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International Journal of Scientific Development and Research - IJSDR
(An International Open Access Journal)
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2455-2631


Issue: January 2022

Volume 7 | Issue 1

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Paper Title: Formulation and evaluation of orodispersible liquisolid tablets of Haloperidol
Authors Name: Duniya Asokan , Dr.Ann Rose Augusthy , Dr.Vipin K V , Abhila V Mukund , Femi Joseph
Unique Id: IJSDR2111010
Published In: Volume 6 Issue 11, November-2021
Abstract: Abstract The present study aimed to enhance the dissolution rate of a poorly water-soluble drug, Haloperidol by adopting liquisolid compact technique and formulating it into an orodispersible system to overcome the gastric metabolism of the drug. Here 12 different formulations of liquisolid compacts of Haloperidol were formulated by varying the concentration of drug solution from 10-30%w/v. Avicel pH 102 and Aerosil 200 was used as carrier and coating material respectively. Crospovidone and SSG in the ratio of 1:1 were added to the formulation for faster disintegration. Prior to the compression of orodispersible tablets all the 12 batches of liquisolid compacts were subjected to precompression evaluations and the results were found to be satisfactory. Further, the prepared powder blends were directly compressed into orodispersible liquisolid tablets. The orodispersible liquisolid tablets were evaluated for the post-compression parameters like weight variation, hardness, friability, disintegration test, wetting time, water absorption ratio, drug content, and in-vitro dissolution studies. From the obtained results, it could be concluded that the formulation LS2 with 10% concentration of drug solution and carrier to coating material in the ratio of 20:1, exhibits quick disintegration and had a maximum drug release of 98.1% at the end of 30 minutes. Liquisolid tablet (LS2) demonstrated a significantly higher drug release rate than those of marketed tablet, which may be due to enhanced wetting properties and increased effective surface area of the drug. The results of the kinetic study revealed that the formulation followed first-order kinetics with a dissolution-controlled release pattern. From the results of stability studies, the batch was found to be stable. In conclusion, the liquisolid compacts technique can be a promising alternative for the formulation of water-insoluble drugs, such as Haloperidol into rapid-release tablets. In conclusion, combining the liquisolid technology and orodispersible system can be used as a promising alternative to improve the dissolution rate of poorly water soluble drugs like Haloperidol.
Keywords: Liquisolid technique, Haloperidol, orodispersible tablets.
Cite Article: "Formulation and evaluation of orodispersible liquisolid tablets of Haloperidol", International Journal of Science & Engineering Development Research (www.ijsdr.org), ISSN:2455-2631, Vol.6, Issue 11, page no.41 - 49, November-2021, Available :http://www.ijsdr.org/papers/IJSDR2111010.pdf
Downloads: 00075629
Publication Details: Published Paper ID: IJSDR2111010
Registration ID:193696
Published In: Volume 6 Issue 11, November-2021
DOI (Digital Object Identifier):
Page No: 41 - 49
Publisher: IJSDR | www.ijsdr.org
ISSN Number: 2455-2631

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