FORMULATION DEVELOPMENT AND IN VITRO EVALUATION OF EXTENDED RELEASE MEBEVERINE HCL PELLETS
Amtun Noor*, P.R.Sathesh Babu, P. Aravind
Abstract
The present study was aimed to formulate and evaluate extended
release mebeverine hydrochloride pellets using fluidized bed coater.
Mebeverine hydrochloride anti spasmodic drug being highly water
soluble drug with a half life of 2 h suitable to develop extended action
for treatment of irritable bowel syndrome. Nine formulations (M1-M9)
of mebeverine hydrochloride pellets were prepared using a
combination of two rate controlling polymers ethyl cellulose and
HPMCP HP 55 and other standard excipients. The prepared pellets
were subjected to micrometric properties and In vitro drug release
studies. The optimized formulation M9 showed 87.91% drug release
after 12 h. Scanning electron microscopy (SEM) studies revealed that
the prepared pellets for mebeverine hydrochloride are spherical in shape. The release profile
for optimized formulation M9 was comparable with that of marketed formulation (MEVA
SR) for mebeverine hydrochloride. The mathematical model was built on the hypotheses that
drug diffusion and drug dissolution in the release environment are the key phenomena
affecting drug release kinetics and it was found to be followed first order and diffusion
mechanism.
Keywords: Mebeverine hydrochloride; extended release; fluidized bed coater; irritable bowel syndrome.
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