journal article·2022Open access

SERS tags derived from silver nanoparticles and aryl diazonium salts for cell Raman imaging

Da Li, Philippe Nizard, Delphine Onidas, Aazdine Lamouri, Jean Pinson, Samia Mahouche-Chergui, Kelly Aubertin, Florence Gazeau, Yun Luo, Claire Mangeney

Nanoscale· Volume 14· Issue 4

Abstract

The surface functionalization of silver nanoparticles (NPs) by Raman reporters has stimulated a wide interest in recent years for the design of Surface-Enhanced Raman Spectroscopy (SERS) labels. However, silver NPs are prone to oxidation and aggregation, which strongly limits their applications. The design of stable SERS tags based on Ag NPs still represents a major challenge for Raman bioimaging. We address this issue herein by taking advantage of aryl diazonium salt chemistry to obtain stable Ag NPs functionalized by multifunctional polyaryl layers bearing different Raman reporters (-NO2, -CN, -CCH). The resulting SERS-encoded Ag NPs were characterized by UV-vis absorption, transmission electron microscopy (TEM) and SERS. The formation of multilayers at the surface of Ag NPs gives access to new spectrally distinguishable SERS codes thus broadening the library of available Raman tags. Proof-of-concept Raman imaging experiments were performed on cancer cells (HeLa) after NP uptake, highlighting the large potentials of diazonium salt chemistry to design Ag NPs-based SERS labels for Raman bioimaging.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Advanced biosensing and bioanalysis techniques · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Address Université de Paris, Lab Chim & Biochim Pharmacolog & Toxicol, UMR 8601, F-75006 Paris, France

Université de Paris, ITODYS, UMR 7086, 75013 Paris, France

Université Paris-Est, ICMPE, UMR7182, 94320 Thiais, France

Université de Paris, MSC, CNRS UMR 7057, 75013 Paris, France

Funding

China Scholarship Council · Agence Nationale de la Recherche

References (45)

Show source-provided references
1. Wallace · Analyst · 2020 · 145 · 716210.1039/D0AN01274B ↗
2. Yao · Chem. Rev. · 2014 · 114 · 613010.1021/cr200359p ↗
3. Han · Nanoscale · 2019 · 11 · 79910.1039/C8NR07769J ↗
4. Mousavi · Drug Metab. Rev. · 2020 · 52 · 29910.1080/03602532.2020.1734021 ↗
5. S. A.Maier , Plasmonics: fundamentals and applications , Springer Science & Business Media , 200710.1007/0-387-37825-1 ↗
6. Lee · Trends Anal. Chem. · 2019 · 117 · 5810.1016/j.trac.2019.05.006 ↗
7. Nguyen · Chem. Mater. · 2016 · 28 · 356410.1021/acs.chemmater.6b00230 ↗
8. Ahmad · Chem. Commun. · 2015 · 51 · 967810.1039/C5CC01489A ↗
9. Mosquera · Adv. Funct. Mater. · 2020 · 30 · 190208210.1002/adfm.201902082 ↗
10. Lenzi · ACS Sens. · 2019 · 4 · 112610.1021/acssensors.9b00321 ↗
11. Alvarez-Puebla · Small · 2010 · 6 · 60410.1002/smll.200901820 ↗
12. Wang · Chem. Rev. · 2017 · 117 · 791010.1021/acs.chemrev.7b00027 ↗
13. M.Tabatabaei , D.McRae and F.Lagugné-Labarthet , Recent advances of plasmon-enhanced spectroscopy at bio-Interfaces , in Frontiers of Plasmon Enhanced Spectroscopy , ACS Publications , 2016 , vol. 2 , pp. 183–20710.1021/bk-2016-1246.ch008 ↗
14. Wokaun · Phys. Rev. Lett. · 1982 · 48 · 95710.1103/PhysRevLett.48.957 ↗
15. Mahmoud · J. Phys. Chem. Lett. · 2013 · 4 · 154110.1021/jz4005015 ↗
16. Kolwas · Opto-Electron. Rev. · 2010 · 18 · 42910.2478/s11772-010-0043-6 ↗
17. Battocchio · J. Phys. Chem. C · 2012 · 116 · 1957110.1021/jp305748a ↗
18. Mir-Simon · Chem. Mater. · 2015 · 27 · 95010.1021/cm504251h ↗
19. Wang · Chem. Rev. · 2013 · 113 · 139110.1021/cr300120g ↗
20. Hamon · J. Colloid Interface Sci. · 2018 · 512 · 83410.1016/j.jcis.2017.10.117 ↗
21. Yu · Anal. Chem. · 2019 · 91 · 527010.1021/acs.analchem.9b00038 ↗
22. Vericat · Chem. Soc. Rev. · 2010 · 39 · 180510.1039/b907301a ↗
23. Walia · Phys. Chem. Chem. Phys. · 2018 · 20 · 23810.1039/C7CP07024A ↗
24. Zhuo · Chem. Mater. · 2020 · 32 · 587910.1021/acs.chemmater.0c01995 ↗
25. Hetemi · Biosensors · 2020 · 10 · 410.3390/bios10010004 ↗
26. Berisha · Langmuir · 2017 · 33 · 873010.1021/acs.langmuir.7b01371 ↗
27. Bouriga · Chem. Mater. · 2013 · 25 · 9010.1021/cm3032994 ↗
28. Nguyen · Chem. Commun. · 2017 · 53 · 1136410.1039/C7CC05974D ↗
29. Nguyen · Nanoscale · 2016 · 8 · 863310.1039/C6NR00744A ↗
30. Pinson · Chem. Soc. Rev. · 2005 · 34 · 42910.1039/b406228k ↗
31. Zhao · Chem. Mater. · 2017 · 29 · 713110.1021/acs.chemmater.7b01106 ↗
32. Cao · ACS Appl. Mater. Interfaces · 2017 · 9 · 503110.1021/acsami.6b16108 ↗
33. Chen · Nanoscale · 2019 · 11 · 1126210.1039/C9NR02543J ↗
34. Kalachyova · ChemistryOpen · 2017 · 6 · 25410.1002/open.201600159 ↗
35. Luo · Chem. Commun. · 2020 · 56 · 682210.1039/D0CC02842H ↗
36. Dai · Biomaterials · 2016 · 83 · 3710.1016/j.biomaterials.2016.01.011 ↗
37. Nguyen · ACS Omega · 2017 · 2 · 194710.1021/acsomega.7b00394 ↗
38. Therien · Nanoscale Adv. · 2021 · 3 · 250110.1039/D0NA00862A ↗
39. Zeng · Appl. Mater. Today · 2019 · 15 · 43110.1016/j.apmt.2019.03.005 ↗
40. Austin · J. Am. Chem. Soc. · 2011 · 133 · 1759410.1021/ja207807t ↗
41. Emeline · FEBS Lett. · 2019 · 593 · 198310.1002/1873-3468.13472 ↗
42. Laurentius · ACS Nano · 2011 · 5 · 421910.1021/nn201110r ↗
43. Mirkhalaf · J. Am. Chem. Soc. · 2006 · 128 · 740010.1021/ja058687g ↗
44. Troian-Gautier · Chem. Commun. · 2016 · 52 · 1049310.1039/C6CC04534K ↗
45. Supur · Anal. Chem. · 2017 · 89 · 646310.1021/acs.analchem.7b00362 ↗