TY - JOUR
T1 - Multiphoton microscopy and fluorescence lifetime imaging provide a novel method in studying drug distribution and metabolism in the rat liver in vivo
AU - Thorling, Camilla A.
AU - Dancik, Yuri
AU - Hupple, Clinton W.
AU - Medley, Gregory
AU - Liu, Xin
AU - Zvyagin, Andrei V.
AU - Robertson, Tom A.
AU - Burczynski, Frank J.
AU - Roberts, Michael S.
PY - 2011/8
Y1 - 2011/8
N2 - Multiphoton microscopy has been shown to be a useful tool in studying drug distribution in biological tissues. In addition, fluorescence lifetime imaging provides information about the structure and dynamics of fluorophores based on their fluorescence lifetimes. Fluorescein, a commonly used fluorescent probe, is metabolized within liver cells to fluorescein mono-glucuronide, which is also fluorescent. Fluorescein and its glucuronide have similar excitation and emission spectra, but different fluorescence lifetimes. In this study, we employed multiphoton fluorescence lifetime imaging to study the distribution and metabolism of fluorescein and its metabolite in vivo in rat liver. Fluorescence lifetime values in vitro were used to interpret in vivo data. Our results show that the mean fluorescence lifetimes of fluorescein and its metabolite decrease over time after injection of fluorescein in three different regions of the liver. In conclusion, we have demonstrated a novel method to study a fluorescent compound and metabolite in vivo using multiphoton fluorescence lifetime imaging.
AB - Multiphoton microscopy has been shown to be a useful tool in studying drug distribution in biological tissues. In addition, fluorescence lifetime imaging provides information about the structure and dynamics of fluorophores based on their fluorescence lifetimes. Fluorescein, a commonly used fluorescent probe, is metabolized within liver cells to fluorescein mono-glucuronide, which is also fluorescent. Fluorescein and its glucuronide have similar excitation and emission spectra, but different fluorescence lifetimes. In this study, we employed multiphoton fluorescence lifetime imaging to study the distribution and metabolism of fluorescein and its metabolite in vivo in rat liver. Fluorescence lifetime values in vitro were used to interpret in vivo data. Our results show that the mean fluorescence lifetimes of fluorescein and its metabolite decrease over time after injection of fluorescein in three different regions of the liver. In conclusion, we have demonstrated a novel method to study a fluorescent compound and metabolite in vivo using multiphoton fluorescence lifetime imaging.
KW - multiphoton microscopy
KW - fluorescence lifetime imaging
KW - fluorescein
KW - fluorescein mono-glucuronide
KW - liver
KW - metabolism
UR - http://www.scopus.com/inward/record.url?scp=80455163065&partnerID=8YFLogxK
U2 - 10.1117/1.3614473
DO - 10.1117/1.3614473
M3 - Article
C2 - 21895325
AN - SCOPUS:80455163065
SN - 1083-3668
VL - 16
SP - 1
EP - 7
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 8
M1 - 086013
ER -