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Intracellular location of radionuclide in In-111 tropolone labelled polymorphonuclear leukocytes

Conference · · J. Nucl. Med.; (United States)
OSTI ID:6782655
Although autologous PMNs labelled with In-111 tropolone (InT) has been successfully used for the detection of inflammatory lesions in humans, the nature of intracellular binding of this agent has not been properly evaluated. In this present investigation, the distribution of radionuclides in different subcellular fractions was studied and the results were compared to those obtained with cells labelled with In-111 Oxine (InO), the currently used agent of choice. Labelled PMNs were homogenized in STM buffer, pH 7.4 at 4/sup 0/C and subjected to differential centrifugation. Nuclear portion of the cells was purified by sucrose (2.4 M) density centrifugation technic. Purity of the mitochondrial and microsomal fractions were checked by assaying the respective marker enzymes. Purity of the DNA preparations were confirmed by estimating the protein to DNA ratios. All the fractions were counted for radioactivity and the percentage distribution was found. About 30% of nuclear activity was associated with DNA fraction for both preparations. After 20 min incubation of PMNs with InT, all the tropolone was quantitatively recovered in the supernatant indicating that tropolone like oxine is used as a carrier to transport the radionuclide into the cells. The authors conclude much higher (about twice) nuclear binding is observed in case of InT labelled cells as compared to InO preparations. A significant portion of the binding is DNA associated suggesting potential use of the InT labelled PMNs in routine clinical situation.
Research Organization:
Long Island Jewish-Hillside Medical Center, New Hyde Park, NY
OSTI ID:
6782655
Report Number(s):
CONF-840619-
Conference Information:
Journal Name: J. Nucl. Med.; (United States) Journal Volume: 25:5
Country of Publication:
United States
Language:
English