Formulation Of Phenytoin Complexes For Dissolution Enhancement

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Inclusion Complexation Using -cyclodextrin And Hp -cyclodextrin

ISBN: 3659537055
ISBN 13: 9783659537059
Autor: Maulika, Patel/Kalpen, Patel
Verlag: LAP LAMBERT Academic Publishing
Umfang: 152 S.
Erscheinungsdatum: 26.08.2014
Auflage: 1/2014
Format: 1 x 22 x 15
Gewicht: 244 g
Produktform: Kartoniert
Einband: Kartoniert
Artikelnummer: 6907157 Kategorie:

Beschreibung

Phenytoin Inclusion complex prepared by microwave method was used for preparation of FDT by different superdisintegrants by direct compression method. From that the cross-povidone (5%) containing inclusion complex was maximum DT, Wetting time and In-vitro drug release. The FDT containing 1:2 ratio complexes and 5% crospovidone give minimum DT and Wetting time. Then 32 full factorial designs were applied and the tablets were synthesized using different proportions of inclusion complex and crospovidone (%) by direct compression technique. The optimum ratio was 1:2 and 5% which produced highest DT (10.01 sec), Wetting time (9.45 sec.) and cumulative percent drug release (99.51% at 40 min). The solubility and dissolution pattern of Phenytoin were found to be carrier ratio dependent. From evaluation parameters and formulation characterization, it can be concluded that solubility of drug was improved by MW method compared to SE method and pure drug. The tablet contain optimum ratio of inclusion complex and optimum concentration of superdisintegrants give maximum drug release in minimum time period.

Autorenporträt

Maulika S Patel, M. Pharmacy in Pharmaceutical Technology in Shree Krishna Institute of Pharmacy, Shankhalpur, becharaji at Gujarat Technological University, Ahmedabad, Gujarat, India.

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