Targeted diagnostic magnetic nanoparticles for medical imaging of pancreatic cancer

Highly aggressive cancer types such as pancreatic cancer possess a mortality rate of up to 80% within the first 6months after diagnosis. To reduce this high mortality rate, more sensitive diagnostic tools allowing an early stage medical imaging of even very small tumours are needed. For this purpose...

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Veröffentlicht in:Journal of controlled release 2015-09, Vol.214, p.76-84
Hauptverfasser: Rosenberger, I., Strauss, A., Dobiasch, S., Weis, C., Szanyi, S., Gil-Iceta, L., Alonso, E., González Esparza, M., Gómez-Vallejo, V., Szczupak, B., Plaza-García, S., Mirzaei, S., Israel, L.L., Bianchessi, S., Scanziani, E., Lellouche, J.-P., Knoll, P., Werner, J., Felix, K., Grenacher, L., Reese, T., Kreuter, J., Jiménez-González, M.
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container_end_page 84
container_issue
container_start_page 76
container_title Journal of controlled release
container_volume 214
creator Rosenberger, I.
Strauss, A.
Dobiasch, S.
Weis, C.
Szanyi, S.
Gil-Iceta, L.
Alonso, E.
González Esparza, M.
Gómez-Vallejo, V.
Szczupak, B.
Plaza-García, S.
Mirzaei, S.
Israel, L.L.
Bianchessi, S.
Scanziani, E.
Lellouche, J.-P.
Knoll, P.
Werner, J.
Felix, K.
Grenacher, L.
Reese, T.
Kreuter, J.
Jiménez-González, M.
description Highly aggressive cancer types such as pancreatic cancer possess a mortality rate of up to 80% within the first 6months after diagnosis. To reduce this high mortality rate, more sensitive diagnostic tools allowing an early stage medical imaging of even very small tumours are needed. For this purpose, magnetic, biodegradable nanoparticles prepared using recombinant human serum albumin (rHSA) and incorporated iron oxide (maghemite, γ-Fe2O3) nanoparticles were developed. Galectin-1 has been chosen as target receptor as this protein is upregulated in pancreatic cancer and its precursor lesions but not in healthy pancreatic tissue nor in pancreatitis. Tissue plasminogen activator derived peptides (t-PA-ligands), that have a high affinity to galectin-1 have been chosen as target moieties and were covalently attached onto the nanoparticle surface. Improved targeting and imaging properties were shown in mice using single photon emission computed tomography–computer tomography (SPECT–CT), a handheld gamma camera, and magnetic resonance imaging (MRI). [Display omitted]
doi_str_mv 10.1016/j.jconrel.2015.07.017
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To reduce this high mortality rate, more sensitive diagnostic tools allowing an early stage medical imaging of even very small tumours are needed. For this purpose, magnetic, biodegradable nanoparticles prepared using recombinant human serum albumin (rHSA) and incorporated iron oxide (maghemite, γ-Fe2O3) nanoparticles were developed. Galectin-1 has been chosen as target receptor as this protein is upregulated in pancreatic cancer and its precursor lesions but not in healthy pancreatic tissue nor in pancreatitis. Tissue plasminogen activator derived peptides (t-PA-ligands), that have a high affinity to galectin-1 have been chosen as target moieties and were covalently attached onto the nanoparticle surface. Improved targeting and imaging properties were shown in mice using single photon emission computed tomography–computer tomography (SPECT–CT), a handheld gamma camera, and magnetic resonance imaging (MRI). 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subjects Animals
Cell Line, Tumor
Ferric Compounds - chemistry
Galectin 1 - chemistry
Galectin 1 - metabolism
Handheld gamma camera
Humans
Maghemite
Magnetic Resonance Imaging
Magnetic resonance imaging (MRI)
Magnetics
Magnetite Nanoparticles
Mice
Pancreatic Neoplasms - diagnosis
Pancreatic Neoplasms - metabolism
Pancreatic Neoplasms - pathology
Radionuclide Imaging
Radiopharmaceuticals
Recombinant Proteins - chemistry
rHSA nanoparticles
Serum Albumin - chemistry
Single photon emission computed tomography–computer tomography (SPECT–CT)
t-PA-ligands to galectins
t-PApeptide1LAC
Tissue Plasminogen Activator - metabolism
Tomography, Emission-Computed, Single-Photon
Xenograft Model Antitumor Assays
title Targeted diagnostic magnetic nanoparticles for medical imaging of pancreatic cancer
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