Formulation, Characterization and Solubility Enhancement of Manidipine Solid Dispersions

DOI:

https://doi.org/10.37285/ijpsn.2019.12.2.3

Authors

  • Laxmi Raj A
  • Y. Shravan Kumar

Abstract

The study was aimed to formulate solid dispersions of Manidipine by using different novel carriers like Labrafac PG, Kolliwax RH 40, Soluplus, Kolliwax GMS II, Kolliphor EL and SLS in drug carrier ratio by using solvent evaporation method. The formulations were characterized for physical appearance, solubility and in vitro dissolution studies. The optimized formulation was characterized and Formulation SD13 was found to be optimized one based on the solubility, dissolution and other parameters using Kolliwax GMS II and SLS.  The drug release of the optimized formulation was found to be 99.41±5.38% within 90 min. Powder X-ray diffraction studies performed on solid dispersion showed that Manidipine existed in the amorphous form within the solid dispersion formulation fabricated using the solvent evaporation process. Additionally, scanning electron microscopy studies suggested the conversion of crystalline Manidipine to an amorphous form. Therefore, the solid dispersions using Kolliwax GMS II as hydrophilic carrier in the combination of SLS can be successfully used for improvement of solubility and dissolution of Manidipine.  

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Keywords:

Manidipine, Solvent Evaporation method, Kolliwax, GMS II, Hypertension

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Published

2019-03-31

How to Cite

1.
A LR, Kumar YS. Formulation, Characterization and Solubility Enhancement of Manidipine Solid Dispersions. Scopus Indexed [Internet]. 2019 Mar. 31 [cited 2024 Dec. 22];12(2):4453-60. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/291

Issue

Vol. 12 No. 2 (2019): March-April 2019

Section

Research Articles
Crossref
Scopus
Google Scholar
Europe PMC

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