The term pellet has
been used by several industries to describe a range of clusters produced from
different and varied raw materials. Many industries have been making use of
pelletization techniques since the 20th century, however
pharmaceutical industry has been showing exquisite interest in this technology in
the later phase owing to the rise in the demand of sustained release
preparations. Pellets for pharmaceuticals of pharma pellets are defined as
semi-spherical or spherical, free slowing solid units. On account of their
numerous advantages, pellets have garnered substantial aid and attention in the
production of both modified as well as immediate release dosage form. The commercial
pellets are formulated with a polymer film coating in order to obtain a
controlled release effect. Presently, the palletization technologies are
getting more intense as they focus on an effective pathway for the manufacture
of oral drug delivery systems. The credit goes to the fact that pellets give
many technological, biopharmaceutical, as well as therapeutic benefits over the
traditional and conventional oral dosage forms.
Pellets developed
through the palletization technique results in better flow, appearance and
mixing properties and thereby preventing development of excess dust particles
and reducing the segregation. It helps in eliminating detrimental properties and
enhances the chemical and physical properties of the fine powders. Pharma
pellets are generated via several techniques such as layering, freeze
palletization, extrusion or spheronization, spray congealing,
cryopelletization, spray drying and compression. Out of all of these
techniques, extrusion or spheronization is the most commonly used technique
owing to its superior efficacy and simple yet rapid processing. Some of the
advantages of pharma pellets are – enhanced safety and efficiency of the active
ingredient, decreased handling hazards and user-friendly transport, lessened hygroscopicity,
little abrasion, no crystallization, uniform size with tapered distribution,
higher drug loading capacity, reduce drug accumulation, pellets disperse
freely, etc. Also, pellets render reduced variations in gastric emptying rate
and intestinal transit time and thus lessen inter and intra subject
variability.
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