Title:Exploration of Neem Gum, Acrylamide Grafted Neem Gum and Carboxymethylated Neem Gum as Retardant in Tablet Formulation
Volume: 16
Issue: 9
Author(s): Rishabha Malviya*
Affiliation:
- Polymer Science Laboratory, Department of Pharmacy, School of Medical & Allied Sciences, Galgotias University, Greater Noida U.P.,India
Keywords:
Binding agent, carboxymethylated polymer, grafted copolymer, neem gum, retardant, tablet.
Abstract:
Background: In the previous study, investigators have synthesized acrylamide grafted and
carboxymethylated derivatives of neem gum and evaluated their potential in the formulation of nanoparticles.
In continuation of previous work, authors have evaluated neem gum polysaccharide (NGP),
acrylamide grafted neem gum polysaccharide (NGP-g-Am) and carboxymethylated neem gum polysaccharide
(CMNGP) as binding agent in the tablet dosage form.
Methods: Diclofenac sodium was used as a model drug while microcrystalline cellulose and talc
were used as excipient in the preparation of granules employing wet granulation technique. NGP,
NGP-g-Am and CMNGP were utilized as binding agent in the preparation of granules. Prepared
granules were characterized for various pre-compression and post-compression parameters.
Results and Discussion: Binding agents were used in the concentration of 4-24%w/w. NGP incorporated
granules showed more bulk density and lower values of tapped density, Carr’s index, bulkiness,
Hausner’s ratio and angle of repose as compared to NGP-g-Am consisting granules. NGP-g-Am consisting
tablets showed more hardness and zero friability as compared to NGP based tablets. Drug
content was found lower for the tablets having grafted polymer in place of NGP. CMNGP were also
utilized to prepare granules but granules were not be able to compress keeping all the compacting parameters
same as used in the case of NGP and NGP-g-Am consisting granules. NGP and NGP-g-Am
were able to sustain drug release up to 6 and 8 h, respectively.
Conclusion: It can be concluded that NGP-g-Am induces better properties when used as a binder in
the tablet formulation than native polymer, while CMNGP cannot be utilized as a binding agent in
the preparation of a tablet.