4.7 Article

Robust and highly adaptable high internal phase gel emulsions stabilized solely by a natural saponin hydrogelator glycyrrhizic acid

Journal

FOOD & FUNCTION
Volume 13, Issue 1, Pages 280-289

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1fo01656c

Keywords

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Funding

  1. National Natural Science Foundation of China [32172347, 31801476]
  2. Natural Science Foundation of Guangdong Province [2021A1515011000]
  3. Fundamental Research Funds for the Central Universities [2020ZYGXZR092]
  4. 111 Project [B17018]

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A new class of high internal phase gel emulsions (gel-HIPEs) with high mechanical strength can be synthesized easily using natural food-grade saponin glycyrrhizic acid (GA) as the sole stabilizer. The formation of fibrillar hydrogel networks in the continuous phase gives rise to unique gel-HIPEs, which exhibit remarkable mechanical performance due to the highly viscoelastic GA nanofibrillar networks actively trapping the emulsion droplets. These robust gel-HIPEs can serve as solid templates for fabricating stable porous materials and are promising long-term delivery vehicles for lipophilic active cargoes.
Herein, we report a new class of high internal phase gel emulsions (gel-HIPEs) that are mechanically robust, adaptable, and processable. They can be synthesized facilely by using the natural food-grade saponin glycyrrhizic acid (GA) as the sole stabilizer, which is shown to be versatile for various oils. The structural properties of these HIPEs including appearance, viscoelasticity and processability are well controlled by simply changing the concentration of GA nanofibrils. When the GA nanofibril concentration exceeds 0.3 wt%, the unique gel-HIPEs can be produced through the formation of fibrillar hydrogel networks in the continuous phase. When the nanofibril concentration only increases to 5 wt%, it is surprising to see that these gel-HIPEs display an extremely high mechanical strength, and the storage moduli as well as the yield stress values can reach 408.5 kPa and 3340 Pa (or even more), respectively. We conjecture that such remarkable mechanical performance is mainly attributed to the highly viscoelastic GA nanofibrillar networks in the continuous phase of gel-HIPEs, which can actively trap the nanofibril-coated emulsion droplets and thus strengthen the gel matrix. Consequently, the robust gel-HIPEs can be used as a solid template to fabricate stable porous materials without the need for crosslinking of the continuous phase, and the open- and closed-cell foam microstructures are controlled by the nanofibril concentration. Furthermore, the nanofibril-based HIPEs are promising long-term delivery vehicles with controlled-release properties for lipophilic active cargoes, since the strong fibrillar networks at the droplet surfaces and in the continuous phase can effectively retard the active release.

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