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The in vitro time and pH dependent release profile of the drug from hydrogel was studied.
In vitro time killing curves were performed to evaluate the pharmacodynamic properties and bactericidal ability.
An in vitro time course study was conducted to determine whether secondary starch particle losses occur during ruminal incubation.
Our in vitro time lapse experiments indicated that few NHKs can attach, proliferate or form NHK colonies on a normal tissue culture plastic surface when single cultured in serum free Greens media (G-FCS).
To examine the DNA-accelerated the aggregation of oxidized SOD1 proteins in vitro, time courses of reactions of the oxidized SOD1 proteins with DNA were monitored by dynamic light scattering (DLS).
Performing in vitro time kinetic studies of PEG minocycline-liposomes in human peripheral blood mononuclear cells (PBMCs), we determined that PEG minocycline-liposome preparations stabilized with CaCl2 are effective in diminishing MMP-9 activity.
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In vitro, time-dependent cell uptake and internalisation showed slower binding kinetics for the PEGylated BN analogue.
The results of ex vivo growth inhibition curves were consistent with the in vitro time-kill study.
The in vitro time-differential release of DOX and ERL from the dual drug-encapsulated nanoliposomes was investigated, and the results are shown in Fig. 8.
The in vitro time-course and co-culture experiments verified that polymer engineered primary myoblasts have the ability to stimulate endothelial proliferation.
In vitro time-lapsed microscopic imaging of living cells is an efficient approach to generating large datasets on dynamic stem cell behavior.
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