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Dingyang Lv

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Open access Aug 2026

Nicandra physalodes (Linn.) Gaertn. Polysaccharide-Stabilized Peanut Oil Body Composite Emulsion Gels: Spontaneous Gelation Behavior, Rheological Properties, and 3D Printing Performance

In this study, peanut oil bodies were stabilized using different concentrations of Nicandra physalodes (Linn.) Gaertn. polysaccharide (NPGP) to fabricate composite emulsion gels. The physical stability, rheological properties, and 3D printing performance of the resulting gels were systematically investigated. The results revealed that the composite systems were capable of self-gelation when the NPGP concentration exceeded 1.0 wt%. Furthermore, the gel hardness and physical stability were improved with the elevation of NPGP concentration. Within the linear viscoelastic region, the samples exhibited dominant elastic responses and maintained solid-like properties throughout the entire test period (G′ > G″). Further 3D printing tests demonstrated that the composite systems possessed favorable formability, with printing precision and printing stability reaching 98.86 ± 0.14% and 97.11 ± 0.07%, respectively. Collectively, as a promising commercial pectin-like polysaccharide resource, NPGP can effectively enhance the stability of peanut oil body emulsions. This study also provides novel strategies and theoretical foundations for the structural regulation and functional utilization of oil bodies.

Si-Qi Sun, Fu-sheng Chen, Dingyang Lv · 0 citations
Aug 2026

Mechanism of non-emulsifying system establishment by NaCl soaking-microwave combined with hexanoic acid in aqueous enzymatic extraction of peanut oil.

Application of aqueous enzymatic extraction (AEE) for peanut oil is hindered by severe emulsification. This study investigated the synergistic effects of NaCl-soaking-microwave (SMW) pretreatment and hexanoic acid (HA) on non-emulsifying AEE and elucidated the mechanisms. SMW disrupted oil body membrane, induced interfacial protein degradation, altered secondary structures, promoted tertiary structure unfolding, and increased surface hydrophobicity, thereby promoting their migration to dreg phase (73.55%). HA further affected lipid molecular arrangement and bound to 18-kDa oleosin (binding energy: -3.84 kcal/mol). These synergistic effects promoted extensive oil droplets coalescence as observed by CLSM of slurries. The residual emulsion exhibited reduced stability with a tendency toward phase inversion, decreased |ζ-potential|, and increased Z-average diameter. Ultimately, SMW combined with 1.5% HA eliminated emulsion formation (from 28.28% to 0%) and increased free oil recovery from 0% to 94.03%. These findings support active suppression of emulsion formation and the development of a non-emulsifying AEE system.

Nan Hai, Dingyang Lv, Fu-sheng Chen et al. · 0 citations