4.7 Article

Fabrication of nanoparticles using partially purified pomegranate ellagitannins and gelatin and their apoptotic effects

Journal

MOLECULAR NUTRITION & FOOD RESEARCH
Volume 55, Issue 7, Pages 1096-1103

Publisher

WILEY-BLACKWELL
DOI: 10.1002/mnfr.201000528

Keywords

Ellagitannin; Gelatin A; Nanoparticle; Pomegranate; Punicalagin

Funding

  1. University of Florida

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Scope: Nanoparticles possess unique chemical and biological properties compared to bulk materials. Bioactive food components encapsulated in nanoparticles may have increased bioavailability and bioactivities. Methods and results: Self-assembled nanoparticles made of partially purified pomegranate ellagitannins (PPE) and gelatin were fabricated using three PPE-to-gelatin mass ratios (1: 5, 5: 5, and 7: 5). The PPE contained 16.6% (w/w) of punicalagin A, 32.5% (w/w) of punicalagin B, and a small amount of ellagic acid-hexoside and ellagic acid (1%, w/w). Nanoparticles fabricated using the ratio 5: 5 had a particle size of 149.3 +/- 1.8 nm, positive zeta-potential of 17.8 +/- 0.9 mV, production efficiency 53.0 +/- 4.2%, and spherical morphology under scanning electron microscopy. Loading efficiency of punicalagin A and punicalagin B in these particles were 94.2 +/- 0.4% and 83.8 +/- 0.5 %, respectively. Loading capacity was 14.8 +/- 1.5% and 25.7 +/- 2.2%, respectively. Only punicalagin anomers were able to bind with gelatin to form nanoparticles, whereas ellagic acid-hexoside or ellagic acid could not. Fourier transform infrared spectroscopy suggested that the interactions between ellagitannins and gelatin were hydrogen bonding and hydrophobic interactions. PPE-gelatin nanoparticle suspension was less effective than PPE in inducing the early stage of apoptosis on human promyelocytic leukemia cells HL-60. But they had similar effects in inducing late stage of apoptosis and necrosis. Conclusion: Pomegranate ellagitannins bind with gelatin to form self-assembled nanoparticles. Ellagitannins encapsulated in nanoparticles had decreased apoptotic effects on leukemia cells HL-60.

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