Sentence examples for release at high from inspiring English sources

Chem-AgNP-treated cells showed significantly higher LDH release at high concentrations compared to untreated cells (Figure 7). Figure 7 Effect of AgNPs on LDH release from A549 human lung epithelial adenocarcinoma cells.

The quantitative measurement of atomic sodium (Na) release, at high concentration, from a burning black liquor droplet has been demonstrated using a planar laser-induced fluorescence (PLIF) technique, corrected for fluorescence trapping.

One product, Palladone SR capsule, which utilizes a coated bead technology demonstrates a slower release at low levels of alcohol (5 15%) and a higher release at high levels of alcohol (35 40%) when compared to the control (0%) release rate (Figs. 5, 6 and 7).

Hydrogels consisting of weakly charged acidic/basic groups are ideal candidates for carriers in oral delivery, as they swell in response to pH changes in the gastrointestinal tract, resulting in drug entrapment at low pH conditions of the stomach and drug release at high pH conditions of the intestine.

Release at high altitudes and night-flying was also part of the training.

Indeed, the effect of time on drug release at high dilution (99%) showed a two phase profile, with a rapid (but still detectable only after 5 min) release of about 53% of the AEA initially entrapped.

The decrease in drug release at higher mole percentage of PVA may be due to its tendency to remain on the surface of the particles even after hardening.

However, DA release at higher burst-like frequencies of axon terminal activation was reduced in the NAc of mice lacking NR1 in DA neurons.

Although spikes are expected to trigger vesicle release at higher instantaneous rates than graded signals, they were infrequent.

In addition, it was demonstrated that norepinephrine is able to inhibit central CRF release at higher concentrations [ 59].

Conversely, the COX inhibitors ASA and indomethacin augment this secretion, whereas the COX-2 specific antagonist celecoxib has differential effects and inhibits CXCR3 ligand release at higher concentrations.