Microparticles for analyzing biomolecules, method for preparing same, kit for analyzing biomolecules, and method for analyzing biomolecules using the kit
The present invention relates to microparticles for analyzing biomolecules, a biomolecule analysis kit comprising the microparticles, and a method for analyzing biomolecules using the analysis kit, the microparticles for analyzing biomolecules comprising: a core including at least one selected from among an optical expression substance, a metallic material, and a magnetic material; a silica coating layer formed on the core; and at least one binding means, linked to the silica coating layer, for binding to an analysis subject biomolecule, wherein the optical expression substance is a fluorescent or a luminescent.
1. A kit for analysis of a biomolecule, comprising:
a first nanoparticle comprising:
a core comprising a metallic material selected from the group consisting of lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium, titanium, lead, cadmium, iron oxide (Fe 3 O 4 ), silicon oxide (SiO 2 ), and titanium oxide (TiO 2 );
a silica coating layer formed on the core; and
a first binding means, linked to the silica coating layer, for binding specifically to the biomolecule to be analyzed, and
a second nanoparticle comprising:
a core comprising a magnetic material;
a silica coating layer formed on the core; and
a second binding means, linked to the silica coating layer, for non-specifically binding to the biomolecule to be analyzed, and
a third nanoparticle comprising a third binding means that specifically binds to the first binding means of the first nanoparticle and comprises a fluorescent substance or a luminescent substance,
wherein the metallic material is an aggregate of single metal atoms ranging in number from 10 4 to 10 6 atoms, and after use of the kit for an analysis, existence and quantity of the biomolecule are identified by an inductively coupled plasma mass spectrometry (ICP-MS),
wherein the core of the first nanoparticle further comprises a fluorescent material or a luminescent material,
wherein the fluorescent material is fluorescein isothiocyanate (FITC) or cyanine (Cy),
wherein the biomolecule is an enrofloxacin, the first binding means is an IgM, the second binding means is an amine group that forms a chemical bond with the biomolecule, and the third binding means is a secondary antibody to an anti-enrofloxacin antibody.
2. The kit of claim 1 , wherein the chemical bond is an amide bond.
3. The kit of claim 1 , wherein the core of the first nanoparticle comprises a combination of lead and fluorescein isothiocyanate (FITC).