Multiphoton microscopy and fluorescence lifetime imaging provide a novel method in studying drug distribution and metabolism in the rat liver in vivo

被引:14
|
作者
Thorling, Camilla A. [2 ]
Dancik, Yuri [2 ]
Hupple, Clinton W. [2 ]
Medley, Gregory
Liu, Xin
Zvyagin, Andrei V. [3 ]
Robertson, Tom A. [2 ]
Burczynski, Frank J. [4 ]
Roberts, Michael S. [1 ,2 ]
机构
[1] Univ Queensland, Princess Alexandra Hosp, Therapeut Res Ctr, Sch Med, Woolloongabba, Qld 4102, Australia
[2] Univ S Australia, Sch Pharm & Biomed Sci, Adelaide, SA 5000, Australia
[3] Macquarie Univ, MQ Biofocus Res Ctr, Sydney, NSW 2109, Australia
[4] Univ Manitoba, Fac Pharm, Winnipeg, MB R3T 2N2, Canada
基金
英国医学研究理事会;
关键词
multiphoton microscopy; fluorescence lifetime imaging; fluorescein; fluorescein mono-glucuronide; liver; metabolism; HEPATIC DISPOSITION; CYTOPLASMIC-BINDING; DISEASED LIVERS; GLUCURONIDE; BILIRUBIN; FIBROSIS; KINETICS; PHARMACOKINETICS; SPECTROSCOPY; RESOLUTION;
D O I
10.1117/1.3614473
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2011 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.3614473]
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页数:7
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