Open AccessA most convenient and patient compliance dosage form- Tablet
Author(s) -
Rajiv Kumar,
Kiranjeet Kaur Batth,
Jaspreet Kaur,
Jaspreet Kaur,
Parminder Nain,
Ravi Dhawan
Publication year - 2020
Publication title -
journal of biomedical and pharmaceutical research
Language(s) - English
Resource type - Journals
eISSN - 2589-8752
pISSN - 2279-0594
DOI - 10.32553/jbpr.v9i6.815
Subject(s) - granulation , diluent , dosage form , dissolution , materials science , patient compliance , process engineering , chromatography , chemistry , composite material , medicine , organic chemistry , engineering , emergency medicine
Tablet is defined as solid pharmaceutical dosage form containing drug substance generally with suitable diluents and prepared by either compression which is given as a single unit and are known as solid unit dosage form. Tablets remain popular as a dosage form because of the advantages afforded, both to the manufacturer (e.g. simplicity and economy of the preparation, stability, and convenience in packing, shipping and dispensing) and the patient. The excipients include diluents, Binders and adhesives, disintegrates, etc. Tablets vary in shape and differ greatly in size and weight depending on the amount of the medicinal substance. The ingredients must be granulated prior to compression to assure an even distribution of the active compound in the final tablet. There are two basic techniques which can be used to granulate powders for compressions into a tablet are wet granulation and dry granulation. In this review article tablet manufacturing and evaluation have been discussed.
Keywords- Tablet, Granulation, Picking and sticking, Dissolution test, weight variation