Fluorescence Lifetime Imaging System for in Vivo Studies
In this article, a fluorescence lifetime imaging system for small animals is presented. Data were collected by scanning a region of interest with a measurement head, a linear fiber array with fixed separations between a single source fiber and several detection fibers. The goal was to localize tumor...
Saved in:
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2007-07-01
|
Series: | Molecular Imaging |
Online Access: | https://doi.org/10.2310/7290.2007.00019 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1841564470173761536 |
---|---|
author | Moinuddin Hassan Jason Riley Victor Chernomordik Paul Smith Randall Pursley Sang Bong Lee Jacek Capala Gandjbakhche Amir H |
author_facet | Moinuddin Hassan Jason Riley Victor Chernomordik Paul Smith Randall Pursley Sang Bong Lee Jacek Capala Gandjbakhche Amir H |
author_sort | Moinuddin Hassan |
collection | DOAJ |
description | In this article, a fluorescence lifetime imaging system for small animals is presented. Data were collected by scanning a region of interest with a measurement head, a linear fiber array with fixed separations between a single source fiber and several detection fibers. The goal was to localize tumors and monitor their progression using specific fluorescent markers. We chose a near-infrared contrast agent, Alexa Fluor 750 (Invitrogen Corp., Carlsbad, CA). Preliminary results show that the fluorescence lifetime for this dye was sensitive to the immediate environment of the fluorophore (in particular, pH), making it a promising candidate for reporting physiologic changes around a fluorophore. To quantify the intrinsic lifetime of deeply embedded fluorophores, we performed phantom experiments to investigate the contribution of photon migration effects on observed lifetime by calculating the fluorescence intensity decay time. A previously proposed theoretical model of migration, based on random walk theory, is also substantiated by new experimental data. The developed experimental system has been used for in vivo mouse imaging with Alexa Fluor 750 contrast agent conjugated to tumor-specific antibodies (trastuzumab [Herceptin]). Three-dimensional mapping of the fluorescence lifetime indicates lower lifetime values in superficial breast cancer tumors in mice. |
format | Article |
id | doaj-art-7ee1606a596248ca966d29e349ec681f |
institution | Kabale University |
issn | 1536-0121 |
language | English |
publishDate | 2007-07-01 |
publisher | SAGE Publishing |
record_format | Article |
series | Molecular Imaging |
spelling | doaj-art-7ee1606a596248ca966d29e349ec681f2025-01-02T22:39:35ZengSAGE PublishingMolecular Imaging1536-01212007-07-01610.2310/7290.2007.0001910.2310_7290.2007.00019Fluorescence Lifetime Imaging System for in Vivo StudiesMoinuddin HassanJason RileyVictor ChernomordikPaul SmithRandall PursleySang Bong LeeJacek CapalaGandjbakhche Amir HIn this article, a fluorescence lifetime imaging system for small animals is presented. Data were collected by scanning a region of interest with a measurement head, a linear fiber array with fixed separations between a single source fiber and several detection fibers. The goal was to localize tumors and monitor their progression using specific fluorescent markers. We chose a near-infrared contrast agent, Alexa Fluor 750 (Invitrogen Corp., Carlsbad, CA). Preliminary results show that the fluorescence lifetime for this dye was sensitive to the immediate environment of the fluorophore (in particular, pH), making it a promising candidate for reporting physiologic changes around a fluorophore. To quantify the intrinsic lifetime of deeply embedded fluorophores, we performed phantom experiments to investigate the contribution of photon migration effects on observed lifetime by calculating the fluorescence intensity decay time. A previously proposed theoretical model of migration, based on random walk theory, is also substantiated by new experimental data. The developed experimental system has been used for in vivo mouse imaging with Alexa Fluor 750 contrast agent conjugated to tumor-specific antibodies (trastuzumab [Herceptin]). Three-dimensional mapping of the fluorescence lifetime indicates lower lifetime values in superficial breast cancer tumors in mice.https://doi.org/10.2310/7290.2007.00019 |
spellingShingle | Moinuddin Hassan Jason Riley Victor Chernomordik Paul Smith Randall Pursley Sang Bong Lee Jacek Capala Gandjbakhche Amir H Fluorescence Lifetime Imaging System for in Vivo Studies Molecular Imaging |
title | Fluorescence Lifetime Imaging System for in Vivo Studies |
title_full | Fluorescence Lifetime Imaging System for in Vivo Studies |
title_fullStr | Fluorescence Lifetime Imaging System for in Vivo Studies |
title_full_unstemmed | Fluorescence Lifetime Imaging System for in Vivo Studies |
title_short | Fluorescence Lifetime Imaging System for in Vivo Studies |
title_sort | fluorescence lifetime imaging system for in vivo studies |
url | https://doi.org/10.2310/7290.2007.00019 |
work_keys_str_mv | AT moinuddinhassan fluorescencelifetimeimagingsystemforinvivostudies AT jasonriley fluorescencelifetimeimagingsystemforinvivostudies AT victorchernomordik fluorescencelifetimeimagingsystemforinvivostudies AT paulsmith fluorescencelifetimeimagingsystemforinvivostudies AT randallpursley fluorescencelifetimeimagingsystemforinvivostudies AT sangbonglee fluorescencelifetimeimagingsystemforinvivostudies AT jacekcapala fluorescencelifetimeimagingsystemforinvivostudies AT gandjbakhcheamirh fluorescencelifetimeimagingsystemforinvivostudies |