1. Nanogel-based nitric oxide-driven nanomotor for deep tissue penetration and enhanced tumor therapy.
- Author
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Wang, Jianhong, Liu, Junjie, Sümbelli, Yiǧitcan, Shao, Jingxin, Shi, Xiangyang, and van Hest, Jan C.M.
- Subjects
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NANOMOTORS , *FLUORESCENT probes , *TUMOR treatment , *DEEP brain stimulation , *TREATMENT effectiveness , *ANTINEOPLASTIC agents , *NANOMEDICINE - Abstract
Antitumor agents often lack effective penetration and accumulation to achieve high therapeutic efficacy in treating solid tumors. Nanomotor-based nanomaterials offer a potential solution to address this obstacle. Among them, nitric oxide (NO) based nanomotors have garnered attention for their potential applications in nanomedicine. However, there widespread clinical adoption has been hindered by their complex preparation processes. To address this limitation, we have developed a NO-driven nanomotor utilizing a convenient and scalable nanogel preparation procedure. These nanomotors, loaded with the fluorescent probe / sonosensitizer chlorin e6 (Ce6), were specifically engineered for sonodynamic therapy. Through comprehensive in vitro investigations using both 2D and 3D cell models, as well as in vivo analysis of Ce6 fluorescent signal distribution in solid tumor models, we observed that the self-propulsion of these nanomotors significantly enhances cellular uptake and tumor penetration, particularly in solid tumors. This phenomenon enables efficient access to challenging tumor regions and, in some cases, results in complete tumor coverage. Notably, our nanomotors have demonstrated long-term in vivo biosafety. This study presents an effective approach to enhancing drug penetration and improving therapeutic efficacy in tumor treatment, with potential clinical relevance for future applications. [Display omitted] • To overcome tissue barriers, biodegradable nanogels were engineered into nanomotors by incorporating L-arginine and Ce6. • Tissue penetration and accumulation were meticulously analyzed and evaluated using 2D/3D cell cultures and in vivo mouse models. • A combination therapy was developed, demonstrating improved therapeutic efficacy and long-term biosafety in vivo. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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