dc.contributor.author
Heing‐Becker, Isabelle
dc.contributor.author
Grötzinger, Carsten
dc.contributor.author
Beindorff, Nicola
dc.contributor.author
Prasad, Sonal
dc.contributor.author
Erdmann, Sarah
dc.contributor.author
Exner, Samantha
dc.contributor.author
Haag, Rainer
dc.contributor.author
Licha, Kai
dc.date.accessioned
2021-04-07T13:54:42Z
dc.date.available
2021-04-07T13:54:42Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/30236
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-29977
dc.description.abstract
Multimodal imaging probes have attracted the interest of ongoing research, for example, for the surgical removal of tumors. Modular synthesis approaches allow the construction of hybrid probes consisting of a radiotracer, a fluorophore and a targeting unit. We present the synthesis of a new asymmetric bifunctional cyanine dye that can be used as a structural and functional linker for the construction of such hybrid probes. 68Ga‐DOTATATE, a well‐characterized radiopeptide targeting the overexpressed somatostatin receptor subtype 2 (SSTR2) in neuroendocrine tumors, was labeled with our cyanine dye, thus providing additional information along with the data obtained from the radiotracer. We tested the SSTR2‐targeting and imaging properties of the resulting probe 68Ga‐DOTA‐ICC‐TATE in vitro and in a tumor xenograft mouse model. Despite the close proximity between dye and pharmacophore, we observed a high binding affinity towards SSTR2 as well as elevated uptake in SSTR2‐overexpressing tumors in the positron emission tomography (PET) scan and histological examination.
en
dc.format.extent
9 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
fluorescence
en
dc.subject
multimodal imaging
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
A Cyanine‐Bridged Somatostatin Hybrid Probe for Multimodal SSTR2 Imaging in Vitro and in Vivo: Synthesis and Evaluation
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/cbic.202000791
dcterms.bibliographicCitation.journaltitle
ChemBioChem
dcterms.bibliographicCitation.number
7
dcterms.bibliographicCitation.pagestart
1307
dcterms.bibliographicCitation.pageend
1315
dcterms.bibliographicCitation.volume
22
dcterms.bibliographicCitation.url
https://doi.org/10.1002/cbic.202000791
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.funding
DEAL Wiley
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1439-7633