4.6 Article

Compact solid-state CMOS single-photon detector array for in vivo NIR fluorescence lifetime oncology measurements

Journal

BIOMEDICAL OPTICS EXPRESS
Volume 7, Issue 5, Pages 1797-1814

Publisher

OPTICAL SOC AMER
DOI: 10.1364/BOE.7.001797

Keywords

-

Funding

  1. CTI
  2. Swiss Federal Administration's Commission for Technology and Innovation [9801.1 PFLS-LS]
  3. Swiss National Foundation [SNF 51NF40-144633]
  4. NCCR MICS

Ask authors/readers for more resources

In near infrared fluorescence-guided surgical oncology, it is challenging to distinguish healthy from cancerous tissue. One promising research avenue consists in the analysis of the exogenous fluorophores' lifetime, which are however in the (sub-)nanosecond range. We have integrated a single-photon pixel array, based on standard CMOS SPADs (single-photon avalanche diodes), in a compact, time-gated measurement system, named FluoCam. In vivo measurements were carried out with indocyanine green (ICG)-modified derivatives targeting the alpha(v)beta(3) integrin, initially on a genetically engineered mouse model of melanoma injected with ICG conjugated with tetrameric cyclic pentapeptide (ICG-E[c(RGDfK)(4)]), then on mice carrying tumour xenografts of U87-MG (a human primary glioblastoma cell line) injected with monomeric ICG c (RGDfK). Measurements on tumor, muscle and tail locations allowed us to demonstrate the feasibility of in vivo lifetime measurements with the FluoCam, to determine the characteristic lifetimes (around 500 ps) and subtle lifetime differences between bound and unbound ICG-modified fluorophores (10% level), as well as to estimate the available photon fluxes under realistic conditions. (C) 2016 Optical Society of America

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available