Literature DB >> 8930102

Quantitative optical spectroscopy for tissue diagnosis.

R Richards-Kortum1, E Sevick-Muraca.   

Abstract

The interaction of light within tissue has been used to recognize disease since the mid-1800s. The recent developments of small light sources, detectors, and fiber optic probes provide opportunities to quantitatively measure these interactions, which yield information for diagnosis at the biochemical, structural, or (patho)physiological level within intact tissues. However, because of the strong scattering properties of tissues, the reemitted optical signal is often influenced by changes in biochemistry (as detected by these spectroscopic approaches) and by physiological and pathophysiological changes in tissue scattering. One challenge of biomedical optics is to uncouple the signals influenced by biochemistry, which themselves provide specificity for identifying diseased states, from those influenced by tissue scattering, which are typically unspecific to a pathology. In this review, we describe optical interactions pursued for biomedical applications (fluorescence, fluorescence lifetime, phosphorescence, and Raman from cells, cultures, and tissues) and then provide a descriptive framework for light interaction based upon tissue absorption and scattering properties. Finally, we review important endogenous and exogenous biological chromophores and describe current work to employ these signals for detection and diagnosis of disease.

Mesh:

Year:  1996        PMID: 8930102     DOI: 10.1146/annurev.physchem.47.1.555

Source DB:  PubMed          Journal:  Annu Rev Phys Chem        ISSN: 0066-426X            Impact factor:   12.703


  210 in total

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Authors:  D J Hawrysz; E M Sevick-Muraca
Journal:  Neoplasia       Date:  2000 Sep-Oct       Impact factor: 5.715

Review 2.  Basic investigations for 2-dimensional time-resolved fluorescence measurements at the fundus.

Authors:  D Schweitzer; A Kolb; M Hammer; E Thamm
Journal:  Int Ophthalmol       Date:  2001       Impact factor: 2.031

3.  A spectrally constrained dual-band normalization technique for protoporphyrin IX quantification in fluorescence-guided surgery.

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4.  Study of the development of the mouse thoracic aorta three-dimensional macromolecular structure using two-photon microscopy.

Authors:  Leah M Zadrozny; Edward B Neufeld; Bertrand M Lucotte; Patricia S Connelly; Zu-Xi Yu; Lam Dao; Li-Yueh Hsu; Robert S Balaban
Journal:  J Histochem Cytochem       Date:  2014-10-31       Impact factor: 2.479

Review 5.  Fluorescence spectroscopy of neoplastic and non-neoplastic tissues.

Authors:  N Ramanujam
Journal:  Neoplasia       Date:  2000 Jan-Apr       Impact factor: 5.715

6.  Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation.

Authors:  Warren R Zipfel; Rebecca M Williams; Richard Christie; Alexander Yu Nikitin; Bradley T Hyman; Watt W Webb
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-19       Impact factor: 11.205

7.  Imaging cells and extracellular matrix in vivo by using second-harmonic generation and two-photon excited fluorescence.

Authors:  Aikaterini Zoumi; Alvin Yeh; Bruce J Tromberg
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-12       Impact factor: 11.205

8.  Determination of myocardium viability on the basis of the spectra of laser-induced fluorescence.

Authors:  V M Fomin; A M Karas'kov; P M Larionov; A N Malov; N A Maslov; A M Orishich
Journal:  Dokl Biol Sci       Date:  2003 Jul-Aug

Review 9.  Optical biopsy: a new frontier in endoscopic detection and diagnosis.

Authors:  Thomas D Wang; Jacques Van Dam
Journal:  Clin Gastroenterol Hepatol       Date:  2004-09       Impact factor: 11.382

10.  Blind spectral decomposition of single-cell fluorescence by parallel factor analysis.

Authors:  Hideki Shirakawa; Shunichi Miyazaki
Journal:  Biophys J       Date:  2004-03       Impact factor: 4.033

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