Synthesis, in vitro evaluation, and 68Ga-radiolabeling of CDP1 toward PET/CT imaging of bacterial infection

dc.contributor.authorDutta, Jyotibon
dc.contributor.authorBaijnath, Sooraj
dc.contributor.authorSomboro, Anou M.
dc.contributor.authorNagiah, Savania
dc.contributor.authorAlbericio, Fernando
dc.contributor.authorDe la Torre, Beatriz G.
dc.contributor.authorMarjanovic-Painter, Biljana
dc.contributor.authorZeevaart, Jan Rijn
dc.contributor.authorSathekge, Mike Machaba
dc.contributor.authorKruger, Hendrik G.
dc.contributor.authorChuturgoon, Anil
dc.contributor.authorNaicker, Tricia
dc.contributor.authorEbenhan, Thomas
dc.contributor.authorGovender, Thavendran
dc.date.accessioned2018-01-15T08:13:11Z
dc.date.issued2017-10
dc.description.abstractBacterial infections are a major concern in the human health sector due to poor diagnosis and development of multidrug-resistant strains. PET/CT provides a means for the non-invasive detection and localization of the infectious foci; however, the radiotracers available are either cumbersome to prepare or their exact contribution toward the imaging is not yet established. Human antimicrobial peptides are of interest for development as PET radiotracers as they are an integral component of the immune system, non-immunogenic toward the recipient, and show selectivity toward pathogens such as bacteria. Herein we report on the potential of LL37, a human cathelicidin antimicrobial peptide, as a radiotracer for bacterial imaging. Bifunctional chelator 1,4,7-triazacyclononane,1-glutaric acid-4,7-acetic acid was utilized to functionalize the antimicrobial peptide, which in turn was capable of chelating gallium. The synthesized natGa-CDP1 showed bacterial selectivity and low affinity toward hepatic cells, which are favorable characteristics for further preclinical application.en_ZA
dc.description.departmentNuclear Medicineen_ZA
dc.description.embargo2018-10-30
dc.description.librarianhj2018en_ZA
dc.description.sponsorshipThe Department of Science and Technology, University of KwaZulu Natal, National Research Foundation and Aspen Pharmacare.en_ZA
dc.description.urihttp://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1747-0285en_ZA
dc.description.urihttp://wileyonlinelibrary.com/journal/cbdden_ZA
dc.identifier.citationDutta, J., Baijnath, S., Somboro, A.M. et al. 2017, 'Synthesis, in vitro evaluation, and 68Ga-radiolabeling of CDP1 toward PET/CT imaging of bacterial infection', Chemical Biology and Drug Design, vol. 90, no. 4, pp. 572-579.en_ZA
dc.identifier.issn1747-0277 (print)
dc.identifier.issn1747-0285 (online)
dc.identifier.other10.1111/cbdd.12980
dc.identifier.urihttp://hdl.handle.net/2263/63536
dc.language.isoenen_ZA
dc.publisherWileyen_ZA
dc.rights© 2017 John Wiley & Sons A/S. This is the pre-peer reviewed version of the following article : 'Synthesis, in vitro evaluation, and 68Ga-radiolabeling of CDP1 toward PET/CT imaging of bacterial infection', Chemical Biology and Drug Design, vol. 90, no. 4, pp. 572-579, 2017, doi : 10.1111/cbdd.12980 . The definite version is available at : http://onlinelibrary.wiley.comjournal/10.1111/(ISSN)1747-0285.en_ZA
dc.subjectSolid-phase peptide synthesisen_ZA
dc.subjectBacteriaen_ZA
dc.subjectCDP1en_ZA
dc.subjectInfectionen_ZA
dc.subjectLL37en_ZA
dc.subjectNODAGAen_ZA
dc.subjectPositron emission tomography (PET)en_ZA
dc.subjectAntimicrobial peptide (AMP)en_ZA
dc.subjectCathelicidinen_ZA
dc.subjectInflamationen_ZA
dc.subjectDiagnosisen_ZA
dc.subjectMedicineen_ZA
dc.subjectRadiotracersen_ZA
dc.subjectProteinen_ZA
dc.titleSynthesis, in vitro evaluation, and 68Ga-radiolabeling of CDP1 toward PET/CT imaging of bacterial infectionen_ZA
dc.typePostprint Articleen_ZA

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