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Thesis submitted 23-03-2012.pdf - University of Limpopo ...

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3.4.3 The fate <strong>of</strong> nanoparticles after administration into the body<br />

The distribution <strong>of</strong> nanoparticles and their loads throughout the body<br />

depends on numerous physicochemical factors: size <strong>of</strong> particles, toxicity,<br />

surface charge, capacity for protein adsorption, surface hydrophobicity,<br />

drug loading and release kinetics, stability, degeneration <strong>of</strong> carrier system,<br />

hydration behavior, electrophoretic mobility, porosity, specific<br />

characteristics, density, crystallinity, contact angle, and molecular<br />

weight. 245 Nevertheless, the fate and consequently the possible toxicity <strong>of</strong><br />

magnetic nanoparticles also depends strongly on the dose and<br />

administration route.<br />

After particles are injected into the blood sream,they are conditioned or<br />

coated by elements like plasma proteins and glycoproteins available in the<br />

circulatory system. This process is called opsonization. The process<br />

makes the nanoparticles recognizable by the major defense system <strong>of</strong> the<br />

body like the macrophages (mainly kupffer cells in the liver) and other<br />

macrophages remove these opsonized particles. Particles having<br />

hydrophobic surface are more efficiently coated, but those having<br />

hydrophilic surface resist coating and are therefore cleared more slowly<br />

from the body. The macrophages take the particles to the endosomes and<br />

lysosomes where they are degraded, so that the drug the particle is<br />

carrying is released and diffused to the circulatory system. The particles<br />

are later excreted from the body or processed further by the body for other<br />

possible metabolic activities.<br />

Where uptake <strong>of</strong> particles by macrophages may be a hinderance in drug<br />

delivery to target area, the particles may be disguised, so that they are not<br />

recognized by the kupffer cells and therefore escape capture by the cells.<br />

The nanoparticles may be disguised partly by making them hydrophilic<br />

(depending on the type <strong>of</strong> treatment) and by stabilizing them using<br />

absorbed polymers which did not allow recognition <strong>of</strong> liposome by<br />

macrophages and thus prevent opsonization. 255<br />

129

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