INVESTIGADORES
ROMERO Eder Lilia
artículos
Título:
99mTc labeling and biological evaluation of conventional liposomes
Autor/es:
GABRIELA NAVARRO; PABLO CABRAL ; MIREL CABRERA; MARCELO FERNÁNDEZ ; JUAN P. GAMBINI; ANTONIO MALANGA; OMAR ALONSO; MARÍA J. MORILLA; EDER ROMERO; EDUARDO SAVIO
Revista:
ALASBIMN JOURNAL
Editorial:
Asociación Latinoamericana de Sociedades de Biología y Medicina Nuclear (Alasbimn)
Referencias:
Año: 2011 vol. 51 p. 1 - 8
ISSN:
0717-4055
Resumen:
Background. Liposomes are self assembled supramolecular systems, composed by phospholipids and cholesterol, designed for the transportation of drugs or radionuclides. Physical properties of 99mTc (pure gamma emitter with E = 140 KeV, t1/2= 6 hours) makes it useful for scintigraphic imaging. Purpose. The goal of this study was to evaluate 99mTc labeled conventional liposomes as potential diagnostic agents for malignant lesions. The goal of this study was to evaluate 99mTc labeled conventional liposomes as potential diagnostic agents for malignant lesions. Methods. The studied liposome composition was hosphatidylcholine: dioleilphosphatidylcholine: cholesterol (1.1:0.4:1molar rate). In order to optimize the labeling, SnF2 was used as reducing agent. Radiochemical purity and labeling efficiency were evaluated using ascending thin layer chromatography. Scintigraphy images were obtained at 1 hour post?]injection of labeled liposomes to healthy mice and with spontaneous breast tumors. The studied liposome composition was hosphatidylcholine: dioleilphosphatidylcholine: cholesterol (1.1:0.4:1molar rate). In order to optimize the labeling, SnF2 was used as reducing agent. Radiochemical purity and labeling efficiency were evaluated using ascending thin layer chromatography. Scintigraphy images were obtained at 1 hour post?]injection of labeled liposomes to healthy mice and with spontaneous breast tumors. Results. Labeled liposomes showed stability during 24 hours, being 138 ?Êg the optimal amount of reducing agent for the technique used. Labeled liposomes showed stability during 24 hours, being 138 ?Êg the optimal amount of reducing agent for the technique used. Conclusions. The described method allows the production of 99mTc labeled liposomes in a simple, efficient and stable way. The radiopharmaceutical showed a physicochemical and biological behavior that allows its potential use as a tumor imaging agent, although further studies are required to confirm this issue. The described method allows the production of 99mTc labeled liposomes in a simple, efficient and stable way. The radiopharmaceutical showed a physicochemical and biological behavior that allows its potential use as a tumor imaging agent, although further studies are required to confirm this issue.