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Magnetic nanoparticles that display high saturation magnetization and high magnetic susceptibility are of great interest for medical applications. Magnetite nanoparticles display strong ferrimagnetic behavior and are less sensitive to oxidation than magnetic transition metal nanoparticles such as cobalt, iron, and nickel. For in vivo applications, well-defined organic coatings are needed to surround the magnetite nanoparticles and prevent any aggregation. The goal of this research was to develop complexes of magnetite nanoparticles coated with well-defined hydrophilic polymers so that they could be dispersed in aqueous fluids. Focal points have included the following: (1) Investigations of polymer systems that bind irreversibly to magnetite at the physiological pH, (2) the design of block copolymers with anchor and tail blocks to enable dispersion in biological fluids, and (3) investigations of copolymer block lengths to maximize the concentration of bound magnetite. Hydrophilic triblock copolymers with controlled concentrations of pendent carboxylic acid binding groups were designed as steric stabilizers for magnetite nanoparticles. These copolymers were comprised of controlled molecular weight poly(ethylene oxide) tail blocks and a central, polyurethane anchor block containing carboxylic acids. Stoichiometric aqueous solutions of FeCl 2 and FeCl 3 were condensed by reaction with NH 4 OH to form magnetite nanoparticles, and then a dichloromethane solution of the block copolymer was added to adsorb the copolymer onto the magnetite surfaces. Stable magnetite dispersions were prepared with all of the triblock copolymers. The polymer-nanomagnetite conjugates described in this paper had a maximum saturation magnetization of 34 emu/g. Magnetization curves showed minimal hysteresis. Powder X-ray diffraction (XRD), selected area electron diffraction (SAED), and high-resolution electron microscopy (HREM) confirmed the magnetite crystal structure. Transmission electron microscopy (TEM) showed that the dispersions contained magnetite particles coated with the polymers with a mean diameter of 8.8 ( S.D. 2.7 nm.

The effect of applied magnetic fields on the deformation of a biocompatible hydrophobic ferrofluid drop suspended in a viscous medium is investigated numerically and compared with experimental data. A numerical formulation for the time-dependent simulation of magnetohydrodynamics of two immiscible non-conducting fluids is used with a volume-of-fluid scheme for fully deformable interfaces. Analytical formulae for ellipsoidal drops and near-spheroidal drops are reviewed and developed for code validation. At low magnetic fields, both the experimental and numerical results follow the asymptotic small deformation theory. The value of interfacial tension is deduced from an optimal fit of a numerically simulated shape with the experimentally obtained drop shape, and appears to be a constant for low applied magnetic fields. At high magnetic fields, on the other hand, experimental measurements deviate from numerical results if a constant interfacial tension is implemented. The difference can be represented as a dependence of apparent interfacial tension on the magnetic field. This idea is investigated computationally by varying the interfacial tension as a function of the applied magnetic field and by comparing the drop shapes with experimental data until a perfect match is found. This estimation method provides a consistent correlation for the variation in interfacial tension at high magnetic fields. A conclusion section provides a discussion of physical effects which may influence the microstructure and contribute to the reported observations.