The Graduate School and University Center of The City University of New York
A Pretargeted Spect Imaging Strategy Employing Technetium-99M Based on Bioorthogonal Diels-Alder Click Chemistry
Abstract
dc:description.abstract<p>A series of related N<sub>3</sub>S <sup>99m</sup>Tc-peptide complexes were synthesized and tested for use in pretargeting SPECT imaging that utilizes the bioorthogonal Diels-Alder click reaction between tetrazine (Tz) and transcyclooctene (TCO). The objective was to optimize the excretory pathways of the <sup>99m</sup>Tc-peptide complexes for maximum tumor targeting with the <em>in vivo </em>“click” and minimum non-target uptake. The <sup>99m</sup>Tc–tetrazine constructs were prepared by reaction of <sup>99m</sup>Tc-peptide complexes (<sup>99m</sup>Tc-FKC, <sup>99m</sup>Tc-FKCR, <sup>99m</sup>Tc-DKC, and <sup>99m</sup>Tc-SKC) with Tz-NHS or Tz-PEG<sub>5</sub>-NHS to form <sup>99m</sup>Tc FK(Tz)C,<sup> 99m</sup>Tc-FK(PEG<sub>5</sub>-Tz)CR, <sup>99m</sup>Tc-DK(PEG<sub>5</sub>-Tz)C, and <sup>99m</sup>Tc-SK(PEG<sub>5</sub>-Tz)C. Log P values were obtained to determine hydrophilicity of each complex. Bovine serum albumin (BSA) was modified with TCO, reacted with each complex, and the “click” reaction was confirmed using Radio-TLC. Biodistributions and blood half-life studies were then performed on healthy athymic mice to determine which complex exhibited the optimal excretory characteristics. The Radio-TLC results indicate that each complex contains a viable Tz moeity. The biodistribution results suggest that <sup>99m</sup>Tc-FK(PEG<sub>5</sub>-Tz)CR has the most promising excretory pathway wherein excretion through the gut and intestines is minimized. The blood half-life values obtained indicated that clearance from the blood is not likely too fast to prevent the <em>in vivo</em> “click” reaction from occurring. Mice bearing xenografted SW1222 tumors were pretargeted with A33-TCO followed by the <sup>99m</sup>Tc-peptide-Tz complexes. SPECT/CT images were obtained and the <em>in vivo</em> “click” was confirmed for both <sup>99m</sup>Tc-FK(Tz)C and <sup>99m</sup>Tc-FK(PEG<sub>5</sub>-Tz)CR. <sup>99m</sup>Tc-FK(PEG<sub>5</sub>-Tz)CR exhibited higher tumor:background ratios than did <sup>99m</sup>Tc-FK(Tz)C but had too high intestinal uptake for translation to the clinic.</p>
Degree
thesis:*- Name thesis:degree_name
- Doctor of Philosophy
- Level thesis:degree_level
- Doctoral
- Discipline thesis:degree_discipline
- Chemistry
- Grantor
- The Graduate School and University Center of The City University of New York
- Year dc:date.available
- 2019
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Walsh, Justin H
- Advisor dc:contributor.advisor
-
- Lynn Francesconi
- Committee members dc:contributor.committeemember
-
- Brian Zeglis
- Jason Lewis
- Maria Contel
Subjects
dc:subject × 10Identifiers
dc:identifier.*- Repository record dc:identifier
- https://academicworks.cuny.edu/gc_etds/3240
- OAI identifier oai:identifier
- oai:academicworks.cuny.edu:gc_etds-4269