Formulation and Evaluation of Sustained Release Matrix Tablet of Itopride
Author(s) - 
G Yaswanth Durga Reddy, 
Ashok Kumar, 
G Girisha, 
Suresh V Kulkarni
Publication year - 2021
Publication title - 
american journal of pharmtech research
Language(s) - English
Resource type - Journals
ISSN - 2249-3387
DOI - 10.46624/ajptr.2021.v11.i5.008
Subject(s) - ethyl cellulose , magnesium stearate , lactose , starch , locust bean gum , granulation , diluent , microcrystalline cellulose , polymer , cellulose , dissolution , chemical engineering , materials science , chromatography , talc , matrix (chemical analysis) , chemistry , solubility , dosage form , nuclear chemistry , organic chemistry , xanthan gum , composite material , rheology , engineering
The  objective  of  this  research  work  was  to  carry  out  design  and  evaluation  of  sustained  release matrix tablets of Itopride by use of natural and synthetic polymers.  Matrix tablets were prepared by wet granulation technique by using natural polymers like Carbopol 934, Tamarind poly saccharide, Locust  bean  gum,  Ethyl  cellulose,  HPMC  K  100  as  matrix  forming  agent  and  excipients  such  as Lactose,  Starch  1500,  Magnesium  stearate,  MCC  and  talc  were  used.  The  dissolution  medium consisted of 900 ml of 0.1 N HCl for first 2 hours and then 7.4 phosphate buffer for remaining 10 hours. The release of Itopride from matrix containing lactose, micro crystalline cellulose and starch 1500 as diluents. The drug release rate was found in order of lactose> micro crystalline cellulose>starch  1500.  The  formulation  was optimized  on the basis of  acceptable tablet  properties and  in-vitro  drug  release.  The  release  data  were  fit  into  different  kinetic  models  (zero-order,  first-order, Higuchi’s equation and Korsmeyer-Peppas  equation).  Optimized  formulation  was tested for their  compatibility  with  Itopride  by  FT-IR  studies,  which  revealed  that  there  is  no  chemical interaction  occurred  with  polymer  and  other  excipients.  The  drug  release  profile  of  the  best formulation was well controlled and uniform throughout the dissolution studies. Keywords: Matrix tablets, Itopride, Carbopol 934, HPMC K 100, Ethyl cellulose.
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