Article
Radio-Opaque and Surface-Functionalized Polymer Microparticles: Potentially Safer Biomaterials for Different Injection Therapies
University of Maastricht.
Eindhoven University of Technology.
To whom correspondence should be addressed. E-mail: l.koole@ bioch.unimaas.nl. Tel.: +31-43-3881531. Fax: +31-43-3884159.
Abstract

Injectable polymer particles with a diameter in the range of 30−300 μm find applications as a biomaterial in different clinical fields, such as cosmetic surgery, reconstructive surgery, and urology. However, clinical effects tend to disappear after several months, either due to migration of the particles away from the injection site (caused by weak adherence with the surrounding soft tissues) or due to fibrosis (caused by excessive encapsulation of the particles by fibrous tissue). Little is known about the fate of injected microparticles, due to the fact that they are extremely difficult to trace in a noninvasive manner. Design, synthesis, and characterization of new polymeric microspheres with two additional features that can enhance safety and can help to overcome drawbacks of existing products are reported. First, the new microparticles feature clear radio-opacity (X-ray visibility) as they are prepared on the basis of a reactive methacrylic monomer that contains covalently bound iodine. Model experiments reveal that the level of X-ray contrast is sufficient for clinical monitoring; they can be visualized both during the injection and afterward. The particles feature excellent cytocompatibility in vitro and in vivo. Second, a method is explored to functionalize the surface of the particles, for example, through immobilization of collagen. Other extracellular matrix proteins can also be immobilized, and this provides a mechanism to control anchoring of the particles in soft tissue. The results are briefly discussed in the context of improved biomaterials, contemporary X-ray imaging, and control over biomaterial−soft tissue interactions in vivo.
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History
- Published In Issue November 13, 2006
- Received April 21, 2006
Revised Manuscript Received July 17, 2006
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