
1.Department of Physics and Astronomy, San Francisco State University, San Francisco, CA, 94132, USA
2.Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37240, USA
3.MOE Key Lab of Weak-Light Nonlinear Photonics, TEDA Applied Physics Institute and School of Physics, Nankai University, Tianjin, 300457, China
4.Guangxi Key Lab for Relativistic Astrophysics, Guangxi Colleges and Universities Key Lab of Novel Energy Materials and Related Technology, School of Physical Science and Technology, Guangxi University, Nanning, Guangxi, 530004, China
5.Department of Physics and Astronomy, California State University Northridge, Northridge, CA, 91330, USA
6.Institut National de la Recherche Scientifique, Université du Québec, Varennes, QC, J3X 1S2, Canada
7.Department of Physics, Chemistry and Biology, Linköping University, Linköping, SE-581 83, Sweden
8.School of Mathematical and Physical Sciences, University of Sussex, Sussex House, Falmer, Brighton, BN1 9RH, UK
9.Department of Biomedical Engineering, University of California Irvine, Irvine, CA, USA
10.Clinical Laboratory Science Program, San Francisco State University, San Francisco, CA, 94132, USA
11.Institute of Fundamental and Frontier Sciences, University of Electronic Science and Tech. of China, Chengdu, 610054, China
12.ITMO University, Saint Petersburg, 197101, Russia
Yinxiao Xiang (yinxiaoermao@nankai.edu.cn)
Yinxiao Xiang (yinxiaoermao@nankai.edu.cn)
Published:2019,
Published Online:13 March 2019,
Received:02 October 2018,
Revised:21 February 2019,
Accepted:22 February 2019
Scan QR Code
Gautam, R. et al. Optical force-induced nonlinearity and self-guiding of light in human red blood cell suspensions. Light: Science & Applications, 8, 279-287 (2019).
Gautam, R. et al. Optical force-induced nonlinearity and self-guiding of light in human red blood cell suspensions. Light: Science & Applications, 8, 279-287 (2019). DOI: 10.1038/s41377-019-0142-1.
Osmotic conditions play an important role in the cell properties of human red blood cells (RBCs)
which are crucial for the pathological analysis of some blood diseases such as malaria. Over the past decades
numerous efforts have mainly focused on the study of the RBC biomechanical properties that arise from the unique deformability of erythrocytes. Here
we demonstrate nonlinear optical effects from human RBCs suspended in different osmotic solutions. Specifically
we observe self-trapping and scattering-resistant nonlinear propagation of a laser beam through RBC suspensions under all three osmotic conditions
where the strength of the optical nonlinearity increases with osmotic pressure on the cells. This tunable nonlinearity is attributed to optical forces
particularly the forward-scattering and gradient forces. Interestingly
in aged blood samples (with lysed cells)
a notably different nonlinear behavior is observed due to the presence of free hemoglobin. We use a theoretical model with an optical force-mediated nonlocal nonlinearity to explain the experimental observations. Our work on light self-guiding through scattering bio-soft-matter may introduce new photonic tools for noninvasive biomedical imaging and medical diagnosis.
Wiersma, D. S. Disordered photonics.Nat. Photon7, 188-196 (2013)..
Yaqoob, Z. et al. Optical phase conjugation for turbidity suppression in biological samples.Nat. Photon2, 110-115 (2008)..
Vellekoop, I. M., Lagendijk, A.&Mosk, A. P. Exploiting disorder for perfect focusing.Nat. Photon4, 320-322 (2010)..
Čižmár, T., Mazilu, M.&Dholakia, K.In situwavefront correction and its application to micromanipulation.Nat. Photon4, 388-394 (2010)..
Katz, O. et al. Focusing and compression of ultrashort pulses through scattering media.Nat. Photon5, 372-377 (2011)..
Mosk, A. P. et al. Controlling waves in space and time for imaging and focusing in complex media.Nat. Photon6, 283-292 (2012)..
Horstmeyer, R., Ruan, H. W.&Yang, C. Guidestar-assisted wavefront-shaping methods for focusing light into biological tissue.Nat. Photon9, 563-571 (2015)..
