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2.
ACS Appl Mater Interfaces ; 10(49): 41935-41946, 2018 Dec 12.
Article in English | MEDLINE | ID: mdl-30465605

ABSTRACT

Magnetic nanoparticles have had a significant impact on a wide range of advanced applications in the academic and industrial fields. In particular, in nanomedicine, the nanoparticles require specific properties, including hydrophilic behavior, uniform and tunable dimensions, and good magnetic properties, which are still challenging to achieve by industrial-scale synthesis. Here, we report a gram-scale synthesis of hydrophilic magnetic nanoclusters based on a one-pot solvothermal system. Using this approach, we achieved the nanoclusters with controlled size composed of magnetite nanocrystals in close-packed superstructures that exhibited hydrophilicity, superparamagnetism, high magnetization, and colloidal stability. The proposed solvothermal method is found to be highly suitable for synthesizing industrial quantities (gram-per-batch level) of magnetic spheres with unchanged structural and magnetic properties. Furthermore, coating the magnetic spheres with an additional silica layer provided further stability and specific functionalities favorable for biological applications. Using in vitro and in vivo studies, we successfully demonstrated both positive and negative separation and the use of the magnetic nanoclusters as a theragnostic nanoprobe. This scalable synthetic procedure is expected to be highly suitable for widespread use in biomedical, energy storage, photonics, and catalysis fields, among others.


Subject(s)
Magnetite Nanoparticles/chemistry , Nanoparticles/chemistry , Silicon Dioxide/chemistry , Theranostic Nanomedicine , Colloids/chemistry
3.
Bioconjug Chem ; 27(1): 59-65, 2016 Jan 20.
Article in English | MEDLINE | ID: mdl-26710682

ABSTRACT

Early diagnosis of infectious diseases is important for treatment; therefore, selective and rapid detection of pathogenic bacteria is essential for human health. We report a strategy for highly selective detection and rapid separation of pathogenic microorganisms using magnetic nanoparticle clusters. Our approach to develop probes for pathogenic bacteria, including Salmonella, is based on a theoretically optimized model for the size of clustered magnetic nanoparticles. The clusters were modified to provide enhanced aqueous solubility and versatile conjugation sites for antibody immobilization. The clusters with the desired magnetic property were then prepared at critical micelle concentration (CMC) by evaporation-induced self-assembly (EISA). Two different types of target-specific antibodies for H- and O-antigens were incorporated on the cluster surface for selective binding to biological compartments of the flagella and cell body, respectively. For the two different specific binding properties, Salmonella were effectively captured with the O-antibody-coated polysorbate 80-coated magnetic nanoclusters (PCMNCs). The synergistic effect of combining selective targeting and the clustered magnetic probe leads to both selective and rapid detection of infectious pathogens.


Subject(s)
Bacteriological Techniques/methods , Nanoparticles/chemistry , Salmonella/isolation & purification , Antibodies, Bacterial/chemistry , Bacteriological Techniques/instrumentation , Magnetic Resonance Spectroscopy , Magnetics/instrumentation , Magnetics/methods , Polysorbates/chemistry , Salmonella/immunology , Serogroup , Spectroscopy, Fourier Transform Infrared
4.
Anal Chim Acta ; 688(1): 70-4, 2011 Feb 28.
Article in English | MEDLINE | ID: mdl-21296207

ABSTRACT

Hydrazide group has a potential of immobilizing an antibody on a sensor surface in a way that ensures an optimal orientation and efficiency of the antibody. However, a multi-step chemical process, required for the preparation of a hydrazide group, is a barrier to its extensive application. This paper describes a new method to introduce a hydrazide group to a sensor surface by a one-step process using dodecanoic hydrazide. The method is based on an ability of the dodecanoic hydrazide to be incorporated into a hybrid bilayer membrane (HBM) layer, thereby presenting its hydrazide group to the surface. Liposome containing dodecanoic hydrazide was added to a hydrophobic self-assembled monolayer surface of a quartz crystal microbalance for the formation of a HBM. Then, the hydrazide group, presented in the surface of the HBM layer, was utilized for the oriented immobilization of an antibody via its carbohydrate moiety which was partially oxidized prior to the conjugation reaction. Activity and stable status of the incorporated dodecanoic hydrazide was revealed by the efficiency and reproducibility of the resulting immunosensor chip.


Subject(s)
Hydrazines/chemistry , Lipid Bilayers/chemistry , Quartz Crystal Microbalance Techniques/methods , Animals , Antibodies, Immobilized/chemistry , Liposomes/chemistry , Oxidation-Reduction , Rabbits , Surface Properties
5.
Biosens Bioelectron ; 24(8): 2522-7, 2009 Apr 15.
Article in English | MEDLINE | ID: mdl-19201593

ABSTRACT

Hybrid bilayer membrane (HBM), comprising a lipid monolayer fused to a hydrophobic self-assembled monolayer (SAM), has a potential capability to provide a convenient tool for the preparation of functionalized sensor surfaces. In this work, the HBM approach was optimized for the preparation of avidin-containing quartz crystal microbalance (QCM) sensor chip which would be available for immobilization of biotinylated molecules. Lipid layer of HBM was composed of background lipid such as egg phosphatidyl choline and biotinylated lipid to which avidin was attached. Highest performance was obtained at 1:1 ratio of the biotinylated lipid and the background lipid, and sensitivity and stability of the resulting sensor chip was comparable to a sensor chip prepared by the conventional carbodiimide reaction. By utilizing the HBM method, construction of a stable avidin sensor chip was achieved within 40 min without any chemical steps. Thus the HBM method was proven to be a convenient and efficient way to immobilize avidin on sensor surfaces.


Subject(s)
Avidin/chemistry , Biosensing Techniques/instrumentation , Biotin/analysis , Immunoassay/instrumentation , Lipid Bilayers/chemistry , Micro-Electrical-Mechanical Systems/instrumentation , Adsorption , Avidin/analysis , Biotin/chemistry , Computer-Aided Design , Equipment Design , Equipment Failure Analysis , Membranes, Artificial , Protein Binding , Reproducibility of Results , Sensitivity and Specificity
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