Tablet Processing
Pharmaceutical products are processed all over the world using the direct compressing, wet granulation, or dry granulation methods. Method chosen depends on the ingredients’ individual characteristics like flow property, compressibility etc. Right choice of method requires thorough investigation of each proposed ingredient in the formula for comprehensive approach for interactions and stability.
Direct compression:
The tablets are made by directly compressing the powdered materials without modifying the physical nature of the materials itself. Direct compression is generally done for the crystalline materials having good physical properties such as flow property, compressibility etc. Main advantages of direct compression are time saving, safety of operations and low cost.
Wet granulation:
This is the most widely used method of tablet preparation. In this method the powders are bound by suitable binder by “adhesion”. The binder is added by diluting with suitable solvent prior to addition to the blended powders to form wet granules which in turn are dried suitably to expel the solvent forming dried granules. The surface tension forces and capillary pressure are primarily responsible for initial granules formation. The main advantage being it meets all the requirements for tablet formation though it is multistage, time consuming.
Dry granulation:
The dry granulation process is used to form granules without using a liquid solution. This type of process is recommended for products, which are sensitive to moister and heat. Forming granules without moisture requires compacting and densifying the powders. Dry granulation can be done on a tablet press using slugging tooling. On large-scale roller compactor commonly referred to as a chilsonator. The compacted mass is called slugs and the process is known as slugging. The slugs are then screened or milled to produce a granular form of tablet materials, which have the good flow properties then original powder mixture. The main advantage of dry granulation is it requires less equipment and eliminates the addition of moisture and the application of heat, as found in wet massing and drying steps of the wet granulation method. The manufacture of oral solid dosage forms such as tablets is a complex multi-stage process under which the starting materials change their physical characteristics a number of times before the final dosage form is produced. Traditionally, tablets have been made by granulation, a process that imparts two primary requisites to formulate: compactibility and fluidity. Both wet granulation and dry granulation (slugging and roll compaction) are used. Regardless of whether tablets are made by direct compression or granulation, the first step, milling and mixing, is the same; subsequent step differ. Numerous unit processes are involved in making tablets, including particle size reduction and sizing, blending, granulation, drying, compaction, and (frequently) coating. Various factors associated with these processes can seriously affect content uniformity, bioavailability, or stability.
0 Comments