Objectives: A common limitation of all H contrast agents is that they only allow indirect visualization through modification of the intrinsic properties of the tissue, making quantification of this effect challenging. F compounds, on the contrary, are measured directly, without any background signal. There is a linear relationship between the amount of F spins and the intensity of the signal. However, non-uniformity of the radiofrequency field may lead to errors in the quantified F signal and should be carefully addressed for any quantitative imaging.
Materials And Methods: Adaptation of the previously introduced [Formula: see text] mapping technique to the problem of quantifying the F signal from perfluoro-15-crown-5-ether (PFCE) is proposed in this work. Initial evaluation of the proposed technique simultaneously accounting for transmit [Formula: see text] and receive [Formula: see text] field inhomogeneities is performed in a PFCE phantom. As a proof of concept, in vivo quantification of the F signal is performed in a murine model after application of custom-designed hollow mesoporous silica spheres (HMSS) loaded with PFCE.
Results: A phantom experiment clearly shows that only compensation for both transmit and receive characteristics outperforms inaccurate quantification based on the non- or partly-corrected signal intensities. Furthermore, an optimized protocol is proposed for in vivo application.
Conclusion: The proposed [Formula: see text]/[Formula: see text] mapping technique represents a simple to implement and easy-to-use solution for quantification of the F signal from PFCE in the presence of B-field inhomogeneities.
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http://dx.doi.org/10.1007/s10334-018-0696-6 | DOI Listing |
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