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Effects of μCT radiation on tissue engineered bone-like constructs.

Thomas P Kraehenbuehl1, Martin Stauber, Martin Ehrbar

  • 1Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.

Biomedizinische Technik. Biomedical Engineering
|June 24, 2010
PubMed
Summary

Micro-computed tomography (μCT) imaging of engineered bone can impact cell survival and function. Even low X-ray doses (1.9 Gy) used for imaging may cause irreparable cellular damage, affecting research outcomes.

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Area of Science:

  • Biomaterials Science
  • Cell Biology
  • Medical Imaging

Background:

  • Micro-computed tomography (μCT) is a non-destructive imaging technique for monitoring tissue-engineered bone constructs in situ.
  • The impact of μCT's X-ray dose on bone development and experimental results is not fully understood.

Purpose of the Study:

  • To develop a model system for assessing the in vitro effects of μCT imaging on engineered bone.
  • To evaluate the impact of μCT irradiation doses on pre-osteoblastic cell survival and function.

Main Methods:

  • Used pre-osteoblastic MC3T3-E1 cells embedded in 3D collagen type I matrices as a model system.
  • Exposed cells to μCT imaging doses of 1.9 Gy and 7.6 Gy.
  • Assessed cell survival at 2 hours and 2 days post-irradiation.

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  • Measured alkaline phosphatase (ALP) activity at 2 and 7 days post-irradiation.
  • Main Results:

    • No significant reduction in cell survival was observed 2 hours after 1.9 Gy irradiation.
    • Cell survival significantly decreased by 15% at 24 hours post-1.9 Gy irradiation.
    • A dose of 7.6 Gy reduced cell survival by approximately 40% at 2 days.
    • Alkaline phosphatase activity was significantly decreased 7 days after 1.9 Gy irradiation.

    Conclusions:

    • μCT imaging, even at low doses (1.9 Gy) necessary for adequate image quality, can induce significant, potentially irreparable, cellular damage.
    • The findings suggest that μCT irradiation may influence the development of tissue-engineered bone constructs.
    • Further research is needed to optimize μCT protocols to minimize biological effects in regenerative medicine applications.