Sentence examples for release extent from inspiring English sources

Exact(4)

This represented a 7-fold increase in release extent when compared to standard pegylated liposomal doxorubicin.

The volume fraction of alginate in EGs did not affect the ultimate free fatty acid (FFA) release extent, but it had a negative correlation with the bioaccessibility of lipophilic nutraceutical.

In UCP2-silenced cells, 15 μ M PA with glucose promoted an insulin release extent, attaining ∼50% of levels in ntgINS-1E cells after 60 min.

It is evident that, in pH 6.8 as the HMPC concentration increased from 7.3 to 20% w/w in F9 to F11, respectively, the drug release extent decreased significantly (P < 0.0001) due to faster water absorption capacities.

Similar(56)

The adsorbed and released extents of the drug onto/from the modified zeolite were determined by UV Vis spectroscopy.

The system was investigated under in vitro conditions for studying its release profile, extent of mucoadhesion and enzymatic degradation over bronchial epithelial cells (16HBE) which further showed a considerable extent of success as compared to conventional carrier molecules.

Question marks also hang over the negotiations that led to his release; the extent, if any, to which the White House violated its obligation to keep Congress informed about a possible release of prisoners from Guantanamo; and the role, if any, that political considerations played in the timing of the deal.

All these studies concluded that hemicellulase activitiy had a beneficial effect on xylose and glucose release, the extent of the gains being highly dependent on the raw materials, the pretreatment and the hemicellulase activity.

With the aim to produce an alternative cementitious material releasing less extent of CO2, utilization of calcium carbonate in the hydrothermal synthesis of a cementitious material would be a unique approach.

For formulations without any release-modifier, the extent and rate of drug release at pH 6.8 was much higher than that at pH 1.0.

Amide-linked conjugates were relatively stable against hydrolysis, whereas the ester-linked conjugates showed pH-dependent release and the extent of release varied with pH from 3% (pH 5) to 38% (pH 8.5) for the 10-day period studied.

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