Rubinsztein-Dunlop, H. et al. Roadmap on structured light.J. Opt.19, 013001 (2017)..
Georgakoudi, I. et al. Optical spectroscopy and imaging for the noninvasive evaluation of engineered tissues.Tissue Eng. Part B: Rev.14, 321-340 (2008)..
Yuan, B. H. et al. A system for high-resolution depth-resolved optical imaging of fluorescence and absorption contrast.Rev. Sci. Instrum.80, 043706 (2009)..
Gather, M. C.&Yun, S. H. Single-cell biological lasers.Nat. Photon5, 406-410 (2011)..
Bahadori, A., Oddershede, L. B.&Bendix, P. M. Hot-nanoparticle-mediated fusion of selected cells.Nano Res10, 2034-2045 (2017)..
Huang, L. et al. Ultralow-power near infrared lamp light operable targeted organic nanoparticle photodynamic therapy.J. Am. Chem. Soc.138, 14586-14591 (2016)..
Barroso, Á. et al. Optical assembly of bio-hybrid micro-robots.Biomed. Micro.17, 26 (2015)..
Villangca, M. J. et al. Light-driven micro-tool equipped with a syringe function.Light.: Sci. Appl.5, e16148 (2016)..
Latimer, P. Light scattering and absorption as methods of studying cell population parameters.Annu. Rev. Biophys. Bioeng.11, 129-150 (1982)..
Jacques, S. L. Optical properties of biological tissues: a review.Phys. Med. Biol.58, 5007 (2013)..
Kuzmin, N. V. et al. Third harmonic generation imaging for fast, label-free pathology of human brain tumors.Biomed. Opt. Express7, 1889-1904 (2016)..
Tolstik, E. et al. Linear and non-linear optical imaging of cancer cells with silicon nanoparticles.Int. J. Mol. Sci.17, 1536 (2016)..
Isobe, K. et al. Background-free deep imaging by spatial overlap modulation nonlinear optical microscopy.Biomed. Opt. Express3, 1594-1608 (2012)..
Bezryadina, A. et al. Nonlinear self-action of light through biological suspensions.Phys. Rev. Lett.119, 058101 (2017)..
Miccio, L. et al. Red blood cell as an adaptive optofluidic microlens.Nat. Commun.6, 6502 (2015)..
Sem'yanov, K. A. et al. Calibration-free method to determine the size and hemoglobin concentration of individual red blood cells from light scattering.Appl. Opt.39, 5884-5889 (2000)..
Zhong, M.-C. et al. Trapping red blood cells in living animals using optical tweezers.Nat. Commun.4, 1768 (2013)..
Steinke, J. M.&Shepherd, A. P. Comparison of Mie theory and the light scattering of red blood cells.Appl. Opt.27, 4027-4033 (1988)..
Pauling, L. et al. Sickle cell anemia, a molecular disease.Science110, 543-548 (1949)..
Gongora, J. S. T.&Fratalocchi, A. Optical force on diseased blood cells: Towards the optical sorting of biological matter.Opt. Lasers Eng.76, 40-44 (2016)..
Kinnunen, M. et al. Effect of the size and shape of a red blood cell on elastic light scattering properties at the single-cell level.Biomed. Opt. Express2, 1803-1814 (2011)..
Ghosh, N. et al. Simultaneous determination of size and refractive index of red blood cells by light scattering measurements.Appl. Phys. Lett.88, 084101 (2006)..
Sinha, A. et al. Single-cell evaluation of red blood cell bio-mechanical and nano-structural alterations upon chemically induced oxidative stress.Sci. Rep.5, 9768 (2015)..
Graydon, O. Detecting malaria.Nat. Photon6, 343 (2012)..
Kim, Y. et al. Profiling individual human red blood cells using common-path diffraction optical tomography.Sci. Rep.4, 6659 (2014)..
Liu, X. S. et al. Rotation and deformation of human red blood cells with light from tapered fiber probes.Nanophotonics6, 309-316 (2017)..
