Photoacoustic imaging of vascular hemodynamics: validation with blood oxygenation level-dependent MR imaging

Radiology. 2015 Apr;275(1):110-8. doi: 10.1148/radiol.14140654. Epub 2014 Nov 20.

Abstract

Purpose: To noninvasively assess vascular hemodynamics with photoacoustic imaging (PAI) and blood oxygenation level-dependent (BOLD) magnetic resonance (MR) imaging in phantoms and in an animal model.

Materials and methods: In vivo studies were performed with institutional animal care and use committee approval. In vitro experiments were performed by using a tissue-mimicking phantom in multiple oxygenation conditions (n = 6) to compare PAI measurements and BOLD MR imaging measurements. PAI and T2-weighted spin-echo-based BOLD MR imaging were performed to assess tumor response to carbogen (95% O2, 5% CO2) in mice with head and neck tumors before (n = 11) and after (n = 9) treatment with a vascular disrupting agent (VDA). Two-tailed Pearson correlation analysis was performed to determine the correlation between the parameters measured with PAI and BOLD MR imaging in vitro. Two-tailed paired t tests were used to compare change in tumor hemoglobin oxygen saturation (sO2) levels and BOLD signal in response to carbogen. Changes in PAI and BOLD signal intensity before and after VDA treatment were analyzed for significance by using analysis of variance with repeated measures.

Results: Phantom measurements yielded good correlation between photoacoustically derived sO2 levels and BOLD signal intensity (r = 0.937, P = .005) and partial pressure of oxygen (r = 0.981, P = .005). In vivo hemodynamic response to carbogen was characterized by a significant increase in tumor sO2 levels (P = .003) and BOLD signal (P = .001). When compared with pretreatment estimates, treatment with VDA resulted in a significant reduction in the tumor hemodynamic response to carbogen at PAI (P = .030).

Conclusion: Carbogen-based functional imaging with PAI and BOLD MR imaging enables monitoring of early changes in tumor hemodynamics after vascular targeted therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzopyrans
  • Carbon Dioxide
  • Carcinoma, Squamous Cell / blood supply*
  • Contrast Media
  • Disease Models, Animal
  • Elasticity Imaging Techniques / methods*
  • Hemodynamics / physiology*
  • Image Processing, Computer-Assisted
  • Magnetic Resonance Imaging / methods*
  • Mice
  • Mice, SCID
  • Oxygen
  • Phantoms, Imaging

Substances

  • Benzopyrans
  • Contrast Media
  • Carbon Dioxide
  • carbogen
  • crolibulin
  • Oxygen