Circular polarization biomicroscopy: a method for determining human corneal stromal lamellar organization in vivo
The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation‐sensitive techniques using linear polarized light alone. A met...
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| Vydané v: | Ophthalmic & physiological optics Ročník 27; číslo 3; s. 256 - 264 |
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| Médium: | Journal Article |
| Jazyk: | English |
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Oxford, UK
Blackwell Publishing Ltd
01.05.2007
Blackwell |
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| ISSN: | 0275-5408, 1475-1313 |
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| Abstract | The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation‐sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15° to the horizontal in a superotemporal–inferonasal direction. |
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| AbstractList | The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation-sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15 degrees to the horizontal in a superotemporal-inferonasal direction. The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation‐sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15° to the horizontal in a superotemporal–inferonasal direction. The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation-sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15 degrees to the horizontal in a superotemporal-inferonasal direction.The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation-sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15 degrees to the horizontal in a superotemporal-inferonasal direction. The theory of polarization biomicroscopy is explored using Stokes vectors and Mueller matrices. It is established that circular polarization can be used to simultaneously detect birefringent elements at any orientation unlike orientation‐sensitive techniques using linear polarized light alone. A method of biomicroscopy using circular polarized light is described and tested in a physical model. The method is then used to investigate the lamellar structure of human corneas in vivo in pairs of eyes of 38 subjects. An approximate confocal elliptic/hyperbolic distribution of stromal fibrils, presumed to be collagen, is clearly identified within central and intermediate areas of the cornea. All subjects tested demonstrate approximate mirror symmetry between pairs of eyes typically with a preferred orientation of central fibrils at approximately 15° to the horizontal in a superotemporal–inferonasal direction. |
| Author | Misson, Gary P. |
| Author_xml | – sequence: 1 givenname: Gary P. surname: Misson fullname: Misson, Gary P. organization: Department of Ophthalmology, Warwick Hospital, South Warwickshire NHS Trust, Lakin Road, Warwick, CV34 5BW, and Optical Engineering Laboratory, School of Engineering, University of Warwick, Coventry, UK |
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| Keywords | Biomicroscopy Human Polarization Cornea Organization corneal stromal structure Stroma Method Polarized light In vivo Mueller matrices collagen lamellae Collagen Ophthalmology Structure circular polarized light |
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| References | Stoller, P., Reiser, K. M., Celliers, P. M. and Rubenchik, A. M. (2002) Polarization-modulated second harmonic generation in collagen. Biophys. J., 82, 3330-3342. Greenfield, D. S., Knighton, R. W. and Huang, X. R. (2000) Effect of corneal polarization axis on assessment of retinal nerve fiber layer thickness by scanning laser polarimetry. Am. J. Ophthalmol., 129, 715-722. Newton, R. H. and Meek, K. M. (1998a) Circumcorneal annulus of collagen fibrils in the human limbus. Invest. Ophthalmol. Vis. Sci., 39, 1125-1134. Shurcliff, W. A. (1962) Polarized Light: Production and Use. Harvard University Press, Cambridge, MA. Stanworth, A. and Naylor, E. J. (1950) The polarization optics of the isolated cornea. Br. J. Ophthalmol., 34, 201-211. Misson, G. P. (2003) A Mueller matrix model of Haidinger's brushes. Ophthalmic Physiol. Opt., 23, 441-447. Koeppe, L. (1921) Die ultra und polarizationsmikroskopische Erforschung des Lebenden Auges und Ihre Ergebnisse. 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M. and Boote, C. (2004) The organization of collagen in the corneal stroma. Exp. Eye Res., 78, 503-512. Rasband, W. S. (19972006) ImageJ. U.S. National Institutes of Health, Bethesda, MD. Morishige, N., Petroll, W. M., Nishida, T., Kenney, M. C. and Jester, J. V. (2006) Noninvasive corneal stromal collagen imaging using two-photon-generated second-harmonic signals. J. Cataract Refract. Surg., 32, 1784-1791. Teng, S.-W., Tan, H.-Y., Peng, J.-L., Lin, H.-H., Kim, K. H., Lo, W., Sun, Y., Lin, W.