Acta Pharmaceutica, Vol. 62 No. 3, 2012.
Original scientific paper
https://doi.org/10.2478/v10007-012-0023-0
Felodipine β-cyclodextrin complex as an active core for time delayed chronotherapeutic treatment of hypertension
KUNAL P. PAGAR
; Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, India
PRADEEP R. VAVIA
; Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, India
Abstract
The present research work deals with the development of a time delayed chronotherapeutic formulation of felodipine (FD) aimed at rapid drug release after a desired lag time in the management of hypertension. The developed system comprises a drug core embedded within a swellable layer and coated with an insoluble, water permeable polymeric system. FD cyclodextrin complex was used as an active core while ethyl cellulose was used as an effective coating layer. Dissolution studies of the complex revealed that there was a 3-fold increase in dissolution of the complex compared to plain FD. This dissolution enhancement and rapid drug release resultedfromFDamorphisation, as confirmed by XRD, DSC and SEM studies. FTIR and 1H NMR studies confirmed the complex formation between FD and cyclodextrin based on the observed hydrogen bond interactions. FD release was adequately adjusted by using a pH independent polymer, i.e., ethyl cellulose, along with dibutyl phthalate as plasticizer. Influence of formulation variables like polymer viscosity, plasticizer concentration, superdisintegrant concentration in the swellable layer and percent coating weight gain was investigated to characterize the lag time. Upon permeation of water, the core tablet swelled, resulting in the rupture of the coating layer, followed by rapid drug release. The developed formulation of FD showed a lag time of 57 h, which is desirable for chronotherapeutic application.
Keywords
felodipine; β-cyclodextrin; chronotherapeutic; ethyl cellulose
Hrčak ID:
81774
URI
Publication date:
30.9.2012.
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