Nuclear Medicine and Biology
Volume 39, Issue 3 , Pages 335-346, April 2012

Insights into the failure of the potential, neutral myocardial imaging agent TcN-NOET: physicochemical identification of by-products and degradation species

  • Francesco Tisato

      Affiliations

    • ICIS-CNR, Corso Stati Uniti, 4, 35127 Padova, Italy
    • Corresponding Author InformationCorresponding author.
  • ,
  • Cristina Bolzati

      Affiliations

    • ICIS-CNR, Corso Stati Uniti, 4, 35127 Padova, Italy
    • Department Pharmaceutical Sciences, University of Padova, Via Marzolo, 5, 35131 Padova, Italy
  • ,
  • Fiorenzo Refosco

      Affiliations

    • ICIS-CNR, Corso Stati Uniti, 4, 35127 Padova, Italy
  • ,
  • Marina Porchia

      Affiliations

    • ICIS-CNR, Corso Stati Uniti, 4, 35127 Padova, Italy
  • ,
  • Roberta Seraglia

      Affiliations

    • ISTM-CNR, Corso Stati Uniti, 4, 35131 Padova, Italy
  • ,
  • Davide Carta

      Affiliations

    • Department Pharmaceutical Sciences, University of Padova, Via Marzolo, 5, 35131 Padova, Italy
  • ,
  • Roberto Pasqualini

      Affiliations

    • IBA Centre de Saclay, B.P. 32, 91192 Gif-sur-Yvette, France

Received 6 June 2011; received in revised form 14 September 2011; accepted 17 September 2011. published online 02 December 2011.

Abstract 

Introduction

The neutral complex [99mTc(N)(NOEt)2], often referred to as TcN-NOET [NOEt=N-ethoxy,N-ethyldithiocarbamate(1−)], was proposed several years ago as a myocardial imaging agent. Despite some favorable clinical properties evidenced during phase I and phase II studies, the overall results of the European and American phase III clinical studies have been judged insufficient for a successful approval process by the regulatory agencies.

Methods

Non-carrier-added and carrier-added experiments using short-lived 99mTc and long-lived 99gTc have been utilized to prepare a series of bis-substituted [Tc(N)(DTC)2] complexes [DTC=dithiocarbamate(1−)]. They have been purified by means of chromatographic techniques (high-performance liquid chromatography and thin-layer chromatography) and identified via double detection (UV-vis and radiometry) by comparison with authenticated samples of 99gTc compounds prepared by conventional coordination chemistry procedures.

Results

The molecular structure of the lipophilic, neutral complex cis-[Tc(N)(NOEt)2] has been assigned by comparison with similar nitrido-Tc(V) complexes already reported in the literature. Novel bis-substituted nitrido-Tc complexes containing hydrolyzed portions of coordinated NOEt, namely, N-ethyldithiocarbamate [NHEt(1−)] and N-hydroxy, N-ethyldithiocarbamate [NOHEt(1−)], have been prepared and characterized by means of multinuclear nuclear magnetic resonance spectroscopy and mass spectrometry.

Conclusions

Despite the identification of these “hydrolyzed” species, it is still unclear whether the failure to reach the clinical goal of the perfusion tracer [99mTc(N)(NOEt)2] is related to the degradation processes evidenced in this study or is the result of the mediocre imaging properties of the tracer.

Keywords: Technetium radiopharmaceuticals, Coordination chemistry, Mass spectrometry, Myocardial imaging

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PII: S0969-8051(11)00228-9

doi:10.1016/j.nucmedbio.2011.09.007

Nuclear Medicine and Biology
Volume 39, Issue 3 , Pages 335-346, April 2012