FORMULATION DEVELOPMENT AND IN-VITRO EVALUATION OF APREMILAST FLOATING TABLET Authors: Rathi SG , PATEL DJ , CHAUDHARY AB, VAGHELA SS, VYAS SS AND KAMANI KR
ABSTRACT
The objective of present work was to prepare a novel sustained release floating formulation
of Apremilast for treatment of psoriatic arthritis. Pre-formulation study had carried out for
possible drug and excipient interactions. Floating tablets were prepared using HPMC K4M
and Carbopol 934 as polymer, Sodium bicarbonate and Citric Acid as gas generating agent,
Starlac as diluents and PVPK 30 used as dry binder. Tablet was prepared by direct
compression method. Initial formulation started with single polymers low to higher
concentration and then combination of the polymers. It was found that combination of
polymer gives good release retarding action in formulation and release the drug for 12 hr
which is desire for formulation. Simultaneously gas generating agent was optimized by
changing its concentration. Formulations were evaluated for Pre-compression parameter and
post compression parameter like Thickness, Hardness, Friability, and Floating lag Time,
Floating Time, Swelling Characteristics, In vitro dissolution studies, Drug release kinetic
study from the results it was concluded that F10 formulation was good release profile than
the others. F10 formulation floated up to 12 hrs and floating time is within a min so F10 is
optimized formulation.
Keyword: Floating Tablet, GRDDS, Apremilast, Psoriasis, Sustain release Publication date: 01/08/2022 https://ijbpas.com/pdf/2022/August/MS_IJBPAS_2022_6279.pdfDownload PDFhttps://doi.org/10.31032/IJBPAS/2022/11.8.6279