1.Department of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98195, USA
2.Department of Otolaryngology- Head and Neck Surgery, Facial Plastic and Reconstructive Surgery, University of Washington, Seattle, WA 98195, USA
3.Department of Pathology, University of Washington, Seattle, WA 98109, USA
4.Center for Cardiovascular Biology, University of Washington, Seattle, WA 98109, USA
5.Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, WA 98109, USA
6.Department of Ophthalmology, University of Washington, Seattle, WA 98105, USA
Ruikang K. Wang (wangrk@uw.edu)
纸质出版日期:2021-12-31,
网络出版日期:2021-11-24,
收稿日期:2021-06-28,
修回日期:2021-10-26,
录用日期:2021-11-10
Scan QR Code
Polarization sensitive optical coherence tomography with single input for imaging depth-resolved collagen organizations[J]. LSA, 2021,10(12):2455-2466.
Tang P.et al. Polarization sensitive optical coherence tomography with single input for imaging depth-resolved collagen organizations. Light: Science & Applications, 10, 2455-2466 (2021).
Polarization sensitive optical coherence tomography with single input for imaging depth-resolved collagen organizations[J]. LSA, 2021,10(12):2455-2466. DOI: 10.1038/s41377-021-00679-3.
Tang P.et al. Polarization sensitive optical coherence tomography with single input for imaging depth-resolved collagen organizations. Light: Science & Applications, 10, 2455-2466 (2021). DOI: 10.1038/s41377-021-00679-3.
Collagen organization plays an important role in maintaining structural integrity and determining tissue function. Polarization-sensitive optical coherence tomography (PSOCT) is a promising noninvasive three-dimensional imaging tool for mapping collagen organization in vivo. While PSOCT systems with multiple polarization inputs have demonstrated the ability to visualize depth-resolved collagen organization
systems
which use a single input polarization state have not yet demonstrated sufficient reconstruction quality. Herein we describe a PSOCT based polarization state transmission model that reveals the depth-dependent polarization state evolution of light backscattered within a birefringent sample. Based on this model
we propose a polarization state tracing method that relies on a discrete differential geometric analysis of the evolution of the polarization state in depth along the Poincare sphere for depth-resolved birefringent imaging using only one single input polarization state. We demonstrate the ability of this method to visualize depth-resolved myocardial architecture in both healthy and infarcted rodent hearts (ex vivo) and collagen structures responsible for skin tension lines at various anatomical locations on the face of a healthy human volunteer (in vivo).
Di Lullo, G. D. et al. Mapping the ligand-binding sites and disease-associated mutations on the most abundant protein in the human, type Ⅰ collagen.J. Biol. Chem.277, 4223–4231 (2002)..
Langer, A. K. On the anatomy and physiology of the skin: I. The cleavability of the cutis.Br. J. Plast. Surg.31, 3–8 (1978)..
Borges, A. F. Relaxed skin tension lines (RSTL) versus other skin lines.Plast. Reconstructive Surg.73, 144–150 (1984)..
Streeter, D. D. Jr. et al. Fiber orientation in the canine left ventricle during diastole and systole.Circulation Res.24, 339–347 (1969)..
Karlon, W. J. et al. Automated measurement of myofiber disarray in transgenic mice with ventricular expression of ras.Anat. Rec.252, 612–625 (1998)..
Yang, B. et al. Structured polarized light microscopy for collagen fiber structure and orientation quantification in thick ocular tissues.J. Biomed. Opt.23, 106001 (2018)..
Jan, N. J., Lathrop, K.&Sigal, I. A. Collagen architecture of the posterior pole: high-resolution wide field of view visualization and analysis using polarized light microscopy.Investigative Ophthalmol. Vis. Sci.58, 735–744 (2017)..
Stoller, P. C. et al. Polarization-dependent optical second-harmonic imaging of rat-tail tendon.J. Biomed. Opt.7, 205–214 (2002)..