Mohanty, S. K., Uppal, A.&Gupta, P. K. Self-rotation of red blood cells in optical tweezers: prospects for high throughput malaria diagnosis.Biotechnol. Lett.26, 971-974 (2004)..
Flormann, D. et al. The buckling instability of aggregating red blood cells.Sci. Rep.7, 7928 (2017)..
Kaneta, T. et al. Theory of optical chromatography.Anal. Chem.69, 2701-2710 (1997)..
Chen, Z. G., Segev, M.&Christodoulides, D. N. Optical spatial solitons: historical overview and recent advances.Rep. Prog. Phys.75, 086401 (2012)..
Gautam, R. et al. Characterization of storage-induced red blood cell hemolysis using raman spectroscopy.Lab. Med.49, 298-310 (2018)..
Friebel, M., Helfmann, J.&Meinke, M. C. Influence of osmolarity on the optical properties of human erythrocytes.J. Biomed. Opt.15, 055005 (2010)..
Ghofraniha, N., Ruocco, G.&Conti, C. Collective thermal diffusion of silica colloids studied by nonlinear optics.Langmuir25, 12495-12500 (2009)..
Lamhot, Y. et al. Self-trapping of optical beams through thermophoresis.Phys. Rev. Lett.105, 163906 (2010)..
Samadi, A. et al. Evaluating the toxic effect of an antimicrobial agent on single bacterial cells with optical tweezers.Biomed. Opt. Express6, 112-117 (2015)..
Bezryadina, A. S. et al. Optical disassembly of cellular clusters by tunable 'tug-of-war' tweezers.Light.: Sci. Appl.5, e16158 (2016)..
Berg-Sørensen, K.&Flyvbjerg, H. Power spectrum analysis for optical tweezers.Rev. Sci. Instrum.75, 594-612 (2004)..
Jones, P. H., Maragò, O. M.&Volpe, G.Optical Tweezers: Principles and Applications. (Cambridge University Press, Cambridge, 2015).
Novotny, L.&Hecht, B.Principles of Nano-Optics. (Cambridge University Press, Cambridge, 2006).
Jonáš, A.&Zemánek, P. Light at work: the use of optical forces for particle manipulation, sorting, and analysis.Electrophoresis29, 4813-4851 (2008)..
Svoboda, K.&Block, S. M. Biological applications of optical forces.Annu. Rev. Biophys. Biomol. Struct.23, 247-285 (1994)..
Man, W. N. et al. Optical nonlinearities and enhanced light transmission in soft-matter systems with tunable polarizabilities.Phys. Rev. Lett.111, 218302 (2013)..
El-Ganainy, R. et al. Nonlinear optical dynamics in nonideal gases of interacting colloidal nanoparticles.Phys. Rev. A.80, 053805 (2009)..
Harada, Y.&Asakura, T. Radiation forces on a dielectric sphere in the Rayleigh scattering regime.Opt. Commun.124, 529-541 (1996)..
Tomaiuolo, G. Biomechanical properties of red blood cells in health and disease towards microfluidics.Biomicrofluidics8, 051501 (2014)..
Hosseini, S. M.&Feng, J. J. How malaria parasites reduce the deformability of infected red blood cells.Biophys. J.103, 1-10 (2012)..
Fardad, S. et al. Plasmonic resonant solitons in metallic nanosuspensions.Nano. Lett.14, 2498-2504 (2014)..
Diez-Silva, M. et al. Shape and biomechanical characteristics of human red blood cells in health and disease.MRS Bull.35, 382-388 (2010)..
Lee, K., Wagner, C.&Priezzhev, A. V. Assessment of the "cross-bridge"-induced interaction of red blood cells by optical trapping combined with microfluidics.J. Biomed. Opt.22, 091516 (2017)..
Schonbrun, E. et al. Quantitative absorption cytometry for measuring red blood cell hemoglobin mass and volume.Cytom. Part A85, 332-338 (2014)..
0
Views
0
Downloads
0
CSCD
Publicity Resources
Related Articles
Related Author
Related Institution
京公网安备11010802024621