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Keynote Speaker - Robotic FluidFM in the Nanobiosensorics Lab: from large-area printing to high-throughput adhesion and injection of single cells - Session Mechanobiology
Dr. Robert HorvathDone
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Keynote Speaker: Online Talk - New Advances in Single Cell Mechanics - Session Material Sciences
Gang-Yu LiuDone
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Characterizing Induced Pluripotent Stem Cell-Derived Cardiomyocytes (iPSC-CMs): Insights from Mass Measurements and Mechanical Properties - Session Mechanobiology
Dr. Angelo GaitasDone
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Transient Changes in Stem Cells Induced by Electrical Stimulation - Session Mechanobiology
Dr. Amy GelmiDone
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Lunch & Poster Session n*1
Done
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Registration & Coffee
Done
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Coffee Break
Done
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Round Table - Live-seq & Biopsies
Done
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Closing note - FluidFM User Conference 2023
Done
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Quantification of micro/nano objects movement under vortex force by Fluidic Force Microscopy - Session Mechanobiology
Dr. Yonghui ZhangDone
C. Müller-Renno, L. Hofherr, D. Remmel, N. Davoudi, A. Elmeligy, C. Ziegler RPTU Kaiserslautern, Department of Physics, Erwin-Schrödinger-Straße 56, 67653 Kaiserslautern
Abstract
The scanning force microscope (SFM), respectively scanning force spectroscopy (SFS) are powerful tools for investigating the interaction of biological molecules and organisms with surfaces. The Fluid-FM addon gives access to many new applications like sucking biological cells or spotting liquids, all under imaging conditions and force control. In this contribution, our emphasis will be given to applications of the Fluid-FM in the field of biomaterials and nanobiotechnology. These include single-cell adhesion measurements [1, 2]. Especially the bacterial cell immobilization on the tip will be compared to a traditional chemical immobilization method. In addition, adhesion measurements of environmentally relevant nanoparticles will be presented. Here, the focus lies on the aspiration and immobilization of optically invisible particles. Nano Spotting of viruses is another application that will be presented [3-5]. Parameters of the solution and the viruses themselves do not only determine the droplet formation and virus attachment to the surface but, together with the properties of the ambient like humidity and temperature, the movement of the particles during the drying process. Here, the Marangoni effect and the Deegan flow together with the other parameters, define whether a coffee ring pattern with or without a central dot or a uniform distribution of the nanoparticles is observed. Last but not least, the type of FluidFM probe used and herewith the geometry of the contact between aperture and substrate play an important role.
References
[1] N. Davoudi et al. Biointerphases, 2017, 12, 05G606.
[2] L. Hofherr et al. Physica Status Solidi A, 2018, 1700846.
[3] A. Lüders et al. Colloids and Surfaces B: Biointerfaces, 2012, 91, 154.
[4] V. Rink et al. Biointerphases, 2017, 12, 04E402.
[5] C. Müller-Renno et al. Physica Status Solidi A, 2021, 2018(18), 210025
Affiliation