Literature DB >> 29665104

Understanding the in vivo fate of radioimmunoconjugates for nuclear imaging.

Delphine Vivier1, Sai Kiran Sharma2, Brian M Zeglis1,2,3.   

Abstract

Over the past 25 years, antibodies have emerged as extraordinarily promising vectors for the delivery of radionuclides to tumors for nuclear imaging. While radioimmunoconjugates often produce very high activity concentrations in target tissues, they also are frequently characterized by elevated activity concentrations in healthy organs as well. The root of this background uptake lies in the complex network of biological interactions between the radioimmunoconjugate and the subject. In this review, we seek to provide an overview of these interactions and thus paint a general picture of the in vivo fate of radioimmunoconjugates. To cover the entire story, we have divided our discussion into 2 parts. First, we will address the path of the entire radioimmunoconjugate as it travels through the body. And second, we will cover the fate of the radionuclide itself, as its course can diverge from the antibody under certain circumstances. Ultimately, our goal is to provide the nuclear imaging field with a resource covering these important-yet often underestimated-pathways.
Copyright © 2018 John Wiley & Sons, Ltd.

Entities:  

Keywords:  FcRn; PET; SPECT; antibodies; copper-64; immunoPET; immunoSPECT; indium-111; monoclonal antibodies; pharmacodynamics; pharmacokinetics; positron emission tomography; radioimmunoconjugates; radioiodine; radiometals; single photon emission computed tomography; zirconium-89

Mesh:

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Year:  2018        PMID: 29665104      PMCID: PMC6432633          DOI: 10.1002/jlcr.3628

Source DB:  PubMed          Journal:  J Labelled Comp Radiopharm        ISSN: 0362-4803            Impact factor:   1.921


  133 in total

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