Improved solubility and bioavailability of cyclolinopeptides by diacylglycerol in the β-cyclodextrin Pickering emulsions.

Food Chem

JNU-UPM International Joint Laboratory on Plant Oil Processing and Safety, Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China. Electronic address:

Published: February 2025

AI Article Synopsis

  • Cyclolinopeptides (CLs) have beneficial properties like anti-inflammatory and anti-tumor effects, but their low solubility limits their use.
  • β-Cyclodextrin (β-CD) emulsions with camellia oil diacylglycerol (CO DAG) enhance the solubility and bioavailability of CLs significantly.
  • The results show that these emulsions not only improve digestibility but also provide higher cellular absorption and anti-inflammatory effects, suggesting their potential use in functional foods and pharmaceuticals.

Article Abstract

Cyclolinopeptides (CLs) have anti-inflammatory, anti-osteoporosis, and anti-tumor effects, however, low water and oil solubility greatly limit their application. Herein, CLs-loaded β-cyclodextrin (β-CD) emulsions were prepared with different oil phases. The in vitro digestibility, cellular absorption, and anti-inflammatory effects were evaluated. Camellia oil diacylglycerol (CO DAG) showed enhanced dissolving ability for CLs due to high polarity. β-CD formed inclusion complexes with DAG through hydrogen bond and the emulsions showed smaller size and higher physical stability with 50 % (w/w) oil. The in vitro digestibility of the DAG emulsion was increased and the CLs' bioavailability was 13.6-fold higher than CLs in oil. The CLs-loaded Pickering emulsion digesta exhibited a higher nitric oxides (NO) inhibition rate (58.62 %) and Caco-2 cell penetration (3.09 × 10 cm/s). Therefore, emulsion formulated with β-cyclodextrin and DAG can effectively improve the solubility and bioavailability of CLs, which has significant potential for application in functional foods and pharmaceutical industry.

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Source
http://dx.doi.org/10.1016/j.foodchem.2024.141553DOI Listing

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