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Azithromycin, as a kind of hydrophobic drug, has a low bioavailability of about 37%% due to its low dissolution rate.
The film with the Ca/P ratio of 1.5 showed an extremely low dissolution rate even in the amorphous state.
A large number of drugs of therapeutic interest present inappropriate physicochemical properties (e.g., low dissolution rate, solubility, or permeability in biological fluids).
In addition, the anodes possess high chemical and physical stabilities: very low dissolution rate of WO3 during the electrolysis and good adhesion to the substrate.
Therefore, pure palladium is non-toxic due to the low dissolution rate of palladium ions (Wataha and Hanks 1996), while pure Co is not stable and thus releases toxic cobalt ions.
In addition, elevated silver content in bioactive glass may also result in low dissolution rate while replacing calcium ions, poor mechanical property, and in vitro behavior [ 7].
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This is expected because quartz, phyllosili-cates, and iron oxides have very low dissolution rates in near-neutral seawater.
However, based on the low dissolution rates of goethite at pH 6 in the presence of EDTA [36] and siderophores [37], the expected dissolved iron concentrations are in the low micromolar range and are not expected to affect the results.
According to various reports, the absorption of BZD anthelmintic drugs in cats, dogs, and humans is substantially limited by their low dissolution rates in gastric fluids [ 26, 27].
The lowest dissolution rate was observed on plains vicinal to the basal plane {0 0 0 1}.
The tablets of β CBZ demonstrated the lowest dissolution rate, while the α form tablets exhibited the highest.
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