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45Ti targeted tracers for PET imaging of PSMA.
Chaple, Ivis F; Houson, Hailey A; Koller, Angus; Pandey, Apurva; Boros, Eszter; Lapi, Suzanne E.
Afiliação
  • Chaple IF; Department of Radiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: ichaple@uab.edu.
  • Houson HA; Department of Radiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Koller A; Department of Chemistry, Stony Brook University, Stony Brook, NY 11794, USA.
  • Pandey A; Department of Chemistry, Stony Brook University, Stony Brook, NY 11794, USA.
  • Boros E; Department of Chemistry, Stony Brook University, Stony Brook, NY 11794, USA.
  • Lapi SE; Department of Radiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: lapi@uab.edu.
Nucl Med Biol ; 108-109: 16-23, 2022.
Article em En | MEDLINE | ID: mdl-35189565
ABSTRACT

PURPOSE:

Positron Emission Tomography is an important molecular imaging technique for detection and diagnoses of various disease states. This work aims to develop novel titanium-45 (t½ = 3.08 h) PET tracers using Prostate Specific Membrane Antigen (PSMA) targeting vectors for imaging of prostate cancer as proof of concept for this relatively unexplored isotope. PROCEDURES Titanium-45 was produced on the University of Alabama at Birmingham (UAB) TR24 cyclotron using proton bombardments on natural scandium foils and separated using procedures described previously [1]. After purification, Titanium-45 was used to radiolabel two PSMA-targeting molecules; DFO-DUPA and LDFC-DUPA. Radiochemical yields were determined via radio-high purity liquid chromatography (radioHPLC). The radiolabeled compounds were tested both in vitro and in vivo using PSMA+ cell lines (LNCaP and 22Rv1) and PSMA- cell lines (PC3).

RESULTS:

Titanium-45 was produced and purified in yields suitable for research studies. Radiochemical yields of up to 98 ± 1% were achieved with DFO-DUPA and 92 ± 7% with LDFC-DUPA. PSMA specific targeting was observed in vitro in PSMA positive cells (LNCaP (0.6% ± 0.05%) and confirmed by blocking (0.15% ± 0.04%) (P < 0.0001)), compared to uptake in the PSMA negative cells (PC3 (0.07% ± 0.008%)) and confirmed by blocking (0.07% ± 0.01%) (P = 0.5253). In vivo studies demonstrated statistically significant uptake in LNCaP tumors (2.3% ± 0.3% ID/g) compared to PC3 tumor uptake (0.1% ± 0.07%).

CONCLUSIONS:

This work shows that titanium-45 can be used to radiolabel PSMA targeting compounds with high radiochemical yields. These radiolabeled compounds remain intact in serum for at least two half-lives of titanium-45, showing that these compounds would be appropriate for implementation in the clinical setting. This study shows the feasibility of using titanium-45 as positron emitting radiometal for use in imaging PSMA+ prostate cancer, and illustrates that further research is in this area is warranted.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Titânio / Glutamato Carboxipeptidase II / Antígenos de Superfície Limite: Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Titânio / Glutamato Carboxipeptidase II / Antígenos de Superfície Limite: Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article