Media.Player

Methods of Using Porous Silicon Nano/Micro-Particles for Time-Gated Fluorescence Imaging

详细技术说明

UC San Diego researchers have developed porous silicon nanoparticles (pSiNP) that can emit visible to near-IR light under photoexcitation, have long luminescence lifetimes (> 10 nanoseconds) and optionally contain quenching/stabilizing molecules that can adjust the luminescence lifetime and intensity from the nanoparticle. The invention also provides methods to fabricate said pSiNP and of time gating the emission of the pSiNP to enable higher fidelity imaging by eliminating background signals (e.g., tissue autofluorescence, spectral bleed through). In contrast to many nanomaterials, pSiNP degrade into renally cleared components in a relatively short period of time with little or no evidence of systemic or cellular toxicity. Moreover, due to their porous nature, the nanoparticles can carry additional species such as drugs, smaller nanoparticles, fluorescence sensitizers or fluorescence quenching agents.

*Abstract

Fluorescence imaging is one of the most versatile and widely used visualization methods in biomedical research because of its high sensitivity, high spatial resolution, low cost, and non-invasive nature. In this method, a fluorescent probe molecule or nanoparticle is used to enhance contrast of the image in desired regions or to identify specific features, molecules, or tissues. However, in vivo fluorescence imaging has not been widely applied in clinical practice due to the lack of specific imaging agents, shallow tissue penetration of the exciting or emitting wavelengths, and ubiquitous background tissue autofluorescence. Conventional fluorescent probes based on organic molecules or quantum dots normally display short fluorescence lifetimes (on the order of a few nanoseconds). These lifetimes are comparable to the lifetimes of naturally occurring species in tissues and cellular media that are responsible for autofluorescence. This makes it hard to separate the fluorescence signal of the probe from background fluorescence in the time domain.

*IP Issue Date

Jun 5, 2014

*Principal Investigation

Name: Luo Gu

Department:

Name: David Hall

Department:

Name: Robert Mattrey

Department:

Name: Michael Sailor

Department:

附加资料

Inventor: SAILOR, Michael, J. | GU, Luo | HALL, David, J. | MATTREY, Robert
Priority Number: WO2012149312A1
IPC Current: G01N002164 | G01N003352
Assignee Applicant: The Regents of the University of California
Title: TIME-GATED FLUORESCENCE IMAGING WITH SI-CONTAINING PARTICLES | IMAGERIE PAR FLUORESCENCE RÉSOLUE DANS LE TEMPS À PARTICULES CONTENANT DU SI
Usefulness: TIME-GATED FLUORESCENCE IMAGING WITH SI-CONTAINING PARTICLES | IMAGERIE PAR FLUORESCENCE RÉSOLUE DANS LE TEMPS À PARTICULES CONTENANT DU SI
Summary: For time-gated fluorescence imaging and tissue (e.g. tumor, brain, cardiac, skin) monitoring; and imaging leverages the fluorescence lifetime of a fluorescent Si-containing particle to distinguish from background fluorescence.
Novelty: Time-gated fluorescence imaging and tissue monitoring involves introducing fluorescent silicon-containing particle into tissue, applying excitation light pulse, and time-gated measuring of responsive luminescence signal to identify particle

主要类别

诊断/治疗

细分类别

癌症/肿瘤

申请号码

2014015184

其他

Intellectual Property Info

The invention has a patent pending and is available for licensing and/or sponsorship.

Tech ID/UC Case

22212/2011-306-0

Related Cases

2011-306-0

国家/地区

美国