Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/1632
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dc.contributor.authorParida, P-
dc.contributor.authorBehera, Ajit-
dc.contributor.authorSwain, S K-
dc.contributor.authorMishra, S C-
dc.date.accessioned2012-02-27T09:54:37Z-
dc.date.available2012-02-27T09:54:37Z-
dc.date.issued2011-12-
dc.identifier.citationNational Conference on Processing and Characterization of Materials (NCPCM-2011), Department of Metallurgical & Materials Engineering, 2-3 December 2011, National Institute of Technology, Rourkelaen
dc.identifier.urihttp://hdl.handle.net/2080/1632-
dc.descriptionCopyright belongs to proceeding publisheren
dc.description.abstractNanoparticles are widely due as sustained drug delivery system. Due to their smaller size of controlled drug release potential, targeting ability, enhancement of therapeutic efficacy and reduction of toxicity. Nifedipine one of the calcium channel blocker use for the management of hypertension. Spray drier technique develops Nifedipine loaded nanoparticle. Primary superimulsion phase contains Drug (Nifedipine), Polymer (Ethylcellulose) & suitable non-aqueous Solvent (Dichloromethane) which are sprayed over secondary phase containing aqueous solvent with dispersing polymers (PVA). Formation of films on the surface of secondary phase dried, sieved & forward to spectroscopic analysis. FTIR spectrometer as an analytical tool shows the final formulation retains its chemical groups with nucleus (dihydropyridine) indicates no fluctuation at drug stability. DSC study shows the glass transition remains likely constanten
dc.format.extent245364 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoen-
dc.subjectNanoparticlesen
dc.subjectDrug Deliveryen
dc.subjectNifedipineen
dc.subjectSpray drier techniqueen
dc.titleCharacterisation of Nanoparticle through SEM, FTIR & DSCen
dc.typeArticleen
Appears in Collections:Conference Papers

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