Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, Alabama 35487-0336, United States.
Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019-0065, United States.
Inorg Chem. 2024 Nov 4;63(44):21323-21335. doi: 10.1021/acs.inorgchem.4c03847. Epub 2024 Oct 23.
In an effort to develop hypoxia-active iridium(III) complexes with long visible-light absorption, we synthesized and characterized five bis(terpyridine) Ir(III) complexes bearing oligothienyl substituents on one of the terpyridine ligands, i.e., ( = 0-4). The UV-vis absorption, emission, and transient absorption spectroscopy were employed to characterize the singlet and triplet excited states of these complexes and to explore the effects of varied number of thienyl units on the photophysical parameters of the complexes. photodynamic therapeutic activities of these complexes were assessed with respect to three melanoma cell lines (SKMEL28, A375, and B16F10) and two breast cancer cell lines (MDA-MB-231 and MCF-7) under normoxia (∼18.5% oxygen tension) and hypoxia (1% oxygen tension) upon broadband visible (400-700 nm), blue (453 nm), green (523 nm), and red (633 nm) light activation. It was revealed that the increased number of thienyl units bathochromically shifted the low-energy absorption bands to the green/orange spectral regions and the emission bands to the near-infrared (NIR) regions. The lowest triplet excited-state lifetimes and the singlet oxygen generation efficiency also increased from to substitution but decreased in and substitution. All complexes exhibited low dark cytotoxicity toward all cell lines, but manifested high photocytotoxicity for all cell lines upon visible, blue, and green light activation under normoxia, with showing the strongest photocytotoxicity toward SKMEL28, MDA-MB-231, and MCF-7 cells, and being the most photocytotoxic one for B16F10 and A375 cells. Singlet oxygen, superoxide anion radicals, and peroxynitrite anions were found to likely be involved in the photocytotoxicity exhibited by the complexes. also showed strong photocytotoxicity upon red-light excitation toward all cell lines under normoxia and retained its photocytotoxicity under hypoxia toward all cell lines upon visible, blue, and green light excitation. The hypoxic activity of along with its green to orange light absorption, NIR emission, and low dark cytotoxicity suggest its potential as a photosensitizer for photodynamic therapy applications.
为了开发具有长可见光吸收的缺氧激活型铱(III)配合物,我们合成并表征了五个带有寡噻吩取代基的双(三联吡啶)Ir(III)配合物,即[Ir(tpy)(2,2'-bpy)(L)]X(X = Cl,L = 2,2':6',2"-三联吡啶-4'-羧酸; = 0-4)。我们采用紫外-可见吸收、发射和瞬态吸收光谱来表征这些配合物的单重态和三重态激发态,并探讨了不同数目的噻吩单元对配合物光物理参数的影响。我们根据三种黑色素瘤细胞系(SKMEL28、A375 和 B16F10)和两种乳腺癌细胞系(MDA-MB-231 和 MCF-7)在常氧(约 18.5%氧张力)和缺氧(1%氧张力)下,用宽带可见光(400-700nm)、蓝光(453nm)、绿光(523nm)和红光(633nm)激发,评估了这些配合物的光动力治疗活性。结果表明,噻吩单元数目的增加使低能量吸收带红移至绿光/橙光光谱区,发射带红移至近红外(NIR)区。最低三重态激发态寿命和单线态氧生成效率也随取代基从[Ir(tpy)(2,2'-bpy)(L)]Cl( = 0)增加到[Ir(tpy)(2,2'-bpy)(L)]( = 3),但在[Ir(tpy)(2,2'-bpy)(L)]( = 4)和[Ir(tpy)(2,2'-bpy)(L)]( = 5)中降低。所有配合物在黑暗条件下对所有细胞系均表现出低细胞毒性,但[Ir(tpy)(2,2'-bpy)(L)]( = 0)在常氧下用可见光、蓝光和绿光激发时,对所有细胞系均表现出高的光细胞毒性,[Ir(tpy)(2,2'-bpy)(L)]( = 0)对 SKMEL28、MDA-MB-231 和 MCF-7 细胞的光细胞毒性最强,[Ir(tpy)(2,2'-bpy)(L)]( = 5)对 B16F10 和 A375 细胞的光细胞毒性最强。单线态氧、超氧阴离子自由基和过氧亚硝酸盐阴离子可能参与了配合物的光细胞毒性。[Ir(tpy)(2,2'-bpy)(L)]( = 0)在常氧下用红光激发时也表现出很强的光细胞毒性,在缺氧下用可见光、蓝光和绿光激发时,对所有细胞系仍保持光细胞毒性。[Ir(tpy)(2,2'-bpy)(L)]( = 0)的缺氧活性以及其绿光到橙光吸收、近红外发射和低细胞毒性暗毒性表明其有潜力作为光动力治疗应用的光敏剂。