Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/643
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dc.contributor.advisorKIKKERI, RAGHAVENDRAen_US
dc.contributor.authorCHERUKURI, KESAVA PHANEENDRAen_US
dc.date.accessioned2016-05-06T11:49:16Z
dc.date.available2016-05-06T11:49:16Z
dc.date.issued2016-05en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/643-
dc.description.abstractThe adhesion of leukocytes to vascular endothelium is a hallmark of the inflammatory process, which play a crucial role in multiple sclerosis (MS), ischemic stroke, and HIV-related dementia. Consequently, diagnoses of this activation are highly desirable. The conventional imaging techniques fail to diagnose the symptom, due to the weak permeability of the molecules through blood brain barrier (BBB). Hence, the delivery of imaging molecules across the BBB is still a major challenging aspect for presymptomatic diagnosis. Herein, we present the design and synthesis of sulfate-lewisx functionalized nanoparticles that allow direct detection of endothelial marker E and P-selectin in acute inflammation. We designed silica-coated iron oxide core, which exhibits superparamagnetic and also provided multiple copies of carbohydrate to increase the avidity during specific carbohydrate-protein interactions. Magnetic resonance imaging studies of these nanoparticles are expected to target E and P selectin in the ischemic brain and potential for translation into the clinic.en_US
dc.language.isoenen_US
dc.subject2016
dc.subjectInflammationen_US
dc.subjectIron nanoparticlesen_US
dc.subjectCarbohydratesen_US
dc.subjectImagingen_US
dc.subjectMRIen_US
dc.titleTargeting Endothelial Inflammation by Superparamagnetic Iron Glyco-Nano Particles.en_US
dc.typeThesisen_US
dc.type.degreeBS-MSen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20111076en_US
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