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Steady state tissue concentrations were reached in all studies within significantly shorter uptake periods compared to fish studies on the same test items.
Even though BrdU labeling assays are characterized by two phases, the shorter uptake or pulse phase (BrdU present for 10 13 days) and a longer chase phase (BrdU absent for up to 306 days), our focus was previously exclusively on BrdU dilution data.
The larger range observed in SUB 3 may reflect that there is more uptake of contrast agent in the breast tissue owing to a longer uptake time; likewise, this may also explain the smaller range observed in SUB 1, on which the amount of contrast enhancement was less owing to a shorter uptake time.
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Regarding the relatively short uptake period (<120 min), lymphatic clearance was considered negligible in the present study.
Thus, our previous results [1] regarding the correlation of SUR and K m (with perfectly standardized and relatively short uptake period) are not necessarily valid for static oncological PET with variable uptake times.
This is particularly desirable when 13C-MRSI is combined with PET tracers using a short uptake time and in cases where a pharmacological challenge or another intervention is employed.
However, due to the perfectly standardized uptake period used for SUR determination and the comparatively short uptake period, these results are not automatically valid and applicable for clinical whole-body examinations in which the uptake periods (T) are distinctly longer and can vary considerably.
A high biosorption capacity of 111 mg/g was obtained within short uptake duration of about 15 min.
Using ultrafiltration and radiotracer techniques we determined silver concentrations and speciation in the EPF of the blue mussel Mytilus edulis after short-term uptake and depuration laboratory experiments.
Simultaneous 123I (c) and 99mTc (d) end-systolic apical short axis uptake for DNM 530c (upper row) and DSPECT (lower row) for LVEF 50% Fig. 4 DNM 530c and DSPECT end-systolic volume rendering, volume (mL), and filling (mL/s).
To measure RBV short-term uptake, cells were treated with SFM (same media type used for infections but without virus) containing 50 µM RBV (1% of which was [3H]RBV).
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