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Imaging tumour distribution of a polymeric drug delivery platform in vivo by PET‐MRI
Author(s) -
Puttick Simon,
Boase Nathan R.B.,
Blakey Idriss,
Thurecht Kristofer J.
Publication year - 2015
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/jctb.4489
Subject(s) - positron emission tomography , drug delivery , molecular imaging , in vivo , biomedical engineering , modalities , preclinical imaging , pet imaging , medicine , magnetic resonance imaging , gadolinium , medical physics , nuclear medicine , radiology , materials science , nanotechnology , social science , microbiology and biotechnology , sociology , metallurgy , biology
BACKGROUND Over the past decade, molecular imaging has played a key role in the progression of drug delivery platforms from concept to commercialization. Of the molecular imaging techniques commonly utilized, positron emission tomography ( PET ) can yield a breadth of information not easily accessible by other methodologies and when combined with other complementary imaging modalities, is a powerful tool for pre‐ and clinical development of therapeutics. However, very little research has focused on the information available from complimentary imaging modalities. This paper reports on the data‐rich methodologies of contrast enhanced PET / CT and PET / MRI for probing efficacy of polymer drug delivery platforms.RESULTS The information available from an ExiTron nano 6000 contrast enhanced PET / CT and a gadolinium (Gd) enhanced PET / MRI image of a 64 Cu labeled HBP in the same mouse was compared qualitatively.CONCLUSIONS Gd contrast enhanced PET / MRI offers a powerful methodology for investigating the distribution of polymer drug delivery platforms in vivo and throughout a tumour volume. Furthermore, information about depth of penetration away from primary blood vessels can be gleaned, potentially leading to development of more efficacious delivery vehicles for clinical use. © 2014 Society of Chemical Industry

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