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Now showing 1 - 5 of 5
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    Ultra-compact tunable fiber laser for coherent anti-Stokes Raman imaging
    (Chichester [u.a.] : Wiley, 2021) Gottschall, Thomas; Meyer-Zedler, Tobias; Schmitt, Michael; Huber, Robert; Popp, Juergen; Tünnermann, Andreas; Limpert, Jens
    This work describes the construction of an ultra-compact narrowband fiber laser source for coherent anti-Stokes Raman scattering microscopy of Raman tags, that is, for addressing Raman resonances of deuterated molecules and alkyne tags in the spectral range from 2080 to 2220 cm−1. A narrowband and fast electronically tunable cw seed source based on a semiconductor optical amplifier (SOA) emitting around 1335 nm has been employed to seed four-wave mixing (FWM) in an endlessly single mode fiber (ESM) pumped by a ps pulse duration Yb-fiber laser. A conversion efficiency of 50% is demonstrated. This compact fiber optical parametric amplifier (FOPA) has been used to perform coherent anti-Stokes Raman imaging experiments of crystalline deuterated palmitic acid.
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    Biochemical Analysis of Leukocytes after In Vitro and In Vivo Activation with Bacterial and Fungal Pathogens Using Raman Spectroscopy
    (Basel : MDPI, 2021) Pistiki, Aikaterini; Ramoji, Anuradha; Ryabchykov, Oleg; Thomas-Rueddel, Daniel; Press, Adrian T.; Makarewicz, Oliwia; Giamarellos-Bourboulis, Evangelos J.; Bauer, Michael; Bocklitz, Thomas; Popp, Juergen; Neugebauer, Ute
    Biochemical information from activated leukocytes provide valuable diagnostic information. In this study, Raman spectroscopy was applied as a label-free analytical technique to characterize the activation pattern of leukocyte subpopulations in an in vitro infection model. Neutrophils, monocytes, and lymphocytes were isolated from healthy volunteers and stimulated with heat-inactivated clinical isolates of Candida albicans, Staphylococcus aureus, and Klebsiella pneumoniae. Binary classification models could identify the presence of infection for monocytes and lymphocytes, classify the type of infection as bacterial or fungal for neutrophils, monocytes, and lymphocytes and distinguish the cause of infection as Gram-negative or Gram-positive bacteria in the monocyte subpopulation. Changes in single-cell Raman spectra, upon leukocyte stimulation, can be explained with biochemical changes due to the leukocyte’s specific reaction to each type of pathogen. Raman spectra of leukocytes from the in vitro infection model were compared with spectra from leukocytes of patients with infection (DRKS-ID: DRKS00006265) with the same pathogen groups, and a good agreement was revealed. Our study elucidates the potential of Raman spectroscopy-based single-cell analysis for the differentiation of circulating leukocyte subtypes and identification of the infection by probing the molecular phenotype of those cells.
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    In vivo coherent anti-Stokes Raman scattering microscopy reveals vitamin A distribution in the liver
    (Weinheim : Wiley-VCH-Verl., 2021) Rodewald, Marko; Bae, Hyeonsoo; Huschke, Sophie; Meyer-Zedler, Tobias; Schmitt, Michael; Press, Adrian Tibor; Schubert, Stephanie; Bauer, Michael; Popp, Juergen
    Here we present a microscope setup for coherent anti-Stokes Raman scattering (CARS) imaging, devised to specifically address the challenges of in vivo experiments. We exemplify its capabilities by demonstrating how CARS microscopy can be used to identify vitamin A (VA) accumulations in the liver of a living mouse, marking the positions of hepatic stellate cells (HSCs). HSCs are the main source of extracellular matrix protein after hepatic injury and are therefore the main target of novel nanomedical strategies in the development of a treatment for liver fibrosis. Their role in the VA metabolism makes them an ideal target for a CARS-based approach as they store most of the body's VA, a class of compounds sharing a retinyl group as a structural motive, a moiety that is well known for its exceptionally high Raman cross section of the C=C stretching vibration of the conjugated backbone.
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    Computational tissue staining of non-linear multimodal imaging using supervised and unsupervised deep learning
    (Washington, DC : OSA, 2021) Pradhan, Pranita; Meyer, Tobias; Vieth, Michael; Stallmach, Andreas; Waldner, Maximilian; Schmitt, Michael; Popp, Juergen; Bocklitz, Thomas
    Hematoxylin and Eosin (H&E) staining is the 'gold-standard' method in histopathology. However, standard H&E staining of high-quality tissue sections requires long sample preparation times including sample embedding, which restricts its application for 'real-time' disease diagnosis. Due to this reason, a label-free alternative technique like non-linear multimodal (NLM) imaging, which is the combination of three non-linear optical modalities including coherent anti-Stokes Raman scattering, two-photon excitation fluorescence and second-harmonic generation, is proposed in this work. To correlate the information of the NLM images with H&E images, this work proposes computational staining of NLM images using deep learning models in a supervised and an unsupervised approach. In the supervised and the unsupervised approach, conditional generative adversarial networks (CGANs) and cycle conditional generative adversarial networks (cycle CGANs) are used, respectively. Both CGAN and cycle CGAN models generate pseudo H&E images, which are quantitatively analyzed based on mean squared error, structure similarity index and color shading similarity index. The mean of the three metrics calculated for the computationally generated H&E images indicate significant performance. Thus, utilizing CGAN and cycle CGAN models for computational staining is beneficial for diagnostic applications without performing a laboratory-based staining procedure. To the author's best knowledge, it is the first time that NLM images are computationally stained to H&E images using GANs in an unsupervised manner.
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    Three step flow focusing enables image-based discrimination and sorting of late stage 1 Haematococcus pluvialis cells
    (San Francisco, Ca. : PLOS, 2021) Kraus, Daniel; Kleiber, Andreas; Ehrhardt, Enrico; Leifheit, Matthias; Horbert, Peter; Urban, Matthias; Gleichmann, Nils; Mayer, Guenter; Popp, Juergen; Henkel, Thomas
    Label-free and gentle separation of cell stages with desired target properties from mixed stage populations are a major research task in modern biotechnological cultivation process and optimization of micro algae. The reported microfluidic sorter system (MSS) allows the subsequent investigation of separated subpopulations. The implementation of a viability preserving MSS is shown for separation of late stage 1 Haematococcus pluvialis (HP) cells form a mixed stage population. The MSS combines a three-step flow focusing unit for aligning the cells in single file transportation mode at the center of the microfluidic channel with a pure hydrodynamic sorter structure for cell sorting. Lateral displacement of the cells into one of the two outlet channels is generated by piezo-actuated pump chambers. In-line decision making for sorting is based on a user-definable set of image features and properties. The reported MSS significantly increased the purity of target cells in the sorted population (94%) in comparison to the initial mixed stage population (19%).