ORGANO MONTMORILLONITE AS DRUG DELIVERY VEHICLE FOR THE EXTENDED RELEASE OF AN ANTIBIOTIC DRUG
Arun Kant and Monika Datta*
ABSTRACT
The aim of the present work was to develop organo Montmorillonite
(OMt) as a drug delivery vehicle for the extended release of an
antibiotic drug, Metronidazole (MTZ). OMt was synthesised by the
modification of the reported procedure.[01] Interaction of MTZ with
OMt was studied as a function of pH of the aqueous solution of the
drug, contact time of batch extraction and initial concentration of MTZ
in the solution. A maximum loading of MTZ was found to be about
1150 μg/50mg of OMt. The adsorption isotherm was well fitted by the
Langmuir model and was observed to follow pseudo-second-order
kinetics. The synthesized OMt-MTZ complex has been characterized
using various appropriate analytical techniques. The in-vitro release behaviour of the drug
from pure MTZ, the commercially available tablets (Metrogyl and Flagyl) and the synthesized
OMt-MTZ complex was investigated in the simulated gastric and intestinal fluids. In the
present case possible bioavailability for pure MTZ, the commercially available tablets and the
OMt-MTZ complex has been calculated from the in- vitro drug release data and it has been
observed that, compared to the pure MTZ and the commercially available tablets performance
of the synthesised OMt-MTZ complex has not only been found superior in terms of probable %
bioavailability but also in terms of availability of the drug in the system for a longer period of time.
Keywords: Montmorillonite, PF68, Adsorption, Isotherm, Kinetics and extended release.
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