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dc.contributor.authorDas, Sathi
dc.contributor.authorTinguely, Jean-Claude
dc.contributor.authorObuobi, Sybil Akua Okyerewa
dc.contributor.authorSkalko Basnet, Natasa
dc.contributor.authorSaxena, Kanchan
dc.contributor.authorAhluwalia, Balpreet Singh
dc.contributor.authorSingh Mehta, Dalip
dc.date.accessioned2024-09-25T07:16:08Z
dc.date.available2024-09-25T07:16:08Z
dc.date.issued2024-03-12
dc.description.abstractProgrammable nanoscale carriers, such as liposomes and DNA, are readily being explored for personalized medicine or disease prediction and diagnostics. The characterization of these nanocarriers is limited and challenging due to their complex chemical composition. Here, we demonstrate the utilization of surface-enhanced Raman spectroscopy (SERS), which provides a unique molecular fingerprint of the analytes while reducing the detection limit. In this paper, we utilize a silver coated nano-bowl shaped polydimethylsiloxane (PDMS) SERS substrate. The utilization of nano-bowl surface topology enabled the passive trapping of particles by reducing mobility, which results in reproducible SERS signal enhancement. The biological nanoparticles’ dwell time in the nano-trap was in the order of minutes, thus allowing SERS spectra to remain in their natural aqueous medium without the need for drying. First, the geometry of the nano-traps was designed considering nanosized bioparticles of 50-150 nm diameter. Further, the systematic investigation of maximum SERS activity was performed using rhodamine 6 G as a probe molecule. The potential of the optimized SERS nano-bowl is shown through distinct spectral features following surface- (polyethylene glycol) and bilayer- (cholesterol) modification of empty liposomes of around 140 nm diameter. Apart from liposomes, the characterization of the highly crosslinked DNA specimens of only 60 nm in diameter was performed. The modification of DNA gel by liposome coating exhibited unique signatures for nitrogenous bases, sugar, and phosphate groups. Further, the unique sensitivity of the proposed SERS substrate displayed distinct spectral signatures for DNA micelles and drug-loaded DNA micelles, carrying valuable information to monitor drug release. In conclusion, the findings of the spectral signatures of a wide range of molecular complexes and chemical morphology of intra-membranes in their natural state highlight the possibilities of using SERS as a sensitive and instantaneous characterization alternative.en_US
dc.identifier.citationDas, Tinguely, Obuobi, Skalko Basnet, Saxena, Ahluwalia, Singh Mehta. Plasmonic nano-bowls for monitoring intra-membrane changes in liposomes, and DNA-based nanocarriers in suspension. Biomedical Optics Express. 2024;15(4):2293-2307en_US
dc.identifier.cristinIDFRIDAID 2253944
dc.identifier.doi10.1364/BOE.517471
dc.identifier.issn2156-7085
dc.identifier.urihttps://hdl.handle.net/10037/34849
dc.language.isoengen_US
dc.publisherOptica Publishing Groupen_US
dc.relation.journalBiomedical Optics Express
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2024 Optica Publishing Groupen_US
dc.titlePlasmonic nano-bowls for monitoring intra-membrane changes in liposomes, and DNA-based nanocarriers in suspensionen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US


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