journal article·2018-08-28

Bright Near-Infrared Aggregation-Induced Emission Luminogens with Strong Two-Photon Absorption, Excellent Organelle Specificity, and Efficient Photodynamic Therapy Potential

Zheng Zheng, Tianfu Zhang, Haixiang Liu, Yuncong Chen, Ryan T. K. Kwok, Chao Ma, Pengfei Zhang, Herman H. Y. Sung, Ian D. Williams, Jacky W. Y. Lam, Kam Sing Wong, Ben Zhong Tang

ACS Nano· Volume 12· Issue 8
Publisher page

Abstract

Far-red and near-infrared (NIR) fluorescent materials possessing the characteristics of strong two-photon absorption and aggregation-induced emission (AIE) as well as specific targeting capability are much-sought-after for bioimaging and therapeutic applications due to their deep penetration depth and high resolution. Herein, a series of dipolar far-red and NIR AIE luminogens with a strong push-pull effect are designed and synthesized. The obtained fluorophores display bright far-red and NIR solid-state fluorescence with a high quantum yield of up to 30%, large Stokes shifts of up to 244 nm, and large two-photon absorption cross-sections of up to 887 GM. A total of three neutral AIEgens show specific lipid droplet (LD)-targeting capability, while the one with cationic and lipophilic characteristics tends to target the mitochondria specifically. All of the molecules demonstrate good biocompatibility, high brightness, and superior photostability. They also serve as efficient two-photon fluorescence-imaging agents for the clear visualization of LDs or mitochondria in living cells and tissues with deep tissue penetration (up to 150 μm) and high contrast. These AIEgens can efficiently generate singlet oxygen upon light irradiation for the photodynamic ablation of cancer cells. All of these intriguing results prove that these far-red and NIR AIEgens are excellent candidates for the two-photon fluorescence imaging of LDs or mitochondria and organelle-targeting photodynamic cancer therapy.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Nanoplatforms for cancer theranostics · Porphyrin and Phthalocyanine Chemistry

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

Affiliations

Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, Institute for Advanced Study, Department of Chemical and Biological Engineering and Division of Life Science, The Hong Kong University of Science and Technology (HKUST), Clear Water Bay, Kowloon, Hong Kong, China

Department of Physics, HKUST, Clear Water Bay, Kowloon, Hong Kong, China

HKUST-Shenzhen Research Institute, No. 9 Yuexing First Road, South Area, Hi-Tech Park, Nanshan, Shenzhen 518057, China

NSFC Center for Luminescence from Molecular Aggregates, SCUT-HKUST Joint Research Institute, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China

Funding

Research Grants Council, University Grants Committee · Innovation and Technology Commission · National Natural Science Foundation of China · Science and Technology Plan of Shenzhen

References (85)

