Photoacoustic imaging of living mouse brain vasculature using hollow gold nanospheres

Biomaterials. 2010 Mar;31(9):2617-26. doi: 10.1016/j.biomaterials.2009.12.007. Epub 2009 Dec 24.

Abstract

Photoacoustic tomography (PAT) also referred to as optoacoustic tomography (OAT) is a hybrid imaging modality that employs nonionizing optical radiation and ultrasonic detection. Here, we describe the application of a new class of optical contrast agents based on mesoscopic hollow gold nanospheres (HAuNS) to PAT. HAuNS are approximately 40 nm in diameter with a hollow interior and consist of a thin gold wall. They display strong resonance absorption tuned to the near-infrared (NIR) range, with an absorption peak at 800 nm, whose photoacoustic efficiency is significantly greater than that of blood. Following surface conjugation with thiolated poly(ethylene glycol), the pegylated HAuNS (PEG-HAuNS) had distribution and elimination half-lives of 1.38 +/- 0.38 and 71.82 +/- 30.46 h, respectively. Compared with PAT images based on the intrinsic optical contrast in nude mice, the PAT images acquired within 2 h after intravenous administration of PEG-HAuNS showed the brain vasculature with greater clarity and detail. The image depicted brain blood vessels as small as approximately 100 mum in diameter using PEG-HAuNS as contrast agents. Preliminary results showed no acute toxicity to the liver, spleen, or kidneys in mice following a single imaging dose of PEG-HAuNS. Our results indicate that PEG-HAuNS are promising contrast agents for PAT, with high spatial resolution and enhanced sensitivity.

Publication types

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

MeSH terms

  • Absorption / drug effects
  • Acoustics*
  • Animals
  • Brain / blood supply*
  • Brain / drug effects
  • Brain Mapping
  • Cell Survival / drug effects
  • Endothelial Cells / cytology
  • Endothelial Cells / drug effects
  • Gold / chemistry*
  • Gold / pharmacokinetics
  • Gold / toxicity
  • Humans
  • Imaging, Three-Dimensional / methods*
  • Light*
  • Mice
  • Nanospheres / chemistry*
  • Nanospheres / toxicity
  • Nanospheres / ultrastructure
  • Organ Specificity / drug effects
  • Polyethylene Glycols / pharmacokinetics
  • Polyethylene Glycols / toxicity
  • Time Factors
  • Tissue Distribution / drug effects
  • Toxicity Tests
  • Umbilical Veins / cytology
  • Umbilical Veins / drug effects

Substances

  • Polyethylene Glycols
  • Gold