Examples of 'dissolution testing' in a sentence

Meaning of "dissolution testing"

dissolution testing: A procedure used in pharmaceutical industry to determine how quickly a drug dissolves in the body. It helps in assessing the bioavailability and effectiveness of the drug

How to use "dissolution testing" in a sentence

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dissolution testing
The capsules were then subjected to dissolution testing.
Dissolution testing should be performed at release.
The tablets are then subjected to dissolution testing.
The dissolution testing is not interrupted by this procedure.
A representative tablet is then subjected to dissolution testing.
Conventional dissolution testing apparatuses have a number of problems.
The finished product was then subjected to dissolution testing.
Dissolution testing was performed in triplicate.
The tablets thus obtained were subjected to dissolution testing.
Method for dissolution testing of solid compositions containing digestive enzymes.
Water was used for dissolution testing.
Potency and dissolution testing were performed on the manufactured CR capsules.
The beads were subjected to dissolution testing.
The results of the dissolution testing confirmed the anticipated in vitro dissolution profile.
The finished product is then subjected to dissolution testing.

See also

Dissolution testing is carried out on capsules using a USP dissolution apparatus.
Such drive systems are known in the art of dissolution testing.
These include USP dissolution testing for immediate release and controlled release solid dosage forms.
The tablets produced were submitted to the lab for dissolution testing.
They are flexible enough to allow dissolution testing for a variety of drug products.
A number of the coated tablets thus prepared were selected for dissolution testing.
Dissolution testing was done in USP II.
For the characterization of the concrete waste leaching and dissolution testing were performed.
Dissolution testing according to example 1 was carried out.
The fluid medium can be any fluid medium suitable for dissolution testing.
Thus, no dissolution testing was performed with this formulation.
Different dosage forms of a formulation also require dissolution testing to determine optimal parameters.
All dissolution testing was performed according to the following method,.
Those prototypes that floated for at least four hours were submitted for dissolution testing.
An apparatus for dissolution testing of a pharmaceutical delivery device, comprising,.
After the tablets had been compressed they were submitted to the lab for dissolution testing.
The results of the defoaming and dissolution testing are reported below,.
A number of the oval-shaped tablets prepared above were selected for dissolution testing.
Bioequivalence can be determined by in vitro dissolution testing and / or in vivo bioequivalence studies.
Prior fiber dissolution studies have discussed acid pH fiber dissolution testing M.
The results of dissolution testing is set forth in Table 2 below.
Example 2 further summarizes the results of dissolution testing.
Dissolution testing was performed and the comparative results are shown in Table 11 below.
In pharmaceutics, sink condition is a term mostly related to the dissolution testing procedure.
Results of the dissolution testing are presented below in Table 5 and graphically represented in Figure 3.
The test was conducted according to the current dissolution testing described in U. S.
The dissolution testing is carried out vía the USP Basket Method, as previously described.
Finished product stage5 Disintegration or dissolution testing Pharmacopoeial or other internationally recognized methods.
Dissolution testing was conducted on the finished products vía USP Apparatus II ( Paddle Method ).
Adopted in 1970 the rotating basket method of dissolution testing was the first official method.
Dissolution testing was performed at a pH of 6.5 in phosphate buffer.
From the specimens created, five ( 5 ) specimens are arbitrarily chosen to be used for dissolution testing.
Basket-type dissolution testing begins with the stirring elements configured at paddle-type stirring elements 104.
A seventh test vessel 106 may be used as an unstirred control vessel during dissolution testing.
In vitro dissolution testing of the samples was done as described in Example 14.

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