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April 18, 20260 citationsOpen Access

Mechanistic insights into the preparation and stabilisation of supersaturated pea protein isolate-curcumin nanoparticles prepared by a pH-driven method

LRLea RohrNSNadine StefanABAstrid Bruckmann

Key Points

  • The research aims to improve the water solubility of curcumin using pea protein isolate nanoparticles prepared via a pH-driven method.
  • Preparation of curcumin-loaded pea protein isolate nanoparticles using a pH-driven method.
  • Assessment of precipitation kinetics, stability, and adsorption/desorption behavior of curcumin.
  • Comparison of supersaturated and stable states to evaluate performance.
  • Supersaturated nanoparticles achieved a solubilization of 96% curcumin within 24 hours.
  • The mass concentration of supersaturated curcumin was 1.39 mg/mL, while stable curcumin concentration was 0.0528 mg/mL.
  • Precipitation kinetics were influenced by factors such as stirring, temperature, and lyophilisation.

Abstract

The water solubility of the polyphenol curcumin was enhanced by preparing pea protein isolate nanoparticles loaded with curcumin using a well-established pH-driven method. This process generated supersaturated nanoparticles, with 96% of the solubilised curcumin precipitating within 24 h. The supersaturated and stable mass concentrations were 1.39 ± 0.093 mg/mL and 0.0528 ± 0.0088 mg/mL, respectively. The study assessed the kinetics, stability, and adsorption and desorption behaviour of curcumin with these nanoparticles, comparing the supersaturated and stable states. A schematic mechanism encompassing all steps from nanoparticle preparation to curcumin precipitation is proposed. The phenomenon is explained by the aggregation or isomerisation of tightly packed curcumin molecules attached to the nanoparticle surface. The precipitation kinetics are influenced by stirring, temperature, and lyophilisation, and are slowed by dilution and the addition of bisdemethoxycurcumin. The studied system is also evaluated from a pharmaceutical perspective and is proposed as a supersaturated drug-delivery system (SDDS).

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Cite This Study

Rohr et al. (2026) studied this question.

synapsesocial.com/papers/69e31ec840886becb653e73bhttps://doi.org/10.5283/epub.79218
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