Material nanosizing effect on living organisms: non-specific, biointeractive, physical size effects

  • Fumio Watari
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Noriyuki Takashi
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Atsuro Yokoyama
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Motohiro Uo
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Tsukasa Akasaka
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Yoshinori Sato
    Graduate School of Environmental Studies, Tohoku UniversitySendai 980-8579, Japan
  • Shigeaki Abe
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Yasunori Totsuka
    Graduate School of Dental Medicine, Hokkaido UniversitySapporo 060-8586, Japan
  • Kazuyuki Tohji
    Graduate School of Environmental Studies, Tohoku UniversitySendai 980-8579, Japan

書誌事項

公開日
2009-04-08
権利情報
  • https://royalsociety.org/journals/ethics-policies/data-sharing-mining/
DOI
  • 10.1098/rsif.2008.0488.focus
公開者
The Royal Society

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説明

<jats:p>Nanosizing effects of materials on biological organisms was investigated by biochemical cell functional tests, cell proliferation and animal implantation testing. The increase in specific surface area causes the enhancement of ionic dissolution and serious toxicity for soluble, stimulative materials. This effect originates solely from materials and enhances the same functions as those in a macroscopic size as a catalyst. There are other effects that become prominent, especially for non-soluble, biocompatible materials such as Ti. Particle size dependence showed the critical size for the transition of behaviour is at approximately 100 μm, 10 μm and 200 nm. This effect has its origin in the biological interaction process between both particles and cells/tissue. Expression of superoxide anions, cytokines tumour necrosis factor-α and interleukin-1β from neutrophils was increased with the decrease in particle size and especially pronounced below 10 μm, inducing phagocytosis to cells and inflammation of tissue, although inductively coupled plasma chemical analysis showed no dissolution from Ti particles. Below 200 nm, stimulus decreases, then particles invade into the internal body through the respiratory or digestive systems and diffuse inside the body. Although macroscopic hydroxyapatite, which exhibits excellent osteoconductivity, is not replaced with natural bone, nanoapatite composites induce both phagocytosis of composites by osteoclasts and new bone formation by osteoblasts when implanted in bone defects. The progress of this bioreaction results in the conversion of functions to bone substitution. Although macroscopic graphite is non-cell adhesive, carbon nanotubes (CNTs) are cell adhesive. The adsorption of proteins and nano-meshwork structure contribute to the excellent cell adhesion and growth on CNTs. Non-actuation of the immune system except for a few innate immunity processes gives the non-specific nature to the particle bioreaction and restricts reaction to the size-sensitive phagocytosis. Materials larger than cell size, approximately 10 μm, behave inertly, but those smaller become biointeractive and induce the intrinsic functions of living organisms. This bioreaction process causes the conversion of functions such as from biocompatibility to stimulus in Ti-abraded particles, from non-bone substitutional to bone substitutional in nanoapatite and from non-cell adhesive to cell adhesive CNTs. The insensitive nature permits nanoparticles that are less than 200 nm to slip through body defence systems and invade directly into the internal body.</jats:p>

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