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End date: 2023 × Start date: 2021 × End date: 2019 × Start date: 2010 × DDC: 600 × Type: Text × Subject: Calibration × WGL Institute: IPHT ×

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    Microparticle Manipulation and Imaging through a Self-Calibrated Liquid Crystal on Silicon Display
    (Basel : MDPI, 2018-11-20) Zhang, Haolin; Lizana, Angel; Van Eeckhout, Albert; Turpin, Alex; Ramirez, Claudio; Iemmi, Claudio; Campos, Juan
    We present in this paper a revision of three different methods we conceived in the framework of liquid crystal on silicon (LCoS) display optimization and application. We preliminarily demonstrate an LCoS self-calibration technique, from which we can perform a complete LCoS characterization. In particular, two important characteristics of LCoS displays are retrieved by using self-addressed digital holograms. On the one hand, we determine its phase-voltage curve by using the interference pattern generated by a digital two-sectorial split-lens configuration. On the other hand, the LCoS surface profile is also determined by using a self-addressed dynamic micro-lens array pattern. Second, the implementation of microparticle manipulation through optical traps created by an LCoS display is demonstrated. Finally, an LCoS display based inline (IL) holographic imaging system is described. By using the LCoS display to implement a double-sideband filter configuration, this inline architecture demonstrates the advantage of obtaining dynamic holographic imaging of microparticles independently of their spatial positions by avoiding the non-desired conjugate images.
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    Single cell analysis in native tissue: Quantification of the retinoid content of hepatic stellate cells
    ([London] : Macmillan Publishers Limited, part of Springer Nature, 2016) Galler, Kerstin; Requardt, Robert Pascal; Glaser, Uwe; Markwart, Robby; Bocklitz, Thomas; Bauer, Michael; Popp, Jürgen; Neugebauer, Ute
    Hepatic stellate cells (HSCs) are retinoid storing cells in the liver: The retinoid content of those cells changes depending on nutrition and stress level. There are also differences with regard to a HSC’s anatomical position in the liver. Up to now, retinoid levels were only accessible from bulk measurements of tissue homogenates or cell extracts. Unfortunately, they do not account for the intercellular variability. Herein, Raman spectroscopy relying on excitation by the minimally destructive wavelength 785 nm is introduced for the assessment of the retinoid state of single HSCs in freshly isolated, unprocessed murine liver lobes. A quantitative estimation of the cellular retinoid content is derived. Implications of the retinoid content on hepatic health state are reported. The Raman-based results are integrated with histological assessments of the tissue samples. This spectroscopic approach enables single cell analysis regarding an important cellular feature in unharmed tissue.