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Journal articles on the topic 'Magnetic microrheology'

Author: Grafiati

Published: 18 May 2024

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1

Peredo-Ortíz, R., and M. Hernández-Contreras. "Diffusion microrheology of ferrofluids." Revista Mexicana de Física 64, no. 1 (2018): 82. http://dx.doi.org/10.31349/revmexfis.64.82.

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We provide a statistical mechanics approach to study the linear microrheology of thermally equilibrated and homogeneous ferrofluids. Theexpressions for the elastic and loss moduli depend on the bulk microstructure of the magnetic fluid determined by the structure factor of thesuspension of magnetic particles. The comparison of the predicted microrheology with computer simulations confirms that as a function ofrelaxation frequency of thermal fluctuations of the particle concentration both theory and simulations have the same trends. At very shortfrequencies the viscous modulus relates to the tr

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2

Kim, Jin Chul, Myungeun Seo, Marc A. Hillmyer, and Lorraine F. Francis. "Magnetic Microrheology of Block Copolymer Solutions." ACS Applied Materials & Interfaces 5, no. 22 (2013): 11877–83. http://dx.doi.org/10.1021/am403569f.

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3

Wang, Hanqing, Tomaž Mohorič, Xianren Zhang, Jure Dobnikar, and Jürgen Horbach. "Active microrheology in two-dimensional magnetic networks." Soft Matter 15, no. 22 (2019): 4437–44. http://dx.doi.org/10.1039/c9sm00085b.

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We study active microrheology in 2D with Langevin simulations of tracer particles pulled through magnetic networks by a constant force. While non-magnetic tracers strongly deform the network in order to be able to move through, the magnetic tracers can do so by deforming the structure only slightly.

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4

Brasovs, Artis, Jānis Cīmurs, Kaspars Ērglis, Andris Zeltins, Jean-Francois Berret, and Andrejs Cēbers. "Magnetic microrods as a tool for microrheology." Soft Matter 11, no. 13 (2015): 2563–69. http://dx.doi.org/10.1039/c4sm02454k.

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The protocol of microrheological measurements consists of recording the dynamics of the orientation of the rod when the magnetic field is applied at an angle to the rod and observing its relaxation after the field is switched off.

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5

Raikher, Yu L., and V. V. Rusakov. "Magnetic rotary microrheology in a Maxwell fluid." Journal of Magnetism and Magnetic Materials 300, no. 1 (2006): e229-e233. http://dx.doi.org/10.1016/j.jmmm.2005.10.086.

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6

Berezney, John P., and Megan T. Valentine. "A compact rotary magnetic tweezers device for dynamic material analysis." Review of Scientific Instruments 93, no. 9 (2022): 093701. http://dx.doi.org/10.1063/5.0090199.

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Here we present a new, compact magnetic tweezers design that enables precise application of a wide range of dynamic forces to soft materials without the need to raise or lower the magnet height above the sample. This is achieved through the controlled rotation of the permanent magnet array with respect to the fixed symmetry axis defined by a custom-built iron yoke. These design improvements increase the portability of the device and can be implemented within existing microscope setups without the need for extensive modification of the sample holders or light path. This device is particularly w

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7

Radiom, Milad, Romain Hénault, Salma Mani, Aline Grein Iankovski, Xavier Norel, and Jean-François Berret. "Magnetic wire active microrheology of human respiratory mucus." Soft Matter 17, no. 32 (2021): 7585–95. http://dx.doi.org/10.1039/d1sm00512j.

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Micrometer-sized magnetic wires are used to study the mechanical properties of human mucus collected after surgery. Our work shows that mucus has the property of a high viscosity gel characterized by large spatial viscoelastic heterogeneities.

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8

Liu, Wei, Xiangjun Gong, To Ngai, and Chi Wu. "Near-surface microrheology reveals dynamics and viscoelasticity of soft matter." Soft Matter 14, no. 48 (2018): 9764–76. http://dx.doi.org/10.1039/c8sm01886c.

