Flow measurements in a blood-perfused collagen vessel using x-ray micro-particle image velocimetry

PLoS One. 2013 Nov 18;8(11):e81198. doi: 10.1371/journal.pone.0081198. eCollection 2013.

Abstract

Blood-perfused tissue models are joining the emerging field of tumor engineering because they provide new avenues for modulation of the tumor microenvironment and preclinical evaluation of the therapeutic potential of new treatments. The characterization of fluid flow parameters in such in-vitro perfused tissue models is a critical step towards better understanding and manipulating the tumor microenvironment. However, traditional optical flow measurement methods are inapplicable because of the opacity of blood and the thickness of the tissue sample. In order to overcome the limitations of optical method we demonstrate the feasibility of using phase-contrast x-ray imaging to perform microscale particle image velocimetry (PIV) measurements of flow in blood perfused hydrated tissue-representative microvessels. However, phase contrast x-ray images significantly depart from the traditional PIV image paradigm, as they have high intensity background, very low signal-to-noise ratio, and volume integration effects. Hence, in order to achieve accurate measurements special attention must be paid to the image processing and PIV cross-correlation methodologies. Therefore we develop and demonstrate a methodology that incorporates image preprocessing as well as advanced PIV cross-correlation methods to result in measured velocities within experimental uncertainty.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Biomimetic Materials / chemistry*
  • Blood Flow Velocity
  • Collagen / chemistry*
  • Diagnostic Imaging / instrumentation
  • Diagnostic Imaging / methods*
  • Humans
  • Image Interpretation, Computer-Assisted
  • Microvessels / anatomy & histology
  • Microvessels / physiology
  • Models, Biological*
  • Neoplasms / blood supply
  • Rheology / instrumentation
  • Rheology / methods*
  • Signal-To-Noise Ratio
  • Tumor Microenvironment
  • X-Rays

Substances

  • Collagen

Grants and funding

Funding for this project was provided by a Clare Boothe Luce Graduate Fellowship, and Virginia Space Grant Consortium Graduate STEM Research Fellowship. The authors gratefully acknowledge support provided by the MBEDS (Multiscale Bio-Engineered Devices and Systems) Center of the Virginia Tech Institute of Critical Technologies and Applied Sciences (ICTAS). Use of the Advanced Photon Source was supported by the U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.