Yasui, T., Tohno, Y.&Araki, T. Characterization of collagen orientation in human dermis by two-dimensional second-harmonic-generation polarimetry.J. Biomed. Opt.9, 259–264 (2004)..
Yasui, T. et al. Observation of dermal collagen fiber in wrinkled skin using polarization-resolved second-harmonic-generation microscopy.Opt. Express17, 912–923 (2009)..
Baumann, B. et al. Swept source / Fourier domain polarization sensitive optical coherence tomography with a passive polarization delay unit.Opt. Express20, 10229–10241 (2012)..
Tang, P. J., Xu, J. J.&Wang, R. K. Imaging and visualization of the polarization state of the probing beam in polarization-sensitive optical coherence tomography.Appl. Phys. Lett.113, 231101 (2018)..
Li, E. et al. Three-dimensional multi-contrast imaging of in vivo human skin by Jones matrix optical coherence tomography.Biomed. Opt. Express8, 1290–1305 (2017)..
Nam, A. S. et al. Wide-field functional microscopy of peripheral nerve injury and regeneration.Sci. Rep.8, 14004 (2018)..
Tuchin, V. V., Wang, L. V.&Zimnyakov, D. A.Optical Polarization in Biomedical Applications. (Berlin: Springer, 2006).
Tuchin, V. V. Polarized light interaction with tissues.J. Biomed. Opt.21, 071114 (2016)..
Fan, C. M.&Yao, G. Imaging myocardial fiber orientation using polarization sensitive optical coherence tomography.Biomed. Opt. Express4, 460–465 (2013)..
Li, Q. Y., Sampson, D. D.&Villiger, M. In vivo imaging of the depth-resolved optic axis of birefringence in human skin.Opt. Lett.45, 4919–4922 (2020)..
Walther, J. et al. Depth-resolved birefringence imaging of collagen fiber organization in the human oral mucosa in vivo.Biomed. Opt. Express10, 1942–1956 (2019)..
Sakai, S. et al. In vivo evaluation of human skin anisotropy by polarization-sensitive optical coherence tomography.Biomed. Opt. Express2, 2623–2631 (2011)..
Fan, C. M.&Yao, G. Mapping local optical axis in birefringent samples using polarization-sensitive optical coherence tomography.J. Biomed. Opt.17, 110501 (2012)..
Park, B. H. et al. Optic axis determination accuracy for fiber-based polarization-sensitive optical coherence tomography.Opt. Lett.30, 2587–2589 (2005)..
Park, B. H. et al. Real-time multi-functional optical coherence tomography.Opt. Express11, 782–793 (2003)..
Saxer, C. E. et al. High-speed fiber-based polarization-sensitive optical coherence tomography of in vivo human skin.Opt. Lett.25, 1355–1357 (2000)..
Villiger, M. et al. Spectral binning for mitigation of polarization mode dispersion artifacts in catheter-based optical frequency domain imaging.Opt. Express21, 16353–16369 (2013)..
Rivet, S. et al. Passive optical module for polarization-sensitive optical coherence tomography systems.Opt. Express25, 14533–14544 (2017)..
Al-Qaisi, M. K.&Akkin, T. Polarization-sensitive optical coherence tomography based on polarization-maintaining fibers and frequency multiplexing.Opt. Express16, 13032–13041 (2008)..
Furuhashi, Y., Kimura, Y.&Yamane, H. Higher order structural analysis of stereocomplex-type poly(lactic acid) melt-spun fibers.J. Polym. Sci. Part B: Polym. Phys.45, 218–228 (2007)..
de Campos Vidal, B.&Mello, M. L. S. Optical anisotropy of collagen fibers of rat calcaneal tendons: an approach to spatially resolved supramolecular organization.Acta Histochemica112, 53–61 (2010)..
