Metalloporphyrin Enhancement of Magnetic Resonance Imaging of Human Tumor Xenografts in Nude Mice

Philip Furmanski, Clifford Longley

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

Paramagnetic metalloporphyrins were examined for their in vivo biodistribution and their ability to enhance nuclear magnetic resonance imaging of human tumor xenografts in nude mice. The metalloporphyrins tested were: manganese tetrasodium-meso-tetra(4-sulfonatophenyl)-porphine (MnTPPS); manganese meso-tetra-4-pyridylporphine; and gadolinium meso-tetra-4-pyridylporphine. All exhibited high molar relaxiv-ities in aqueous solution. In vivo, at a dose of 2 mg/mouse, MnTPPS depressed the longitudinal relaxation time, T1, significantly in the kidney and less in lung and blood. Manganese meso-tetra-4-pyridylporphine depressed T1 in the kidney, lung and liver, while gadolinium meso-tetra-4-pyridylporphine caused large T1 depressions in the blood, liver, brain and tumor, probably due to dissociation of the metalloporphyrin and binding of Gd to plasma or tissue proteins. At a dose of 10 mg/mouse, MnTPPS caused marked T1 depressions of all tissues tested within 5 min of inoculation, but 48–72 h later, T1 values of normal tissues had returned to near normal, while those of the tumors remained significantly depressed. MnTPPS was able to significantly enhance the intensity of nuclear magnetic resonance images of MX-1 and ZR-75 human breast tumors and CX-1 and LS174T human colon tumor xenografts in nude mice. The results demonstrate that paramagnetic metalloporphyrins, because of their high relaxivities and retention in tumors, have the potential for use as tumor-selective contrast agents for nuclear magnetic resonance imaging.

Original languageEnglish (US)
Pages (from-to)4604-4610
Number of pages7
JournalCancer Research
Volume48
Issue number16
StatePublished - Aug 15 1988
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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