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Optical Biopsy - a new armamentarium to detect disease using light

机译:光学活检-一种使用光检测疾病的新型武器库

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Optical spectroscopy has been considered a promising method for cancer detection for past thirty years because of its advantages over the conventional diagnostic methods of no tissue removal, minimal invasiveness, rapid diagnoses, less time consumption and reproducibility since the first use in 1984. It offers a new armamentarium. Human tissue is mainly composed of extracellular matrix of collagen fiber, proteins, fat, water, and epithelial cells with key molecules in different structures. Tissues contain a number of key fingerprint native endogenous fluorophore molecules, such as tryptophan, collagen, elastin, reduced nicotinamide adenine dinucleotide (NADH), flavin adenine dinucleotide (FAD) and porphyrins. It is well known that abnormalities in metabolic activity precede the onset of a lot of main diseases: carcinoma, diabetes mellitus, atherosclerosis, Alzheimer, and Parkinson's disease, etc. Optical spectroscopy may help in detecting various disorders. Conceivably the biochemical or morphologic changes that cause the spectra variations would appear earlier than the histological aberration. Therefore, "optical biopsy" holds a great promise as clinical tool for diagnosing early stage of carcinomas and other deceases by combining with available photonic technology (e.g. optical fibers, photon detectors, spectrographs spectroscopic ratiometer, fiber-optic endomicroscope and nasopharyngoscope) for in vivo use. This paper focuses on various methods available to detect spectroscopic changes in tissues, for example to distinguish cancerous prostate tissues and/or cells from normal prostate tissues and/or cells. The methods to be described are fluorescence, stokes shift, scattering, Raman, and time-resolved spectroscopy will be reviewed. The underlying physical and biological basis for these optical approaches will be discussed with examples. The idea is to present some of the salient works to show the usefulness and methods of Optical Biopsy for cancer detection and show new directions.
机译:自从1984年首次使用光谱技术以来,它比不清除组织,侵入性最小,诊断迅速,耗时少且可重现性的常规诊断方法更具优势,在过去三十年中,光谱被认为是一种有前途的癌症检测方法。新的军备库。人体组织主要由胶原纤维,蛋白质,脂肪,水和上皮细胞的细胞外基质组成,其关键分子具有不同的结构。组织包含许多关键的指纹天然内源性荧光团分子,例如色氨酸,胶原蛋白,弹性蛋白,烟酰胺还原腺嘌呤二核苷酸(NADH),黄素腺嘌呤二核苷酸(FAD)和卟啉。众所周知,代谢活动异常先于许​​多主要疾病的发作:癌,糖尿病,动脉粥样硬化,阿尔茨海默氏病和帕金森氏病等。光谱学可以帮助发现各种疾病。可以想象,引起光谱变化的生物化学或形态学变化会比组织学畸变更早出现。因此,“光学活检”通过结合可用的光子技术(例如光纤,光子检测器,光谱仪,光谱比仪,光纤内窥镜和鼻咽镜),有望作为诊断癌症早期发作和其他疾病的临床工具。采用。本文关注于可用于检测组织中光谱变化的各种方法,例如,将癌性前列腺组织和/或细胞与正常前列腺组织和/或细胞区分开。将要描述的方法是荧光,斯托克斯频移,散射,拉曼光谱和时间分辨光谱。这些光学方法的潜在物理和生物学基础将通过示例进行讨论。这个想法是要提出一些突出的工作,以证明光学活检对癌症检测的有用性和方法,并显示出新的方向。

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