Show source-provided references
1. 10.1038/nature0691710.1038/nature06917 ↗
2. 10.1021/ar200044b10.1021/ar200044b ↗
3. 10.1021/acs.chemrev.5b0014810.1021/acs.chemrev.5b00148 ↗
4. 10.1038/8668410.1038/86684 ↗
5. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
6. 10.1038/nchem.150010.1038/nchem.1500 ↗
7. 10.1038/nnano.2009.32610.1038/nnano.2009.326 ↗
8. 10.1039/C4CS00275J10.1039/C4CS00275J ↗
9. 10.1021/cr200410310.1021/cr2004103 ↗
10. 10.1016/j.cbpa.2009.10.02210.1016/j.cbpa.2009.10.022 ↗
11. 10.1039/C2CS35313J10.1039/C2CS35313J ↗
12. 10.1039/C3CS60271K10.1039/C3CS60271K ↗
13. 10.1039/C4CS00011K10.1039/C4CS00011K ↗
14. 10.1021/am506750m10.1021/am506750m ↗
15. 10.1039/C8NR00066B10.1039/C8NR00066B ↗
16. 10.1021/acsnano.7b0771610.1021/acsnano.7b07716 ↗
17. 10.1002/0471142956.cy1227s6010.1002/0471142956.cy1227s60 ↗
18. 10.1016/j.biomaterials.2011.06.02410.1016/j.biomaterials.2011.06.024 ↗
19. 10.1016/j.cbpa.2003.08.00710.1016/j.cbpa.2003.08.007 ↗
20. Birks, J. B. Photophysics of Aromatic Molecules, Wily-Interscience: London, England, 1970; pp 528–537.
21. 10.1039/b105159h10.1039/b105159h ↗
22. 10.1039/c2jm32405a10.1039/c2jm32405a ↗
23. 10.1039/C4CC02564D10.1039/C4CC02564D ↗
24. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
25. 10.1039/C7QM00032D10.1039/C7QM00032D ↗
26. 10.1002/adfm.20110219110.1002/adfm.201102191 ↗
27. 10.1002/adfm.20130211410.1002/adfm.201302114 ↗
28. 10.1039/C6CC01797E10.1039/C6CC01797E ↗
29. 10.1002/chem.20160012510.1002/chem.201600125 ↗
30. 10.1002/adfm.20150001010.1002/adfm.201500010 ↗
31. 10.1002/anie.20150703110.1002/anie.201507031 ↗
32. Shao A. · Angew. Chem., Int. Ed. · 2015 · 54 · 738310.1002/ange.201501478 ↗
33. 10.1039/C5NR05051K10.1039/C5NR05051K ↗
34. 10.1039/C7QM00024C10.1039/C7QM00024C ↗
35. 10.1002/adhm.20120024310.1002/adhm.201200243 ↗
36. 10.1039/C4CC02767A10.1039/C4CC02767A ↗
37. 10.1002/adma.20170054810.1002/adma.201700548 ↗
38. 10.1038/nbt89910.1038/nbt899 ↗
39. 10.1021/cr500442510.1021/cr5004425 ↗
40. 10.1002/smll.20160087210.1002/smll.201600872 ↗
41. 10.1002/adfm.20170694510.1002/adfm.201706945 ↗
42. 10.1101/cshperspect.a00471310.1101/cshperspect.a004713 ↗
43. 10.1002/pmic.20080058410.1002/pmic.200800584 ↗
44. 10.1016/j.cell.2009.11.00510.1016/j.cell.2009.11.005 ↗
45. 10.1038/nrm191210.1038/nrm1912 ↗
46. 10.1172/JCI4606910.1172/JCI46069 ↗
47. 10.1073/pnas.121373811010.1073/pnas.1213738110 ↗
48. 10.1146/annurev-biochem-061009-10243010.1146/annurev-biochem-061009-102430 ↗
49. 10.1038/nrm369910.1038/nrm3699 ↗
50. 10.1016/j.plefa.2010.02.00510.1016/j.plefa.2010.02.005 ↗
51. 10.1002/emmm.20110067110.1002/emmm.201100671 ↗
52. 10.1038/nm.223810.1038/nm.2238 ↗
53. 10.1155/2017/165605310.1155/2017/1656053 ↗
54. 10.1016/j.canlet.2017.05.00210.1016/j.canlet.2017.05.002 ↗
55. 10.1039/C4AN01875C10.1039/C4AN01875C ↗
56. 10.1016/j.mam.2004.03.00110.1016/j.mam.2004.03.001 ↗
57. 10.1038/nature0529210.1038/nature05292 ↗
58. 10.1073/pnas.88.23.1061410.1073/pnas.88.23.10614 ↗
59. 10.1038/nrn186810.1038/nrn1868 ↗
60. 10.2217/nnm.14.16110.2217/nnm.14.161 ↗
61. 10.3892/ijo.12.1.14110.3892/ijo.12.1.141 ↗
62. 10.1016/j.biomaterials.2017.10.03410.1016/j.biomaterials.2017.10.034 ↗
63. 10.1021/jacs.6b1339910.1021/jacs.6b13399 ↗
64. 10.1039/C6CC01797E10.1039/C6CC01797E ↗
65. 10.1039/C6SC04842K10.1039/C6SC04842K ↗
66. 10.1039/C7SC01400G10.1039/C7SC01400G ↗
67. 10.1002/adfm.20170403910.1002/adfm.201704039 ↗
68. 10.1021/jacs.7b1281710.1021/jacs.7b12817 ↗
69. 10.1021/cr050054x10.1021/cr050054x ↗
70. 10.1002/anie.20080525710.1002/anie.200805257 ↗
71. 10.1021/jo400116j10.1021/jo400116j ↗
72. 10.1039/C6CC09471F10.1039/C6CC09471F ↗
73. 10.1039/C5SC01733E10.1039/C5SC01733E ↗
74. 10.1039/c3sc22325f10.1039/c3sc22325f ↗
75. 10.1021/cm102190510.1021/cm1021905 ↗
76. 10.1021/acs.analchem.7b0071010.1021/acs.analchem.7b00710 ↗
77. 10.1002/adfm.20160280810.1002/adfm.201602808 ↗
78. 10.1146/annurev.arplant.55.031903.14170110.1146/annurev.arplant.55.031903.141701 ↗
79. 10.1016/S0010-8545(02)00034-610.1016/S0010-8545(02)00034-6 ↗
80. 10.1021/cr60272a00410.1021/cr60272a004 ↗
81. 10.1039/C4NR05574H10.1039/C4NR05574H ↗
82. 10.1021/acs.jmedchem.6b0035210.1021/acs.jmedchem.6b00352 ↗
83. 10.1002/chem.20140303610.1002/chem.201403036 ↗
84. 10.1039/c3tc30759j10.1039/c3tc30759j ↗
85. 10.1021/jo01277a04210.1021/jo01277a042 ↗