Label-free fluorescence lifetime spectroscopy detects radiation-induced necrotic changes in live brain in real-time

被引:6
作者
Hartl, Brad A. [1 ]
Ma, Htet S. W. [1 ]
Sridharan, Shamira [1 ]
Hansen, Katherine S. [2 ]
Kent, Michael S. [2 ]
Gorin, Fredric [3 ]
Fragoso, Ruben C. [4 ]
Marcu, Laura [1 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Vet Med, Dept Surg & Radiol Sci, Davis, CA 95616 USA
[3] Univ Calif Davis, Sch Med, Dept Neurol, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Sch Med, Dept Radiat Oncol, Sacramento, CA 95817 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2018年 / 9卷 / 08期
基金
美国国家卫生研究院;
关键词
THIAMINE-DEFICIENCY; MALIGNANT GLIOMAS; NADH; NECROSIS; MICROSCOPY; AUTOFLUORESCENCE; DIFFERENTIATION; METABOLISM; TUMOR; DECAY;
D O I
10.1364/BOE.9.003559
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Current clinical imaging modalities do not reliably identify brain tissue regions with necrosis following radiotherapy. This creates challenges for stereotaxic biopsies and surgical decision making. Time-resolved fluorescence spectroscopy (TRFS) provides a means to rapidly identify necrotic tissue by its distinct autofluorescence signature resulting from tissue breakdown and altered metabolic profiles in regions with radiation damage. Studies conducted in a live animal model of radiation necrosis demonstrated that necrotic tissue is characterized by respective increases of 27% and 108% in average lifetime and redox ratio, when compared with healthy tissue. Moreover, radiation-damaged tissue not visible by MRI but confirmed by histopathology, was detected by TRFS. Current results demonstrate the ability of TRFS to identify radiation-damaged brain tissue in real-time and indicates its potential to assist with surgical guidance and MRI-guided biopsy procedures. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:3559 / 3580
页数:22
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