TY - JOUR
T1 - Magnetic/photothermal dual-driven micro/nanorobots for synergistic NO-mediated photothermal thrombolysis
AU - Kang, Wenjia
AU - Li, Jinhua
AU - Li, Song
AU - Yang, Yingting
AU - Gao, Shanqing
AU - Wei, Shuangying
AU - Sofer, Zdenek
AU - Zhang, Jiatao
AU - Zhou, Huaijuan
N1 - Publisher Copyright:
© 2026 The Authors
PY - 2026/6
Y1 - 2026/6
N2 - Thrombotic vascular obstruction, a leading cause of cardiovascular/cerebrovascular events and global mortality, poses a severe threat to human health, while conventional thrombolytic agents suffer from inherent limitations, including short half-lives, poor targeting, low utilization efficiency, and suboptimal therapeutic outcomes. Nitric oxide (NO)-supported gas therapy exhibits significant potential in synergistic thrombolysis but is hindered by its ultra-short half-life and challenges in targeted delivery and spatiotemporal control. Herein, we developed dual-driven rGO@Fe3O4-βCD-BNN6 micro/nanorobots for NO-mediated targeted photothermal thrombus ablation, with the advantages of site-specific accumulation, controlled therapeutic agent release, and enhanced therapeutic specificity. Reduced graphene oxide (rGO) served as the core photothermal agent with excellent photothermal conversion efficiency (44.2%), while Fe3O4 nanoparticles endowed the micro/nanorobots with magnetic responsiveness for precise directional targeting. β-Cyclodextrin (βCD) enhanced the loading capacity and biocompatibility of the NO donor BNN6 (N,N′-di-sec-butyl-N,N′-dinitroso-1,4-phenylene diamine), which underwent photothermal-induced thermal decomposition to release NO in situ, disrupting fibrin networks and synergistically boosting thrombolysis. The micro/nanorobots achieved a remarkable thrombolytic efficacy of up to 88.8%, significantly outperforming conventional drugs. Comprehensive hemolysis and cytotoxicity assays confirmed their excellent biocompatibility. This dual-driven, photothermal-gas synergistic micro/nanorobotic platform provides a novel and safe strategy to overcome the limitations of traditional thrombolysis, paving the way for advancing micro/nanorobotic thrombotic intervention.
AB - Thrombotic vascular obstruction, a leading cause of cardiovascular/cerebrovascular events and global mortality, poses a severe threat to human health, while conventional thrombolytic agents suffer from inherent limitations, including short half-lives, poor targeting, low utilization efficiency, and suboptimal therapeutic outcomes. Nitric oxide (NO)-supported gas therapy exhibits significant potential in synergistic thrombolysis but is hindered by its ultra-short half-life and challenges in targeted delivery and spatiotemporal control. Herein, we developed dual-driven rGO@Fe3O4-βCD-BNN6 micro/nanorobots for NO-mediated targeted photothermal thrombus ablation, with the advantages of site-specific accumulation, controlled therapeutic agent release, and enhanced therapeutic specificity. Reduced graphene oxide (rGO) served as the core photothermal agent with excellent photothermal conversion efficiency (44.2%), while Fe3O4 nanoparticles endowed the micro/nanorobots with magnetic responsiveness for precise directional targeting. β-Cyclodextrin (βCD) enhanced the loading capacity and biocompatibility of the NO donor BNN6 (N,N′-di-sec-butyl-N,N′-dinitroso-1,4-phenylene diamine), which underwent photothermal-induced thermal decomposition to release NO in situ, disrupting fibrin networks and synergistically boosting thrombolysis. The micro/nanorobots achieved a remarkable thrombolytic efficacy of up to 88.8%, significantly outperforming conventional drugs. Comprehensive hemolysis and cytotoxicity assays confirmed their excellent biocompatibility. This dual-driven, photothermal-gas synergistic micro/nanorobotic platform provides a novel and safe strategy to overcome the limitations of traditional thrombolysis, paving the way for advancing micro/nanorobotic thrombotic intervention.
KW - Dual-driven
KW - Micro/nanorobots
KW - Nitric oxide release
KW - Photothermal therapy
KW - Thrombosis treatment
UR - https://www.scopus.com/pages/publications/105037607841
U2 - 10.1016/j.mtbio.2026.103179
DO - 10.1016/j.mtbio.2026.103179
M3 - Article
AN - SCOPUS:105037607841
SN - 2590-0064
VL - 38
JO - Materials Today Bio
JF - Materials Today Bio
M1 - 103179
ER -