A Novel Method to Radiolabel Stealth Liposome through 1,2- dimyristoyl-sn-glycero-3-phosphoethanolamine-N-DTPA with 99mTc and Biological Evaluation
- Authors
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Mirel Cabrera
Arera de Radiofarmacia, Centro de Investigaciones Nucleares, Facultad de Ciencias, Universidad de la República. Mataojo 2055, 11400 Montevideo, Uruguay -
Alejandra Medrano
Departamento de Ciencia y Tecnología de Alimentos, Facultad de Química, Universidad de la República. General Flores 2124, 11800, Montevideo, Uruguay -
Nicole Lecot
Arera de Radiofarmacia, Centro de Investigaciones Nucleares, Facultad de Ciencias, Universidad de la República. Mataojo 2055, 11400 Montevideo, Uruguay -
Marcelo Fernandez
Arera de Radiofarmacia, Centro de Investigaciones Nucleares, Facultad de Ciencias, Universidad de la República. Mataojo 2055, 11400 Montevideo, Uruguay -
Maria Moreno
Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República. Av.Alfredo Navarro 3051, 11600, Montevideo, Uruguay -
Jose A Chabalgoity
Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República. Av.Alfredo Navarro 3051, 11600, Montevideo, Uruguay -
Juan Pablo Gambini
Centro de Medicina Nuclear, Hospital de Clínicas “Dr. Manuel Quintela”, Facultad de Medicina, Universidad de la República. Av. Italia s/n, 11600, Montevideo, Uruguay -
Omar Alonso
Centro de Medicina Nuclear, Hospital de Clínicas “Dr. Manuel Quintela”, Facultad de Medicina, Universidad de la República. Av. Italia s/n, 11600, Montevideo, Uruguay -
Henia Balter
Arera de Radiofarmacia, Centro de Investigaciones Nucleares, Facultad de Ciencias, Universidad de la República. Mataojo 2055, 11400 Montevideo, Uruguay -
Pablo Cabral
Arera de Radiofarmacia, Centro de Investigaciones Nucleares, Facultad de Ciencias, Universidad de la República. Mataojo 2055, 11400 Montevideo, Uruguay
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- Keywords:
- Liposome, nanomedicine, diagnostic oncology
- Abstract
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Purpose: To study surface technetium labeling of stealth DTPA-Liposomeand to evaluate its potential as a molecular imaging tracer for both normal and melanoma-bearing mice.
The radiolabeling yield of liposomes was greater than 90%and showed good chemical and biological stability. Biodistribution studies in normal mice showed blood clearance with hepatic and renal depuration. Melanoma-bearing mice showed a similar pattern of biodistribution with high tumor uptake allowing tumor imaging.
The developed method of surface radiolabeled DTPA-PEG-Liposomes with 99mTc was effective and stable in vivo.
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- 2013-01-14
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- Vol. 2 No. 1 (2013)
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