FORMULATION AND IN VITRO EVALUATION OF MUCOADHESIVE BUCCAL TABLET OF LOSARTAN POTASSIUM USING SYNTHETIC AND NATURAL POLYMERS
Raut D.B., Sakhare R.S. *, Kankudte A.D., Muli P.N, Bharkad V.B.
Abstract
The objective of this study was to develop mucoadhesive buccal tablets
of Losartan Porassium using both Synthetic and Natural mucoadhesive
polymers and evaluate results of both polymers. Losartan Potassium is
Angiotensin receptor blocker having short biological half-life (2hr),
high first-pass metabolism and poor oral bioavailability (33%), hence
an ideal candidate for buccal delivery system. The buccal tablets of
150 mg were prepared by using synthetic (Carbopol 934p as primary
and HPMC K15M and SCMC as secondary polymer) and natural
polymers (Sodium Alginate as primary and Guar Gum and Xanthan
Gum as secondary polymers) separately in various concentrations by
direct compression method, eight batches were prepared. Estimation of
Losartan potassium was carried out spectrophotometrically at 205 nm. FTIR spectroscopy
method revealed that there was no interaction between Losartan potassium and polymers. The
tablets were evaluated for hardness, thickness, weight variation, friability, drug content,
surface pH, swelling index, in vitro drug release, mucoadhesive strength and in vitro
Residence time. Among synthetic polymers FS2 and among natural polymers FX2 batches
showed better results. Data of in-vitro release from tablets were fed into kinetic models (Zero
order, first order, Higuchi and Korsmeyer-Peppas models) to explain release profiles. The
optimized formulations showed zero order release.
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