Deuteration of Hyperpolarized 13 C-Labeled Zymonic Acid Enables Sensitivity-Enhanced Dynamic MRI of pH

Aberrant pH is characteristic of many pathologies such as ischemia, inflammation or cancer. Therefore, a non-invasive and spatially resolved pH determination is valuable for disease diagnosis, characterization of response to treatment and the design of pH-sensitive drug-delivery systems. We recently...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemphyschem 2017-09, Vol.18 (18), p.2422-2425
Hauptverfasser: Hundshammer, Christian, Düwel, Stephan, Köcher, Simone S, Gersch, Malte, Feuerecker, Benedikt, Scheurer, Christoph, Haase, Axel, Glaser, Steffen J, Schwaiger, Markus, Schilling, Franz
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Aberrant pH is characteristic of many pathologies such as ischemia, inflammation or cancer. Therefore, a non-invasive and spatially resolved pH determination is valuable for disease diagnosis, characterization of response to treatment and the design of pH-sensitive drug-delivery systems. We recently introduced hyperpolarized [1,5- C ]zymonic acid (ZA) as a novel MRI probe of extracellular pH utilizing dissolution dynamic polarization (DNP) for a more than 10000-fold signal enhancement of the MRI signal. Here we present a strategy to enhance the sensitivity of this approach by deuteration of ZA yielding [1,5- C , 3,6,6,6-D ]zymonic acid (ZA ), which prolongs the liquid state spin lattice relaxation time (T ) by up to 39 % in vitro. Measurements with ZA and ZA on subcutaneous MAT B III adenocarcinoma in rats show that deuteration increases the signal-to-noise ratio (SNR) by up to 46 % in vivo. Furthermore, we demonstrate a proof of concept for real-time imaging of dynamic pH changes in vitro using ZA , potentially allowing for the characterization of rapid acidification/basification processes in vivo.
ISSN:1439-4235
1439-7641
DOI:10.1002/cphc.201700779