dc.contributor.author | Das, Sathi | |
dc.contributor.author | Tinguely, Jean-Claude | |
dc.contributor.author | Obuobi, Sybil Akua Okyerewa | |
dc.contributor.author | Skalko Basnet, Natasa | |
dc.contributor.author | Saxena, Kanchan | |
dc.contributor.author | Ahluwalia, Balpreet Singh | |
dc.contributor.author | Singh Mehta, Dalip | |
dc.date.accessioned | 2024-09-25T07:16:08Z | |
dc.date.available | 2024-09-25T07:16:08Z | |
dc.date.issued | 2024-03-12 | |
dc.description.abstract | Programmable 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.citation | Das, 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):2293-2307 | en_US |
dc.identifier.cristinID | FRIDAID 2253944 | |
dc.identifier.doi | 10.1364/BOE.517471 | |
dc.identifier.issn | 2156-7085 | |
dc.identifier.uri | https://hdl.handle.net/10037/34849 | |
dc.language.iso | eng | en_US |
dc.publisher | Optica Publishing Group | en_US |
dc.relation.journal | Biomedical Optics Express | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2024 Optica Publishing Group | en_US |
dc.title | Plasmonic nano-bowls for monitoring intra-membrane changes in liposomes, and DNA-based nanocarriers in suspension | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |