Hesperidin-loaded emulsions stabilized by genipin-crosslinked protein particles

What is it about?

The present work aimed to fabricate genipin-crosslinked ovotransferrin (OVT) particle-stabilized Pickering emulsions as delivery vehicles for hesperidin. Nearly monodisperse ovotransferrin colloidal particles were prepared by employing genipin crosslinking, and reaction mechanism for the crosslinking of ovotransferrin with genipin was proposed. Genipin-crosslinked OVT particles were found to be efficient Pickering stabilizers at different oil fractions, and high internal phase Pickering emulsions (oil fraction φ = 0.75) with emulsified phase volume fraction of 100% could be solely stabilized by these particles. Visual observation and microscopic image indicated that genipin-crosslinked OVT particle-stabilized high internal phase Pickering emulsion (particle concentration c = 2.0 wt%, oil fraction φ = 0.75) was stable during one-month storage at room temperature. Optical microscopy and rheological measurements revealed that microstructures and rheological properties of genipin-crosslinked OVT particle-stabilized Pickering emulsions were dependent on both protein particle concentration and internal oil phase volume fraction. Genipin-crosslinked OVT particle-stabilized high internal phase Pickering emulsions were also stable at various pHs (2.0–4.0) and ionic strengths (0–200 mM). Optical microscopy showed that increase of pH or ionic strength resulted in a slight decrease in emulsion droplet sizes. In vitro digestion study showed that these OVT particles-stabilized high internal phase Pickering emulsions could improve both extent of lipolysis and hesperidin bioaccessibility significantly.

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Why is it important?

1. Nearly monodisperse ovotransferrin (OVT) colloidal particles were prepared with genipin crosslinking. 2. Genipin-crosslinked OVT particles were efficient Pickering stabilizers. 3. Stable high internal phase Pickering emulsions were fabricated with genipin-crosslinked OVT particles. 4. Genipin-crosslinked OVT particle-stabilized Pickering emulsions were stable at various pHs and ionic strengths。 5. The Pickering emulsions improved both extent of lipolysis and hesperidin bioaccessibility.

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