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We report the development of a microrheology technique that incorporates a magnetic-field-induced simulator on total internal reflection microscopy (TIRM) to probe the near-surface dynamics and viscoelastic behaviors of soft matter like polymer solution/gels and colloidal dispersions.

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9

Preece, Daryl, Rebecca Warren, R. M. L. Evans, et al. "Optical tweezers: wideband microrheology." Journal of Optics 13, no. 4 (2011): 044022. http://dx.doi.org/10.1088/2040-8978/13/4/044022.

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10

Berret, Jean François. "Microrheology of viscoelastic solutions studied by magnetic rotational spectroscopy." International Journal of Nanotechnology 13, no. 8/9 (2016): 597. http://dx.doi.org/10.1504/ijnt.2016.079661.

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11

Rebêlo, L. M., J. S. de Sousa, J. Mendes Filho, J. Schäpe, H. Doschke, and M. Radmacher. "Microrheology of cells with magnetic force modulation atomic force microscopy." Soft Matter 10, no. 13 (2013): 2141–49. http://dx.doi.org/10.1039/c3sm52045e.

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12

Lin, Jun, and Megan T. Valentine. "Ring-shaped NdFeB-based magnetic tweezers enables oscillatory microrheology measurements." Applied Physics Letters 100, no. 20 (2012): 201902. http://dx.doi.org/10.1063/1.4717988.

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13

Besseris, George J., and Donovan B. Yeates. "Rotating magnetic particle microrheometry in biopolymer fluid dynamics: Mucus microrheology." Journal of Chemical Physics 127, no. 10 (2007): 105106. http://dx.doi.org/10.1063/1.2766947.

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14

Behrend, Caleb J., Jeffrey N. Anker, Brandon H. McNaughton, and Raoul Kopelman. "Microrheology with modulated optical nanoprobes (MOONs)." Journal of Magnetism and Magnetic Materials 293, no. 1 (2005): 663–70. http://dx.doi.org/10.1016/j.jmmm.2005.02.072.

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15

Helseth, L. E., and T. M. Fischer. "Fundamental limits of optical microrheology." Journal of Colloid and Interface Science 275, no. 1 (2004): 322–27. http://dx.doi.org/10.1016/j.jcis.2004.01.052.

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16

Lin, Jun, and Megan T. Valentine. "High-force NdFeB-based magnetic tweezers device optimized for microrheology experiments." Review of Scientific Instruments 83, no. 5 (2012): 053905. http://dx.doi.org/10.1063/1.4719916.

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17

Kollmannsberger, Philip, Claudia Mierke, and Ben Fabry. "Nonlinear mechanical response of adherent cells measured by magnetic bead microrheology." Bone 46 (March 2010): S50—S51. http://dx.doi.org/10.1016/j.bone.2010.01.115.

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18

Rich, Jason P., Jan Lammerding, Gareth H. McKinley, and Patrick S. Doyle. "Nonlinear microrheology of an aging, yield stress fluid using magnetic tweezers." Soft Matter 7, no. 21 (2011): 9933. http://dx.doi.org/10.1039/c1sm05843f.

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19

Puig-De-Morales, Marina, Mireia Grabulosa, Jordi Alcaraz, et al. "Measurement of cell microrheology by magnetic twisting cytometry with frequency domain demodulation." Journal of Applied Physiology 91, no. 3 (2001): 1152–59. http://dx.doi.org/10.1152/jappl.2001.91.3.1152.

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Magnetic twisting cytometry (MTC) (Wang N, Butler JP, and Ingber DE, Science260: 1124–1127, 1993) is a useful technique for probing cell micromechanics. The technique is based on twisting ligand-coated magnetic microbeads bound to membrane receptors and measuring the resulting bead rotation with a magnetometer. Owing to the low signal-to-noise ratio, however, the magnetic signal must be modulated, which is accomplished by spinning the sample at ∼10 Hz. Present demodulation approaches limit the MTC range to frequencies <0.5 Hz. We propose a novel demodulation algorithm to expand the frequenc

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20

Huang, Derek E., and Roseanna N. Zia. "Sticky, active microrheology: Part 1. Linear-response." Journal of Colloid and Interface Science 554 (October 2019): 580–91. http://dx.doi.org/10.1016/j.jcis.2019.07.004.

