Tissue Engineering And Nanotheranostics

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b2815 Tissue Engineering and Nanotheranostics “9.61x6.69”

174 Tissue Engineering and Nanotheranostics


5.2. Particle Plasmon-Coupled Localized Surface


Plasmon Resonance


Advances in DNA nanotechnology allow us to organize nanoparticles


with specific distance, and this distance change also affects their plas­


monic effect. For example, when two plasmonic particles approach


each other within one particles’ diameter, these particles’ plasmon


couples, resulting in enhancing the electromagnetic field between two


nanoparticles and a visible red­shift in the scattering spectral.


Therefore, DFM and Rayleigh spectroscopy find great applications in


determination of the distance between each other.


5.2.1. Applications in assembles and disassembles


Taking advantage of the color change of AuNPs solution from red to


blue caused by the aggregation of AuNPs,126–128 Fan et al. developed


a series of aptamer sensors to exploit interactions between aptamers


and AuNPs by observing its color change, such as potassium ion­


specific G­quartet probe, T­rich DNA probe, C­rich DNA probe,


anti­ATP aptamer and anticocaine aptamer.129–131 For example, Fan


et al. developed a biosensor assay based on cocaine–AuNPs to identify


cocaine in latent fingerprints (LFPs).^132 Briefly, two pieces of rationally


engineered anticocaine aptamers were attached to different AuNPs.


The presence of cocaine in LFPs, working as a molecular linker,


induces the aggregation of AuNPs by reassembling the two pieces of


aptamers, resulting in green­to­red color change of the scattered light


in DFM images (Fig. 4). This strategy provides a quasi­quantitative


method to identify cocaine loadings in LFPs. Similarly, Long’s group


designed a sensor through the status of AuNPs aggregation to moni­


tor Cu+­catalyzed click reaction at the single­nanoparticle level by


DFM.^133 By contrast, Lee and the coworkers applied a core­satellite


nanoassembled substrate for colorimetric biomolecular detection


through red­to­green changes in the DFM images.^134 In the presence


of target biomolecules, the core­satellite nanoassembled substrate dis­


assembled and a blue shift in the spectrum was demonstrated by


DFM. Furthermore, stepwise peak shifts in LSPR were monitored by

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