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本文引用的文献

1
A dual-modality optical coherence tomography and fluorescence lifetime imaging microscopy system for simultaneous morphological and biochemical tissue characterization.一种用于同时进行形态学和生化组织表征的双模态光学相干断层扫描和荧光寿命成像显微镜系统。
Biomed Opt Express. 2010 Jul 16;1(1):186-200. doi: 10.1364/BOE.1.000186.
2
Automated analysis of fluorescence lifetime imaging microscopy (FLIM) data based on the Laguerre deconvolution method.基于拉盖尔反卷积法的荧光寿命成像显微镜(FLIM)数据的自动分析。
IEEE Trans Biomed Eng. 2011 Jan;58(1):172-81. doi: 10.1109/TBME.2010.2084086. Epub 2010 Oct 7.
3
High-speed multispectral fluorescence lifetime imaging implementation for in vivo applications.用于体内应用的高速多光谱荧光寿命成像实现。
Opt Lett. 2010 Aug 1;35(15):2558-60. doi: 10.1364/OL.35.002558.
4
Carcinogenic effects of MGP-7 and B[a]P on the hamster cheek pouch.
Toxicol Pathol. 2009 Oct;37(6):733-40. doi: 10.1177/0192623309344203. Epub 2009 Aug 13.
5
Endoscopic optical coherence tomography and laser-induced fluorescence spectroscopy in a murine colon cancer model.小鼠结肠癌模型中的内镜光学相干断层扫描和激光诱导荧光光谱分析
Lasers Surg Med. 2006 Apr;38(4):305-13. doi: 10.1002/lsm.20305.
6
Fluorescence guided optical coherence tomography for the diagnosis of early bladder cancer in a rat model.荧光引导光学相干断层扫描在大鼠模型中用于早期膀胱癌的诊断
J Urol. 2005 Dec;174(6):2376-81. doi: 10.1097/01.ju.0000180413.98752.a1.
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Spectroscopic detection and evaluation of morphologic and biochemical changes in early human oral carcinoma.早期人类口腔癌形态学和生化变化的光谱检测与评估
Cancer. 2003 Apr 1;97(7):1681-92. doi: 10.1002/cncr.11255.

口腔上皮癌的体内形态与生化同时光学成像。

In vivo simultaneous morphological and biochemical optical imaging of oral epithelial cancer.

机构信息

Department of Biomedical Engineering, Texas A&M University, College Station, TX 77840, USA.

出版信息

IEEE Trans Biomed Eng. 2010 Oct;57(10):2596-9. doi: 10.1109/TBME.2010.2060485. Epub 2010 Jul 23.

DOI:10.1109/TBME.2010.2060485
PMID:20656649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4795161/
Abstract

Early detection of cancer is key to reducing morbidity and mortality. Morphological and chemical biomarkers presage the transition from normal to cancerous tissue. We have developed a noninvasive imaging system incorporating optical coherence tomography (OCT) and fluorescence lifetime imaging microscopy (FLIM) into a single optical system for the first time, in order to acquire both sets of biomarkers. OCT can provide morphological images of tissue with high resolution, while FLIM can provide biochemical tissue maps. Coregistered OCT volumes and FLIM images have been acquired simultaneously in an in vivo hamster cheek pouch model of oral cancer. The OCT images indicate morphological biomarkers for cancer including thickening of the epithelial layer and loss of the layered structure. The FLIM images indicate chemical biomarkers including increased nicotinamide adenine dinucleotide and reduced collagen emission. While both sets of biomarkers can differentiate normal and cancerous tissue, we believe their combination will enable the discrimination of benign lesions possessing some of the indicated biomarkers, e.g., scarring or inflammation.

摘要

癌症的早期检测是降低发病率和死亡率的关键。形态和化学生物标志物预示着正常组织向癌变组织的转变。我们首次开发了一种将光学相干断层扫描(OCT)和荧光寿命成像显微镜(FLIM)集成到单个光学系统中的非侵入性成像系统,以便同时获取这两种生物标志物。OCT 可以提供具有高分辨率的组织形态图像,而 FLIM 可以提供生化组织图谱。我们在体内仓鼠颊囊口腔癌模型中同时获取 OCT 体积和 FLIM 图像。OCT 图像显示了癌症的形态学生物标志物,包括上皮层增厚和分层结构的丧失。FLIM 图像显示了包括烟酰胺腺嘌呤二核苷酸增加和胶原蛋白发射减少在内的化学生物标志物。虽然这两种生物标志物都可以区分正常组织和癌变组织,但我们相信它们的组合将能够区分具有某些指示生物标志物的良性病变,例如疤痕或炎症。