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21

Sohn, I. S., R. Rajagopalan, and A. C. Dogariu. "Spatially resolved microrheology through a liquid/liquid interface." Journal of Colloid and Interface Science 269, no. 2 (2004): 503–13. http://dx.doi.org/10.1016/s0021-9797(03)00728-8.

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22

Wu, Chenjun, Qingxu Zhang, Yihu Song, and Qiang Zheng. "Microrheology of magnetorheological silicone elastomers during curing process under the presence of magnetic field." AIP Advances 7, no. 9 (2017): 095004. http://dx.doi.org/10.1063/1.5002121.

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23

Aprelev, Pavel, Bonni McKinney, Chadwick Walls, and Konstanin G. Kornev. "Magnetic stage with environmental control for optical microscopy and high-speed nano- and microrheology." Physics of Fluids 29, no. 7 (2017): 072001. http://dx.doi.org/10.1063/1.4989548.

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24

Raikher, Yu L., and V. V. Rusakov. "Rotational Microrheology of Viscoelastic Fluid: Orientational Kinetics of Magnetic Particles in the Inertialess Approximation." Colloid Journal 67, no. 5 (2005): 610–24. http://dx.doi.org/10.1007/s10595-005-0140-2.

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25

García Daza, Fabián A., Antonio M. Puertas, Alejandro Cuetos, and Alessandro Patti. "Microrheology of colloidal suspensions via dynamic Monte Carlo simulations." Journal of Colloid and Interface Science 605 (January 2022): 182–92. http://dx.doi.org/10.1016/j.jcis.2021.07.088.

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26

Medronho, B., A. Filipe, C. Costa, et al. "Microrheology of novel cellulose stabilized oil-in-water emulsions." Journal of Colloid and Interface Science 531 (December 2018): 225–32. http://dx.doi.org/10.1016/j.jcis.2018.07.043.

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27

Gan, Tiansheng, Xiangjun Gong, Holger Schönherr, and Guangzhao Zhang. "Microrheology of growing Escherichia coli biofilms investigated by using magnetic force modulation atomic force microscopy." Biointerphases 11, no. 4 (2016): 041005. http://dx.doi.org/10.1116/1.4968809.

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28

Inoue, Masao, and Akira Yoshimori. "Effects of interactions between particles on dynamics in microrheology." Journal of Molecular Liquids 200 (December 2014): 81–84. http://dx.doi.org/10.1016/j.molliq.2014.05.029.

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29

Meng, Xianghe, Xiaomo Wu, Jianmin Song, Hao Zhang, Mingjun Chen, and Hui Xie. "Quantification of the Microrheology of Living Cells Using Multi-Frequency Magnetic Force Modulation Atomic Force Microscopy." IEEE Transactions on Instrumentation and Measurement 71 (2022): 1–9. http://dx.doi.org/10.1109/tim.2022.3153994.

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30

Malgaretti, Paolo, Antonio M. Puertas, and Ignacio Pagonabarraga. "Active microrheology in corrugated channels: Comparison of thermal and colloidal baths." Journal of Colloid and Interface Science 608 (February 2022): 2694–702. http://dx.doi.org/10.1016/j.jcis.2021.10.193.

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31

Liu, Wei, Yuwei Zhu, Tong Zhang, Hui Zhu, Chuanxin He, and To Ngai. "Microrheology of thermoresponsive poly(N-isopropylacrylamide) microgel dispersions near a substrate surface." Journal of Colloid and Interface Science 597 (September 2021): 104–13. http://dx.doi.org/10.1016/j.jcis.2021.03.181.

