Volume 3, Issue 3, June 2017, Page: 37-48
Use of Solid Dispersions and Inclusion Complexation for Enhancing Oral Bioavailability of Ziprasidone in Treating Schizophrenia
Poonam Mogal, Department of Pharmaceutics, M. V. P. S’ College of Pharmacy, Nashik, India
Deeliprao Derle, Department of Pharmaceutics, M. V. P. S’ College of Pharmacy, Nashik, India
Received: May 19, 2017;       Accepted: Jun. 21, 2017;       Published: Jul. 25, 2017
DOI: 10.11648/j.jddmc.20170303.12      View  2648      Downloads  131
In modern times, people are suffering from many mental health disorders like schizophrenia, bipolar disorders and many psychoses. Hence, it is essential to treat these mental disorders using medications as well as with assistance from caregivers for the social well being of person. This study was focussed on improving solubility & dissolution of poorly soluble drug Ziprasidone using different formulation approaches like solid dispersion & inclusion complexation. Different solubility enhancing techniques like physical mixing, solvent evaporation, microwave irradiation, lyophilization & spray drying were used for the along with four different polymers i.e Kollidon, Soluplus, Pluronic and HPβCD. The prepared formulations were evaluated for saturated solubility, dissolution, ATR, SEM, XRD, pharmacodynamic and pharmacokinetic in vivo study. The prepare formulations showed increment in solubility as well as dissolution. The order of solubility enhancement for the studied polymers was found to be of following order: Soluplus >HPβCD >Kollidon >Pluronic. In the pharmacodynamic study, the optimized solid dispersion showed the calming effect on mice when compared to pure Ziprasidone. The pharmacokinetic study demonstrated the increase in oral absorption of Ziprasidone in all prepared formulations and it followed the same order as that solubility & dissolution enhancement. The Soluplus-solid dispersion prepared by spray drying technique was found to be suitable in enhancing oral absorption with significant (p < 0.05) enhancement in Cmax & AUC than pure Ziprasidone. Hence, comparative study was helpful in increasing oral bioavailability Of Ziprasidone in choosing the suitable polymer with decreasing the dose and increasing patient adherence to therapy.
Ziprasidone, Solubility, Kollidon, Soluplus, Pluronic, HPβCD, Solid Dispersion
To cite this article
Poonam Mogal, Deeliprao Derle, Use of Solid Dispersions and Inclusion Complexation for Enhancing Oral Bioavailability of Ziprasidone in Treating Schizophrenia, Journal of Drug Design and Medicinal Chemistry. Vol. 3, No. 3, 2017, pp. 37-48. doi: 10.11648/j.jddmc.20170303.12
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