Document Detail


Uptake of 153Sm-DTPA-bis-biotin and 99mTc-DTPA-bis-biotin in rat as-30D-hepatoma cells.
MedLine Citation:
PMID:  12623112     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Labeled biotin has been used mainly for pretargeted therapy, an approach for increasing the amount of radioactivity delivered to a cancer cell. The aim of this investigation was to prepare (153)Sm-DTPA-bis-biotin and (99m)Tc-DTPA-bis-biotin in order to study their in vitro and in vivo uptake in rat AS-30D hepatoma cells found in ascites and in implanted tumor. DTPA-bis-biotin (pH 8) was (153)Sm labeled with (153)SmCl(3) and (99m)Tc-DTPA-bis-biotin was prepared via SnCl(2) reduction. Radiochemical purity was >98% in both cases. AS-30D hepatoma cells were obtained from ascites of a rat with hepatoma and were propagated in the peritoneum cavity of normal rats. In vitro ascites cell (153)Sm-DTPA-bis-biotin uptake was compared with (153)SmCl(3) cell uptake. The ratio cell (153)Sm-DTPA-bis-biotin/(153) SmCl(3) was 39.6 and when avidin was added it increased to 50. The ratio (99m)Tc-DTPA-bis-biotin/TcO(4)Na was 8.7. Concentration of (153)Sm-DTPA-bis-biotin in tumor 2, 3 and 24 h after administration, was 5, 15 and 3 times higher than in normal muscle (T/nT). Biodistribution in a 0.083-24 h time period showed that (153)Sm-DTPA-bis-biotin was taken up only by ascites tumor cells and hepatoma cells. Two and 3 h ratio ascites/liver (As/Lv) was 6.4 and 6.0. For (99m)Tc-DTPA-bis-biotin 2 and 3 h T/nT was 15.7 and 4.7 and 2 h As/Lv was 1.4. In conclusion, both radiopharmaceuticals show high uptake in rat AS-30D hepatoma cells in ascites and in implanted tumor. Since lung, thyroid, kidney, liver or pancreas carcinomas are ascites producing cancers (153)Sm-DTPA-bis-biotin would be an adequate therapeutic radiopharmaceutical for these patients whose life quality would be enhanced with control of ascites, and a reduction of the primary tumor and its metastases.
Authors:
Luis Correa-González; Consuelo Arteaga de Murphy; Guillermina Ferro-Flores; Martha Pedraza-López; Eduardo Murphy-Stack; Dolores Mino-León; Graciela Pérez-Villaseñor; Yaneth Díaz-Torres; Rodrigo Muñóz-Olvera
Publication Detail:
Type:  Comparative Study; Evaluation Studies; Journal Article    
Journal Detail:
Title:  Nuclear medicine and biology     Volume:  30     ISSN:  0969-8051     ISO Abbreviation:  Nucl. Med. Biol.     Publication Date:  2003 Feb 
Date Detail:
Created Date:  2003-03-07     Completed Date:  2003-10-27     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9304420     Medline TA:  Nucl Med Biol     Country:  England    
Other Details:
Languages:  eng     Pagination:  135-40     Citation Subset:  IM    
Affiliation:
Servicio de Medicina Nuclear, Hospital de Especialidades, Instituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Mexico.
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MeSH Terms
Descriptor/Qualifier:
Animals
Biotin / analogs & derivatives*,  diagnostic use*,  pharmacokinetics*
Carcinoma, Hepatocellular / metabolism*,  pathology,  radionuclide imaging*
Female
Liver Neoplasms / metabolism,  pathology,  radionuclide imaging
Neoplasm Transplantation
Organ Specificity
Organotechnetium Compounds / diagnostic use*,  pharmacokinetics*
Pentetic Acid / analogs & derivatives*,  diagnostic use*,  pharmacokinetics*
Radiopharmaceuticals / chemical synthesis,  diagnostic use,  pharmacokinetics
Rats
Rats, Wistar
Reference Values
Tissue Distribution
Tumor Cells, Cultured
Chemical
Reg. No./Substance:
0/DTPA-bis-biotin; 0/Organotechnetium Compounds; 0/Radiopharmaceuticals; 0/technetium 99m DTPA-bisbiotin; 58-85-5/Biotin; 67-43-6/Pentetic Acid

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