journal article·2026-01-09Open access

N -Acetylcysteine-Functionalized Gold Nanoparticles via Photoclick Reaction as Antioxidant Nanomedicine

Yang Zhang, Greta Malavasi, Philippe Nizard, Virginie Gueguen, Cédric Chauvierre, Fan Sun, Pauline Cornette, Miryana Hémadi, Aazdine Lamouri, Claire Mangeney, Graciela Pavon-Djavid, Yun Luo

ACS Applied Nano Materials· Volume 9· Issue 1

Abstract

Reactive oxygen species (ROS) are highly reactive molecules regulated by a balance of enzymatic and nonenzymatic antioxidant systems. In the heart, ROS play crucial roles in maintaining cellular homeostasis, influencing processes such as cell proliferation, differentiation, and excitation–contraction coupling. However, when ROS levels surpass the antioxidant defense capacity, oxidative stress occurs, leading to cellular and molecular damage that can ultimately result in cardiac dysfunction. In this study, we developed an antioxidant nanomedicine based on gold nanoparticles (Au NPs) functionalized with N -acetylcysteine (NAC), designed to counteract oxidative stress in the heart. NAC is an essential endogenous antioxidant that can effectively prevent local ROS formation and protect human endothelial and stem cells from oxidative stress. Using a thiol–yne photoclick chemistry approach, NAC was efficiently grafted onto Au NPs prefunctionalized with 4-ethynylbenzene diazonium salts. The resulting Au NPs exhibit excellent biocompatibility, along with significant antioxidant activity, good compatibility with human endothelial cells, and efficient cellular internalization.
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Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanoplatforms for cancer theranostics · Advanced Nanomaterials in Catalysis

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

Affiliations

Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques

Université Paris Cité, CNRS

Université Sorbonne Paris Nord, Université Paris Cité, Nanotechnologies for Vascular Medicine and Imaging Team

INSERM U1148, Laboratory for Vascular Translational Science

IRCP, Chimie Paris Tech, CNRS UMR 8247, PSL Université, 11, Rue Pierre et Marie Curie, 75005 Paris, France

Université Paris Cité, ITODYS, CNRS-UMR 7086

Funding

Agence Nationale de la Recherche · Università Degli Studi di Modena e Reggio Emila · China Scholarship Council · Université Paris Cité

References (50)

Show source-provided references
1. 10.1016/j.cub.2014.03.03410.1016/j.cub.2014.03.034 ↗
2. 10.1016/j.stem.2021.02.01110.1016/j.stem.2021.02.011 ↗
3. 10.3390/antiox1307083210.3390/antiox13070832 ↗
4. 10.1007/BF0106142210.1007/BF01061422 ↗
5. 10.1002/jbm.a.3546910.1002/jbm.a.35469 ↗
6. 10.1002/slct.20210087310.1002/slct.202100873 ↗
7. 10.3390/nano1106143410.3390/nano11061434 ↗
8. 10.1021/acs.nanolett.5c0105410.1021/acs.nanolett.5c01054 ↗
9. 10.1016/j.nantod.2025.10282010.1016/j.nantod.2025.102820 ↗
10. 10.1002/anie.20241203110.1002/anie.202412031 ↗
11. 10.1002/adma.20250326110.1002/adma.202503261 ↗
12. 10.1016/j.biomaterials.2024.12300810.1016/j.biomaterials.2024.123008 ↗
13. 10.1038/s41467-024-53824-y10.1038/s41467-024-53824-y ↗
14. 10.1021/acsnano.4c0740610.1021/acsnano.4c07406 ↗
15. 10.1039/D0CC02842H10.1039/D0CC02842H ↗
16. 10.1039/D2NA00572G10.1039/D2NA00572G ↗
17. 10.3390/s1909211010.3390/s19092110 ↗
18. 10.1039/df951110005510.1039/df9511100055 ↗
19. 10.1021/ac070208410.1021/ac0702084 ↗
20. 10.1016/j.diamond.2008.04.00310.1016/j.diamond.2008.04.003 ↗
21. 10.1002/cphc.20170079810.1002/cphc.201700798 ↗
22. 10.1002/celc.20180119110.1002/celc.201801191 ↗
23. 10.1021/jf011660610.1021/jf0116606 ↗
24. 10.1155/2017/807379810.1155/2017/8073798 ↗
25. 10.1002/jat.347010.1002/jat.3470 ↗
26. 10.3390/pharmaceutics1110053210.3390/pharmaceutics11100532 ↗
27. 10.1021/acs.langmuir.3c0067610.1021/acs.langmuir.3c00676 ↗
28. 10.1021/cm070055110.1021/cm0700551 ↗
29. 10.1021/acs.langmuir.4c0136110.1021/acs.langmuir.4c01361 ↗
30. 10.1021/jp906367t10.1021/jp906367t ↗
31. 10.1021/la301110310.1021/la3011103 ↗
32. 10.1016/S0301-0104(97)00337-610.1016/S0301-0104(97)00337-6 ↗
33. 10.1021/acs.jafc.5b0473910.1021/acs.jafc.5b04739 ↗
34. 10.1016/j.foodchem.2008.09.03310.1016/j.foodchem.2008.09.033 ↗
35. 10.1039/P2996000074710.1039/P29960000747 ↗
36. 10.3390/molecules2701007510.3390/molecules27010075 ↗
37. 10.1016/j.polymdegradstab.2023.11058510.1016/j.polymdegradstab.2023.110585 ↗
38. 10.1021/acs.orglett.5c0074710.1021/acs.orglett.5c00747 ↗
39. 10.1016/j.jphotobiol.2016.04.00310.1016/j.jphotobiol.2016.04.003 ↗
40. 10.1016/j.colsurfb.2019.01.03010.1016/j.colsurfb.2019.01.030 ↗
41. 10.1016/j.freeradbiomed.2007.06.01110.1016/j.freeradbiomed.2007.06.011 ↗
42. 10.1016/j.msec.2019.11017010.1016/j.msec.2019.110170 ↗
43. 10.1016/j.jcis.2018.02.06910.1016/j.jcis.2018.02.069 ↗
44. 10.3390/pharmaceutics1406128810.3390/pharmaceutics14061288 ↗
45. 10.1002/slct.20220028110.1002/slct.202200281 ↗
46. 10.1021/ja00077a04210.1021/ja00077a042 ↗
47. 10.1002/asia.20120093310.1002/asia.201200933 ↗
48. International Organization for Standardization. ISO 10993–5:2009/(R)2022, Biological Evaluation of Medical Devices─Part 5: Tests for in Vitro Cytotoxicity , Geneva: ISO; 2009, reaffirmed 2022.
49. 10.1038/s41598-017-04229-z10.1038/s41598-017-04229-z ↗
50. 10.1039/c4tx00061g10.1039/c4tx00061g ↗