<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 2 Issue 1</issue_number>
<issue_period>2011 (January - March) </issue_period>
<title>Formulation and evaluation of mouth dissolving tablets of carvedilol</title>
<abstract>The aim of the present research work was to enhance the solubility of Carvedilol by solid dispersion method and to formulate a mouth dissolving tablet. Drugs are more frequently taken by oral administration. The solubility of Carvedilol enhanced with different ratios of PVP by the solvent evaporation method .In-vitro release profile of solid dispersion obtained in SGF with out enzymes and Ph 6.8 phosphate buffer indicate that 100% drug release found within 20 min. These solid dispersion were directly compressed into tablets using crospovidone, sodium starch glycol ate, croscarmellose sodium and polacrilin potassium in different concentrations as a superdisintgrants. The prepared tablets containing the solid dispersion of Carvedilol having sufficient strength of 2.5-4 kg/cm2. The disintegranted in the oral cavity with in 21 sec. contain crospovidone (5%) as super disintegrant. </abstract>
<authors>Himmat Singh,Swatantra Ku. Mishra,Rakesh Varma,Sandeep Singh Parihar</authors>
<keywords>Carvedilol, PVP, Super Disintegrants, Mouth Dissolving Tablet. </keywords>
<pages>232-239</pages>
</article>
</Journal>
