Computed tomographic enhancement of the liver, liver abscesses, spleen, and major vessels with perfluorooctylbromide emulsion. Influence of dosage and injection velocity in an animal model

Invest Radiol. 1992 Sep;27(9):698-705. doi: 10.1097/00004424-199209000-00008.

Abstract

Rationale and objectives: Computed tomographic (CT) enhancement of the liver, liver abscess, spleen, and major vessels was investigated between 2 and 48 hours after intravenous administration of perfluorooctylbromide (PFOB emulsion) in an animal model of 63 rabbits.

Methods: Twenty-one animals received 3 g/kg PFOB as a fast bolus injection. Using a slow infusion rate, the same number of animals received either the same dose (3 g/kg) or half the dose (1.5 g/kg).

Results: Vascular enhancement was best after bolus injection of 3 g/kg emulsion. The density peak occurred after 2 hours. A continuous enhancement of approximately 100 Hounsfield units (HU) was observed up to 24 hours in the animals receiving 3 g/kg, independent of the injection velocity. A density peak of 70 HU was found 2 hours after the infusion of 1.5 g/kg. The density peak of the liver, the spleen, and the abscess wall was observed 48 hours after emulsion administration in all groups receiving 3 g/kg. The peak was approximately 150 HU for the liver, 400 HU for the spleen, and 150 HU for the abscess wall. In animals receiving only 1.5 g/kg perflubron, the peak density of the abscess wall was 132 HU after 12 hours, approximately 80 HU for the liver between 2 and 48 hours, and approximately 280 HU after 48 hours for the spleen.

Conclusions: PFOB emulsion produces the highest vascular enhancement within the first 2 hours after the bolus injection of 3 g/kg. For spleen and abscess wall imaging, even the relatively low dose of 1.5 g/kg produced a satisfactory enhancement level for a significant length of time, whereas liver enhancement was best after administration of the higher dose.

MeSH terms

  • Animals
  • Aorta, Abdominal / diagnostic imaging*
  • Contrast Media / administration & dosage*
  • Disease Models, Animal*
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Emulsions
  • Escherichia coli Infections / diagnostic imaging*
  • Fluorocarbons / administration & dosage*
  • Hydrocarbons, Brominated
  • Injections, Intravenous
  • Liver / diagnostic imaging*
  • Liver Abscess / diagnostic imaging*
  • Rabbits
  • Spleen / diagnostic imaging*
  • Time Factors
  • Tomography, X-Ray Computed* / instrumentation
  • Tomography, X-Ray Computed* / methods
  • Vena Cava, Inferior / diagnostic imaging*

Substances

  • Contrast Media
  • Emulsions
  • Fluorocarbons
  • Hydrocarbons, Brominated
  • perflubron