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Cancer Theranostic Nanoparticles Self-Assembled from Amphiphilic Small Molecules with Equilibrium Shift-Induced Renal
Yuan Ma1, Quanbing Mou1, Mo Sun1
11. School of Chemistry and Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, P. R. China.
Abstract:
Nano drug delivery systems have emerged as promising candidates for cancer therapy, whereas their uncertainly complete elimination from the body within specific timescales restricts their clinical translation. Compared with hepatic clearance of nanoparticles, renal excretion of small molecules is preferred to minimize the agent-induced toxicity. Herein, we construct in vivo renal-clearable nanoparticles, which are self-assembled from amphiphilic small molecules holding the capabilities of magnetic resonance imaging (MRI) and chemotherapy. The assembled nanoparticles can accumulate in tumor tissues for their nano-characteristics, while the small molecules dismantled from the nanoparticles can be efficiently cleared by kidneys. The renal-clearable nanoparticles exhibit excellent tumor-inhibition performance as well as low side effects and negligible chronic toxicity. These results demonstrate a potential strategy for small molecular nano drug delivery systems with obvious anticancer effect and low-toxic metabolism pathway for clinical applications.
Insights
Researchers developed novel renal-clearable nanoparticles for cancer therapy. These nanoparticles effectively target tumors and are safely eliminated by the kidneys, minimizing toxicity for improved clinical translation.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Nano drug delivery systems show promise for cancer treatment but face challenges with complete body elimination.
- Renal excretion is a preferred pathway for minimizing toxicity compared to hepatic clearance of nanoparticles.
Purpose of the Study:
- To design and evaluate in vivo renal-clearable nanoparticles for enhanced cancer therapy.
- To develop a nano drug delivery system that combines chemotherapy and magnetic resonance imaging (MRI) with a safe metabolic pathway.
Main Methods:
- Self-assembly of amphiphilic small molecules into nanoparticles capable of MRI and chemotherapy.
- Evaluation of nanoparticle accumulation in tumor tissues and subsequent renal clearance of dismantled small molecules.
- Assessment of tumor inhibition efficacy, side effects, and chronic toxicity in vivo.
Main Results:
- The constructed nanoparticles effectively accumulated in tumor tissues.
- Dismantled small molecules were efficiently cleared by the kidneys, demonstrating renal-clearability.
- The nanoparticles exhibited significant tumor inhibition with low side effects and negligible chronic toxicity.
Conclusions:
- In vivo renal-clearable nanoparticles offer a promising strategy for cancer therapy.
- This approach facilitates efficient tumor targeting and safe elimination, reducing agent-induced toxicity.
- The developed system presents a potential pathway for clinical translation of nano drug delivery systems with anticancer effects and low-toxic metabolism.
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