practical

Wednesday, 18 December 2013


Experiment 2: Tablet friability


Objective
To test the friabitily of the chosen tablets

Introduction
The friability test is closely related to tablet hardness and is designed to evaluate the ability of the tablet to withstand abrasion in packaging, handling and shipping. It is usually measured by the use of the Roche friabilator. A number of tablets are weighed and placed in the apparatus where they are exposed to rolling and repeated shocks as they fall 6 inches in each turn within the apparatus.
Materials
10 of chosen tablets
Apparatus
the Roche friabilator

Procedures
1.     Select 10 tablets and weigh.






2. Put all tablets into the drum of the tablet abration and friability tester. Set the rate of rotation to 100 rpm, time to 10 minutes and start the operation.

3. At the end of the operation, remove all the tablets and ensure freedom from dust or powder (use the brush). Reweigh the tablets. Determine the percentage loss of weight.

4. Compressed tablet should nor lose more than 1% of its weight.

Result
Weight of tablet
Before                                   after
6.6062 g                               6.5628 g
Weight loss = 6.6062g -6.5628g          
                     = 0.0434 g

Percentage of loss
0.0434 g/ 6.6062g x 100 = 0.66 %

Discussion
After 10 minutes of this treatment or 100 revolutions, the tablets are weighed and the weight compared with the initial weight. The loss due to abrasion is a measure of the tablet friability. The value is expressed as a percentage. A maximum weight loss of not more than 1% of the weight of the tablets being tested during the friability test is considered generally acceptable and any broken or smashed tablets are not picked up . Normally, when capping occurs, friability values are not calculated. A thick tablet may have less tendency to cap whereas thin tablets of large diameter often show extensive capping, thus indicating that tablets with greater thickness have reduced internal stress.

 Conclusion
The weight loss of tablet is less than 1% which is 0.66%.  this mean that the tablets have good friability.

References
Aulton, M.E. 2002. Pharmaceutics: The Science of Dosage form Design. Edinburgh Churchill Livingstone.  (pg 441-445)


            

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