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23 Na Triple-quantum signal of in vitro human liver cells, liposomes, and nanoparticles: Cell viability assessment vs. separation of intra- and extracellular signal.

M. Hoesl, D. Kleimaier, R. Hu, M. Malzacher, C. Nies, E. Gottwald and L. Schad

J Magn Reson Imaging,, p.in Press

Triple-quantum (TQ) filtered sequences have become more popular in sodium MR due to the increased usage of scanners with field strengths exceeding 3T. Disagreement as to whether TQ signal can provide separation of intra- and extracellular compartments persists. To provide insight into TQ signal behavior on a cellular level. Prospective. Cell-phantoms in the form of liposomes, encapsulated 0 mM, 145 mM, 154 mM Na+ in a double-lipid membrane similar to cells. Poly(lactic-co-glycolic acid) nanoparticles encapsulated 154 mM Na+ within a single-layer membrane structure. Two microcavity chips with each 6 × 10 human HEP G2 liver cells were measured in an MR-compatible bioreactor. Spectroscopic TQ sequence with time proportional phase-increments at 9.4T. The TQ signal of viable, dead cells, and cell-phantoms was assessed by a fit in the time domain and by the amplitude in the frequency domain. The noise variance (?) was evaluated to express the deviation of the measured TQ signal amplitude from noise. TQ signal >20? was found for liposomes encapsulating sodium ions. Liposomal encapsulation of 0 mM Na+ and 154 mM Na+ encapsulation in the nanoparticles resulted in <2? TQ signal. Cells under normal perfusion resulted in >9? TQ signal. Compared with TQ signal under normal perfusion, a 56% lower TQ signal of was observed (25?) during perfusion stop. TQ signal returned to 92% of the initial signal after reperfusion. Our measurements indicate that TQ signal in liposomes was observed due to the trapping of ions within the double-lipid membrane rather than from the intraliposomal space. Transfer to the cell results suggests that TQ signal was observed from motion restriction equivalent to trapping. 1 Technical Efficacy: Stage 3 J. Magn. Reson. Imaging 2019.

Contact: Dr. Frank Zöllner last modified: 17.04.2019
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