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dc.contributor.authorShah, Jigar N.-
dc.date.accessioned2015-01-23T05:25:31Z-
dc.date.available2015-01-23T05:25:31Z-
dc.date.issued2013-
dc.identifier.urihttp://hdl.handle.net/123456789/5325-
dc.descriptionPharma Science Monitor, Vol - 4, Isue - 4, Jul-Sept 2013en_US
dc.description.abstractPulmonary route as a targeted drug delivery system cuts the edge over other routes of administration in terms of local, site specific, patient friendly, and needle free drug delivery. Pulmonary route minimizes the systemic toxicity of drugs administered and facilitates accomplishment of optimal drug concentrations at the site of action in asthma and allied pulmonary disorders. Montelukast sodium (MS), a leukotriene receptor antagonist (LTRA) is used for the maintenance therapy of asthma & providing symptomatic relief from seasonal allergies. The objective of the present investigation was to formulate biodegradable polymeric nanoparticles (PNP) for controlled delivery of MS to broncho alveolar tract for management of asthma. To achieve the same, we have hypothesized to prepare drug loaded biodegradable and biocompatible nanoparticles using PLGA by solvent evaporation method which leads to long term site specific controlled release of the encapsulated drug over the treatment period in management of asthma. The prepared Montelukast sodium (MS) loaded PLGA nanoparticles were evaluated on the basis of particle size, zeta potential, % entrapment efficiency (%EE), Scanning Electron Microscopy analysis, In-vitro Drug release study.en_US
dc.publisherhttp://www.pharmasm.com/en_US
dc.relation.ispartofseriesIPFP0133;-
dc.subjectMontelukast Sodium (MS)en_US
dc.subjectPolymeric Nanoparticlesen_US
dc.subjectPulmonary Drug deliveryen_US
dc.subjectPLGA (poly lactic-co-glycolic acid)en_US
dc.titleMontelukast Sodium (MS), Polymeric Nanoparticles, Pulmonary Drug delivery, PLGA (poly lactic-co-glycolic acid)en_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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