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A lower concentration range was used initially and was increased in the second case.
A systematic investigation reveals that unique particle shapes can be obtained by electroprocessing within this lower concentration range.
Stable isotope technique is sufficiently sensitive to determine the uptake of Zn at an exposure equivalent to lower concentration range (<15 μg g−1).
The apparent binding constants (Kapp) has been obtained 3.9 and 10.9 × 104 M−1 at lower concentration range and 1.03 and 1.59 × 104 M−1 at higher concentration range for complexes (1) and (2), respectively.
Moreover, the two most potent apoptosis inducers displayed antiproliferative profile identical to several known advanced p53 activators: they inhibited the growth of p53+/+ HCT116 cells in much lower concentration range compared to p53−/− HCT116 cells.
The hydrate formation rate of xenon increased with the addition of the surfactants in the lower concentration range, and the acceleration showed a maximum at a certain concentration, but decreased with further concentration increases.
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Smaller particle sizes and larger concentrations (>50 g/m3) increase turbulent burning velocity compared with larger particle sizes and lower concentration ranges.
An increase in Mw enhanced affinity between membrane proteins and surfactants, thereby allowing effective solubilization, even for lower concentration ranges (<0.0005 wt %).
We conclude that binary combinations of PFAAs behave additively at the lower concentration ranges in activating PPARα in this in vitro system.
Dual-energy quantification systematically overestimated concentrations in lower concentration ranges and underestimated concentrations in higher concentration ranges.
ZnO CTS NPs prepared through nano spray dying and precipitation methods showed significant (p < 0.05) biofilm inhibition activity against M. luteus and S. aureus at a lower concentration ranging from 0.625 to 0.156 mg/ml.
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