusually rapid growth of Ag NSs was attributed to a significant increase in the reduction potential of the Ag(+) ions in ethylene glycol (EG) through the formation of an Ag/EG complex, which in turn led to their facile reduction by octylamine, even at room temperature. A substantial enhancement in the surface-enhanced Raman scattering (SERS) of the prepared Ag NSs was demonstrated. The Ag NSs were also utilized as SERS-active nanostructures for label-free detection of the pesticide thiram. The Ag NS-based SERS approach successfully detected thiram on apple peel down to the level of 38 ng/cm(2) in a label-free manner, which is very promising with respect to its potential use for the on-site detection of residual pesticides.

Target-specific near-IR induced drug release and photothermal therapy with accumulated Au/Ag hollow nanoshells on pulmonary cancer cell membranes.

Au/Ag hollow nanoshells (AuHNSs) were developed as multifunctional therapeutic agents for effective, targeted, photothermally induced drug delivery under near-infrared (NIR) light. AuHNSs were synthesized by galvanic replacement reaction. We further conjugated antibodies against the epidermal growth factor receptor (EGFR) to the PEGylated AuHNS, followed by loading with the antitumor drug doxorubicin (AuHNS-EGFR-DOX) for lung cancer treatment. AuHNSs showed similar photothermal efficiency to gold nanorods under optimized NIR laser power. The targeting of AuHNS-EGFR-DOX was confirmed by light-scattering images of A549 cells, and doxorubicin release from the AuHNSs was evaluated under low pH and NIR-irradiated conditions. Multifunctional AuHNS-EGFR-DOX induced photothermal ablation of the targeted lung cancer cells and rapid doxorubicin release following irradiation with NIR laser. Furthermore, we evaluated the effectiveness of AuHNS-EGFR-DOX drug delivery by comparing two drug delivery methods: receptor-mediated endocytosis and cell-surface targeting. Accumulation of the AuHNS-EGFR-DOX on the cell surfaces by targeting EGFR turned out to be more effective for lung cancer treatments than uptake of AuHNS-EGFR-DOX. Taken together, our data suggest a new and optimal method of NIR-induced drug release via the accumulation of targeted AuHNS-EGFR-DOX on cancer cell membranes.

Synthesis and dual biological effects of hydroxycinnamoyl phenylalanyl/prolyl hydroxamic acid derivatives as tyrosinase inhibitor and antioxidant.

We previously reported that caffeoyl-amino acidyl-hydroxamic acid (CA-Xaa-NHOH) acted as both a good antioxidant and tyrosinase inhibitor, in particular when caffeic acid was conjugated with proline or amino acids having aromatic ring like phenylalanine. Here, various hydroxycinnamic acid (HCA) derivatives were further conjugated with phenylalanyl hydroxamic acid and prolyl hydroxamic acid (HCA-Phe-NHOH and HCA-Pro-NHOH) to study the structure and activity relationship as both antioxidants and tyrosinase inhibitors. When their biological activities were evaluated, all HCA-Phe-NHOH and HCA-Pro-NHOH exhibited enhanced antioxidant activity compared to HCA alone. Moreover, derivatives of caffeic acid, ferulic acid, and sinapic acid inhibited lipid peroxidation more efficiently than vitamin E analogue (Trolox). In addition, derivatives of caffeic acid and sinapic acid efficiently inhibited tyrosinase activity and reduced melanin content in melanocytes Mel-Ab cell.

Ag Shell−Au Satellite Hetero-Nanostructure for Ultra-Sensitive, Reproducible, and Homogeneous NIR SERS Activity

It is critical to create isotropic hot spots in developing a reproducible, homogeneous, and ultrasensitive SERS probe. Here, an Ag shell-Au satellite (Ag-Au SS) nanostructure composed of an Ag shell and surrounding Au nanoparticles was developed as a near-IR active SERS probe. The heterometallic shell-satellite structure based SERS probe produced intense and uniform SERS signals (SERS enhancement factor ∼1.4 × 10(6) with 11% relative standard deviation) with high detectability (100% under current measurement condition) by 785 nm photoexcitation. This signal enhancement was independent of the laser polarizations, which reflects the isotropic feature of the SERS activity of Ag-Au SS from the three-dimensional (3D) distribution of SERS hot spots between the shell and the surrounding satellite particles. The Ag-Au SS nanostructure shows a great potential as a reproducible and quantifiable NIR SERS probe for in vivo targets.

