Formulation Development And Evaluation Of Nanosponges For Topical Application

dc.contributor.guideNagoba Shivappa N.
dc.coverage.spatialNanosponges
dc.creator.researcherShaikh Nasheer Shadulla
dc.date.accessioned2022-12-12T06:00:54Z
dc.date.available2022-12-12T06:00:54Z
dc.date.awarded2022
dc.date.completed2022
dc.date.registered2017
dc.description.abstractAtopic dermatitis is a hyperproliferative, autoimmune skin disorder. Regardless of the newlineavailability of drugs and advances in therapies, no fast cure is seen in atopic dermatitis newlinepatients. Drugs available for atopic dermatitis treatment have several disadvantages. To newlineovercome this, Nanotechnologically prepared (nanosponges) drug therapy has been practiced newlinewhich has several advantages in atopic dermatitis treatment. newlineNanosponges are nanosized microscopic particles with wide cavities, during which an newlineoversized sort of substances may be encapsulated. These particles possess the flexibility to newlinehold each lipotropic and deliquescent substance and thereby raising the solubility of poorly newlinewater-soluble molecules. Medicine encapsulated inside the nanosponges pores secures newlinepremature destruction and stability of the drug is increased. newlinePresent study aims to formulate Crisaborole-loaded nanosponges utilizing a variety of newlinepolymers for anti-inflammatory research and to ensure a consistent and predictable release of newlinethe medication. The negative effects of this formulation were decreased, as were the newlinefrequency of dosage and the dose. newlineObjective newlineTo formulate nanosponges (NS) and nanosponges based topical hydrogel gels of for newlinefacilitated treatment of atopic dermatitis newlineMethod newlineNS were prepared using polymers ethyl cellulose and HPMC K35 by emulsion solvent newlinediffusion method. Full Factorial design (32) (FFD) was constructed in a fully randomized newlinemanner to formulate and evaluate all nine possible experimental runs. Detailed evaluation newlinestudies for NS and optimized NS were conducted. Optimized nanosponges were incorporated newlinein topical hydrogels. Also, factorial design (32) in a fully randomized manner was constructed newlineto formulate hydrogels and evaluate all nine possible experimental runs. Detailed evaluation newlinestudies for nanosponges based hydrogel and optimized NS based hydrogels were conducted. newlineIn vivo animal studies were also done for optimized formulation. newlineResults newlineThe physical and chemical characteristics displayed by the prepared NS (CF1-C
dc.description.note
dc.format.accompanyingmaterialNone
dc.format.dimensions
dc.format.extent207p
dc.identifier.urihttp://hdl.handle.net/10603/424302
dc.languageEnglish
dc.publisher.institutionDepartment of Pharmacy
dc.publisher.placeNanded
dc.publisher.universitySwami Ramanand Teerth Marathwada University
dc.relation196b
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 Evaluation Of Nanosponges For Topical Application
dc.title.alternative
dc.type.degreePh.D.

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