4.8 Article

Long-Term Fate of Magnetic Particles in Mice: A Comprehensive Study

Journal

ACS NANO
Volume 15, Issue 7, Pages 11341-11357

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c00687

Keywords

iron oxide nanoparticles; biodegradation; biodistribution; nanotoxicity; magnetic particle detection; noninvasive detection

Funding

  1. Russian Science Foundation [19-14-00112, 19-19-00716]
  2. Russian Foundation for Basic Research [19-29-04012, 19-515-06010, 20-04-60552, 19-33-51011]
  3. Russian Science Foundation [19-19-00716] Funding Source: Russian Science Foundation

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Safe application of nanoparticles in medicine requires a full understanding of their pharmacokinetics and degradation in the organism. In this study, a magnetic spectral approach was used for in vivo monitoring of magnetic particle degradation, revealing the significant influence of parameters such as dose, size, surface coating, and internal architecture on the degradation process. These findings provide deeper insights into particle degradation in vivo, potentially facilitating the rational design of nano- and microparticles with predictable long-term fate in vivo.
Safe application of nanoparticles in medicine requires full understanding of their pharmacokinetics including catabolism in the organism. However, information about nanoparticle degradation is still scanty due to difficulty of long-term measurements by invasive techniques. Here, we describe a magnetic spectral approach for in vivo monitoring of magnetic particle (MP) degradation. The method noninvasiveness has allowed performing of a broad comprehensive study of the 1-year fate of 17 types of iron oxide particles. We show a long-lasting influence of five parameters on the MP degradation half-life: dose, hydrodynamic size,.-potential, surface coating, and internal architecture. We observed a slowdown in MP biotransformation with an increase of the injected dose and faster degradation of the particles of a small hydrodynamic size. A comparison of six types of 100 nm particles coated by different hydrophilic polymer shells has shown that the slowest (t(1/2) = 38 +/- 6 days) and the fastest (t(1/2) = 15 +/- 4 days) degradations were achieved with a polyethylene glycol and polyglucuronic acid coatings, respectively. The most significant influence on the MP degradation was due to the internal architecture of the particles as the coverage of magnetic cores with a solid 39 nm polystyrene layer slowed down the half-life of the core-shell MPs from 48 days to more than 1 year. The revealed deeper insights into the particle degradation in vivo may facilitate rational design of nano- and microparticles with predictable long-term fate in vivo.

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