One-step synthesis of silver nanoshells with bumps for highly sensitive near-IR SERS nanoprobes

A seedless, one-step synthetic route to uniform bumpy silver nanoshells (AgNSs) as highly NIR sensitive SERS substrates is reported. These substrates can incorporate Raman label compounds and biocompatible polymers on their surface. AgNS based NIR-SERS probes are successfully applied to cell tracking in a live animal using a portable Raman system.

Direct Identification of On-Bead Peptides Using Surface-Enhanced Raman Spectroscopic Barcoding System for High-Throughput Bioanalysis

Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been reported to identify those libraries. In this paper, a simple and efficient surface-enhanced Raman spectroscopic (SERS) barcoding method using highly sensitive SERS nanoparticles (SERS ID) is presented. The 44 kinds of SERS IDs were able to generate simple codes and could possibly generate more than one million kinds of codes by incorporating combinations of different SERS IDs. The barcoding method exhibited high stability and reliability under bioassay conditions. The SERS ID encoding based screening platform can identify the peptide ligand on the bead and also quantify its binding affinity for specific protein. We believe that our SERS barcoding technology is a promising method in the screening of one-bead-one-compound (OBOC) libraries for drug discovery.

Double-Layer Magnetic Nanoparticle-Embedded Silica Particles for Efficient Bio-Separation

Superparamagnetic Fe3O4 nanoparticles (NPs) based nanomaterials have been exploited in various biotechnology fields including biomolecule separation. However, slow accumulation of Fe3O4 NPs by magnets may limit broad applications of Fe3O4 NP-based nanomaterials. In this study, we report fabrication of Fe3O4 NPs double-layered silica nanoparticles (DL MNPs) with a silica core and highly packed Fe3O4 NPs layers. The DL MNPs had a superparamagnetic property and efficient accumulation kinetics under an external magnetic field. Moreover, the magnetic field-exposed DL MNPs show quantitative accumulation, whereas Fe3O4 NPs single-layered silica nanoparticles (SL MNPs) and silica-coated Fe3O4 NPs produced a saturated plateau under full recovery of the NPs. DL MNPs are promising nanomaterials with great potential to separate and analyze biomolecules.

Plasmon-enhanced dye-sensitized solar cells using SiO2 spheres decorated with tightly assembled silver nanoparticles

SiO2 spheres decorated with tightly assembled silver nanoparticles were incorporated into the photoanode of a dye-sensitized solar cell. Localized surface plasmon resonance from the assembled Ag nanoparticles increased the light absorption throughout the wide visible light range. This plasmon-enhanced light absorption resulted in a significant improvement in the device performance.

Fabrication of mono-dispersed silica-coated quantum dot-assembled magnetic nanoparticles†

Multifunctional nanoparticles (NPs) with magnetic and luminescent properties have garnered considerable attention in various fields of biomedical and physiological applications. In this study, we report the fabrication of QD-embedded silica NPs with an iron oxide NP core (Fe3O4@SiO2@QDs NPs) that has dual functional properties. The Fe3O4@SiO2@QDs NPs were mono-dispersed in size and exhibited super-paramagnetic and highly fluorescent properties. Most of the Fe3O4@SiO2@QDs NPs were naturally internalized into MDA-MB-231 human breast cancer cells, and the NP containing cells were successfully sorted by utilizing both fluorescence flow cytometry and a magnetic field. Results indicate that the Fe3O4@SiO2@QDs NPs have great potential for multimodal cell separation.

Chemical modulation of bioactive compounds via oligopeptide or amino acid conjugation.

Conjugation of an oligopeptide or an amino acid to bioactive compounds is one of the simplest chemical modifications to modulate the biological functions of the compounds. Recently, numerous methods have been proposed for the modification of their properties, including the alteration of their chemical and physical properties, and of their original bioactivities. We review the current knowledge of the adaptability of oligopeptide or amino acid conjugation for modulating the biological activities of biomolecules.