High internal phase pickering emulsions stabilized by pea protein isolate-high methoxyl pectin-EGCG complex: Interfacial properties and microstructure
Introduction
Pickering emulsions (PEs) were stabilized by solid particles that adsorb onto the oilwater interface, and the stability was dependent on the physicochemical properties of the adsorbent particles and the viscoelastic behavior of the interface layer (Gao et al., 2014, Van Hooghten et al., 2017). The applicability of inorganic particles in the food industry was limited. Therefore, it was necessary to develop ecofriendly particles which are of great value to food system. Some edible particles have been found to stabilize emulsions, such as cellulose nanocrystals (Chen et al., 2018), modified starch (Li, Zhang, Li, Fu, & Huang, 2020) and zein (Wang et al., 2016). The development of protein-based PEs has been promising for the establishment and wide application of emulsion-based ingredients. Compared with individual protein particles, protein-polysaccharide complexes have shown improved surface wettability, enhanced interfacial properties (Wang et al., 2016), promotion the interfacial adsorption and accumulation, and the formation of a stable interfacial layer (Zeng et al., 2017).
High internal phase Pickering emulsions (HIPPEs) are characterized by enrichment of the internal dispersed phase to more than 0.74 by volume, and exhibit high loading efficiency for active substances and nutrients (Wei et al., 2020a, Wei et al., 2020b, Wei et al., 2020c). HIPPEs stabilized by alcohol-soluble proteins, including zein (Zhou et al., 2018) and gliadin (Zeng et al., 2017), were usually prepared via organic solvent-mediated precipitation, which limited their application in the food industry. Therefore, there is considerable interest in developing effective PE/HIPPE stabilizers with water-soluble plant proteins or protein-polysaccharide-polyphenol complexes.
PPI is a plant protein with a high nutritive value. At present, the utilization of PPI is limited, mainly due to low water-solubility and aggregation near the isoelectric point (Guo et al., 2020). The addition of the polysaccharide (HMP) enhanced the viscosity of aqueous phase and prevented protein aggregation. Meanwhile, many studies have reported on the effect of HMP on stabilizing plant protein dispersion (Wei et al., 2020a, Wei et al., 2020b, Wei et al., 2020c) and the preparation of the alcohol-soluble protein-pectin complex (Zhou et al., 2018). Some researchers pointed out that the addition of EGCG can improve the wettability of the protein-based complex and further enhance the stability of the PEs (Liu et al., 2019, Zhang et al., 2020). Also, polyphenols can participate in the regulation and manipulation of the interfacial layer to stabilize PEs (Zembyla et al., 2019, Zou et al., 2015). Furthermore, the combination of protein, polysaccharide and EGCG can enhance the hydrophobicity of the protein through the interactions between EGCG and protein (Yang et al., 2018). There are some studies on PEs stabilization using plant-derived protein-pectin/polyphenol complexes, such as zein-pectin complex (Jiang et al., 2020) and zein-EGCG complex (Zhang et al., 2020). However, there have been no reports on the usage of the PPI-HMP-EGCG complex as the stabilizer for PEs and HIPPEs.
The objective of this study was to investigate the impact of interfacial rheological properties on the interfacial microstructure, bulk rheology and stability of PEs and HIPPEs. The relationship between EGCG content and interfacial properties were illustrated using surface wettability, interfacial shear rheology and interfacial intension. The PEs and HIPPEs were prepared with PPI-HMP-EGCG complex as the stabilizer, and the formation and stability mechanism of emulsions were explored through the interfacial behaviors.
Section snippets
Materials and chemicals
Commercial PPI (85% proteins) was obtained from Yantai Oriental Protein Tech Co. Ltd. (Shandong, China). HMP (type APC147, DE value 72%) was purchased from Yantai Andre Pectin Co. Ltd. (Shandong, China). EGCG (purity ≥ 98%) was bought from Yuanye Biological Technology Co. Ltd. (Shanghai, China). Tea camellia seed oil was supplied by Junda Natural Flavor Oil Co. Ltd. (Jiangxi, China). Nile red (purity ≥ 95%) and Nile blue A (dye content ≥ 75%) dyes were provided by Aladdin Biochemical Technology
Interfacial wettability properties of PPI-HMP-EGCG complex
The interfacial wettability of the PPI-HMP-EGCG complex was measured to evaluate its potential as a PE stabilizer. As shown in Fig. 1A, the θ of PPI was 39.4 ± 0.6°, which was consistent with its hydrophilic nature. The PPI-HMP complex on the other hand was hydrophobic, as indicated by the higher θ value of 77.8 ± 0.2° (Fig. 1B). The emulsions prepared with 1% PPI at φ 0.52 or 0.74 had an excessive amount of oil in the upper phase, and separated after 2 h at room temperature (Fig. 1A). In
Conclusions
The PPI-HMP-EGCG complex exhibited interfacial wettability, shear rheology and tension properties, and produced a thick and ordered viscoelastic interface layer around the oil droplets that prevented the aggregation of the oil droplets and stabilized the emulsions. PEs and HIPPEs was prepared using the PPI-HMP-EGCG complex as a partial wettability (81.6 ± 0.4°) stabilizer. The PEs (φ between 0.52 and 0.72) and HIPPEs (φ up to 0.83) showed an excellent stability against a 30-day storage period
CRediT authorship contribution statement
Tingting Feng: Investigation, Data curation, Methodology, Writing - original draft, Software. Xuejiao Wang: Investigation, Validation. Xingwei Wang: Validation. Xiaoming Zhang: Validation. Yao Gu: Validation. Shuqin Xia: Visualization, Investigation, Supervision, Writing - review & editing. Qingrong Huang: Visualization, Investigation, Supervision, Writing - review & editing.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgements
All authors acknowledge the National key R & D program (2017YFD0400105), and the National First-class Discipline of Food Science and Technology (JUFSTR20180204).
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