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Stimulated Raman Spectroscopy and Microscopy with an All-Electronic Spectrometer

技術優勢
Provides built-in rejection of fluorescence that can mask the weaker Raman signals Achieves ultra-fast temporal sampling using time-division multiplexing (TDM) Achieves simultaneous fine spatial resolution Raman imaging and single-shot fine temporal resolution with the spatial localization inherent in nonlinear optical interactions Allows the study, direct probing, and potential control of molecular dynamics and chemical reactions
技術應用
Detection of chemical compounds, biomolecules, and rare cell types (e.g., cancer cells) Single-shot study of chemical reactions without needing repetitive analysis Spatio-temporal Raman microscopy with sub-wavelength resolution Biochemical sensing with matched detection for efficient and effective bio-detectors Combinatorial chemistry synthesis with matched detection High-throughput detection and study of biological molecules and macromolecules (proteins, DNA, RNA, hormones, etc.), microbes, and pathogens (viruses, bacteria) Cancer screening and rare-cell detection without needing fluorescent dye preparation
詳細技術說明
The novel analysis method and apparatus can measure stimulated Raman scattering (SRS), coherent anti-stokes Raman scattering (CARS), and coherent Stokes Raman scattering (CSRS). It can analyze samples that are rapidly and irreversibly evolving, or destroyed by continuous exposure used in conventional techniques. Its extremely fast image acquisition times enable high throughput and can be used to directly monitor temporal dynamics of ultra-fast reactions, even capturing the Raman spectrum of a single molecule as it evolves.
*Abstract

UCLA Researchers in the Electrical Engineering Department have developed a novel spectroscopy and microscopy method and apparatus for extremely fast image acquisition. It eliminates the need for a traditional optical spectrometer and requires no moving parts, enabling high-throughput 4D imaging snapshots for fast and efficient sample identification.

*IP Issue Date
Oct 26, 2010
*Principal Investigation

Name: Jason Chou

Department:


Name: Bahram Jalali

Department:


Name: Daniel Solli

Department:

附加資料
Patent Number: US7821633B2
Application Number: US2008210656A
Inventor: Jalali, Bahram | Solli, Daniel | Chou, Jason
Priority Date: 28 Mar 2006
Priority Number: US7821633B2
Application Date: 15 Sep 2008
Publication Date: 26 Oct 2010
IPC Current: G01J000344
US Class: 356301 | 3560731
Assignee Applicant: The Regents of the University of California
Title: Apparatus and method for Raman spectroscopy and microscopy with time domain spectral analysis
Usefulness: Apparatus and method for Raman spectroscopy and microscopy with time domain spectral analysis
Summary: Used for performing stimulated Raman spectroscopy e.g. spontaneous Raman scattering, coherent anti-stokes Raman scattering and coherent stokes Raman scattering, of a sample such as biochemical molecule and rare cell type e.g. cancer cell, and also for acquiring spectral snapshots of the reaction at specific time intervals.
Novelty: Sample`s e.g. biochemical molecule, stimulated Raman spectroscopy e.g. coherent anti-stokes Raman scattering, performing method for acquiring spectral snapshot, involves exposing sample to beams of pulsed probe light
主要類別
診斷/治療
細分類別
癌症/腫瘤
申請號碼
7821633
其他

Background

Known analysis techniques, such as conventional repetitive-waveform probe spectroscopy, are unable to attain very high scan rates. This limits throughput and prevents molecular spectra measuring at any one moment in time. Thus, existing sample identification and cancer screening techniques are slow and have some margin of error. Furthermore, known optical spectrometers are physically bulky, which prevents their use in some applications.


Additional Technologies by these Inventors


Tech ID/UC Case

20147/2006-526-0


Related Cases

2006-526-0

國家/地區
美國

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