<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Masihzadeh O</submitter><funding>NIDDK NIH HHS</funding><pagination>036009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5997970</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(3)</volume><pubmed_abstract>The development of technologies to characterize the ocular aqueous outflow system (AOS) is important for the understanding of the pathophysiology of glaucoma. Multiphoton microscopy (MPM) offers the advantage of high-resolution, label-free imaging with intrinsic image contrast because the emitted signals result from the specific biomolecular content of the tissue. Previous attempts to use MPM to image the murine irido-corneal region directly through the sclera have suffered from degradation in image resolution due to scattering of the focused laser light. As a result, transscleral MPM has limited ability to observe fine structures in the AOS. In this work, the porcine irido-corneal angle was successfully imaged through the transparent cornea using a gonioscopic lens to circumvent the highly scattering scleral tissue. The resulting high-resolution images allowed the detailed structures in the trabecular meshwork (TM) to be observed. Multimodal imaging by two-photon autofluorescence and second harmonic generation allowed visualization of different features in the TM without labels and without disruption of the TM or surrounding tissues. MPM gonioscopy is a promising noninvasive imaging tool for high-resolution studies of the AOS, and research continues to explore the potential for future clinical applications in humans.</pubmed_abstract><journal>Journal of biomedical optics</journal><pubmed_title>Direct trabecular meshwork imaging in porcine eyes through multiphoton gonioscopy.</pubmed_title><pmcid>PMC5997970</pmcid><funding_grant_id>K25 DK095232</funding_grant_id><pubmed_authors>Lei TC</pubmed_authors><pubmed_authors>Ammar DA</pubmed_authors><pubmed_authors>Kahook MY</pubmed_authors><pubmed_authors>Gibson EA</pubmed_authors><pubmed_authors>Masihzadeh O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Direct trabecular meshwork imaging in porcine eyes through multiphoton gonioscopy.</name><description>The development of technologies to characterize the ocular aqueous outflow system (AOS) is important for the understanding of the pathophysiology of glaucoma. Multiphoton microscopy (MPM) offers the advantage of high-resolution, label-free imaging with intrinsic image contrast because the emitted signals result from the specific biomolecular content of the tissue. Previous attempts to use MPM to image the murine irido-corneal region directly through the sclera have suffered from degradation in image resolution due to scattering of the focused laser light. As a result, transscleral MPM has limited ability to observe fine structures in the AOS. In this work, the porcine irido-corneal angle was successfully imaged through the transparent cornea using a gonioscopic lens to circumvent the highly scattering scleral tissue. The resulting high-resolution images allowed the detailed structures in the trabecular meshwork (TM) to be observed. Multimodal imaging by two-photon autofluorescence and second harmonic generation allowed visualization of different features in the TM without labels and without disruption of the TM or surrounding tissues. MPM gonioscopy is a promising noninvasive imaging tool for high-resolution studies of the AOS, and research continues to explore the potential for future clinical applications in humans.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Mar</publication><modification>2024-02-14T02:20:47.454Z</modification><creation>2019-03-26T22:40:54Z</creation></dates><accession>S-EPMC5997970</accession><cross_references><pubmed>23515864</pubmed><doi>10.1117/1.JBO.18.3.036009</doi></cross_references></HashMap>