Examples of using Dissolution test in English and their translations into French
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Colloquial
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Official
Dissolution test.
Scientists perform dissolution test.
The dissolution test carried out was the following.
These capsules comply with USP Dissolution Test 1.
The dissolution test gives a very poor result.
In vitro tests( dissolution test.
Dissolution test for solid dosage forms… 5.7-4805 2.9.40.
Complies with USP dissolution Test 2.
The dissolution test is carried out with the whole mantles.
This product meets USP Dissolution Test 3.
The dissolution test gives the same result as in Example 1.
Powder Analysis Protocol: Dissolution Test Operating Conditions.
Dissolution test was performed on the products obtained in examples 7.1 and 7.2.
It turns out that the microcapsules were not modified externally by the dissolution test.
A dissolution test will now be required for both cutaneous and transdermal patches;
The solid obtained after the procedure was subjected to the dissolution test in Example 1 of the present invention.
The dissolution test is carried out and gives a positive result for the 5 pieces.
The UV/Vis spectrophotometers SPECORD PLUS can be easily connected with any commercially available online dissolution test system.
The dissolution test gives the same negative result as in Comparison Example(a) above.
The UV/Vis spectrophotometers SPECORD® PLUS can be easily connected with any commercially available online dissolution test system.
Dissolution test for lipophilic solid dosage forms previously included in chapter 2.9.3.
Not less than 85% of the labelled amountis released within 15 minutes or less during a product dissolution test under the conditions specified in this guidance.
With each batch, the dissolution test gives a result almost as good as that obtained in Example 1.
A product in which not less than 85% of the labelled amountis released within 30 minutes or less during a product dissolution test under the conditions specified in this guidance.
The dissolution test is carried out with the whole mantles and gives good results.
The release profile of the whole tablet used in the comparative bioavailability study should be used as the reference and the dissolution test condition should be the one proposed in the regulatory submission.
A dissolution test of the film in THF confirmed that reticulation occurred under the conditions used.
Considering the dissolution test, both strengths of the test product can be classified as“very rapid dissolving tablets.
Further, the dissolution test, namely more than 70% over 8 hours, is adapted to the frequency of administration.
FIG. 5 shows a dissolution test in the FaSSIF fluid comparing formulations 5 to 8 of the Invention with Plavix®;