Anticancer evaluation of Co(III) complex derived from 1-isonicotinoyl-4-(4-nitrophenyl)-3-thiosemicarbazide: Structural characterization, photophysical, and Hirshfeld studies

IF 4.4 3区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Communications Pub Date : 2024-11-15 DOI:10.1016/j.inoche.2024.113521
Ram Nayan Gautam , Alok Shukla , Suryansh Chandra , Sundeep Kumar , A. Acharya , Mamata Singh , R.J. Butcher , M.K. Bharty
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Abstract

A new cationic complex, [Co((intph)(en)2]Cl, derived from the 1-isonicotinoyl-4-(4-nitrophenyl)-3-thiosemicarbazide (H2intph), is reported. The synthesized ligand and its corresponding Co(III) complex were successfully characterized by applying FT-IR and UV–visible spectroscopic techniques and single crystal ray diffraction data. Molecular geometries of the ligand and its Co(III) complex were accurately determined from their respective X-ray crystallographic analysis. The ligand and [Co((intph)(en)2]Cl crystallize in Triclinic and monoclinic systems with space groups P-1 and P 21/n, respectively. The crystal structures of H2intph and [Co((intph)(en)2]Cl are stabilized by weak C-H⋯O, N-H⋯O, and C-H⋯Cl hydrogen bonding interactions. Hirshfeld surface analysis was accomplished to investigate intermolecular hydrogen bonding interactions found in ligand H2intph and [Co((intph)(en)2]Cl. The cytotoxicity of the ligand and the complex [Co((intph)(en)2]Cl was assessed for their anticancer potential against human glioblastoma (U87) and Dalton lymphoma (DL) cell lines. The complex exhibited IC50 values of 100 μg/mL for U87 cells and 120 μg/mL for DL cells, indicating the concentration at which 50 % of cell viability was inhibited. In comparison, the ligand was less effective in the MTT assay against both U87 and DL cells. These results suggest that the complex [Co((intph)(en)2]Cl significantly reduces glioblastoma cell viability. Treatment with the complex induced cell death through both apoptotic and necrotic pathways, as evidenced by Hoechst/PI double staining. Additionally, there was an increase in intracellular reactive oxygen species (ROS), highlighting the role of oxidative stress in the anticancer activity of the [Co((intph)(en)2]Cl complex. Furthermore, fluorescence studies were carried out which revealed the order of fluorescence behaviors between the ligand and the Co(III) complex to be Co(III) complex > H2intph.

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1-isonicotinoyl-4-(4-nitrophenyl)-3-thiosemicarbazide 的 Co(III) 复合物的抗癌评估:结构表征、光物理和 Hirshfeld 研究
报告了一种新的阳离子配合物[Co((intph)(en)2]Cl,由 1-异烟酰胺基-4-(4-硝基苯基)-3-硫代氨基脲(H2intph)衍生而来。通过应用傅立叶变换红外光谱、紫外可见光谱技术和单晶射线衍射数据,成功地对合成的配体及其相应的 Co(III) 复合物进行了表征。配体及其 Co(III)配合物的分子几何形状是通过各自的 X 射线晶体分析准确确定的。配体和[Co((intph)(en)2]Cl分别在空间群为 P-1 和 P 21/n 的三斜系和单斜系中结晶。H2intph和[Co((intph)(en)2]Cl的晶体结构通过微弱的C-H⋯O、N-H⋯O和C-H⋯Cl氢键相互作用而稳定。为了研究配体 H2intph 和[Co((intph)(en)2]Cl 中发现的分子间氢键相互作用,我们进行了 Hirshfeld 表面分析。评估了配体和[Co((intph)(en)2]Cl 复合物对人类胶质母细胞瘤(U87)和道尔顿淋巴瘤(DL)细胞系的抗癌潜力。该复合物对 U87 细胞的 IC50 值为 100 μg/mL,对 DL 细胞的 IC50 值为 120 μg/mL,即抑制 50% 细胞活力的浓度。相比之下,配体在 MTT 试验中对 U87 和 DL 细胞的抑制作用较弱。这些结果表明,[Co((intph)(en)2]Cl 复合物能显著降低胶质母细胞瘤细胞的活力。Hoechst/PI 双染色法证明,用该复合物处理可通过凋亡和坏死两种途径诱导细胞死亡。此外,细胞内活性氧(ROS)也有所增加,凸显了氧化应激在[Co((intph)(en)2]Cl 复合物抗癌活性中的作用。此外,还进行了荧光研究,结果显示配体与 Co(III)络合物之间的荧光行为顺序为 Co(III)络合物 > H2intph。
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来源期刊
Inorganic Chemistry Communications
Inorganic Chemistry Communications 化学-无机化学与核化学
CiteScore
5.50
自引率
7.90%
发文量
1013
审稿时长
53 days
期刊介绍: Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.
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