DMSO对DMPC和DPPC脂质体悬浮体结构性质的影响
Luísa M P F Amaral1, Maria Rangel2, Margarida Bastos3
1REQUIMTE, LAQV, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, R. do Campo Alegre, 4169-007 Porto, Portugal.
Journal of functional biomaterials
|March 27, 2024
概括
高达10%的二甲基硫氧化物 (DMSO) 对脂质模型膜的影响最小. 较高的DMSO度稳定了脂质相,增加了膜流动性,可能会影响药物输送.
科学领域:
- 生物物理学的生物物理.
- 材料科学 材料科学 材料科学
- 药理学 药理学是指药理学的学科.
背景情况:
- 生物膜是药物开发中的关键障碍.
- 脂质体增强药物溶解性,生物可用性和向性输送.
- 甲基二硫氧化物 (DMSO) 通常用于改善脂质体制备的药物溶解性.
研究的目的:
- 为了研究DMSO对二聚胺酸胆 (DPPC) 和五聚胺酸胆 (DMPC) 模型膜的生物物理性质的影响.
- 评估DMSO如何影响药物膜相互作用,并根据不同的化合物疏水性.
主要方法:
- 差分扫描热量计 (DSC) 用于分析热带性质.
- 电子磁共振 (EPR) 谱学用于研究膜流动性和动态.
- 研究DMPC和DPPC脂质模型膜的DMSO度不同.
主要成果:
- 在高达10%的DMSO中,DMPC和DPPC脂质体的双层流动性或热otropic特性没有显著变化.
- 较高的DMSO度 (10%以上) 导致凝和纹凝相的稳定.
- 在较高的DMSO度下,观察到双层流动性和膜透性增加.
结论:
- 在脂质体配方中的DMPC和DPPC模型膜中,高达10%的DMSO度通常是安全的.
- 较高的DMSO水平可以改变膜性质,可能影响药物透和输送效率.
- 了解DMSO的影响对于优化脂质体药物配方和预测体内行为至关重要.
关键词:
不同扫描热量计 (DSC)二甲基硫氧化物 (DMSO) 的使用五基克里斯托酸胆 (DMPC) 的使用双基酸胆 (DPPC) 是一种电子偏磁共振 (EPR) 是一种电子偏磁共振.脂质体是一种脂质体.更多相关视频
相关概念视频
Detergent Purification of Membrane Proteins
5.2K
Detergents are used to purify the integral proteins of the membrane. The hydrophobic portion of the detergent can replace membrane phospholipids while solubilizing the membrane proteins. When detergent monomers reach a specific concentration in a solution called critical micelle concentration (CMC), they form micelles. Above CMC, the concentration of the detergent monomers remains in equilibrium with the micelle. The number of detergent monomers present in the CMC varies for each detergent, and...
5.2K
Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH
1.3K
Drug absorption within the gastrointestinal (GI) tract is a complex process influenced by several critical factors, including the site pH, the drug's dissociation constant (pKa), and the drug's lipophilicity. The GI tract exhibits a pH gradient, with an acidic environment in the stomach and a more alkaline environment in the small intestine. This pH variation directly affects the ionization state of drugs.
A drug's pKa and the pH of the gastrointestinal (GI) tract play crucial roles...
A drug's pKa and the pH of the gastrointestinal (GI) tract play crucial roles...
1.3K
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
304
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...
304


