Enhancing stability and anti-inflammatory properties of curcumin in ulcerative colitis therapy using liposomes mediated colon-specific drug delivery system.

Food Chem Toxicol

Key Laboratory of Food Processing Technology and Quality Control in Shandong Province, College of Food Science and Engineering, Shandong Agricultural University, Tai'an, Shandong Province, 271018, PR China. Electronic address:

Published: May 2021

AI Article Synopsis

  • Curcumin liposomes (CUR-LPs) were analyzed for their properties, revealing particle diameter of 167 nm and a zeta potential of -34 mV, which indicates good stability.
  • These liposomes exhibit pseudo-pH sensitivity, allowing them to remain stable in gastric fluid while gradually releasing curcumin in intestinal fluid, with 21.82% and 27.32% consumption in SGF and SIF, respectively.
  • CUR-LPs show promise in alleviating symptoms of ulcerative colitis, including weight loss and intestinal damage, while also reducing markers of inflammation in an animal model.

Article Abstract

Curcumin liposomes (CUR-LPs) was identified by evaluating morphology, appearance, zeta potential, particle diameter, and drug encapsulation efficiency. The results indicated that particle diameter, surface charge and polydispersity index (PDI) of curcumin (CUR)-loaded anionic liposomes were 167 nm, -34 mV and 0.09, respectively. CUR-LPs is high stable pseudo-pH-sensitive nanoparticles system which has a favorable stability in simulated gastric fluid and slower degradation rate allowing CUR sustained release for prolonged times in simulated intestinal fluid. Within 1 h, the CUR consumption was 21.82% in simulated gastric fluid (SGF) and 27.32% in simulated intestinal fluid (SIF), respectively. CUR-LPs could attenuate clinical symptoms including weight loss, diarrhea and fecal bleeding. Especially, it could also prevent dextran sulfate sodium salt (DSS)-inducedcolon tissue damage and colon shortening, and reduce the production of malondialdehyde (MDA), colonic myeloperoxidase (MPO), Interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in animal model. Our study illustrated that liposomes (LPs) was a potential carrier to develop the colon-specific drug delivery system incorporating CUR for treating ulcerative colitis.

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http://dx.doi.org/10.1016/j.fct.2021.112123DOI Listing

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