Examples of 'in vitro release' in a sentence

Meaning of "in vitro release"

in vitro release - This phrase is often used in scientific or medical contexts, particularly in pharmacology or drug development. It refers to the process of measuring or studying the release of substances from a controlled environment, such as a laboratory setting or artificial model

How to use "in vitro release" in a sentence

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in vitro release
All in vitro release studies were set up in duplicate.
Protein integrity and activity after in vitro release.
In vitro release of leuprolide from injectable polymeric formulations.
Study of in vitro release.
In vitro release of the therapeutic agent.
Before a sample was withdrawn the in vitro release vessel was gently shaken.
The in vitro release was tested as follows.
This method is used in conjunction with the in vitro release studies.
The in vitro release profile is reported in the table hereinbelow.
Good agreement was found between in vivo and in vitro release profiles.
In vitro release studies were performed using a centrifugal ultrafiltration device.
The formulations of the invention have a prolonged in vitro release rate.
In vitro release profile.
Quality control was ensured by measuring the in vitro release rate of every fifth device.
The in vitro release studies were initiated within a few days of preparation.

See also

The resulting tablets were tested for the in vitro release rate immediately after production.
In vitro release rate is determined by a standard dissolution test as described above.
The pharmaceutical composition of the present invention has a particularly advantageous in vitro release profile.
Taxol in vitro release.
Example 1 shows the influence of maltodextrin on the in vitro release kinetics.
The sterility and in vitro release kinetics of the microspheres obtained are monitored.
Figure 7 is a graphical illustration of the in vitro release profile of a coated stent.
Our in vitro release rates seem to be predictive of the in vivo release rate.
These pieces were used for in vitro release tests, as further described below.
The in vitro release of ACh from cortical slices was inhibited by all four agents.
Figure 2 is a plot depicting the in vitro release of various protein loaded microparticles.
In vitro release and stability of peptides and biodegradable polymer in liquid polymeric compositions.
Formulations having the desired in vitro release profiles produce the desired plasma concentration levels.
In vitro release studies were performed with these microparticles in a buffer medium under physiological conditions.
Figure 1 shows the in vitro release of human growth hormone.
In vitro release is preferably determined in accordance with Ph.
Figure 3 shows the in vitro release curves for each batch.
In vitro release studies were performed using Franz diffusion cells.
Example 1 shows the influence of the constituents on the kinetics of in vitro release.
Experimental in vitro release data is shown for a hyaluronic acid formulation with gentamicin.
The test product was shown to exhibit the following in vitro release profile,.
The in vitro release was determined according to Ph.
From this powder mix, samples for in vitro release tests were moulded and cured.
The in vitro release is depicted in FIG.
Therefore, the commercially available patch exelon ¿ was evaluated using in vitro release and permeation methods.
The in vitro release rates are set forth below in Table III.
Figure 10 shows in silico predicted PK profiles for various in vitro release profiles.
Average in vitro release rates over 7 batches were.
The nanoprecipitated BDNF was encapsulated in FN-PAMs and the in vitro release profile was evaluated.
Kinetics of in vitro release are shown in figure 1.
FIG . 4 is a graphical depiction illustrating the solvent effect on in vitro release kinetics in tilmicosin.
In vitro release studies were reviews by gas chromathografy ¿ mass spectrum gc-ms.
Figure 5 demonstrates the cumulative in vitro release of dopamine from a variety of polymer configurations.
In vitro release studies according to example 8 were carried out on system 4 described above.
In a separate experiment, the in vitro release profiles were determined as described in Example 3.

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