_1568962289 1568962289 Editor editor.jddt@gmail.com UJPR Universal Journal of Pharmaceutical Research Univ J Pharm Res 2456-8058 04 11 2018 Ankush Kumar Kapil Kumar Improving oral bioavailability of drugs those given as solid dosage forms remains a challenge for the formulation scientists due to solubility problems. Over the years a variety of solubilization techniques have been studied and widely used, as maximum drugs are poorly water soluble in pharmaceutical field.  The enhancement of dissolution rate and oral bioavailability is one of the greatest challenges in the development of poorly water soluble drugs. Solid dispersions have attracted many researchers as an efficient means of improving the dissolution rate and hence the bioavailability of a range of poorly water-soluble drugs. The term solid dispersion refers to a group of solid products consisting of at least two different components, generally a hydrophilic inert carrier or matrix and a hydrophobic drug. Solid dispersion can form either a eutectic mixture or solid solution or glass solution or amorphous precipitation in a crystalline carrier or compound or complex formation.   The focus of this review article is on the advantages, limitations, various methods of preparation and characterization of the solid dispersion. Google Scholar 09 01 2017 10.22270/ujpr.v2i5.RW4 http://ujpr.org/index.php/journal/article/view/93 http://ujpr.org/index.php/journal/article/download/93/71 http://ujpr.org/index.php/journal/article/download/93/253 http://ujpr.org/index.php/journal/article/download/93/71 http://ujpr.org/index.php/journal/article/download/93/253