Examples of 'release kinetics' in a sentence

Meaning of "release kinetics"

Release kinetics is a term used in the fields of chemistry and pharmacology to describe the rate at which a substance or drug is released from a dosage form or delivery system over time. It refers to the pattern or profile of the release, which can be controlled to achieve desired therapeutic effects

How to use "release kinetics" in a sentence

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release kinetics
Release kinetics of carotenes from microparticles in oil.
The use of different polymers affected release kinetics.
Variable release kinetics and mass recoveries were observed.
The morphology did not seem to influence the release kinetics.
This can improve the release kinetics of the agent.
Release kinetics were improved by the addition of larger amounts of thrombin.
Adjustment of the release kinetics.
These release kinetics of these compounds were evaluated in aqueous solutions at increasing pH.
Biodegradation rate directly impacts therapeutic agent release kinetics.
Controlled release kinetics.
Biodegradation rate directly impacts active agent release kinetics.
Release kinetics in vitro.
Relative release kinetics.
Release kinetics and gastric protection of carotene microparticles in digestive juices.
The method of placement may influence the drug release kinetics.

See also

The sterility and in vitro release kinetics of the microspheres obtained are monitored.
The drug load had also a significant influence on release kinetics.
They exhibit very advantageous release kinetics when they are administered to man.
The release kinetics can be controlled by the structure of the nucleophilic amines.
Many active ingredients require specific release kinetics or prolonged release.
The release kinetics were characterized by a burst release which was followed by a plateau release.
The prepared suspensions are accepted by children and retain good release kinetics.
Drug release kinetics can be regulated by different pore sizes of the material.
The selection of the form of the drug may impact release kinetics.
Proper loading and release kinetics of the gel are being developed along the way.
Such combinations provide yet a further mechanism for controlling release kinetics.
Systematically the drug release kinetics increases in aqueous acid and ethanol media.
Using this method resulted in polymer samples with undesirable release kinetics.
The data obtained from the release kinetics of sulforhodamine are quantified by mathematical models.
Thus a great deal of control is available on the release kinetics of the fiber.
The overall release kinetics of the more complicated mechanism is substantially linear in time.
It is also challenging to obtain a sustained release kinetics from these small fibers.
The desired release kinetics will also depend upon the specific treatment.
The method of placement may influence the therapeutic component or drug release kinetics.
Release kinetics of tablets obtained by different degrees of compression showed a decrease of drug release.
The blends are mentioned in order to control the drug release kinetics particularly of proteins.
This type of release kinetics might be inappropriate for an efficient and safe drug treatment.
Barrier layers can be used to control beneficial agent release kinetics in more sophisticated ways.
The release kinetics obtained for the lyophilized leuprolide alone are typically variable and slow.
The particles can include a material which enhances the release kinetics of the medicament.
Preferably, release kinetics is not zero order.
Physical processing of the formed electroprocessed collagen matrix is another way to manipulate release kinetics.
The nature of X plays an important role in the release kinetics of the odoriferous molecule.
The release profile of the BMP crystals may be manipulated to give desired release kinetics.
These embodiments also exhibit the desired release kinetics with minimal prolonged HPA axis suppression.
The drug release data from emulsions appears to fit a first order release kinetics model.
The question of release kinetics is a multi-factored problem.
Hydration of the core and not the geometry of the cavity controls the release kinetics.
In-vitro study relating to the release kinetics of the active constituent.
The differences in methods of loading had significant effects on the release kinetics for MTX.

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Examples of using Kinetics
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He taught biomolecular kinetics and cellular dynamics
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Examples of using Release
Press again to release the hold state
Release buttons when the motor unit
Read the press release online here
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