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Their identification has been studied with the method of gamma spectroscopy.
A 2-step method of gamma dose rate calculation was used for shutdown dose rates in CAD-based Multi-Functional 4D Neutronics Simulation System (VisualBUS).
The novel method for quantification of the optical tracer IRDye800CW gives similar results as the reference method of gamma ray quantification.
Therefore, we employed the method of gamma ray response and relative abundance of sand versus shale to separate upper shoreface sands with middle to lower shoreface sands (Fig. 10).
To employ the new method for quantification of fluorescent probes in tissues and, at the same time, to enable the comparison with the reference method of gamma ray quantification, a dual-labeled probe was produced.
In order to apply both methods for assessment of the biodistribution, i.e., the quantification of IR fluorescence and the reference method of gamma ray quantification, the following setup was employed: a group of six mice was injected with 120 μL containing 106 μg of 89Zr-cetuximab-IR, i.e., the biodistribution probe.
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During this study, we aimed to develop a methodology of mass flow rate measurement to replace the existing limited method of gamma-densitometer, as the irregularities noticed during various phase measurement reduce the reliability of this technique.
We conclude that this observer-based method of visual gamma correction is useful to estimate the OETF for LCD displays.
The purpose of our study was to evaluate the 1.5-to-1 ratiometric threshold criteria method versus the three-sigma statistical threshold criteria method for determination of gamma detection probe positivity for intraoperative in situ identification of presumed abnormal F-FDG-avid tissue sites in a manner that was independent of the specific type of gamma detection probe used.
The three-sigma statistical threshold criteria method was significantly better than the 1.5-to-1 ratiometric threshold criteria method for determination of gamma detection probe positivity for intraoperative in situ detection of presumed abnormal F-FDG-avid tissue sites during radioguided oncologic surgery.
Therefore, we have suggested that improved intraoperative in situ identification of F-FDG-avid tissue sites can be accomplished by the use of the three-sigma statistical threshold criteria method for determination of gamma detection probe positivity [ 2].
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