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Multimodal Nonlinear Imaging of the Human Cornea
- Source :
- Investigative Ophthalmology & Visual Science, Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (5), pp.2459-2465. ⟨10.1167/iovs.09-4586⟩, Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (5), pp.2459-2465. 〈10.1167/iovs.09-4586〉
- Publication Year :
- 2010
- Publisher :
- HAL CCSD, 2010.
-
Abstract
- PURPOSE. To evaluate the potential of third-harmonic generation (THG) microscopy combined with second-harmonic generation (SHG) and two-photon excited fluorescence (2PEF) microscopies for visualizing the microstructure of the human cornea and trabecular meshwork based on their intrinsic nonlinear properties. METHODS. Fresh human corneal buttons and corneoscleral discs from an eye bank were observed under a multiphoton microscope incorporating a titanium-sapphire laser and an optical parametric oscillator for the excitation, and equipped with detection channels in the forward and backward directions. RESULTS. Original contrast mechanisms of THG signals in cornea with physiological relevance were elucidated. THG microscopy with circular incident polarization detected microscopic anisotropy and revealed the stacking and distribution of stromal collagen lamellae. THG imaging with linear incident polarization also revealed cellular and anchoring structures with micrometer resolution. In edematous tissue, a strong THG signal around cells indicated the local presence of water. Additionally, SHG signals reflected the distribution of fibrillar collagen, and 2PEF imaging revealed the elastic component of the trabecular meshwork and the fluorescence of metabolically active cells. CONCLUSIONS. The combined imaging modalities of THG, SHG, and 2PEF provide key information about the physiological state and microstructure of the anterior segment over its entire thickness with remarkable contrast and specificity. This imaging method should prove particularly useful for assessing glaucoma and corneal physiopathologies. (Invest Ophthalmol Vis Sci. 2010;51:2459‐2465) DOI:10.1167/iovs.09-4586
- Subjects :
- Materials science
Microscope
genetic structures
Corneal Stroma
Glaucoma
Fluorescence Polarization
Eye Banks
01 natural sciences
law.invention
Cornea
010309 optics
03 medical and health sciences
0302 clinical medicine
Trabecular Meshwork
law
0103 physical sciences
Microscopy
medicine
Humans
[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]
[ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]
Corneal Edema
Endothelium, Corneal
Resolution (electron density)
Epithelium, Corneal
Eye bank
Anatomy
medicine.disease
Tissue Donors
eye diseases
Microscopy, Fluorescence, Multiphoton
medicine.anatomical_structure
030221 ophthalmology & optometry
Collagen
Trabecular meshwork
sense organs
Sclera
Fluorescence anisotropy
Biomedical engineering
Subjects
Details
- Language :
- English
- ISSN :
- 01460404 and 15525783
- Database :
- OpenAIRE
- Journal :
- Investigative Ophthalmology & Visual Science, Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (5), pp.2459-2465. ⟨10.1167/iovs.09-4586⟩, Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2010, 51 (5), pp.2459-2465. 〈10.1167/iovs.09-4586〉
- Accession number :
- edsair.doi.dedup.....41291fc8c1b17572fe592284e0fc2f25