Characterization of superparamagnetic nanoparticle interactions with extracellular matrix in an in vitro system.

Kuhn SJ, Hallahan DE, Giorgio TD
Ann Biomed Eng. 2006 34 (1): 51-8

PMID: 16477503 · DOI:10.1007/s10439-005-9004-5

Controlled dispersion of therapeutic agents within liquid- and gel-filled cavities represents a barrier to treatment of some cancers and other pathological states. Interstitial delivery is compromised by the poor mobility of macromolecules and larger nanoscale structures. We developed an in vitro system to quantify the suitability of superparamagnetic nanoparticles (SPM NPs) as a site-specific therapeutic vehicle for delivery through fluid- and gel-based systems. SPM NP motion was induced by an external magnetic field. NP migration was modulated by NP concentration and surface coating. 135 nanometer radius PEGylated NPs moved through the extracellular matrix with an average velocity of 1.5 mm h(-1), suitable for some clinical applications. Increasing the SPM NP radius to 400 nm while maintaining the same per NP magnetic susceptibility resulted in a greater than 1,000-fold reduction in magnetic mobility, to less than 0.01 mm h(-1). The critical influence of NP size on gel permeation was also observed in silica-coated 135 nm SPM NPs that aggregated under the experimental conditions. Aggregation played a critical role in determining the behavior of the nanoparticles. SPM NPs allow significant free-solution mobility to specific sites within a cavity and generate sufficient force to penetrate common in vivo gels.

MeSH Terms (12)

Animals Biocompatible Materials Drug Carriers Drug Delivery Systems Extracellular Matrix Humans Magnetics Models, Biological Nanostructures Nanotechnology Polyethylene Glycols Surface Properties

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