相关实验视频
Updated: Sep 11, 2025

08:44
Assembly and Characterization of Polyelectrolyte Complex Micelles
Published on: March 2, 2020
10.9K
核心菌体表面单个循环菌素的排列和动态
I S Vaskan1, V A Dimitreva1,2, A A Piryazev3
1Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997, Russia. vaskan.ivan@inbox.ru.
Physical chemistry chemical physics : PCCP
|August 15, 2025
概括
纳米颗粒上的循环德克斯特林 (CD) 显示药物负载较差,这是由于不利的方向和集群. 优化CD密度和间隔结构是有效的纳米药物药物递送系统的关键.
科学领域:
- 纳米医学是一种纳米医学.
- 材料科学 材料科学 材料科学
- 生物技术是生物技术.
背景情况:
- 纳米粒子 (NP) 药物递送面临效率降低,向失效和不良生物反应等挑战.
- 环极素 (CDs) 可以增强NP特性,促进药物加载/释放,但它们的表面呈现是至关重要的.
研究的目的:
- 评价核心菌体的结构和动态特性,其核心菌体与循环菌素 (CDs) 装饰.
- 评估CD局部化,定向和流动性对药物输送的NP功能的影响.
主要方法:
- 使用了传输电子显微镜 (TEM),小角度X射线散射 (SAXS) 和分子动力学 (MD) 模拟的组合.
- 分析了NP地形地图的自我组装的,装饰着α-或β-CDs,通过水友空间器与DOPE结合.
主要成果:
- 大多数CD残留物表现出不利的方向和集群,限制了进入CD腔的机会.
- 由于间隔器相互作用,CD显示出低流动性,形成静态表面层.
- 减少CD和间隔器密度提高了连接体宿主可访问性,而不会改变CD的方向或移动性.
结论:
- CD残留物的功能取决于间隔结构和最佳CD密度.
- 这些发现为先进,高效的基于纳米粒子的药物输送系统的合理设计提供了洞察力.
相关概念视频
Stability of Substituted Cyclohexanes
13.0K
This lesson discusses the stability of substituted cyclohexanes with a focus on energies of various conformers and the effect of 1,3-diaxial interactions.
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
13.0K
Pinching-off of Coated Vesicles
3.2K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.2K
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
263
Orally administered drugs primarily enter the systemic circulation via passive diffusion through the intestinal membranes. The drug's absorption is influenced by drug stability in the gastrointestinal GI tract, membrane permeability, the surface area available for absorption, luminal drug concentration, and residence time in the lumen. Drug permeability can be enhanced by adjusting the lipophilicity, polarity, or molecular size of the drug, promoting its passive transport across intestinal...
263
Colloids
17.9K
Children at play often make suspensions such as mixtures of mud and water, flour and water, or a suspension of solid pigments in water known as tempera paint. These suspensions are heterogeneous mixtures composed of relatively large particles that are visible to the naked eye or can be seen with a magnifying glass. They are cloudy, and the suspended particles settle out after mixing. On the other hand, a solution is a homogeneous mixture in which no settling occurs and in which the dissolved...
17.9K
Factors Affecting Dissolution: Particle Size and Effective Surface Area
1.0K
Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are...
1.0K
Mechanisms of Membrane Domain Formation
3.2K
Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
Another mechanism for membrane domain formation involves membrane proteins interacting with...
3.2K

