Bright Near-Infrared-Emitting Organic Nanoparticles Based on Small-Molecule Ionic Isolation Lattices
Source abstract
Abstract
Near infrared (NIR) fluorescence imaging has received significant attention. However, it remains challenging to develop NIR emitters with a high brightness. Herein, we report a supramolecular approach to formulate NIR fluorescent molecular nanoparticles from cationic NIR fluorophores and cyanostar receptors using their charge-by-charge packing in small-molecule ionic isolation lattices (SMILES). Four types of cationic NIR fluorophores were successfully used to form NIR SMILES nanoparticles. The NIR nanoparticles show fluorescence quantum yields (FQYs) of ∼1% and are over 60 times brighter than those of single fluorophores. Four different surface capping agents were examined and found to generate stable nanoparticles with slight changes in FQY. Femtosecond transient absorption spectroscopy reveals the low FQY originates from nonradiative decay introduced by interfluorophore coupling. Introduction of inert molecular cations into the SMILES structures raises the FQY to ∼7%. The NIR SMILES nanoparticles were used for in vivo tumor imaging and are thus promising for bioimaging applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Nanocluster Synthesis and Applications · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nano-Science Center and Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark
Department of Clinical Physiology, Nuclear Medicine & PET and Cluster for Molecular Imaging, Department of Biomedical Sciences, Rigshospitalet
University of Copenhagen
Department of Chemical Physics and NanoLund
Lund University
Department of Chemistry
Indiana University
Funding
Danmarks Frie Forskningsfond · Novo Nordisk Fonden · China Scholarship Council · National Science Foundation · Lundbeck Foundation
References (72)
Show source-provided references
1. 10.1186/s12951-022-01648-710.1186/s12951-022-01648-7 ↗
2. 10.1038/nrm253110.1038/nrm2531 ↗
3. 10.1118/1.156897710.1118/1.1568977 ↗
4. 10.1039/C6CS00908E10.1039/C6CS00908E ↗
5. 10.1002/adom.20160044610.1002/adom.201600446 ↗
6. 10.1016/j.cbpa.2003.08.00710.1016/j.cbpa.2003.08.007 ↗
7. 10.1021/acs.nanolett.5c0175410.1021/acs.nanolett.5c01754 ↗
8. 10.1021/cm202836710.1021/cm2028367 ↗
9. 10.34133/research.053410.34133/research.0534 ↗
10. 10.1007/s44211-025-00735-710.1007/s44211-025-00735-7 ↗
11. 10.2174/010929867336247725022611523810.2174/0109298673362477250226115238 ↗
12. 10.1038/nnano.2009.32610.1038/nnano.2009.326 ↗
13. 10.1002/jso.2194310.1002/jso.21943 ↗
14. 10.1117/1.JBO.26.3.03090110.1117/1.JBO.26.3.030901 ↗
15. 10.1039/D1NA00649E10.1039/D1NA00649E ↗
16. 10.1021/acsmaterialslett.0c0015710.1021/acsmaterialslett.0c00157 ↗
17. 10.1016/j.ccr.2025.21655110.1016/j.ccr.2025.216551 ↗
18. 10.1021/acsabm.4c0013710.1021/acsabm.4c00137 ↗
