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Titolo:
Tumoral distribution of long-circulating dextran-coated iron oxide nanoparticles in a rodent model
Autore:
Moore, A; Marecos, E; Bogdanov, A; Weissleder, R;
Indirizzi:
Massachusetts Gen Hosp, Dept Radiol, Ctr Mol Imaging Res, Charlestown, MA 02129 USA Massachusetts Gen Hosp Charlestown MA USA 02129 Charlestown, MA 02129 USA
Titolo Testata:
RADIOLOGY
fascicolo: 2, volume: 214, anno: 2000,
pagine: 568 - 574
SICI:
0033-8419(200002)214:2<568:TDOLDI>2.0.ZU;2-V
Fonte:
ISI
Lingua:
ENG
Soggetto:
MONOCYTE CHEMOATTRACTANT PROTEIN-1; CONTRAST AGENTS; EXPRESSION; GLIOMAS; CELLS; MACROPHAGES; METASTASES; PARTICLES; DELIVERY; BRAIN;
Keywords:
animals; brain, iron; brain neoplasms; brain neoplasms, MR; contrast media, experimental studies; iron; neoplasms, experimental studies;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
30
Recensione:
Indirizzi per estratti:
Indirizzo: Weissleder, R Massachusetts Gen Hosp, Dept Radiol, Ctr Mol Imaging Res, Bldg 149,13th St5403, Charlestown, MA 02129 USA Massachusetts Gen Hosp Bldg 149,13th St 5403 Charlestown MA USA 02129
Citazione:
A. Moore et al., "Tumoral distribution of long-circulating dextran-coated iron oxide nanoparticles in a rodent model", RADIOLOGY, 214(2), 2000, pp. 568-574

Abstract

PURPOSE: To investigate the accumulation and cellular uptake of long-circulating dextran-coated iron oxide (LCDIO) particles in malignant neoplasms in vivo. MATERIALS AND METHODS: A gliosarcoma rodent model was established to determine the distribution of a model LCDIO preparation in tumors. LCDIO accumulation in tissue sections was evaluated with multichannel fluorescence microscopy with rhodaminated LCDIO, green fluorescent protein as a tumor marker,and Hoechst 33258 dye as an intravital endothelial stain. Uptake into tumor cells was corroborated with results of immunohistochemical and cell culture uptake experiments. The effect of intratumoral LCDIO uptake on magnetic resonance (MR) imaging signal intensity was evaluated with a 1.5-T superconducting magnet. RESULTS: Tumoral accumulation of LCDIO was 0.11% +/- 0.06 of the injected dose per gram of tissue in brain tumors and was sufficient for detection atMR imaging. In tumor sections, LCDIO was preferentially localized in tumorcells (49.0% +/- 4.6) but was also taken up by macrophages in tumors (21.0% +/- 3.1) and by endothelial cells in the areas of active angiogenesis (6.5% +/- 1.4). In cell culture, LCDIO uptake was strongly correlated with growth rate of tumor cell lines. CONCLUSION: Tumoral LCDIO accumulation was not negligible and helped explain MR imaging signal intensity changes observed in clinical trials. Microscopically, LCDIO accumulated predominantly in tumor cells and tumor-associated macrophages. Uptake into tumor cells appeared to be directly proportional to cellular proliferation rates.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/12/20 alle ore 01:20:35