的光激活抗癌活性 (III) 复合物与天然存在的黄酸 (chrysin) 和酸 (silibinin) 复合
Jyotirmoy Dutta1, Arpan Bera2, Aarti Upadhyay2
1Department of Chemistry, Handique Girls' College, Guwahati, Assam, 781001, India.
Chembiochem : a European journal of chemical biology
|July 4, 2024
概括
新的 (III) 复合物与天然黄化合物显示出对癌症光动力学治疗 (PDT) 的前景. 复合物Co5和Co6有效地向癌细胞,对正常细胞的毒性最小,通过单片氧生成诱导细胞亡.
科学领域:
- 协调化学 协调化学
- 光动力学疗法 光动力学疗法
- 癌症研究 癌症研究
背景情况:
- 使用生物必需的过渡金属和天然化剂的光活性金属复合物正在成为癌症光动力疗法 (PDT) 的光细胞毒剂.
- 开发具有增强疗效和选择性的新型综合体对于推进PDT应用至关重要.
研究的目的:
- 合成和表征六种新的 (III) 复合物,其中含有天然黄的混合合物配方.
- 评估这些复杂物对癌细胞的光细胞毒性,稳定性和作用机制.
主要方法:
- 六个 (III) 复合物的合成 ([CoB2L]ClO4) 2) 与N,N-捐赠者α-二胺联体 (phen,dpq,dppz) 和天然黄 (chrysin,silibinin).
- 用光谱分析 (UV-Vis) 来确定吸收波段 (500-700 nm).
- 在可见光照射下对HeLa和A549癌细胞和HPL1D正常细胞进行细胞毒性测定 (IC50值).
- 流细胞计和ROS生成试验以阐明细胞死亡机制.
主要成果:
- 复合物Co5和Co6,包括二氧化和黄联体,对宫 (HeLa) 和肺 (A549) 癌细胞表现出显著的光细胞毒性 (IC50:2.3-3.4μM).
- 这些复合体对正常的肺上皮细胞 (HPL1D) 具有低毒性.
- 光动力学作用涉及诱导亡和在可见光照射后单点氧气生成.
结论:
- (III) 复合物Co5和Co6表现出极好的光细胞毒性活性和选择性,使它们成为癌症光动力学治疗的有希望的候选者.
- 天然的黄类和二氧化类联体有助于增强这些金属复合物的治疗潜力.
更多相关视频
13:17In Vitro and In Vivo Evaluation of Photocontrolled Biologically Active Compounds - Potential Drug Candidates for Cancer Photopharmacology
Published on: September 29, 2023
2.3K
10:21Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
8.4K
相关概念视频
Electron Transport Chain: Complex I and II
12.8K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
12.8K
Targeted Cancer Therapies
7.5K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
There are several types of targeted therapies against...
7.5K
Inhibition of Cdk Activity
4.7K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
4.7K
Colors and Magnetism
11.6K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
11.6K
