Label-free biosensing with singular-phase-enhanced lateral position shift based on atomically thin plasmonic nanomaterials.
Journal
Light, science & applications
ISSN: 2047-7538
Titre abrégé: Light Sci Appl
Pays: England
ID NLM: 101610753
Informations de publication
Date de publication:
01 Jan 2024
01 Jan 2024
Historique:
received:
02
07
2023
accepted:
24
11
2023
revised:
18
11
2023
medline:
2
1
2024
pubmed:
2
1
2024
entrez:
31
12
2023
Statut:
epublish
Résumé
Rapid plasmonic biosensing has attracted wide attention in early disease diagnosis and molecular biology research. However, it was still challenging for conventional angle-interrogating plasmonic sensors to obtain higher sensitivity without secondary amplifying labels such as plasmonic nanoparticles. To address this issue, we developed a plasmonic biosensor based on the enhanced lateral position shift by phase singularity. Such singularity presents as a sudden phase retardation at the dark point of reflection from resonating plasmonic substrate, leading to a giant position shift on reflected beam. Herein, for the first time, the atomically thin layer of Ge
Identifiants
pubmed: 38161210
doi: 10.1038/s41377-023-01345-6
pii: 10.1038/s41377-023-01345-6
doi:
Types de publication
Journal Article
Langues
eng
Pagination
2Informations de copyright
© 2024. The Author(s).
Références
Siegel, R. L. et al. Cancer statistics, 2022. CA: A Cancer J. Clin. 72, 7–33 (2022).
Adler, O. et al. Reciprocal interactions between innate immune cells and astrocytes facilitate neuroinflammation and brain metastasis via lipocalin-2. Nat. Cancer 4, 401–418 (2023).
doi: 10.1038/s43018-023-00519-w
Cheng, C. P. et al. Gremlin1 is a therapeutically targetable FGFR1 ligand that regulates lineage plasticity and castration resistance in prostate cancer. Nat. Cancer 3, 565–580 (2022).
doi: 10.1038/s43018-022-00380-3
Lima, L. G. et al. Tumor microenvironmental cytokines bound to cancer exosomes determine uptake by cytokine receptor-expressing cells and biodistribution. Nat. Commun. 12, 3543 (2021).
doi: 10.1038/s41467-021-23946-8
Au, L. et al. Cytokine release syndrome in a patient with colorectal cancer after vaccination with BNT162b2. Nat. Med. 27, 1362–1366 (2021).
doi: 10.1038/s41591-021-01387-6
Lippitz, B. E. Cytokine patterns in patients with cancer: a systematic review. Lancet Oncol. 14, e218–e228 (2013).
doi: 10.1016/S1470-2045(12)70582-X
Kanchanawong, P. & Calderwood, D. A. Organization, dynamics and mechanoregulation of integrin-mediated cell–ECM adhesions. Nat. Rev. Mol. Cell Biol. 24, 142–161 (2023).
doi: 10.1038/s41580-022-00531-5
Aksorn, N. & Chanvorachote, P. Integrin as a molecular target for anti-cancer approaches in lung cancer. Anticancer Res. 39, 541–548 (2019).
doi: 10.21873/anticanres.13146
Kechagia, J. Z., Ivaska, J. & Roca-Cusachs, P. Integrins as biomechanical sensors of the microenvironment. Nat. Rev. Mol. Cell Biol. 20, 457–473 (2019).
doi: 10.1038/s41580-019-0134-2
Anker, J. N. et al. Biosensing with plasmonic nanosensors. Nat. Mater. 7, 442–453 (2008).
doi: 10.1038/nmat2162
Zeng, S. et al. Graphene–gold metasurface architectures for ultrasensitive plasmonic biosensing. Adv. Mater. 27, 6163–6169 (2015).
doi: 10.1002/adma.201501754
Zeng, S. W. et al. Nanomaterials enhanced surface plasmon resonance for biological and chemical sensing applications. Chem. Soc. Rev. 43, 3426–3452 (2014).
doi: 10.1039/c3cs60479a
Sreekanth, K. V. et al. Excitation of surface electromagnetic waves in a graphene-based Bragg grating. Sci. Rep. 2, 737 (2012).
doi: 10.1038/srep00737
Szymanska, B. et al. An immunosensor for the determination of carcinoembryonic antigen by Surface Plasmon Resonance imaging. Anal. Biochem. 609, 113964 (2020).
doi: 10.1016/j.ab.2020.113964
Vashist, S. K., Schneider, E. M. & Luong, J. H. Surface plasmon resonance-based immunoassay for human C-reactive protein. Analyst 140, 4445–4452 (2015).
doi: 10.1039/C5AN00690B
Beeg, M. et al. A surface plasmon resonance-based assay to measure serum concentrations of therapeutic antibodies and anti-drug antibodies. Sci. Rep. 9, 2064 (2019).
doi: 10.1038/s41598-018-37950-4
Zeng, Y. J. et al. Phase interrogation SPR sensing based on white light polarized interference for wide dynamic detection range. Opt. Express 28, 3442–3450 (2020).
doi: 10.1364/OE.382242
Li, M. C. et al. A simple phase-sensitive surface plasmon resonance sensor based on simultaneous polarization measurement strategy. Sensors 21, 7615 (2021).
doi: 10.3390/s21227615
Goos, F. & Hänchen, H. Ein neuer und fundamentaler Versuch zur Totalreflexion. Ann. Phys. 436, 333–346 (1947).
doi: 10.1002/andp.19474360704
Schwefel, H. G. L. et al. Direct experimental observation of the single reflection optical Goos-Hänchen shift. Opt. Lett. 33, 794–796 (2008).
doi: 10.1364/OL.33.000794
Olaya, C. M. et al. Angular Goos–Hänchen shift sensor using a gold film enhanced by surface plasmon resonance. J. Phys. Chem. A 125, 451–458 (2021).
doi: 10.1021/acs.jpca.0c09373
Gilles, H., Girard, S. & Hamel, J. Simple technique for measuring the Goos–Hänchen effect with polarization modulation and a position-sensitive detector. Opt. Lett. 27, 1421–1423 (2002).
doi: 10.1364/OL.27.001421
Artmann, K. Berechnung der seitenversetzung des totalreflektierten strahles. Ann. Phys. 437, 87–102 (1948).
doi: 10.1002/andp.19484370108
Wild, W. J. & Giles, C. L. Goos-Hänchen shifts from absorbing media. Phys. Rev. A 25, 2099–2101 (1982).
doi: 10.1103/PhysRevA.25.2099
Sreekanth, K. V. et al. Biosensing with the singular phase of an ultrathin metal-dielectric nanophotonic cavity. Nat. Commun. 9, 369 (2018).
doi: 10.1038/s41467-018-02860-6
Malassis, L. et al. Topological darkness in self‐assembled plasmonic metamaterials. Adv. Mater. 26, 324–330 (2014).
doi: 10.1002/adma.201303426
Kravets, V. G. et al. Singular phase nano-optics in plasmonic metamaterials for label-free single-molecule detection. Nat. Mater. 12, 304–309 (2013).
doi: 10.1038/nmat3537
Tselikov, G. I. et al. Topological darkness: how to design a metamaterial for optical biosensing with ultrahigh sensitivity. ACS Nano 17, 19338–19348 (2023).
doi: 10.1021/acsnano.3c06655
West, P. R. et al. Searching for better plasmonic materials. Laser Photon. Rev. 4, 795–808 (2010).
doi: 10.1002/lpor.200900055
de Bruijn, H. E., Kooyman, R. P. H. & Greve, J. Choice of metal and wavelength for surface-plasmon resonance sensors: some considerations. Appl. Opt. 31, 440_1–442_1 (1992).
doi: 10.1364/AO.31.0440_1
Sreekanth, K. V., Han, S. & Singh, R. Ge
doi: 10.1002/adma.201706696
Wu, F. et al. Giant enhancement of the Goos-Hänchen shift assisted by quasibound states in the continuum. Phys. Rev. Appl. 12, 014028 (2019).
doi: 10.1103/PhysRevApplied.12.014028
Zhou, X. et al. Precise control of positive and negative Goos-Hänchen shifts in graphene. Carbon 149, 604–608 (2019).
doi: 10.1016/j.carbon.2019.04.064
Haynes, W. M., Lide, D. R. & Bruno, T. J. CRC Handbook of Chemistry and Physics (ed Haynes, W. M.) (CRC Press, 2016).
Kang, J. H. et al. Goos-Hänchen shift and even–odd peak oscillations in edge-reflections of surface polaritons in atomically thin crystals. Nano Lett. 17, 1768–1774 (2017).
doi: 10.1021/acs.nanolett.6b05077
Wang, Y. Y. et al. Targeted sub-attomole cancer biomarker detection based on phase singularity 2D nanomaterial-enhanced plasmonic biosensor. Nano-Micro Lett. 13, 96 (2021).
doi: 10.1007/s40820-021-00613-7
Karawdeniya, B. I. et al. Surface functionalization and texturing of optical metasurfaces for sensing applications. Chem. Rev. 122, 14990–15030 (2022).
doi: 10.1021/acs.chemrev.1c00990
Domínguez, R. A. S., Jiménez, M. Á. D. & Díaz, A. O. Antibody immobilization in zinc oxide thin films as an easy-handle strategy for Escherichia coli detection. ACS Omega 5, 20473–20480 (2020).
doi: 10.1021/acsomega.0c02583
Sheen-Chen, S. M. et al. Serum concentration of tumor necrosis factor in patients with breast cancer. Breast Cancer Res. Treat. 43, 211–215 (1997).
doi: 10.1023/A:1005736712307
Jablonska, E., Piotrowski, L. & Grabowska, Z. Serum Levels of IL-lβ, IL-6, TNF-α, sTNF-RI and CRP in Patients with oral cavity cancer. Pathol. Oncol. Res. 3, 126–129 (1997).
doi: 10.1007/BF02907807
Knüpfer, H. & Preiß, R. Significance of interleukin-6 (IL-6) in breast cancer (review). Breast Cancer Res. Treat. 102, 129–135 (2007).
doi: 10.1007/s10549-006-9328-3
Yanagawa, H. et al. Serum levels of interleukin 6 in patients with lung cancer. Br. J. Cancer 71, 1095–1098 (1995).
doi: 10.1038/bjc.1995.212
Zhang, K. & Chen, J. F. The regulation of integrin function by divalent cations. Cell Adhes. Migr. 6, 20–29 (2012).
doi: 10.4161/cam.18702
Hughes, P. E. & Pfaff, M. Integrin affinity modulation. Trends Cell Biol. 8, 359–364 (1998).
doi: 10.1016/S0962-8924(98)01339-7
Sun, Z. Q., Costell, M. & Fässler, R. Integrin activation by talin, kindlin and mechanical forces. Nat. Cell Biol. 21, 25–31 (2019).
doi: 10.1038/s41556-018-0234-9
Yin, X. B. & Hesselink, L. Goos-Hänchen shift surface plasmon resonance sensor. Appl. Phys. Lett. 89, 261108 (2006).
doi: 10.1063/1.2424277
Barth, I. et al. Common-path interferometric label-free protein sensing with resonant dielectric nanostructures. Light Sci. Appl. 9, 96 (2020).
doi: 10.1038/s41377-020-0336-6
Yesilkoy, F. et al. Phase-sensitive plasmonic biosensor using a portable and large field-of-view interferometric microarray imager. Light Sci. Appl. 7, 17152 (2018).
doi: 10.1038/lsa.2017.152
Kabashin, A. V., Kravets, V. G. & Grigorenko, A. N. Label-free optical biosensing: going beyond the limits. Chem. Soc. Rev. 52, 6554–6585 (2023).
doi: 10.1039/D3CS00155E
Treps, N. et al. A quantum laser pointer. Science 301, 940–943 (2003).
doi: 10.1126/science.1086489