Nanocomposites are undoubtedly making an impact in many fields of technology, where profound advantages over conventional composites can be readily identified. Whether they have a role in medical technology is yet to be determined. The answer may lie in the degree of subtly that is brought to the underlying scientific issues.
The era of composite materials
When I was a young man, what we now know as materials science departments at universities were called metallurgy departments and metals ruled the world. Polymers, which gave rise to those inferior things we called plastics, were just being introduced and high performance ceramics barely existed. Within the then imperious world of metals, profound technologies were established that allowed major strengthening and toughening mechanisms to be developed that gave us ultrahigh performance alloys. Their strengthening mechanisms often depended on phase changes and precipitates, which were deliberately introduced to control plastic deformation and crack propagation. However, those magnificent alloys were expensive and heavy, and applications in areas such as aerospace and consumer electronic goods became limited. Before long, the same types of structural features were introduced into the polymer and ceramic fields and often gave good increases in strength to the intrinsically weak polymers, and acceptable increases in toughness to the inherently brittle ceramics. Foremost amongst the mechanisms were those associated with the development of multi-phase materials and the introduction of fillers into plastics and ceramics; the era of composite materials was born. In general, the principles of resistance to plastic deformation that were applied to the alloys also applied to these composites; the distributed particles or fibres acted as barriers to moving cracks and to plastic flow. Of equal importance was the fact that the fillers such as silica were often extremely cheap, which provided even greater cost savings.
However, with the vast majority of implantable devices this was not the case. There were two major reasons for this. First, for
those materials where inertness and long-term performance were essential, the presence of a microscopic second phase could be detrimental; the release of small particles in this phase, often of micron dimensions, could stimulate a foreign body response far in excess of that associated with the principle matrix phase. It really did not matter what this second phase was made of, because small particles stimulate inflammation by virtue of their size and shape not their chemistry. The massive tissue reactions and appalling clinical consequences associated with the use of the polytetrafluoroethylene-alumina or polytetrafluoroethylene-carbon composites as components of temporomandibular joint prostheses in the 1980s showed just how bad an idea this could be. It should be noted that one area of healthcare has benefitted enormously from particulate resin based composites and that is dentistry. We would not have light-cured white fillings without these materials; the biological safety issues of swallowing the occasional microparticle released from a filling are nowhere near the same order of magnitude. The second reason that militated against implantable composites was the fact that the frequently claimed improvement in bioactivity was difficult to demonstrate or justify. If it is claimed that a dispersed second phase made of a putative bioactive material such as hydroxyapatite or a glass-ceramic improves the bioactivity (for example, bone-bonding activity) of a material, then we have to question how much of that second material actually occupies sites at the surface of the composite where they could exert their biological effect. It is unlikely that it will be a high percentage.
A great deal has to be learnt about the biological activity of nanoparticles and nanotopographies and, as usual, there is still time for us to get this all wrong again. But at least we have some hope now that the inspiration of nature can be put to really good effect.
1812–1816 (2008).
Brussels 1000, Belgium, tel. +32 4 7597 0556
e-mail: peggy@morgan-masterson.com [5], www.morgan-masterson.com [6]

Professor David Williams DSc, FREng
Professor Williams retired from the University of Liverpool, after 40 years, at the end of 2007. He retains the position of Emeritus Professor there and now has a series of professorial appointments in the USA, Australia, South Africa and China. In the USA he is Director of International Affairs for the Wake Forest Institute of Regenerative Medicine. He offers consulting services from his company Morgan & Masterson, based in Brussels, Belgium. He is Editor-in-Chief of Biomaterials, the leading journal in the biomaterials field.