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Systematic Review of Cancer Targeting by Nanoparticles Revealed a Global Association between Accumulation in Tumors
Andrey S Drozdov1, Petr I Nikitin2, Julian M Rozenberg3
1Laboratory of Nanobiotechnology, Moscow Institute of Physics and Technology, 141700 Dolgoprudny, Russia.
Abstract:
Active targeting of nanoparticles toward tumors is one of the most rapidly developing topics in nanomedicine. Typically, this strategy involves the addition of cancer-targeting biomolecules to nanoparticles, and studies on this topic have mainly focused on the localization of such formulations in tumors. Here, the analysis of the factors determining efficient nanoparticle targeting and therapy, various parameters such as types of targeting molecules, nanoparticle type, size, zeta potential, dose, and the circulation time are given. In addition, the important aspects such as how active targeting of nanoparticles alters biodistribution and how non-specific organ uptake influences tumor accumulation of the targeted nanoformulations are discussed. The analysis reveals that an increase in tumor accumulation of targeted nanoparticles is accompanied by a decrease in their uptake by the spleen. There is no association between targeting-induced changes of nanoparticle concentrations in tumors and other organs. The correlation between uptake in tumors and depletion in the spleen is significant for mice with intact immune systems in contrast to nude mice. Noticeably, modulation of splenic and tumor accumulation depends on the targeting molecules and nanoparticle type. The median survival increases with the targeting-induced nanoparticle accumulation in tumors; moreover, combinatorial targeting of nanoparticle drugs demonstrates higher treatment efficiencies. Results of the comprehensive analysis show optimal strategies to enhance the efficiency of actively targeted nanoparticle-based medicines.
Insights
Active targeting of nanoparticles enhances tumor accumulation and survival by reducing spleen uptake, especially in immune-competent mice. Optimal strategies involve careful selection of nanoparticle type and targeting molecules for improved cancer therapy.
Area of Science:
- Nanomedicine
- Biomaterials Science
- Cancer Therapy
Background:
- Active targeting of nanoparticles using cancer-targeting biomolecules is a key strategy in nanomedicine.
- Research has primarily focused on nanoparticle localization within tumors.
Purpose of the Study:
- To analyze factors influencing efficient nanoparticle targeting and therapy.
- To investigate how active targeting alters biodistribution and non-specific organ uptake.
- To identify optimal strategies for enhancing actively targeted nanoparticle-based medicines.
Main Methods:
- Analysis of various parameters: targeting molecule type, nanoparticle type, size, zeta potential, dose, and circulation time.
- Evaluation of nanoparticle biodistribution and organ uptake.
- Correlation analysis between tumor accumulation, spleen depletion, and survival rates in different mouse models.
Main Results:
- Increased tumor accumulation of targeted nanoparticles correlates with decreased spleen uptake.
- The spleen depletion effect is significant in immune-competent mice but not in nude mice.
- Targeting molecule and nanoparticle type influence splenic and tumor accumulation.
- Median survival increases with nanoparticle accumulation in tumors; combinatorial targeting shows higher efficiency.
Conclusions:
- Optimizing nanoparticle type and targeting molecules is crucial for enhancing tumor accumulation and therapeutic efficacy.
- Understanding the interplay between spleen uptake and tumor targeting is vital for effective nanomedicine design.
- Actively targeted nanoparticles offer promising strategies for improved cancer treatment outcomes.

