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The release of the model protein BSA from these new systems was studied.
Sustained release of the model proteins from the biodegradable matrices was observed.
Microspheres allowing the controlled release of the model oligonucleotide pdT16 were designed.
The in vitro release of the model drug from scaffold containing the peptide drug-binding domains was measured.
Once the amount of drug encapsulated in each type of microparticle was determined, the rate of release of the model drug could be evaluated.
Since the release of the model by Itasca, it has not been validated for fluid flow application in porous media, especially in case of petroleum reservoir.
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The release of this model marks the beginning of the 3rd generation of NEC's line of ultramobile notebooks.
The accumulative release percent of the model drug reached 85.6% after 48 h and the drug release was controlled by the swelling and the degradation of the hydrogels.
The Scuba Series HD 320 model shipped a few months after the release of the VideoMask model 310.
These results demonstrate that the model drug electronegativity, estimated as Taft values, has a significant influence on the release rate of the model drug.
The structure of the spacer in the vicinity of the hydrazone bond significantly influenced the release rate of the model drug.
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