Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7762
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dc.contributor.authorBHOGE, PREETI RAVINDRAen_US
dc.contributor.authorMARDHEKAR, SANDHYAen_US
dc.contributor.authorTORASKAR, SURAJen_US
dc.contributor.authorSUBRAMANI, BALAMURUGANen_US
dc.contributor.authorKIKKERI, RAGHAVENDRAen_US
dc.date.accessioned2023-04-27T10:11:18Z-
dc.date.available2023-04-27T10:11:18Z-
dc.date.issued2022-12en_US
dc.identifier.citationACS Applied Bio Materials, 5(12), 5675–5681.en_US
dc.identifier.issn2576-6422en_US
dc.identifier.urihttps://doi.org/10.1021/acsabm.2c00716en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7762-
dc.description.abstractNanotechnology-based vaccine development necessitates understanding the crucial biophysical properties of nanostructures that alter immune responses. In this study, we demonstrate the synergistic effect of gold nanoparticles (AuNPs) shapes with toll-like receptor (TLR) agonists in immune modulation activity. Our results showed that CpG- and imidazoquinoline-conjugated rod-shaped AuNPs display relatively fast uptake by bone marrow-derived macrophage cells but exhibit poor immunogenic responses compared to their spherical and star-shaped AuNP counterparts. Surprisingly, star-shaped AuNPs exhibited intense pro-inflammatory cytokine secretion. Further mechanistic studies showed that star-shaped AuNPs were abundantly localized in the late endosome and lysosomal regions, whereas rod-shaped AuNPs were majorly sequestered in the mitochondrial region. These findings reveal that the shape of the nanostructures plays a pivotal role in driving the adjuvant molecules toward their receptors and altering immune responses.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectGold nanoparticlesen_US
dc.subjectToll-like receptoren_US
dc.subjectImmunomodulationen_US
dc.subjectCpGen_US
dc.subjectImidazoquinolineen_US
dc.subject2022en_US
dc.titlePairing Nanoparticles Geometry with TLR Agonists to Modulate Immune Responses for Vaccine Developmenten_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleACS Applied Bio Materialsen_US
dc.publication.originofpublisherForeignen_US
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