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Solvating Effects02:12

Solvating Effects

7.6K
An understanding of the solvating effect helps rationalize the relation between solvation and acidity of the compound. In addition, this also explains the relative stability of conjugate bases for compounds with different pKa values. This lesson details, in-depth, the principle of solvating effects. The strength of an acid and the stability of its corresponding conjugate base are determined using pKa values. This observed relationship is a consequence of solvation, which is the interaction...
7.6K
Factors Affecting Solubility04:01

Factors Affecting Solubility

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Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Chȃtelier’s principle. Consider the dissolution of silver iodide:
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Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry01:20

Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry

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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...
260
Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH01:21

Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH

1.9K
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...
1.9K
Solubility of Ionic Compounds02:55

Solubility of Ionic Compounds

64.1K
Solubility is the measure of the maximum amount of solute that can be dissolved in a given quantity of solvent at a given temperature and pressure. Solubility is usually measured in molarity (M) or moles per liter (mol/L). A compound is termed soluble if it dissolves in water.
64.1K
Solubility Equilibria03:07

Solubility Equilibria

53.2K
Solubility equilibria are established when the dissolution and precipitation of a solute species occur at equal rates. These equilibria underlie many natural and technological processes, ranging from tooth decay to water purification. An understanding of the factors affecting compound solubility is, therefore, essential to the effective management of these processes. This section applies previously introduced equilibrium concepts and tools to systems involving dissolution and precipitation.
The...
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Updated: Sep 9, 2025

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
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Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs

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使用深溶性溶剂改善阿托瓦斯的溶性

Yoga Windhu Wardhana1,2, Insan Sunan Kurniawansyah1,2, Taofik Rusdiana1,2

  • 1Department of Pharmaceutics and Pharmaceuticals Technology, Faculty of Pharmacy, Universitas Padjadjaran (UNPAD), Jatinangor, Indonesia.

Journal of advanced pharmaceutical technology & research
|September 3, 2025
PubMed
概括

深度溶解剂 (DES) 增强了阿托瓦斯三酸盐 (ATCH) 的溶解性. 在基醇 (PG) 中的尼古丁胺被证明是ATCH可溶性的最佳,与水相比显著改善.

关键词:
亚托瓦斯三水合物深层溶解剂药物的可溶性

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Last Updated: Sep 9, 2025

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科学领域:

  • 制药科学
  • 材料科学

背景情况:

  • 深度溶解剂 (DES) 在药物中具有潜力,但需要安全性和可用性评估.
  • 提高药物溶解度对于有效的药物输送和配方至关重要.

研究的目的:

  • 调查DES增强阿托瓦斯三酸盐 (ATCH) 溶解性的可能性.
  • 在DES系统中探索ATCH和尼古丁胺 (NA) 等共构体之间的性相互作用.

主要方法:

  • 使用联合结晶的原理来形成优化混合物.
  • 采用极化显微镜,富里埃变换红外光谱 (FT-IR) 和差分扫描热量计 (DSC) 进行分析.
  • 在DES中评估了ATCH,尼古丁胺 (NA) 和基醇 (PG) 之间的相互作用.

主要成果:

  • 鉴定了使用尼古丁胺 (NA) 在基醇 (PG) 中的最佳DES系统.
  • 通过FT-IR和DSC确认ATCH和DES组件之间形成键 (H键).
  • 与水 (0.000597 ± 0.003 mg/mL) 相比,在DES系统中ATCH溶解度显著增加.

结论:

  • 深度溶解剂,特别是用尼古丁胺作为基的辅制剂,有效地增强了阿托瓦斯三水合物的溶解性.
  • 这项研究证实了使用DES作为改善ATCH等难溶药物的可行策略.
  • 在DES系统中观察到的增强溶解度的关键是结相互作用.