Academic Journal

Pt(II)‐Phenanthroline‐Ln(III)‐DOTA d–f Hybrids as Small‐Molecule Theranostics

التفاصيل البيبلوغرافية
العنوان: Pt(II)‐Phenanthroline‐Ln(III)‐DOTA d–f Hybrids as Small‐Molecule Theranostics
المؤلفون: Brito, Beatriz, Price, Thomas W., Bañobre‐López, Manuel, Gallo, Juan, Stasiuk, Graeme J.
المساهمون: University of Hull, Engineering and Physical Sciences Research Council
المصدر: European Journal of Inorganic Chemistry ; volume 27, issue 17 ; ISSN 1434-1948 1099-0682
بيانات النشر: Wiley
سنة النشر: 2024
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: 1,10‐Phenanthroline d‐ or f‐ metal complexes can be utilised in biomedical applications such as imaging or therapeutics. Herein, we designed bimetallic d ‐block metal‐phenanthroline f ‐block metal‐1,4,7,10‐tetraazacyclododecane‐1,4,7,1,0‐tetraacetic acid (DOTA) conjugates as theranostic agents to simultaneously achieve both of these applications. Luminescence studies show the 1,10‐phenanthroline‐Eu(III)‐DOTA complexes displayed an off/on/off pH‐dependent switch, demonstrating their potential as pH‐responsive lanthanide luminescence probes. Relaxometry studies showed that the 1,10‐phenanthroline‐Gd(III)‐DOTA complexes present a r 1 of 5.15±0.05 mM −1 s −1 and could thus be used as magnetic resonance (MR) contrast agents. Complexation of Pt(II) by the 1,10‐phenanthroline moiety resulted in quenching of the Eu(III) luminescence, but an enhancement of the Gd(III) relaxivity ( r 1 =7.53±0.69 mM −1 s −1 ). Cell viability studies of the d–f hybrids in a cancer cell line showed the potential of these complexes as anticancer agents, as the IC 50 for the Pt(II)/Gd(III) complex (IC 50 =24.9 μM) was lower than that of cisplatin (IC 50 =31.6 μM). As such, Pt(II)‐1,10‐phenanthroline‐Gd(III)‐DOTA complexes are promising theranostic agents for cancer therapy.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/ejic.202400063
الاتاحة: http://dx.doi.org/10.1002/ejic.202400063
Rights: http://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.4C1B7DC4
قاعدة البيانات: BASE