Journal of Biomaterials Science Polymer Edition· 2026Q2
Development and characterization of a natural amphiphilic complex from soy lecithin and fenugreek extract for improved drug solubility and delivery
- 0citations
- Q2SCImago
- 2026year
Short summary
A novel natural amphiphilic complex, formed from soy lecithin and fenugreek extract, was developed to improve the solubility of hydrophobic drugs, offering a biodegradable and biocompatible alternative to synthetic polymers.
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Key points
- A natural amphiphilic complex was synthesized from soy lecithin and fenugreek extract using solvent-assisted self-assembly.
- The complex formed stable spherical nanostructures with an average particle diameter of 201 nm and a zeta potential of -44.51 mV.
- Fourier Transform Infrared (FTIR) spectroscopy confirmed molecular interactions within the complex.
- Transmission Electron Microscopy (TEM) revealed spherical nanostructures ranging from 55-160 nm.
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Abstract
The low water solubility of hydrophobic drugs continues to be a critical challenge in drug formulations due to its impact on bioavailability and efficacy. While synthetic amphiphilic polymers are commonly applied to increase solubility, their toxicity, immunogenicity or environmental impact restricts their use. Here, a new natural amphiphilic complex was prepared from soy lecithin and fenugreek extract as biodegradable and biocompatible materials. The amphiphilic complex was prepared using a solvent-assisted self-assembly method, in which the fenugreek extract (prepared by Soxhlet extraction) was mixed with soy lecithin and then probe sonicated, precipitated and dried. The delivery system was evaluated using dynamic light scattering (DLS), zeta potential, FTIR, transmission electron microscopy (TEM), UV-vis and differential scanning calorimetry (DSC). The amphiphilic complex had an average particle diameter of 201 nm, polydispersity index (PDI) of 0.43, and a zeta potential of -44.51 mV, suggesting stability. FTIR spectroscopy demonstrated the presence of interactions between the molecules, and TEM showed spherical nanostructures (55-160 nm). The CMC was approximately determined at 2.5-3.0 mL of the sample volume in the dilution series (mean value 2.75 mL), (roughly 0.025-0.030 mg/mL), indicating favourable self-assembly. The system was soluble and had a near-neutral pH (6.5 ± 0.2). The material is a self-assembled amphiphilic complex (rather than a copolymer) formed through non-covalent bonding. In conclusion, the complex has good promising physicochemical properties and the future potential of being developed as a nanocarrier; drug loading, release and biological testing should be studied to establish its efficacy as a drug delivery system.
The authors' abstract, as published at the source. Journal of Biomaterials Science Polymer Edition, 2026 · DOI ↗
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Field: Pharmaceutical Science
Pharmaceutical SciencePharmacology, Toxicology and Pharmaceutics