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Size-controlled synthesis, surface functionalization, and biological applications of thiol-organosilica particles
Copyright policy )Thiol-organosilica particles of a narrow size distribution, made from 3-mercaptopropyltrimethoxysilane (MPMS), were prepared by means of a one-pot synthesis. We examined three synthetic conditions at high temperature (100 degrees C), including the Stöber synthesis and two entirely aqueous syntheses. Under all conditions, the sizes of MPMS particles were well controlled, and the average of the coefficient of variation for the size distribution was less than 20%. The incubation times required for formation of MPMS particles were shorter at high temperature than at low temperature. MPMS particles internally functionalized with fluorescent dye were also prepared by means of the same one-pot synthesis. On flow cytometry analysis these MPMS particles showed distinct peaks of scattering due to well-controlled sizes of particles as well as due to fluorescence signals. Real-time observation of interaction between fluorescent MPMPS particles and cultured cells could be observed under fluorescent microscopy with bright light. The surface of the as-prepared MPMS particles contained exposed mercaptopropyl residues, and the ability to adsorb proteins was at least 6 times higher than that of gold nanopaticles. In addition, fluorescein-labeled proteins adsorbed to the surface of the particles were quantitatively detected at the pg/ml level by flow cytometry. MPMS particles surface functionalized with anti-CD20 antibody using adsorption could bind with lymphoma cells expressing CD20 specifically. In this paper, we demonstrated the possibility of size-controlled thiol-organosilica particles for wild range of biological applications.
Microsoft Academic Graph classification: Thiol chemistry.chemical_classification chemistry Analytical chemistry Chemical engineering Adsorption Aqueous solution Surface modification Fluorescence Fluorescence microscope Range (particle radiation) Scattering
Colloid and Surface Chemistry, Physical and Theoretical Chemistry, Surfaces and Interfaces, General Medicine, Biotechnology, Animals, Antigens, CD20, Cell Line, Tumor, Cells, Cultured, Green Fluorescent Proteins, Humans, Mice, Mice, Inbred C57BL, Microscopy, Electron, Transmission, Microscopy, Fluorescence, Nanoparticles, Organosilicon Compounds, Particle Size, Protein Binding, Silanes, Surface Properties, Temperature, Time Factors
Colloid and Surface Chemistry, Physical and Theoretical Chemistry, Surfaces and Interfaces, General Medicine, Biotechnology, Animals, Antigens, CD20, Cell Line, Tumor, Cells, Cultured, Green Fluorescent Proteins, Humans, Mice, Mice, Inbred C57BL, Microscopy, Electron, Transmission, Microscopy, Fluorescence, Nanoparticles, Organosilicon Compounds, Particle Size, Protein Binding, Silanes, Surface Properties, Temperature, Time Factors
Microsoft Academic Graph classification: Thiol chemistry.chemical_classification chemistry Analytical chemistry Chemical engineering Adsorption Aqueous solution Surface modification Fluorescence Fluorescence microscope Range (particle radiation) Scattering
- University of Tokushima Japan
- University of Tokushima Japan
Thiol-organosilica particles of a narrow size distribution, made from 3-mercaptopropyltrimethoxysilane (MPMS), were prepared by means of a one-pot synthesis. We examined three synthetic conditions at high temperature (100 degrees C), including the Stöber synthesis and two entirely aqueous syntheses. Under all conditions, the sizes of MPMS particles were well controlled, and the average of the coefficient of variation for the size distribution was less than 20%. The incubation times required for formation of MPMS particles were shorter at high temperature than at low temperature. MPMS particles internally functionalized with fluorescent dye were also prepared by means of the same one-pot synthesis. On flow cytometry analysis these MPMS particles showed distinct peaks of scattering due to well-controlled sizes of particles as well as due to fluorescence signals. Real-time observation of interaction between fluorescent MPMPS particles and cultured cells could be observed under fluorescent microscopy with bright light. The surface of the as-prepared MPMS particles contained exposed mercaptopropyl residues, and the ability to adsorb proteins was at least 6 times higher than that of gold nanopaticles. In addition, fluorescein-labeled proteins adsorbed to the surface of the particles were quantitatively detected at the pg/ml level by flow cytometry. MPMS particles surface functionalized with anti-CD20 antibody using adsorption could bind with lymphoma cells expressing CD20 specifically. In this paper, we demonstrated the possibility of size-controlled thiol-organosilica particles for wild range of biological applications.