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Andre C. Stiel

Publications and source records attributed to Andre C. Stiel.

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Model-based temporal unmixing towards quantitative photo-switching optoacoustic tomography

Optoacoustic (OA) imaging combined with reversibly photoswitchable proteins has emerged as a promising technology for the high-sensitivity and multiplexed imaging of cells in live tissues in preclinical research. Through carefully-designed illumination schedules of ON and OFF laser pulses, the resulting OA signal is a multiplex of different reporter species and the background. We propose a model-based variational framework to computationally unmix and image different species of photo-switching reporters using optoacoustic tomography. It is based on a detailed mathematical description of the photo-switching mechanism, which models how relevant physical parameters such as the kinetic constants and light fluence impact the switching signal. We introduce an algorithm that operates on images, as opposed to traditional pixelwise approaches. It takes the form of an iterative inversion combined with tailored $\ell_1$ and total-variation regularization to increase the robustness to noise and to improve the unmixing quality. We show that our method is able to disentangle multiple spatially overlapping labels and to recover continuous maps of quantities of interest on controlled phantoms and mice experiments.

physics.optics

Optoacoustic flow-cytometry with light scattering referencing

In analogy to the development of fluorescent proteins, innovative tools for screening optoacoustic cell labels could lead to tailored protein labels for OA, imparting novel ways to visualize biological structure and function. Optoacoustic imaging emerges towards a highly promising modality for life sciences and medical practise with advantageous capabilities such as great accessible depth, and 3D studying of living tissue. The development of novel labels with molecular specificity could significantly enhance the optoacoustic contrast, specificity, and sensitivity and allow optoacoustic to interrogate tissues not amenable to the fluorescence method. We report on an optoacoustic flow cytometer (OAFC) prototype, developed for screening optoacoustic reporter genes. The cytometer concurrently records light scattering for referencing purposes. Since recording light scattering is completely independent from OA, we believe it to be a more reliable referencing method than e.g. fluorescence or ultrasound-backscatter. Precise characterization of our OAFC prototype showcases its ability to optoacoustically characterize objects in-flow that are in the size range of single cells. We apply the OAFC to distinguish individual E. coli cells based on optoacoustic properties of their expressed chromoproteins read in-flow using microfluidic arrangements and achieved precisions over 90%. We discuss how the light scattering referenced OAFC method offers a critical step towards routine measurement of optoacoustic properties of single-cells and could pave the way for identifying genetically encoded optoacoustic reporters, by transferring working concepts of the fluorescence field.

physics.bio-ph