Abstract:
본 발명은 실리카 중심 입자; 및 상기 실리카 중심 입자 주변을 둘러싸고 있는 할로우 금속 나노입자층;을 포함하여 이루어진 근적외선 광학영상용 나노-표지 입자, 그 제조방법 및 그를 이용한 생체 내 광학 검출방법에 관한 것으로, 본 발명은 근적외선 광학영상용 나노-표지 입자는 근적외선 영역의 파장을 이용하여 생체 내, 예를 들어 피하 조직의 광학영상을 확인할 수 있고, 표면증강 라만산란 강도가 뛰어나며, 생체적합성 및 안정성이 뛰어나므로, 생체 내 다중 광학영상을 얻기 위한 나노 프로브로서 활용될 수 있다.
Abstract:
A nanoprobe based on biomass for enabling self-duplication comprises: a combining element which exists in a first area of the biomass and is able to be unusually coupled to a target substance; and nanoparticles which exist in a second area of the biomass and provide an optical detection signal. The nanoprobe enables the quantitative analysis and multiplexed analysis of the target substance and facilitates mass production.
Abstract:
PURPOSE: A nano-tagging particle for near infrared optical image is provided to check the in vivo optical image using a spectrum range of near infrared ray, and to have the excellent enrichment Raman scattering intensity, biocompatibility, and stability. CONSTITUTION: A nano-tagging particle for near infrared optical image comprises a silica core particle and a hollow metal nanoparticle layer surrounding the silica core particle. The average particle size of the silica core particle is 50-300 nm. The hollow metal nanoparticle is a hollow metal nanosphere. The hollow metal nanoparticle is a hollow gold nanoparticle, a hollow gold, and a silver nanoparticle. The surface of the hollow metal nanoparticle in the hollow metal nanoparticle layer is coated with a marker. A manufacturing method of the nano-tagging particle for near infrared optical image is as follows. The silica core particle is manufactured. The silver nanoparticle layer is formed on the surface of the silica core particle. The silica particle, in which the silver nanoparticle layer is formed, is reacted with gold ion so that the silica particle, in which the hollow gold and the silver nanoparticle layer are formed by Galvanic displacement reaction, is manufactured.
Abstract:
PURPOSE: A medical imaging method for simultaneous detection of multiplex targets using a fluorescent and a raman signal and an apparatus for simultaneously detecting multiplex targets of fluorescent and raman signal using thereof are provided to obtain more accurate diagnosis result in real time. CONSTITUTION: A light source(10) projects a laser light. An image guide part(21) guides the optical signal of an incident light emitted from a surface particle. A scanner(30) scans the optical signal collected from an optical collection unit(20). A light division unit includes a beam splitter projecting the incident light through a first path and a second path. A fluorescence signal detection unit detects a fluorescence signal from an optical signal in the first path.
Abstract:
PURPOSE: A qualitative method of a multiple marker is provided to performing qualitation of high sensitivity and selectivity using F-SERS dots. CONSTITUTION: A qualitative method for a multiple marker comprises: a step of treating multiple marker-specific fluorescence-surface enhanced raman scattering(SERS) dot mixture to a sample; and a step of measuring raman signal corresponding to the multiple marker to calculate relative amount of the multiple marker. The SERS dot comprises: a metal nanoparticle layer containing a metal on the surface of silica nanoparticle; a raman probe and fluorescence probe layer formed at the metal nanoparticle layer; a functional layer; and a reaction molecule attached on the functional layer. The diameter of the silica nanoparticle is 50-300nm. The metal is gold, silver, palladium, platinum, aluminum, iridium, osmium, rhodium or ruthenium. The functional group is thiol group(-SH), amine group(-NH_2) or carboxyl group(-COOH).
Abstract:
PURPOSE: A method for isolating cells using M-SERS dots(Magnetic surface enhanced raman spectroscopic dots) is provided to isolated rare cells in organs. CONSTITUTION: A method for isolating cells comprises: a step of treating a sample with antibody-conjugated M-SERS dots; a step of applying magnetic force to collect marker-positive cells; and a step of performing FACS(Fluorescence activated cell sorter) to isolate target cells from the collected cells. The target cells are cancer stem cells. The cancer stem cells are BASCs(bronchioalveolar stem cells) and the marker is CD34.