2012
DOI: 10.1016/j.nantod.2012.02.008
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Multiplex targeted in vivo cancer detection using sensitive near-infrared SERS nanotags

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Cited by 168 publications
(142 citation statements)
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“…In comparison with non-targeted NPs, it was shown that the targeted probes were sufficiently distributed at the tumour, but also to the liver and spleen, though mostly avoided accumulation in the brain, kidneys, lungs and muscle. Other in vivo studies include multiplex SERS probes for in vivo imaging [341] and using NIRspecific probes [342]. An instrument specifically designed for handling small animals has also been developed for rapid multiplexed SERS imaging using four different Raman reporter particles, with the ability to scan 1 cm 2 in 6 minutes [343].…”
Section: Applicationsmentioning
confidence: 99%
“…In comparison with non-targeted NPs, it was shown that the targeted probes were sufficiently distributed at the tumour, but also to the liver and spleen, though mostly avoided accumulation in the brain, kidneys, lungs and muscle. Other in vivo studies include multiplex SERS probes for in vivo imaging [341] and using NIRspecific probes [342]. An instrument specifically designed for handling small animals has also been developed for rapid multiplexed SERS imaging using four different Raman reporter particles, with the ability to scan 1 cm 2 in 6 minutes [343].…”
Section: Applicationsmentioning
confidence: 99%
“…[13] Further in vivo applications have been demonstrated by Maiti et al [103][104][105] In the first of their in vivo experiments nanotags were injected into a mouse model and successfully imaged using SERS. [103] The only difference being that the antibody functionalised nanotags were actively bound to cancerous cells prior to their introduction, highlighting the opportunity to successfully image the nanotags in vivo even after participation in a disease recognition event.…”
Section: In Vivo Imaging and Disease Detectionmentioning
confidence: 99%
“…[104] In the most recent of their work, the group elegantly demonstrated the selectivity of their targeting nanotags. [105] In this study the xenograft was composed of oral squamous cell carcinoma (OSCC) cells which exhibit a differential level of expression of EGFR and HER2. EGFR receptors are present at a much higher level than HER2 receptors on the surface of the OSCC cells.…”
Section: In Vivo Imaging and Disease Detectionmentioning
confidence: 99%
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“…2,3 Examples for the successful use of the Raman labeling approach are the discrimination of different cell types, viruses, and other lab-on-a-chip applications. [4][5][6][7][8][9] Also in vivo, these SERS-active structures, such as nanorods or nanospheres, have shown the potential to discriminate these labels inside different tissues. 10,11 Gold nanoparticles have been extensively studied as potential SERS contrast agents for cancer diagnosis.…”
Section: Introductionmentioning
confidence: 99%