[HTML][HTML] Histidine-based ionizable cationic surfactants: novel biodegradable agents for hydrophilic macromolecular drug delivery

I Polidori, D To, G Kali, A Bernkop-Schnürch - Drug Delivery and …, 2024 - Springer
The aim of this study was to design surfactants based on histidine (His) for hydrophobic ion-
pairing and evaluate their safety and efficacy. Lauryl, palmitoyl and oleyl alcohol, as well as …

[HTML][HTML] Oral formulations for highly lipophilic drugs: Impact of surface decoration on the efficacy of self-emulsifying drug delivery systems

M Sandmeier, J Hoeng, SS Jensen… - Journal of Colloid and …, 2025 - Elsevier
Aim To evaluate the impact of the surface decoration of cannabidiol (CBD) loaded self-
emulsifying drug delivery systems (SEDDS) on the efficacy of the formulations to cross the …

[HTML][HTML] Interactions of oral permeation enhancers with lipid membranes in simulated intestinal environments

NW Larsen, S Kostrikov, MB Hansen… - International Journal of …, 2024 - Elsevier
The oral bioavailability of therapeutic peptides is generally low. To increase peptide
transport across the gastrointestinal barrier, permeation enhancers are often used. Despite …

QbD Approach-Based Preparation and Optimization of Hydrophobic Ion-Pairing Complex of Lysozyme with Sodium Dodecyl Sulphate to Enhance Stability in Lipid …

AAA Hassan, T Sovány, K Pamlényi, M Deák, V Hornok… - Pharmaceutics, 2024 - mdpi.com
Hydrophobic ion pairing (HIP) complexation was found to be an efficient approach in
modulating the release and enhancing the stability and encapsulation of hydrophilic …

Re-engineering lysozyme solubility and activity through surfactant complexation

J Mu, L Mao, G Andrews, S Carmali - 2024 - chemrxiv.org
Hydrophobic ion-pairing is an established solubility engineering technique that uses
amphiphilic surfactants to modulate drug lipophilicity and facilitate encapsulation in …