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Updated: Aug 12, 2026

Green Synthesis, Characterization, Encapsulation, and Measurement of the Release Potential of Novel Alkali Lignin Micro-/Submicron Particles
Published on: March 1, 2024
Ulvan Microparticles for Encapsulation of Eucalyptus Essential Oil: Characterization, Release Behavior, and Stability
Nikoletta Tricha1,2, Chrysanthos Stergiopoulos1, Sofia Papadaki2
1Laboratory of Process Analysis and Design, School of Chemical Engineering, National Technical University of Athens, Iroon Polytechneiou 9, Athens 157 80, Greece, ntua.gr.
Abstract:
Ulvan-lecithin microstructures were developed as a delivery platform for eucalyptus essential oil (EEO) in functional aquafeeds to improve phytobiotic retention, modulate gastrointestinal release, and enhance pellet stability during storage. Preliminary formulation screening compared ulvan-only and ulvan-lecithin systems containing different lecithin levels. Among the tested formulations, ulvan-1%-lecithin-EEO (U-L1-EEO) showed the most favorable overall profile, with the highest encapsulation efficiency (EE%, 76.4% ± 1.2%), the lowest surface-associated EEO fraction (23.6% ± 1.2%), a median particle size of 145.2 ± 4.8 μm, a narrow size distribution (span = 1.33 ± 0.04), and a negative ζ-potential (-31.6 ± 1.8 mV). Fourier-transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC) analyses supported the formation of a physically stabilized ulvan-lecithin matrix and the incorporation of EEO through mainly noncovalent interactions. In PBS (pH 7.4), U-L1-EEO exhibited sustained release, reaching ~90% after 24 h, with Higuchi and Korsmeyer-Peppas modeling indicating diffusion-governed and anomalous transport behavior during the initial release phase. Under simulated Dicentrarchus labrax gastrointestinal conditions, release was limited during the gastric phase (~12.7% at 90 min, pH 2.5) and increased markedly under intestinal conditions (~82% at 360 min, pH 7.5 with pancreatin and bile salts), indicating preferential intestinal release under the applied in vitro conditions. When incorporated into commercial aquafeed pellets at equivalent EEO inclusion (0.1% w/w), the encapsulated formulation improved accelerated storage stability (45°C, 70% RH, 28 days), reducing moisture uptake and peroxide value (PV) development while improving lipid and ω-3 retention, antioxidant capacity, total phenolic content (TPC), pellet durability, hardness, fines resistance, and water stability. Ulvan-lecithin microencapsulation appears to be a promising proof-of-concept strategy for stabilizing volatile phytobiotics and improving the storage performance of functional aquafeeds, although in vivo validation and process-scale assessment are required before biological efficacy and industrial applicability can be confirmed.
