Maggioni Daniela, Galli Marco, D'Alfonso Laura, Inverso Donato, Dozzi Maria Vittoria, Sironi Laura, Iannacone Matteo, Collini Maddalena, Ferruti Paolo, Ranucci Elisabetta, D'Alfonso Giuseppe
Dipartimento di Chimica, Università degli Studi di Milano , Via Golgi 19, 20133 Milano, Italy.
Inorg Chem. 2015 Jan 20;54(2):544-53. doi: 10.1021/ic502378z. Epub 2015 Jan 2.
A polymer complex (1P) was synthesized by binding bis(cyclometalated) Ir(ppy)2(+) fragments (ppy = 2-phenylpyridyl) to phenanthroline (phen) pendants of a poly(amidoamine) copolymer (PhenISA, in which the phen pendants involved ∼6% of the repeating units). The corresponding molecular complex Ir(ppy)2(bap) (1M, bap = 4-(butyl-4-amino)-1,10-phenanthroline) was also prepared for comparison. In water solution 1P gives nanoaggregates with a hydrodynamic diameter of 30 nm in which the lipophilic metal centers are presumed to be segregated within polymer tasks to reduce their interaction with water. Such confinement, combined with the dilution of triplet emitters along the polymer chains, led to 1P having a photoluminescence quantum yield greater than that of 1M (0.061 vs 0.034, respectively, in an aerated water solution) with a longer lifetime of the (3)MLCT excited states and a blue-shifted emission (595 nm vs 604 nm, respectively). NMR data supported segregation of the metal centers. Photoreaction of O2 with 1,5-dihydroxynaphthalene showed that 1P is able to sensitize (1)O2 generation but with half the quantum yield of 1M. Cellular uptake experiments showed that both 1M and 1P are efficient cell staining agents endowed with two-photon excitation (TPE) imaging capability. TPE microscopy at 840 nm indicated that both complexes penetrate the cellular membrane of HeLa cells, localizing in the perinuclear region. Cellular photodynamic therapy tests showed that both 1M and 1P are able to induce cell apoptosis upon exposure to Xe lamp irradiation. The fraction of apoptotic cells for 1M was higher than that for 1P (74 and 38%, respectively) 6 h after being irradiated for 5 min, but cells incubated with 1P showed much lower levels of necrosis as well as lower toxicity in the absence of irradiation. More generally, the results indicate that cell damage induced by 1M was avoided by binding the iridium sensitizers to the poly(amidoamine).
通过将双(环金属化)铱(ppy)₂⁺片段(ppy = 2 - 苯基吡啶基)与聚(酰胺胺)共聚物(PhenISA,其中菲咯啉侧基占重复单元的约6%)的菲咯啉(phen)侧基结合,合成了一种聚合物配合物(1P)。还制备了相应的分子配合物[Ir(ppy)₂(bap)]⁺(1M,bap = 4 - (丁基 - 4 - 氨基) - 1,10 - 菲咯啉)用于比较。在水溶液中,1P形成流体动力学直径为30 nm的纳米聚集体,其中亲脂性金属中心被认为在聚合物结构域内隔离,以减少它们与水的相互作用。这种限制,再加上三线态发射体沿聚合物链的稀释,导致1P的光致发光量子产率高于1M(在曝气水溶液中分别为0.061和0.034),具有更长寿命的³MLCT激发态和蓝移发射(分别为595 nm和604 nm)。核磁共振数据支持金属中心的隔离。O₂与1,5 - 二羟基萘的光反应表明,1P能够敏化单线态氧(¹O₂)的产生,但量子产率是1M的一半。细胞摄取实验表明,1M和1P都是具有双光子激发(TPE)成像能力的高效细胞染色剂。840 nm的TPE显微镜检查表明,两种配合物都能穿透HeLa细胞的细胞膜,定位于核周区域。细胞光动力疗法测试表明,1M和1P在暴露于氙灯照射时都能够诱导细胞凋亡。照射5分钟后6小时,1M的凋亡细胞比例高于1P(分别为74%和38%),但用1P孵育的细胞在无照射时坏死水平低得多,毒性也较低。更普遍地说,结果表明通过将铱敏化剂与聚(酰胺胺)结合,避免了1M诱导的细胞损伤。