Cytotoxic and Nitric Oxide Inhibition Activities of Propolis Extract along with Microencapsulation by Complex

Rabia Onbas1, Aslihan Kazan1, Ayse Nalbantsoy1

  • 1Department of Bioengineering, Faculty of Engineering, Ege University, 35100 Bornova-, Izmir, Turkey.

Insights

Ethanol extract of propolis (EEP) shows potent anti-inflammatory and cytotoxic effects against cancer cells. Encapsulation via complex coacervation improved its properties, yielding high encapsulation efficiency and retaining bioactivity for potential use as a natural supplement.

Area of Science:

  • Natural Products Chemistry
  • Pharmacology
  • Materials Science

Background:

  • Ethanol extract of propolis (EEP) possesses notable cytotoxic and anti-inflammatory properties.
  • Challenges such as low solubility and bitter taste limit the application of EEP as a natural supplement.
  • Encapsulation is a promising strategy to enhance the delivery and applicability of EEP.

Purpose of the Study:

  • To evaluate the cytotoxicity of EEP against various cancer cell lines and its nitric oxide inhibition.
  • To develop an encapsulated form of EEP using complex coacervation to improve its physicochemical properties.
  • To assess the bioactivity of the encapsulated EEP.

Main Methods:

  • Cytotoxicity was assessed using the MTT assay on multiple cancer cell lines (PC-3, U87MG, A-549, mPANC96, CaCo-2, MCF-7, HeLa, MDA-MB-231) and a non-tumor cell line (HEK293).
  • Inducible nitric oxide synthase (iNOS) inhibition was determined in RAW 264.7 macrophage cells post-lipopolysaccharide (LPS) treatment.
  • Complex coacervation was employed to encapsulate EEP, optimizing parameters like polymer ratio (alginate:gelatin), stirring rate, and core material concentration.

Main Results:

  • EEP demonstrated significant cytotoxic and nitric oxide inhibitory activities, with an IC50 value of 0.1 ± 0.1 μg/ml, indicating anti-inflammatory potential.
  • Microparticles achieved a high encapsulation efficiency of 98.77% for EEP, with a mean particle size of 36.44 μm.
  • EEP-loaded microparticles retained similar cytotoxic effects on MCF-7 and MDA-MB-231 cancer cells as free EEP.

Conclusions:

  • Encapsulated EEP effectively overcomes solubility and taste limitations, preserving its cytotoxic and anti-inflammatory bioactivity.
  • The developed microencapsulation technique shows high efficiency and potential for enhancing the use of propolis extract.
  • This study supports the industrial application of propolis extract as a functional ingredient in supplements and potentially therapeutics.

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