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癌症治疗中的生物材料:通过计算、光谱和生物学分析研究山奈酚与锌离子之间的相互作用

Biomaterials in Cancer Therapy: Investigating the Interaction between Kaempferol and Zinc Ions through Computational, Spectroscopic and Biological Analyses.

作者信息

Golonko Aleksandra, Olichwier Adam Jan, Paszko Adam, Świsłocka Renata, Szczerbiński Łukasz, Lewandowski Włodzimierz

机构信息

Clinical Research Centre, Medical University of Bialystok, 15-276 Bialystok, Poland.

Prof. Wacław Dąbrowski Institute of Agricultural and Food Biotechnology-State Research Institute, 02-532 Warsaw, Poland.

出版信息

Materials (Basel). 2024 May 24;17(11):2526. doi: 10.3390/ma17112526.

DOI:10.3390/ma17112526
PMID:38893790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11172956/
Abstract

A complex of the natural flavonoid kaempferol with zinc (Kam-Zn) was synthesized, and its physicochemical properties were investigated using spectroscopic methods such as Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-Vis) spectroscopy and theoretical chemistry. Biological studies were conducted to evaluate the cytotoxic and antiproliferative effects of these complexes on MCF-7 breast cancer cells. Treatment with Kam 100 µM (84.86 ± 7.79%; 64.37 ± 8.24%) and Kam-Zn 100 µM (91.87 ± 3.80%; 87.04 ± 13.0%) showed no significant difference in proliferation between 16 h and 32 h, with the gap width remaining stable. Both Kam-Zn 100 μM and 200 μM demonstrated effective antiproliferative and cytotoxic activity, significantly decreasing cell viability and causing cell death and morphology changes. Antioxidant assays revealed that Kam (IC50 = 5.63 ± 0.06) exhibited higher antioxidant potential compared to Kam-Zn (IC50 = 6.80 ± 0.075), suggesting that zinc coordination impacts the flavonoid's radical scavenging activity by the coordination of metal ion to hydroxyl groups. Computational studies revealed significant modifications in the electronic structure and properties of Kam upon forming 1:1 complexes with Zn ions. Spectroscopy analyses confirmed structural changes, highlighting shifts in absorption peaks and alterations in functional group vibrations indicative of metal-ligand interactions. FT-IR and UV-Vis spectra analysis suggested that Zn coordinates with the 3-OH and 4C=O groups of ligand. These findings suggest that the Kam-Zn complex exhibits interesting antiproliferative, cytotoxic and modified antioxidant effects on MCF-7 cells, providing valuable insights into their structural and anticancer properties.

摘要

合成了天然黄酮类化合物山奈酚与锌的配合物(Kam-Zn),并使用傅里叶变换红外光谱(FT-IR)、紫外可见(UV-Vis)光谱等光谱方法以及理论化学对其物理化学性质进行了研究。开展生物学研究以评估这些配合物对MCF-7乳腺癌细胞的细胞毒性和抗增殖作用。用100 μM的山奈酚(84.86±7.79%;64.37±8.24%)和100 μM的Kam-Zn处理(91.87±3.80%;87.04±13.0%)显示,在16小时至32小时之间增殖无显著差异,间隙宽度保持稳定。100 μM和200 μM的Kam-Zn均表现出有效的抗增殖和细胞毒性活性,显著降低细胞活力并导致细胞死亡和形态变化。抗氧化分析表明,与Kam-Zn(IC50 = 6.80±0.075)相比,山奈酚(IC50 = 5.63±0.06)表现出更高的抗氧化潜力,这表明锌配位通过金属离子与羟基的配位影响黄酮类化合物的自由基清除活性。计算研究表明,山奈酚与锌离子形成1:1配合物后,其电子结构和性质发生了显著变化。光谱分析证实了结构变化,突出了吸收峰的移动和官能团振动的改变,表明存在金属-配体相互作用。FT-IR和UV-Vis光谱分析表明,锌与配体的3-OH和4C=O基团配位。这些发现表明,Kam-Zn配合物对MCF-7细胞表现出有趣的抗增殖、细胞毒性和改变的抗氧化作用,为其结构和抗癌特性提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/993039c3c2c8/materials-17-02526-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/3385c7b9fa5f/materials-17-02526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/5c9e713a6976/materials-17-02526-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/1a1a927fb825/materials-17-02526-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/993039c3c2c8/materials-17-02526-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/54c25acb8358/materials-17-02526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/ca4c5082de51/materials-17-02526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/61a8835f6629/materials-17-02526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/0073d73712e3/materials-17-02526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/3385c7b9fa5f/materials-17-02526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/5c9e713a6976/materials-17-02526-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/1a1a927fb825/materials-17-02526-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e56/11172956/993039c3c2c8/materials-17-02526-g008.jpg

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