Zaffar, M.&Pradhan, A. Assessment of anisotropy of collagen structures through spatial frequencies of Mueller matrix images for cervical pre-cancer detection.Appl. Opt.59, 1237–1248 (2020)..
de Visser, S. K. et al. Anisotropy of collagen fibre alignment in bovine cartilage: comparison of polarised light microscopy and spatially resolved diffusion-tensor measurements.Osteoarthr. Cartil.16, 689–697 (2008)..
Ariga, R. et al. Identification of myocardial disarray in patients with hypertrophic cardiomyopathy and ventricular arrhythmias.J. Am. Coll. Cardiol.73, 2493–2502 (2019)..
Wang, Y. et al. Histology validation of mapping depth-resolved cardiac fiber orientation in fresh mouse heart using optical polarization tractography.Biomed. Opt. Express5, 2843–2855 (2014)..
Alhamdi, A. A. Facial skin lines.Iraqi JMS13, 103–107 (2015)..
Piérard, G.&Lapière, C. Microanatomy of the dermis in relation to relaxed skin tension lines and langer's lines.Am. J. Dermatopathol.9, 219–224 (1987)..
Borges, A. F. Relaxed skin tension lines.Dermatologic Clin.7, 169–178 (1989)..
Mao, J. R.&Bristow, J. The Ehlers-Danlos syndrome: on beyond collagens.J. Clin. Investig.107, 1063–1069 (2001)..
Krieg, T. et al. Collagen synthesis in scleroderma: selection of fibroblast populations during subcultures.Arch. Dermatological Res.277, 373–376 (1985)..
Oh, W. Y. et al. High-speed polarization sensitive optical frequency domain imaging with frequency multiplexing.Opt. Express16, 1096–1103 (2008)..
Lurie, K. L., Moritz, T. J.&Ellerbee, A. K. Design considerations for polarization-sensitive optical coherence tomography with a single input polarization state.Biomed. Opt. Express3, 2273–2287 (2012)..
Louis-Dorr, V. et al. Linear dichroism of the cornea.Appl. Opt.43, 1515–1521 (2004)..
Park, J. et al. Differential geometry of normalized stokes vector trajectories in anisotropic media.J. Optical Soc. Am. A23, 679–690 (2006)..
Chen, D. S. et al. Study of optical clearing in polarization measurements by Monte Carlo simulations with anisotropic tissue-mimicking models.J. Biomed. Opt.21, 081209 (2016)..
Chen, D. S. et al. Mueller matrix polarimetry for characterizing microstructural variation of nude mouse skin during tissue optical clearing.Biomed. Opt. Express8, 3559–3570 (2017)..
Xu, X. Q.&Wang, R. K. Synergistic effect of hyperosmotic agents of dimethyl sulfoxide and glycerol on optical clearing of gastric tissue studied with near infrared spectroscopy.Phys. Med. Biol.49, 457–468 (2004)..
Deegan, A. J. et al. Optical coherence tomography angiography of normal skin and inflammatory dermatologic conditions.Lasers Surg. Med.50, 183–193 (2018)..
Lu, J. et al. Application of OCT-derived attenuation coefficient in acute burn-damaged skin.Lasers Surg. Med.53, 1192–1200 (2021)..
Pitre, J. J. Jr. et al. Nearly-incompressible transverse isotropy (NITI) of cornea elasticity: model and experiments with acoustic micro-tapping OCE.Sci. Rep.10, 12983 (2020)..
Hu, S. W., Lundgren, M.&Niemi, A. J. Discrete Frenet frame, inflection point solitons, and curve visualization with applications to folded proteins.Phys. Rev. E83, 061908 (2011)..
Nam, A.Development and translation of label-free functional microscopy based on optical coherence tomography(PhD thesis, Massachusetts Institute of Technology, Massachusetts, 2017).
Kemp,N. J. et al. High-sensitivity determination of birefringence in turbid media with enhanced polarization-sensitive optical coherence tomography.J. Optical Soc. Am. A22, 552–560 (2005)..
0
浏览量
0
Downloads
0
CSCD
关联资源
相关文章
相关作者
相关机构