Formulation Development and Pharmacological Evaluation of Sustained Release Poly Herbal Formulation for Anti Diabetic Activity

dc.contributor.guideDr. Nitu Singh
dc.coverage.spatial
dc.creator.researcherVinod Kumar
dc.date.accessioned2023-01-19T16:02:07Z
dc.date.available2023-01-19T16:02:07Z
dc.date.awarded2022
dc.date.completed2022
dc.date.registered2018
dc.description.abstractIn the following research Alstonia scholaris, Centella asiatica, Corchorus newlinetrilocularis, and Morinda pubescens leaves were selected for the development of newlinePolyherbal antidiabeticsustained Release Matrix Tablets. All Polyherbal extract newlinedeliver their favourable antidiabetic action under blood glucose level examination newlinefrom the induction of diabetes to the final day of polyherbal extract treatment. newlineWhen comparing diabetic control non-treated animals to all formulations with two newlinedifferent dose regimens (200 andamp; 400 mg/kg), the dose 200 mg/kg of formulation D newlineexhibited a more potent favorable blood glucose reducing effect and other newlinebiochemical parameters. Polyethylene oxide (PEO WSR coagulant), Xanthan gum, newlineand hydroxyl propyl methyl cellulose (HPMC K100 LV) (HPMC K4M) and other newlineexcipients were used to make Poly Herbal Extract (PHE) sustained release tablets newlineutilizing the dry granulation process. The purity of excipients is determined using newlineDSC thermograms. Pre, post-compression, quality control, and dissolution newlineinvestigations were performed on the granules and produced tablets. The newlinecumulative medication release of all of the formulations were compared to that of newlineconventional medicine Diamicron SR newlinetablets.Fromthecumulativedrugreleaseanddrugcontentinvestigation,theHPMC- newline10batchwas chosen as the optimized batch. The IR spectra of a mixture of newlineDicalcium phosphate anhydrous, Maltodextrin, Hydroxy propyl methylcellulose newline(HPMC K100 LV), Hydroxy propyl methylcellulose (HPMC K 4 M), Magnesium newlinestearate in formulation reveal no changes in these key peaks. The peaks in the newlineformulation spectra corresponded to the peaks in the polyherbal extract. The newlinePolyherbal sustained-release tablet formulation employing ingredients was shown newlineto newlinehavethesuperlativedissolvingprofileofpolyherbalextractswhenlikenedtothedischarge newlineoutline newlineofDiamicronSRTablet.Thedissolutionprofileoftheformulationdemonstrated95.1perc newlineentdrug release after 10 hours. Results of present study demonstrated that newlinemethodology successfully employed for formulation
dc.description.note
dc.format.accompanyingmaterialDVD
dc.format.dimensions
dc.format.extent
dc.identifier.urihttp://hdl.handle.net/10603/450213
dc.languageEnglish
dc.publisher.institutionPharmacy
dc.publisher.placeIndore
dc.publisher.universityOriental University
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.titleFormulation Development and Pharmacological Evaluation of Sustained Release Poly Herbal Formulation for Anti Diabetic Activity
dc.title.alternative
dc.type.degreePh.D.

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