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Synthesis and evaluation of 99mTc-N-sulfanilamide ferrocene carboxamide as bacterial infections detector.

Abstract
A technetium-99m-labeled derivative from sulfanilamide, further referred to as (99m)Tc-N-SFC, targeting infections in experimental animals, has been synthesized. The biological features of this radioactive agent have also been studied. The N-sulfanilamide ferrocene carboxamide (N-SFC) was chemically synthesized and then labeled with technetium-99m. It has been confirmed through this work that it is stable and obtained with radiolabelling yield (>87%). Radiochemical analyses of (99m)Tc-N-SFC revealed that the molecule was labeled rapidly (within 2 min) and effectively with little free pertechnetate in the preparations containing purified compound. Furthermore, in vitro investigations were conducted and the label's stability in serum was observed up to 24 h of testing. Uptake of the tracer with live and heat/killed bacteria was compared in physiological conditions and was about 69% and 61.9% for the Escherichia coli and Staphylococcus aureus strains, respectively. We concluded that synthesis and labeling of Sulfanilamide derivative with (99m-)Tc by this method is rapid, efficient and safe. Biodistribution studies demonstrated that our radiolabeled compound is accumulated rapidly and significantly (P<.05) at infection sites. The comparison of the (99m)Tc-N-SFC accumulation at sites of S. aureus-infected animals, which is expressed as target-to-non-target ratio, (2.88 ± 0.10) with other radiotracers was discussed.
AuthorsImen Essouissi, Wafa Ghali, Nadia Malek Saied, Mouldi Saidi
JournalNuclear medicine and biology (Nucl Med Biol) Vol. 37 Issue 7 Pg. 821-9 (Oct 2010) ISSN: 1872-9614 [Electronic] United States
PMID20870157 (Publication Type: Journal Article)
CopyrightCopyright © 2010 Elsevier Inc. All rights reserved.
Chemical References
  • Ferrous Compounds
  • Metallocenes
  • Organotechnetium Compounds
  • Radiopharmaceuticals
  • technetium 99m N-sulfanilamide ferrocene carboxamide
Topics
  • Animals
  • Ferrous Compounds (chemical synthesis, pharmacokinetics)
  • Metallocenes
  • Mice
  • Organotechnetium Compounds (chemical synthesis, pharmacokinetics)
  • Radionuclide Imaging
  • Radiopharmaceuticals (chemical synthesis, pharmacokinetics)
  • Staphylococcal Infections (diagnostic imaging, microbiology)
  • Staphylococcus aureus (physiology)
  • Tissue Distribution

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