相关实验视频
Updated: May 15, 2025

11:53
Crystallization of Membrane Proteins in Lipidic Mesophases
Published on: March 28, 2011
31.2K
在同形切莱可西布 - 卡尔巴马西系统中依赖摩尔比率的结晶:热力学和运动学的相互作用
Minqian Luo1, An Chen2, Shiyu Shan1
1Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Molecular pharmaceutics
|May 13, 2025
概括
摩尔比率极大地影响了共形赛莱可西布-卡巴马泽 (CEL-CBZ) 的稳定性. 热力学,而不是动力学,控制结晶,为药物输送系统提供了洞察力.
科学领域:
- 制药科学 制药科学
- 材料科学 材料科学 材料科学
- 物理化学 物理化学
背景情况:
- 同形药物递送系统提高了水溶性较差的药物的溶性和生物可用性.
- 构成分子比对于同形系统的物理稳定性至关重要.
- 了解结晶行为是开发稳定的同形配方的关键.
研究的目的:
- 为了研究赛莱可西布-卡巴马泽 (CEL-CBZ) 同形系统的结晶行为.
- 确定不同摩尔比对CEL-CBZ同形系统的稳定性和结晶性的影响.
- 阐明同形结晶中的动力学和热力学之间的相互作用.
主要方法:
- 准备不同摩尔比率的赛莱可西布-卡巴马泽 (CEL-CBZ) 同形系统.
- 对赛莱科西布,卡巴马西平和CEL-CBZ共晶体的晶体生长速度的观察.
- 分析各种摩尔比率的结晶趋势.
主要成果:
- CEL,CBZ和CEL-CBZ共晶体的晶体生长率显示出明显的依赖于摩尔比率.
- 受摩尔比率影响的热力学驱动力是结晶的主要驱动力.
- 热力学在CEL-CBZ的同形结晶中表现出比动力学更为主导的作用.
结论:
- 摩尔比率通过对分子流动性和热力学驱动力的影响显著影响同形系统结晶.
- 在同形CEL-CBZ系统的结晶过程中,热力学在动力学上占据主导地位.
- 这项研究提供了对多元组件无形系统复杂结晶机制的基本见解.
更多相关视频
相关概念视频
Recrystallization: Solid–Solution Equilibria
994
Recrystallization is a purification technique used to separate impurities from solid compounds. In this technique, no chemical reactions occur. Instead, it exploits physical properties only, specifically, the solubility differences between the desired compound and impurities, either at a single temperature or at different temperatures, and under other selected conditions. The solid-solution equilibrium (solubility equilibrium) of each component in the solution represents a binary phase...
994
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
258
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
258
Cycloaddition Reactions: MO Requirements for Thermal Activation
3.5K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
3.5K
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
158
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...
158
Thermal Electrocyclic Reactions: Stereochemistry
1.9K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
1.9K
Factors Influencing Drug Absorption: Drug Dissolution
378
The pharmacokinetic journey of drugs from solid oral dosage forms into systemic circulation is multifaceted. It begins with disintegration, a prerequisite ensuring a solid dosage form's subdivision into minute particles. Dissolution occurs next as these granulated entities solubilize in gastrointestinal fluids. This solubilization is crucial for the succeeding stage, permeation, which describes the traversal of the drug across the intestinal membrane and its subsequent entry into the blood...
378

