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               Clinical Pharmacy-Pharm D        Level Three        2  Semester       2024/2025      Pharmaceutical Technology (PT 607)


               II) Tablet Friability:


               Tablet friability is the evaluation of the ability of tablets to withstand abrasion, packaging,
               handling and shipping. It can also be defined as the phenomenon whereby tablet surfaces are

               damaged and /or show evidence of lamination or breakage when subjected to mechanical shock

               or attrition. To monitor the resistance of tablets to such stress and to decide on their suitability
               for further processing such as coating, tablets are routinely subjected to friability test.


               Apparatus: Roche Friabilator.






























               Method:

               1- Select 10 tablets and weigh them, then place in the friabilator.

               2- The friabilator operates for 100 revolutions (25 rpm for 4 minutes).

               3- At the end of the operation, remove all the tablets and ensure freedom from dust or powder.
                  The tablets are reweighed then determine the percentage loss of weight.



                                     % Friability = [                             −                         ]  X 100
                                                                                       
               Limits:

               •  Conventional compressed tablets that lose up to 1 % in weight are generally acceptable.

               •  Some chewable tablets & most effervescent  tablets would have higher friability weight

                   losses, which accounts for the special stack packaging that may be required.
               •  When  capping  is  observed  during  friability  testing,  the  tablet  shouldn't  be  considered

                   acceptable, regardless of what the % weight loss result in.



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