Related Experiment Video
Updated: May 9, 2026

Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
Published on: July 27, 2022
Formulation and stability of a soap microemulsion and the apparent pK(A) herein
Julien Marcus1, Didier Touraud, Werner Kunz
1Institute of Physical and Theoretical Chemistry, University of Regensburg, 93040 Regensburg, Germany. julien1.marcus@chemie.uni-regensburg.de
Abstract:
The influence of composition, and added salts and polyols on the stability of an oil-in-water microemulsion formulation and on the apparent pKA (apKA) of the used oleate surfactant is investigated. High temperature favours a decrease of the apKA and leads to the formation of more hydrated micelles. The apKA decreases also when the percentage of ethanol increases. Citronellol molecules do not significantly influence the apKA at concentrations between 0% and 2% w/w. By contrast, with increasing limonene concentration, the apKA increases. It was observed that anions of sodium salts destabilize the microemulsion and high temperatures are needed to recover it. By increasing the concentration of NaCl, a slight increase of the apKA is observed, which can be associated with a non-specific, electrostatic (Debye-Hückel) effect. Cations of chloride salts have different effects depending on their ability to exchange with Na(+) near the carboxylate group. Li(+), Na(+) and K(+) have apparently a salting-out effect. Tetramethylammonium chloride and choline chloride have salting-in effects until respectively 0.6 and 0.4 mol kg(-1). The associations of sorbitol or glycerol with ethanol lead to a salting-in effect and to a decrease of the apKA of Na-Oleate.
Related Concept Videos
Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH
A drug's pKa and the pH of the gastrointestinal (GI) tract play crucial roles in drug...
Bioavailability Enhancement: Drug Solubility Enhancement
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
Colloids
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence
