Enhanced osseointegration of endosseous implants by predictable sustained release properties of strontium

J Biomed Mater Res B Appl Biomater. 2015 Jul;103(5):1099-106. doi: 10.1002/jbm.b.33279. Epub 2014 Sep 25.

Abstract

Studies have shown that strontium (Sr) incorporated into surfaces may enhance osseointegration. Thus, we suggested that a sustained Sr release from implant surfaces could improve bone healing. This study verifies and further investigates the effect of a novel Ti-Sr-O functionalized implant surface prepared from a magnetron co-sputtering platform with a continuous release of Sr.

Materials and methods: Four experimental Ti-Sr-O groups, which differed from each other in Sr contents and pre-wash procedures, were tested. Implants were prepared with a Ti-Sr-O coating by means of magnetron co-sputtering and compared to Grade 4 titanium. Composition, morphology and mechanical stability were analyzed; Sr-release data were gained from in vitro washout experiments. In vivo investigations were carried out in a rat model and analyzed histologically regarding bone-to-implant contact and new bone formation 30 days after implantation.

Results: Structural differences were detected between the two basis Ti-Sr-O coatings with 6.7 at.% and 8.9 at.% Sr, respectively. Different release profiles were observed with 8.9 at.% Sr coating exhibiting the highest long-term release of Sr. Median values of new bone formation and bone-to-implant contact was found to be 60.1% and 91.6%, respectively, for the best group compared to 16.6% and 70.6% for the Grade 4 titanium reference. The increase in new bone formation was found to correlate with the amount of Sr released in vitro.

Conclusion: The results show that sputtered Ti-Sr-O coatings with sustained release of Sr may improve osseointegration, and could thus have impact on practical applications for medical implants.

Keywords: implant; in vivo; osseointegration; strontium; sustained release; titanium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Substitutes* / chemistry
  • Bone Substitutes* / pharmacokinetics
  • Bone-Implant Interface*
  • Delayed-Action Preparations / chemistry
  • Delayed-Action Preparations / pharmacokinetics
  • Female
  • Fracture Healing / drug effects*
  • Osseointegration*
  • Rats
  • Rats, Wistar
  • Strontium* / chemistry
  • Strontium* / pharmacokinetics

Substances

  • Bone Substitutes
  • Delayed-Action Preparations
  • Strontium