具有基悬挂的抗氧化聚合物用于缓解细胞氧化应激
Anushree Mondal, Arpita Pal, Subhasish Sarkar1
1Department of General Surgery, College of Medicine and Sagore Dutta Hospital, Kamarhati, Kolkata - 700058, West Bengal, India.
Biomacromolecules
|February 8, 2024
概括
新的水溶性聚合物带有胆醇悬挂有效地清除反应性氧物种 (ROS). 这些新型抗氧化剂可以透细胞并减少氧化应激,为ROS相关疾病提供了有前途的治疗策略.
科学领域:
- 聚合物化学 聚合物化学
- 生物材料科学 生物材料科学
- 氧化压力研究研究 氧化压力研究
背景情况:
- 反应性氧物种 (ROS) 的过度生产会导致细胞损伤和疾病.
- 传统的抗氧化剂 (多,维生素) 由于溶解性和生物可用性差,有效性有限.
- 需要新的,水溶性抗氧化剂,增强细胞透.
研究的目的:
- 为了合成和表征水溶性抗氧化聚合物与烯酸悬挂.
- 评估这些新型聚合物的*体外*和细胞抗氧化特性.
主要方法:
- 通过RAFT聚合,合成四种共聚合物 (P1-P4) 与不同的替代剂.
- 使用DPPH,ABTS,TMB和β-胡卜素试验评估的*体外*抗氧化活性.
- 用EPR光谱和H2O2诱导的ROS测量在巨细胞中评估的细胞抗氧化疗效.
主要成果:
- 合成的聚合物 (P1-P4) 具有所需的分子质量和狭窄的分散性.
- 罗链聚合物显示出显著的ROS清除和激光灭能力.
- 在非有毒度下,胆吊聚合物有效地降低了巨细胞中H2O2诱导的ROS.
结论:
- 水溶性聚合物带有胆醇悬挂是有效的抗氧化剂.
- 这些聚合物显示出减轻细胞氧化应激的潜力.
- 开发的聚合物代表了治疗ROS相关疾病的有前途的战略.
更多相关视频
09:33Imaging Approaches to Assessments of Toxicological Oxidative Stress Using Genetically-encoded Fluorogenic Sensors
Published on: February 7, 2018
7.5K
04:53Detection of Total Reactive Oxygen Species in Adherent Cells by 2',7'-Dichlorodihydrofluorescein Diacetate Staining
Published on: June 23, 2020
30.5K
相关概念视频
Oxidation of Phenols to Quinones
3.0K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
3.0K
Radical Autoxidation
2.1K
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
2.1K
Radical Chain-Growth Polymerization: Overview
2.4K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.4K
Radical Reactivity: Steric Effects
1.9K
The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic...
Along with electronic...
1.9K
Peroxisomes
12.4K
Peroxisomes are specialized organelles present in fungi, plant, and animal cells. It can vary in number, size, morphology, and activity depending on the type of tissue and the nutritional state of the cell. For example, cells with active lipid metabolism, such as adipocytes, neurons, and hepatocytes, have more peroxisomes than other cells in the body. Besides their primary role in breaking down complex organic molecules, peroxisomes can also synthesize specific macromolecules and participate in...
12.4K
