ABSTRACT
A key challenge of central nervous system tumor surgery is to discriminate between brain regions infiltrated by tumor cells and surrounding healthy tissue. Although monitoring of autofluorescence could potentially be an efficient way to provide reliable information for these regions, we found little information on this subject, and thus we conducted studies of brain tissue optical properties. This particular study focuses on the different optical quantitative responses of human central nervous system tumors and their corresponding controls. Measurements were performed on different fixed human tumoral and healthy brain samples. Four groups of central nervous system tumors (glioblastoma, diffuse glioma, meningioma and metastasis) were discriminated from healthy brain and meninx control tissues. A threshold value was found for the scattering and absorption coefficient between tumoral and healthy groups. Emission Spectra of healthy tissue had a significant higher intensity than tumoral groups. The redox and optical index ratio were thenn calculated and these also showed significant discrimination. Two fluorescent molecules, NADH and porphyrins, showed distinct lifetim values among the different groups of samples. This study defines several optical indexes that can act as combinated indicators to discriminate healthy from tumoral tissues.
Subject(s)
Brain Neoplasms/diagnosis , Brain/pathology , Glioblastoma/diagnosis , Glioma/diagnosis , Meningeal Neoplasms/diagnosis , Meningioma/diagnosis , Optical Imaging/methods , Algorithms , Brain Neoplasms/classification , Case-Control Studies , Cohort Studies , Computer Simulation , Glioblastoma/classification , Glioma/classification , Humans , Meningeal Neoplasms/classification , Meningioma/classification , Spectrometry, FluorescenceABSTRACT
We present a customized small-core double-clad photonic crystal fiber for spectral and fluorescence lifetime measurements of human samples. In this Letter, the new fiber has been characterized on different fluorophores and samples of human brain tumor; a comparison to a bi-fiber homemade system and a commercial fiber probe was made.
ABSTRACT
We report a study of gradient index (GRIN) lenses as a miniaturized micro-objective for in vivo imaging in the context of the development of a nonlinear endomicroscope. A numerical study of the parameters influencing the lateral resolution, excitation, and collection efficiency, when GRIN lens is coupled with a double clad fiber (DCF), is exposed. Four commercial DCFs, previously identified from the literature as potential endoscopic fibers, are simulated. Then, an experimental study characterizes two GRIN lenses (one commercial, one homemade) by their dispersion and nonlinear effects, potential intrinsic fluorescence, and use for fluorescence lifetime measurements. Images of neural cells from brain tissues of mice through a GRIN lens are presented.