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32

Molaei, Mehdi, and John C. Crocker. "Interfacial microrheology and tensiometry in a miniature, 3-d printed Langmuir trough." Journal of Colloid and Interface Science 560 (February 2020): 407–15. http://dx.doi.org/10.1016/j.jcis.2019.09.112.

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33

Bausch, Andreas R., Ulrike Hellerer, Markus Essler, Martin Aepfelbacher, and Erich Sackmann. "Rapid Stiffening of Integrin Receptor-Actin Linkages in Endothelial Cells Stimulated with Thrombin: A Magnetic Bead Microrheology Study." Biophysical Journal 80, no. 6 (2001): 2649–57. http://dx.doi.org/10.1016/s0006-3495(01)76234-0.

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34

Huang, Shilin, Kornelia Gawlitza, Regine von Klitzing, et al. "Microgels at the Water/Oil Interface: In Situ Observation of Structural Aging and Two-Dimensional Magnetic Bead Microrheology." Langmuir 32, no. 3 (2016): 712–22. http://dx.doi.org/10.1021/acs.langmuir.5b01438.

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35

Aponte-Rivera, Christian, and Roseanna N. Zia. "The confined Generalized Stokes-Einstein relation and its consequence on intracellular two-point microrheology." Journal of Colloid and Interface Science 609 (March 2022): 423–33. http://dx.doi.org/10.1016/j.jcis.2021.11.037.

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36

Chu, Henry C. W., and Roseanna N. Zia. "Toward a nonequilibrium Stokes-Einstein relation via active microrheology of hydrodynamically interacting colloidal dispersions." Journal of Colloid and Interface Science 539 (March 2019): 388–99. http://dx.doi.org/10.1016/j.jcis.2018.12.055.

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37

Huang, Derek E., and Roseanna N. Zia. "Sticky-probe active microrheology: Part 2. The influence of attractions on non-Newtonian flow." Journal of Colloid and Interface Science 562 (March 2020): 293–306. http://dx.doi.org/10.1016/j.jcis.2019.11.057.

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38

Chen, Yin-Quan, Chia-Yu Kuo, Ming-Tzo Wei, et al. "Intracellular viscoelasticity of HeLa cells during cell division studied by video particle-tracking microrheology." Journal of Biomedical Optics 19, no. 1 (2013): 011008. http://dx.doi.org/10.1117/1.jbo.19.1.011008.

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39

Habibi, Ahlem, Christophe Blanc, Nadia Ben Mbarek, and Taoufik Soltani. "Passive and active microrheology of a lyotropic chromonic nematic liquid crystal disodium cromoglycate." Journal of Molecular Liquids 288 (August 2019): 111027. http://dx.doi.org/10.1016/j.molliq.2019.111027.

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40

Moschakis, Thomas, Brent S. Murray, and Eric Dickinson. "On the kinetics of acid sodium caseinate gelation using particle tracking to probe the microrheology." Journal of Colloid and Interface Science 345, no. 2 (2010): 278–85. http://dx.doi.org/10.1016/j.jcis.2010.02.005.

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41

Neckernuss, T., L. K. Mertens, I. Martin, T. Paust, M. Beil, and O. Marti. "Active microrheology with optical tweezers: a versatile tool to investigate anisotropies in intermediate filament networks." Journal of Physics D: Applied Physics 49, no. 4 (2015): 045401. http://dx.doi.org/10.1088/0022-3727/49/4/045401.

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42

Alves, Luis, Bruno Medronho, Alexandra Filipe, et al. "New Insights on the Role of Urea on the Dissolution and Thermally-Induced Gelation of Cellulose in Aqueous Alkali." Gels 4, no. 4 (2018): 87. http://dx.doi.org/10.3390/gels4040087.

