Imaging ex vivo and in vitro brain morphology in animal models with ultrahigh resolution optical coherence tomography
- PMID: 15250758
- DOI: 10.1117/1.1756920
Imaging ex vivo and in vitro brain morphology in animal models with ultrahigh resolution optical coherence tomography
Abstract
The feasibility of ultrahigh resolution optical coherence tomography (UHR OCT) to image ex vivo and in vitro brain tissue morphology on a scale from single neuron cells to a whole animal brain was investigated using a number of animal models. Sub-2-microm axial resolution OCT in biological tissue was achieved at different central wavelengths by separately interfacing two state-of-the-art broad bandwidth light sources (titanium:sapphire, Ti:Al2O3 laser, lambdac=800 nm, Deltalambda=260 nm, Pout=50 mW and a fiber laser light source, lambdac=1350 nm, Deltalambda=470 nm, Pout=4 mW) to free-space or fiber-based OCT systems, designed for optimal performance in the appropriate wavelength regions. The ability of sub-2-microm axial resolution OCT to visualize intracellular morphology was demonstrated by imaging living ganglion cells in cultures. The feasibility of UHR OCT to image the globular structure of an entire animal brain as well as to resolve fine morphological features at various depths in it was tested by imaging a fixed honeybee brain. Possible degradation of OCT axial resolution with depth in optically dense brain tissue was examined by depositing microspheres through the blood stream to various depths in the brain of a living rabbit. It was determined that in the 1100 to 1600-nm wavelength range, OCT axial resolution was well preserved, even at depths greater than 500 microm, and permitted distinct visualization of microspheres 15 microm in diameter. In addition, the OCT image penetration depth and the scattering properties of gray and white brain matter were evaluated in tissue samples from the visual cortex of a fixed monkey brain.
Similar articles
-
Advances in broad bandwidth light sources for ultrahigh resolution optical coherence tomography.Phys Med Biol. 2004 Apr 7;49(7):1235-46. doi: 10.1088/0031-9155/49/7/011. Phys Med Biol. 2004. PMID: 15128201
-
Enhanced visualization of choroidal vessels using ultrahigh resolution ophthalmic OCT at 1050 nm.Opt Express. 2003 Aug 25;11(17):1980-6. doi: 10.1364/oe.11.001980. Opt Express. 2003. PMID: 19466083
-
Ultrahigh-resolution optical coherence tomography with a fiber laser source at 1 microm.Opt Lett. 2005 May 15;30(10):1171-3. doi: 10.1364/ol.30.001171. Opt Lett. 2005. PMID: 15945143
-
[Methodological advancements. Ultrahigh-resolution OCT].Ophthalmologe. 2004 Aug;101(8):804-12. doi: 10.1007/s00347-004-1057-6. Ophthalmologe. 2004. PMID: 15459789 Review. German.
-
Ultrahigh-resolution optical coherence tomography.J Biomed Opt. 2004 Jan-Feb;9(1):47-74. doi: 10.1117/1.1629679. J Biomed Opt. 2004. PMID: 14715057 Review.
Cited by
-
Review of optical coherence tomography in oncology.J Biomed Opt. 2017 Dec;22(12):1-23. doi: 10.1117/1.JBO.22.12.121711. J Biomed Opt. 2017. PMID: 29274145 Free PMC article. Review.
-
Capability of physically reasonable OCT-based differentiation between intact brain tissues, human brain gliomas of different WHO grades, and glioma model 101.8 from rats.Biomed Opt Express. 2020 Oct 28;11(11):6780-6798. doi: 10.1364/BOE.409692. eCollection 2020 Nov 1. Biomed Opt Express. 2020. PMID: 33282523 Free PMC article.
-
Localization of cortical tissue optical changes during seizure activity in vivo with optical coherence tomography.Biomed Opt Express. 2015 Apr 22;6(5):1812-27. doi: 10.1364/BOE.6.001812. eCollection 2015 May 1. Biomed Opt Express. 2015. PMID: 26137382 Free PMC article.
-
Thinned-skull cortical window technique for in vivo optical coherence tomography imaging.J Vis Exp. 2012 Nov 19;(69):e50053. doi: 10.3791/50053. J Vis Exp. 2012. PMID: 23183913 Free PMC article.
-
Dual-modality optical diagnosis for precise in vivo identification of tumors in neurosurgery.Theranostics. 2019 Apr 13;9(10):2827-2842. doi: 10.7150/thno.33823. eCollection 2019. Theranostics. 2019. PMID: 31244926 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources