PuSH - Publikationsserver des Helmholtz Zentrums München: Optimization of <em>in vivo</em> murine X-ray dark-field computed tomography.

Informationen

Hinweise zu Qualitätskriterien von Zeitschriften

Open-Access-Richtlinie der Helmholtz-Gemeinschaft 2016

CC Licencences

Metriken für Publikationen

Navigation

Startseite

English

EVA: Veröffentlichen

Neuer EVA Antrag

Recherche

Erweiterte Suche

Durchblättern nach ...

... HMGU-Autoren/Konsortien

... Organisationsstruktur

... Zeitschriften

... Publikationstypen

... Forschungsdaten

... Arbeitsgruppen

... Erscheinungsjahr

Publikationen im Überblick

Statistik

HGF Fortschrittsbericht

OA Publikationen

Eintragen

Neue Publikation eintragen

Neue Publikation holen aus...

...EVA

Fehlende Publikation melden

Highlights

Suche

Hilfe & Kontakt

Ansprechpartner

Hilfe

Datenschutz

Helmholtz Open Science

Bibliometrische Indikatoren

SHERPA/RoMEO

DOAJ

Export:

Text

Endnote (RIS) BIB

BibTeX

Umkehrer, S.* ; Birnbacher, L.* ; Burkhardt, R. ; Von Teuffenbach, M.* ; Yildirim, A.Ö. ; Pfeiffer, D.* ; Herzen, J.* ; Pfeiffer, F.*

Optimization of in vivo murine X-ray dark-field computed tomography.

Rev. Sci. Instruments 90:103103 (2019)

Postprint

DOI

	Open Access Green

Abstract
Metriken
Zusatzinfos

Grating-based dark-field interferometry can be realized with lab-based, low-brilliance X-ray sources and provides scattering information of sample structures below the detector pixel size. This unique property allows promising medical imaging applications, especially for lung diseases. Structural damage in lung tissue caused by pulmonary emphysema or pulmonary carcinoma could be observed in radiographs by changes in the dark-field signal with high sensitivity at early stages, in contrast to the conventional absorption signal. Currently, the standard for diagnosis in the clinical routine of pulmonary diseases is absorption computed tomography (CT). The assessment of a larger number of samples with in vivo dark-field CT is limited by the rather long scan times, the order of 2 h, that are required to obtain sufficient CT data quality. In this work, a prototype in vivo, small-animal, dark-field CT is optimized with respect to CT measurements with the following: usage of an iterative reconstruction algorithm for the reduction of undersampling artifacts, a rearranged data acquisition scheme with reduced amount of dead time, and thinned gratings and curved grating geometry for more efficient utilization of the 37 kV X-ray flux. The device performance is evaluated with noise-effective dose measurements, image contrast-to-noise ratio, interferometry visibility across the field-of-view, and a reduced measurement time of 40 min with a deposited dose of 85 mGy.

Impact Factor

Scopus SNIP

Web of Science
Times Cited

Scopus
Cited By

Altmetric

1.587

1.090