19. 10.1016/j.dyepig.2024.11204410.1016/j.dyepig.2024.112044 ↗
20. 10.1002/asia.20200134810.1002/asia.202001348 ↗
21. 10.1002/adhm.20190026010.1002/adhm.201900260 ↗
22. 10.1002/wnan.7710.1002/wnan.77 ↗
23. 10.1002/adhm.20200128910.1002/adhm.202001289 ↗
24. 10.1016/j.ccr.2024.21637910.1016/j.ccr.2024.216379 ↗
25. Matsumura Y. · Cancer Res. · 1986 · 46 · 6387
26. Alasvand N. · 2017 · 24510.1016/B978-0-323-52725-5.00013-7 ↗
27. 10.1021/nn800448r10.1021/nn800448r ↗
28. 10.1021/acsmaterialslett.0c0007810.1021/acsmaterialslett.0c00078 ↗
29. 10.1021/acsami.7b1229210.1021/acsami.7b12292 ↗
30. 10.1002/adfm.20180515710.1002/adfm.201805157 ↗
31. 10.1021/jacs.8b0584010.1021/jacs.8b05840 ↗
32. 10.1038/s41566-017-0001-710.1038/s41566-017-0001-7 ↗
33. 10.1002/smll.20170158210.1002/smll.201701582 ↗
34. 10.1021/acsnano.0c0150510.1021/acsnano.0c01505 ↗
35. 10.1021/acsnano.0c0634810.1021/acsnano.0c06348 ↗
36. 10.1039/b105159h10.1039/b105159h ↗
37. 10.1002/adma.20180106510.1002/adma.201801065 ↗
38. 10.1002/adom.20200002710.1002/adom.202000027 ↗
39. 10.1002/anie.20200084510.1002/anie.202000845 ↗
40. 10.1016/j.cej.2025.16069210.1016/j.cej.2025.160692 ↗
41. 10.1002/anie.20200752510.1002/anie.202007525 ↗
42. 10.1002/adma.20170685610.1002/adma.201706856 ↗
43. 10.1002/adma.20180076610.1002/adma.201800766 ↗
44. 10.1002/anie.20201242710.1002/anie.202012427 ↗
45. 10.1021/acsnano.1c0892810.1021/acsnano.1c08928 ↗
46. 10.1016/j.partic.2022.06.00110.1016/j.partic.2022.06.001 ↗
47. 10.1016/j.chempr.2020.06.02910.1016/j.chempr.2020.06.029 ↗
48. 10.1002/anie.20210095010.1002/anie.202100950 ↗
49. 10.1038/nchem.166810.1038/nchem.1668 ↗
50. 10.1002/anie.20100635610.1002/anie.201006356 ↗
51. 10.1002/smll.20150339610.1002/smll.201503396 ↗
52. 10.1039/D2CS00464J10.1039/D2CS00464J ↗
53. 10.1021/acs.analchem.3c0195810.1021/acs.analchem.3c01958 ↗
54. 10.1021/acsphotonics.3c0154710.1021/acsphotonics.3c01547 ↗
55. 10.1021/jacs.2c0854010.1021/jacs.2c08540 ↗
56. 10.1021/acsanm.2c0189910.1021/acsanm.2c01899 ↗
57. 10.1039/D3SC05496A10.1039/D3SC05496A ↗
58. 10.1002/anie.20241232010.1002/anie.202412320 ↗
59. 10.1039/D4SC01352B10.1039/D4SC01352B ↗
60. 10.1002/anie.20170473910.1002/anie.201704739 ↗
61. 10.1039/b904381k10.1039/b904381k ↗
62. 10.1016/S0169-4332(00)00834-510.1016/S0169-4332(00)00834-5 ↗
63. 10.1039/D0SC05431C10.1039/D0SC05431C ↗
64. 10.1002/adom.20230167110.1002/adom.202301671 ↗
65. 10.1002/smll.20070059510.1002/smll.200700595 ↗
66. 10.1021/acs.chemrev.1c0048410.1021/acs.chemrev.1c00484 ↗
67. 10.1007/s11307-022-01736-y10.1007/s11307-022-01736-y ↗
68. 10.1038/s41467-023-40324-810.1038/s41467-023-40324-8 ↗
69. 10.7602/jmis.2021.24.3.11310.7602/jmis.2021.24.3.113 ↗
70. 10.23736/S0390-5616.19.04753-210.23736/S0390-5616.19.04753-2 ↗
71. 10.1039/c8pp00064f10.1039/c8pp00064f ↗
72. 10.1371/journal.pone.014742810.1371/journal.pone.0147428 ↗