Inhibition of restenosis after balloon injury in rabbit vessels by integrin αvβ3-targeted 10058-F4 nanoparticles

This study investigated whether 10058-F4, a small molecule inhibitor of the c-Myc gene, could play a corresponding inhibitory role in the vascular proliferation process. The efficacy and targeting ability of the synthesised drug-loaded nanoparticles were first measured at the cellular level, while 16 rabbit femoral arteries were then balloon damaged to establish a vascular model and treated locally with targeted αvβ3-10058-F4 nanoparticles (experimental group) and αvβ3 nanoparticles (control group), and vascular specimens were obtained after 4 weeks for analysis. The vascular specimens were found to have a vascular lumen area of 0.34 mm2 ± 0.12 mm2 in the experimental group compared to 0.79 mm2 + 0.21 mm2 in the control group (p < 0.05), and in terms of neovascular smooth muscle area, 0.22 mm2 + 0.12 mm2 in the experimental group compared to 0.64 mm2 ± 0.17 mm2 in the control group (p < 0.05), indicating a significant inhibition of vascular proliferation after drug application. The small molecule inhibitor of the c-Myc gene, 10058-F4, can play a significant inhibitory role in the process of vascular proliferation, and the locally targeted nano-delivery method allows the drug to be activated within the smooth muscle cell layer to prevent stenosis and does not retard endothelial healing.

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Publication Details

Journal
Journal of Experimental Nanoscience
Published
2024-08-15
DOI
https://doi.org/10.1080/17458080.2024.2388539
Citations
1
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
0.38
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article

Inhibition of restenosis after balloon injury in rabbit vessels by integrin αvβ3-targeted 10058-F4 nanoparticles

Chang Dong, Qiang Fu, Wei Li, Po Song Yang et al.
1 citations
Journal of Experimental Nanoscience
Cell Adhesion Molecules Research
0.38
article

Inhibition of restenosis after balloon injury in rabbit vessels by integrin αvβ3-targeted 10058-F4 nanoparticles

Chang Dong, Qiang Fu, Wei Li, Po Song Yang, Wenling Man, Yujia Wang
article en
1 citations

Abstract

This study investigated whether 10058-F4, a small molecule inhibitor of the c-Myc gene, could play a corresponding inhibitory role in the vascular proliferation process. The efficacy and targeting ability of the synthesised drug-loaded nanoparticles were first measured at the cellular level, while 16 rabbit femoral arteries were then balloon damaged to establish a vascular model and treated locally with targeted αvβ3-10058-F4 nanoparticles (experimental group) and αvβ3 nanoparticles (control group), and vascular specimens were obtained after 4 weeks for analysis. The vascular specimens were found to have a vascular lumen area of 0.34 mm2 ± 0.12 mm2 in the experimental group compared to 0.79 mm2 + 0.21 mm2 in the control group (p < 0.05), and in terms of neovascular smooth muscle area, 0.22 mm2 + 0.12 mm2 in the experimental group compared to 0.64 mm2 ± 0.17 mm2 in the control group (p < 0.05), indicating a significant inhibition of vascular proliferation after drug application. The small molecule inhibitor of the c-Myc gene, 10058-F4, can play a significant inhibitory role in the process of vascular proliferation, and the locally targeted nano-delivery method allows the drug to be activated within the smooth muscle cell layer to prevent stenosis and does not retard endothelial healing.

Journal of Experimental NanoscienceVol. 19(1)
Harbin Medical University (CN), Yuhuangding Hospital (CN), Fourth Affiliated Hospital of Harbin Medical University (CN)
Openalex Percentile: Top 37%
Cell Adhesion Molecules Research
0.38
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Inhibition of restenosis after balloon injury in rabbit vessels by integrin αvβ3-targeted 10058-F4 nanoparticles — Chang Dong, Qiang Fu, et al. · Journal of Experimental Nanoscience (2024) | TGRS Research Map | TGRS