Lipid-based blood-pool CT imaging of the liver

Acad Radiol. 1998 Apr:5 Suppl 1:S16-9; discussion S28-30. doi: 10.1016/s1076-6332(98)80047-0.

Abstract

Rationale and objectives: We have recently developed an iodinated lipid-based contrast agent capable of residing in the blood pool for extended periods of time relative to conventional water-soluble contrast agents. The purpose of this study was to examine the effects of combining this new blood-pool agent (ITG-PEG) with a hepatocyte-selective agent (ITG-LE; Molecular Biosystems) for accurate CT detection of small (< 10 mm) VX2 tumors in rabbit liver.

Materials and methods: Preliminary pharmacokinetic analyses were conducted in SD rats (12) by injection of either I-125-labeled ITG-PEG or I-125-labeled ITG-LE followed by subsequent blood collection and quantification of radioactivity. Preliminary CT studies were conducted in both normal (3) and tumor-bearing NZW rabbits (2). Tumor-bearing rabbits were laparotomized and VX2 cells injected directly into the hepatic parenchyma to produce a total of eight focal lesions (2-10 mm diameter). Animals underwent CT scanning 10 days later with multiple techniques including noncontrast and helical i.v. enhanced (600 mg I/kg iohexol), and then 24 hours later using both ITG-PEG and ITG-LE (200 mg I/kg). Tissue density measurements (HU) of liver, tumor, and blood (descending aorta) were acquired in each case for comparison. Tumor morphology was verified by gross pathologic inspection.

Results: Pharmacokinetic analysis in rats as well as CT studies in normal rabbits revealed that ITG-PEG remains in the blood-pool phase for more than 2 hours following i.v. administration. In fact, blood density in normal rabbit obtained with ITG-PEG was 95.1 HU +/- 5.8 at 120 minutes compared to 90.7 HU +/- 6.1 immediately after injection. Although liver enhancement was greater with iohexol (67 HU within 1 minute of injection), than for ITG-PEG/ITG-LE (32 HU, 60 minutes postinjection), liver to lesion ratios favored ITG-PEG/ITG-LE due to significant enhancement of tumor itself with iohexol (+40 HU). Tumor enhancement was minimal with ITG-PEG/ITG-LE. Lesions were subjectively much better defined with ITG-PEG/ITG-LE with sharper edge definition.

Conclusion: In these animal models, a new iodinated lipid-based contrast agent composed of both blood pool and hepatocyte-selective components afforded favorable CT imaging results compared to a conventional urographic agent, albeit at one-third the total iodine dose.

MeSH terms

  • Animals
  • Cholesterol / administration & dosage
  • Cholesterol / pharmacokinetics
  • Contrast Media / administration & dosage*
  • Contrast Media / pharmacokinetics
  • Emulsions / administration & dosage*
  • Emulsions / pharmacokinetics
  • Female
  • Liver Neoplasms, Experimental / diagnostic imaging*
  • Polyethylene Glycols / administration & dosage
  • Polyethylene Glycols / pharmacokinetics
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Tomography, X-Ray Computed*
  • Triglycerides / administration & dosage
  • Triglycerides / pharmacokinetics
  • Triolein / administration & dosage
  • Triolein / pharmacokinetics

Substances

  • 2-oleoylglycerol-1,3-bis(7-(3-amino-2,4-6-triiodophenyl)heptanoate)
  • Contrast Media
  • Emulsions
  • Triglycerides
  • Triolein
  • Polyethylene Glycols
  • monomethoxypolyethylene glycol
  • Cholesterol