-C., Lin, S.-J., Jee, S.-H., So, P. T. C. and Dong, C.-Y. (2006) Multiphoton autofluorescence and second-harmonic generation imaging of the ex vivo porcine eye. Invest. Ophthalmol. Vis. Sci., 47, 1216-1224. Van Blokland, G. J. (1985) Ellipsometry of the human retina in vivo: preservation of polarization. J. Opt. Soc. Am. A, 2, 72-75. Mishima, S. (1960) The use of polarized light in the biomicroscopy of the eye. Report I. Bibl. Ophthalmol., 55, 1-20. Meek, K. M., Blamires, T., Elliott, G. F., Gyi, T. J. and Nave, C. (1987) The organisation of collagen fibrils in the human corneal stroma: a synchrotron X-ray diffraction study. Curr. Eye Res., 6, 841-846. Wang, B. G. and Halbhuber, K. J. (2006) Corneal multiphoton microscopy and intratissue optical nanosurgery by nanojoule femtosecond near-infrared pulsed lasers. Ann. Anat., 188, 395-409. Newton, R. H. and Meek, K. M. (1998b) The integration of the corneal and limbal fibrils in the human eye. Biophys. J., 75, 2508-2512. Clarke, D. and Grainger, J. F. (1971) Polarized Light and Optical Measurement. Pergamon Press, Oxford. 1960; 55 2006; 32 1985; 2 1987; 4 1987; 6 1997 1998b; 75 1971 1993 2002; 82 1991 1979 1998a; 39 1950; 34 2002; 120 2000; 129 1999; 16 2002; 43 2006; 69 2004; 78 2006; 47 1921 1997; 38 1962 1852; 9 19972006 1958; 2 1938; 138 1969 2006; 188 1974; 250 2003; 23 Bron A. J. (e_1_2_6_5_1) 1997 e_1_2_6_32_1 e_1_2_6_10_1 e_1_2_6_30_1 Mishima S. (e_1_2_6_18_1) 1958; 2 Knighton R. W. (e_1_2_6_11_1) 2002; 43 Bour L. J. (e_1_2_6_4_1) 1991 Rasband W. S. (e_1_2_6_24_1) 1997 Clarke D. (e_1_2_6_6_1) 1971 Wahlstrom E. E. (e_1_2_6_31_1) 1979 Newton R. H. (e_1_2_6_22_1) 1998; 39 Daxer A. (e_1_2_6_8_1) 1997; 38 e_1_2_6_13_1 e_1_2_6_14_1 e_1_2_6_33_1 e_1_2_6_17_1 Koeppe L. (e_1_2_6_12_1) 1921 e_1_2_6_16_1 e_1_2_6_21_1 e_1_2_6_20_1 Collett E. (e_1_2_6_7_1) 1993 Mishima S. (e_1_2_6_19_1) 1960; 55 e_1_2_6_9_1 e_1_2_6_25_1 Stokes G. G. (e_1_2_6_28_1) 1852; 9 e_1_2_6_3_1 Maurice D. M. (e_1_2_6_15_1) 1969 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_27_1 e_1_2_6_26_1 |
| References_xml | – reference: Shute, C. C. (1974) Haidinger's brushes and predominant orientation of collagen in corneal stroma. Nature, 250, 163-164. – reference: Hunter, D. G., Sandruck, J. C., Sau, S., Patel, S. N. and Guyton, D. L. (1999) Mathematical modeling of retinal birefringence scanning. J. Opt. Soc. Am. A, 16, 2103-2111. – reference: Kokott, W. (1938) Uber mechanisch-funktionelle Strukturen des Auges. Albrecht Von Graefes Arch. Ophthalmol., 138, 424-485. – reference: Shurcliff, W. A. (1962) Polarized Light: Production and Use. Harvard University Press, Cambridge, MA. – reference: Meek, K. M. and Boote, C. (2004) The organization of collagen in the corneal stroma. Exp. Eye Res., 78, 503-512. – reference: Rasband, W. S. (19972006) ImageJ. U.S. National Institutes of Health, Bethesda, MD. – reference: Knighton, R. W., Huang, X. R. and Greenfield, D. S. (2002) Analytical model of scanning laser polarimetry for retinal nerve fiber layer assessment. Invest. Ophthalmol. Vis. Sci., 43, 383-392. – reference: Stokes, G. G. (1852) On the composition and resolution of streams of polarized light from different sources. Trans. Cambridge Phil. Soc., 9, 399-416. – reference: Morishige, N., Petroll, W. M., Nishida, T., Kenney, M. C. and Jester, J. V. (2006) Noninvasive corneal stromal collagen imaging using two-photon-generated second-harmonic signals. J. Cataract Refract. Surg., 32, 1784-1791. – reference: Newton, R. H. and Meek, K. M. (1998b) The integration of the corneal and limbal fibrils in the human eye. Biophys. J., 75, 2508-2512. – reference: Lo, W., Teng, S.-W., Tan, H.-Y., Kim, K. H., Chen, H.-C., Lee, H.-S., Chen, Y.-F., So, P. T. C. and Dong, C.-Y. (2006) Intact corneal stroma visualization of GFP mouse revealed by multiphoton imaging. Microsc. Res. Tech., 69, 973-975. – reference: Newton, R. H. and Meek, K. M. (1998a) Circumcorneal annulus of collagen fibrils in the human limbus. Invest. Ophthalmol. Vis. Sci., 39, 1125-1134. – reference: Collett, E. 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| SubjectTerms | Adult Aged Aged, 80 and over Biological and medical sciences biomicroscopy circular polarized light Collagen - ultrastructure collagen lamellae cornea Cornea - physiology Corneal Stroma - ultrastructure corneal stromal structure Eye and associated structures. Visual pathways and centers. Vision Female Fundamental and applied biological sciences. Psychology Humans Male Microscopy, Polarization - methods Middle Aged Models, Biological Mueller matrices Ocular Physiological Phenomena Vertebrates: nervous system and sense organs |
| Title | Circular polarization biomicroscopy: a method for determining human corneal stromal lamellar organization in vivo |
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