4.7 Article

β-Sitosterol Loaded Nanostructured Lipid Carrier: Physical and Oxidative Stability, In Vitro Simulated Digestion and Hypocholesterolemic Activity

Journal

PHARMACEUTICS
Volume 12, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics12040386

Keywords

beta-sitosterol; nanostructured lipid carrier; hypocholesterolemic activity; digestion; bioaccessibility; in vitro release

Funding

  1. Isfahan University of Technology (Iran)
  2. Chemistry Department of Florence University (Italy)

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The objective of the present study was to explore the potential of nanostructured lipid carriers (NLCs) for improving the oral delivery of beta-sitosterol, a poorly water-soluble bioactive component with hypocholesterolemic activity. Two beta-sitosterol formulations with different solid lipid compositions were prepared by melt emulsification, followed by the sonication technique, and the effect of storage conditions and simulated digestion on the physical, chemical and oxidative stability, bioaccessibility and release were extensively studied. Both NLC preparations remained relatively stable during the four weeks of storage at different conditions (4, 25 and 40 degrees C), with more superior stability at lower temperatures. The in vitro digestion experiment indicated a high physical stability after exposure to the simulated mouth and stomach stages and an improved overall beta-sitosterol bioaccessibility at the end of the digestion. The NLCs presented an increased solubility and gradual release which could be justified by the remarkable affinity of beta-sitosterol to the complex lipid mixture. An in vivo study demonstrated an improved reduction in the total cholesterol and low-density lipoprotein cholesterol plasma levels in mice compared with the drug suspension. These investigations evidenced the potential of the developed NLC formulations for the enhancement of solubility and in vivo performance of beta-sitosterol.

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