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新型镧系(III)-姜黄素/二酮配合物用于光动力疗法的光物理、理论及光细胞毒性评估

Photo-physical, theoretical and photo-cytotoxic evaluation of a new class of lanthanide(iii)-curcumin/diketone complexes for PDT application.

作者信息

Musib Dulal, Pal Mrityunjoy, Raza Md Kausar, Roy Mithun

机构信息

Department of Chemistry, National Institute of Technology Manipur, Langl-795004, Imphal, Manipur, India.

Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore-560012, India.

出版信息

Dalton Trans. 2020 Aug 11;49(31):10786-10798. doi: 10.1039/d0dt02082f.

Abstract

Herein we report the synthesis, characterization, photophysical and photocytotoxicity studies of a new class of curcumin-based lanthanide(iii) complexes of general molecular formula [La(1,10-phen)2(L)(NO3)2] (1-4), where L = 1-phenylbutane-1,3-dione (L1, 1), 1-(anthracen-9-yl)butane-1,3-dione (L2, 2), 1-(3a1,5a1-dihydropyren-1-yl)butane-1,3-dione (L3, 3) and curcumin (L4, 4). Complex 1 was characterized by single-crystal X-ray crystallography and it exhibited the N4O6 coordination of La(iii). The presence of the low-lying and long-lived triplet excited state enabled the luminescent complexes (2-4) to generate singlet oxygen (1O2) in high yield when the complex was activated with visible light (400-700 nm, 10 J cm-2), which could be responsible for the photo-ablation of cancer cells. Complexes (2-4) exhibited remarkable photocytotoxicity in HeLa and MCF-7 cells with photocytotoxicity index 4-50 in the presence of visible light (400-700 nm, 10 J cm-2), while they were non-toxic in the dark with an IC50 value of >100 μM. The significantly lower toxicity (IC50 > 100 μM in the dark; IC50 in visible light ∼60 μM) of the complexes in MCF-10A (normal cells) in the dark and in visible light suggested their potential for targeting anticancer activity. Further studies showed that complex 4 induced caspase-dependent apoptosis through mitochondrial damage, mitochondrial respiration inhibition and reactive oxygen species (ROS) elevation. The cytosolic localization of complex 4 in HeLa cells, having a curcumin moiety as a fluorophore, was proved from the confocal microscopic studies. The photocytotoxicity of the complexes (1-4) was directly correlated to the efficacy of the complexes to generate singlet oxygen, which resulted in the photocytotoxicity order of 4 > 3>2 ≫ 1. Photo-physical studies revealed that the chelation of curcumin by La(iii) facilitated intersystem crossing in curcumin by reducing the energy gap of the singlet to triplet excited state. Therefore, the presence of low-lying and long-lived triplet excited state was responsible for increasing the generation of singlet oxygen and, thereby, photo-cytotoxicity in HeLa and MCF-7 cells. The present study has given an overall (Chemistry to Biology) perspective on the effect of La(iii) on the photo-cytotoxicity of selected photo-active curcumin-based β-diketonate ligands.

摘要

在此,我们报告了一类新的通式为[La(1,10 - 菲啰啉)₂(L)(NO₃)₂] (1 - 4)的基于姜黄素的镧系(iii)配合物的合成、表征、光物理和光细胞毒性研究,其中L = 1 - 苯基丁烷 - 1,3 - 二酮(L1, 1)、1 - (蒽 - 9 - 基)丁烷 - 1,3 - 二酮(L2, 2)、1 - (3a1,5a1 - 二氢芘 - 1 - 基)丁烷 - 1,3 - 二酮(L3, 3)和姜黄素(L4, 4)。配合物1通过单晶X射线晶体学进行了表征,它呈现出La(iii)的N₄O₆配位。当配合物用可见光(400 - 700 nm,10 J cm⁻²)激活时,低位且长寿命的三重激发态的存在使发光配合物(2 - 4)能够高产率地产生单线态氧(¹O₂),这可能是癌细胞光消融的原因。配合物(2 - 4)在HeLa和MCF - 7细胞中表现出显著的光细胞毒性,在可见光(400 - 700 nm,10 J cm⁻²)存在下光细胞毒性指数为4 - 50,而在黑暗中它们无毒,IC50值>100 μM。配合物在MCF - 10A(正常细胞)中黑暗和可见光条件下显著更低的毒性(黑暗中IC50 > 100 μM;可见光中IC50 ∼60 μM)表明它们具有靶向抗癌活性的潜力。进一步研究表明,配合物4通过线粒体损伤、线粒体呼吸抑制和活性氧(ROS)升高诱导半胱天冬酶依赖性凋亡。共聚焦显微镜研究证明了配合物4在HeLa细胞中的胞质定位,其具有姜黄素部分作为荧光团。配合物(1 - 4)的光细胞毒性与配合物产生单线态氧的效率直接相关,这导致光细胞毒性顺序为4 > 3 > 2 ≫ 1。光物理研究表明,La(iii)与姜黄素的螯合通过减小单重态到三重态激发态的能隙促进了姜黄素中的系间窜越。因此,低位且长寿命的三重激发态的存在导致单线态氧生成增加,从而在HeLa和MCF - 7细胞中产生光细胞毒性。本研究从整体(化学到生物学)角度阐述了La(iii)对所选具有光活性的基于姜黄素的β - 二酮配体光细胞毒性的影响。

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