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The gelation of cellulose in alkali solutions is quite relevant, but still a poorly understood process. Moreover, the role of certain additives, such as urea, is not consensual among the community. Therefore, in this work, an unusual set of characterization methods for cellulose solutions, such as cryo-transmission electronic microscopy (cryo-TEM), polarization transfer solid-state nuclear magnetic resonance (PTssNMR) and diffusion wave spectroscopy (DWS) were employed to study the role of urea on the dissolution and gelation processes of cellulose in aqueous alkali. Cryo-TEM reveals that the

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43

Jones, Dustin P., William Hanna, Gwendolyn M. Cramer, and Jonathan P. Celli. "In situ measurement of ECM rheology and microheterogeneity in embedded and overlaid 3D pancreatic tumor stroma co-cultures via passive particle tracking." Journal of Innovative Optical Health Sciences 10, no. 06 (2017): 1742003. http://dx.doi.org/10.1142/s1793545817420032.

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Tumor growth is regulated by a diverse set of extracellular influences, including paracrine crosstalk with stromal partners, and biophysical interactions with surrounding cells and tissues.Studies elucidating the role of physical force and the mechanical properties of the extracellular matrix (ECM) itself as regulators of tumor growth and invasion have been greatly catalyzed by the use of in vitro three-dimensional (3D) tumor models. These systems provide the ability to systematically isolate, manipulate, and evaluate impact of stromal components and extracellular mechanics in a platform that

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44

Wilhelm, C., J. Browaeys, A. Ponton, and J. C. Bacri. "Rotational magnetic particles microrheology: The Maxwellian case." Physical Review E 67, no. 1 (2003). http://dx.doi.org/10.1103/physreve.67.011504.

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45

Mao, Yating, Paige Nielsen, and Jamel Ali. "Passive and Active Microrheology for Biomedical Systems." Frontiers in Bioengineering and Biotechnology 10 (July 5, 2022). http://dx.doi.org/10.3389/fbioe.2022.916354.

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Microrheology encompasses a range of methods to measure the mechanical properties of soft materials. By characterizing the motion of embedded microscopic particles, microrheology extends the probing length scale and frequency range of conventional bulk rheology. Microrheology can be characterized into either passive or active methods based on the driving force exerted on probe particles. Tracer particles are driven by thermal energy in passive methods, applying minimal deformation to the assessed medium. In active techniques, particles are manipulated by an external force, most commonly produc

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46

Berret, Jean-François. "Comment on “Bilayer aggregate microstructure determines viscoelasticity of lung surfactant suspensions” by C. O. Ciutara and J. A. Zasadzinski, Soft Matter, 2021, 17, 5170–5182." Soft Matter, 2022. http://dx.doi.org/10.1039/d2sm00653g.

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This note discusses the possible causes of the discrepancy between two studies and suggests that for pulmonary surfactant substitutes, the microrheology technique known as rotational magnetic spectroscopy can provide valuable results.

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47

Wilhelm, C., F. Gazeau, and J. C. Bacri. "Rotational magnetic endosome microrheology: Viscoelastic architecture inside living cells." Physical Review E 67, no. 6 (2003). http://dx.doi.org/10.1103/physreve.67.061908.

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48

"Viscoelasticity of the bacteriophage Pf1 network measured by magnetic microrheology." Magnetohydrodynamics 46, no. 1 (2010): 23–30. http://dx.doi.org/10.22364/mhd.46.1.2.

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49

Chevry, L., N. K. Sampathkumar, A. Cebers, and J. F. Berret. "Magnetic wire-based sensors for the microrheology of complex fluids." Physical Review E 88, no. 6 (2013). http://dx.doi.org/10.1103/physreve.88.062306.

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50

Wilhelm, Claire. "Effective temperature inside living cells." MRS Proceedings 1227 (2009). http://dx.doi.org/10.1557/proc-1227-jj05-03.

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AbstractThe combination of active and passive microrheology using magnetic probes engulfed inside living cells demonstrates the violation of the fluctuation dissipation theorem in cells. It is proposed to quantify the deviation from the in equilibrium situation with an effective temperature. Each magnetic probe then serves as a local thermometer within the cells. The response of pairs of magnetic beads of two diameters (1 and 2.8 μm) to an oscillating magnetic field is analyzed to measure the viscoelastic complex modulus in the beads environment (active measurement). The spontaneous motion of

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