Chemical Evaluation of Liquidambar styraciflua L. Fruits Extracts and Their Potential as Anticancer Drugs.
Rafaela G PozzobonRenata RutckeviskiJuliane CarlottoVanessa S SchneiderLucimara Mach Côrtes CordeiroGraziele Francine Franco MancarzLauro M de SouzaRosiane Guetter MelloFhernanda Ribeiro SmiderlePublished in: Molecules (Basel, Switzerland) (2023)
Liquidambar styraciflua L. is an aromatic species, popularly used in traditional Chinese medicine to treat diarrhea, dysentery, coughs, and skin sores. The present study was designed to investigate the chemical composition and biological potential of extracts obtained from the fruits of this plant. For the chemical evaluation, it was used mainly liquid and gas chromatography, plus NMR, and colorimetric methods. The aqueous extract (EA) originated two other fractions: an aqueous (P-EA) and an ethanolic (S-EA). The three extracts were composed of proteins, phenolic compounds, and carbohydrates in different proportions. The analyses showed that the polysaccharide extract (P-EA) contained pectic polysaccharides, such as acetylated and methyl esterified homogalacturonans together with arabinogalactan, while the fraction S-EA presented phenolic acids and terpenes such as gallic acid, protocathecuic acid, liquidambaric acid, combretastatin, and atractyloside A. EA, P-EA, and S-EA showed antioxidant activity, with IC 50 values of 4.64 µg/mL, 16.45 µg/mL, and 3.67 µg/mL, respectively. The cytotoxicity followed the sequence S-EA > EA > P-EA, demonstrating that the toxic compounds were separated from the non-toxic ones by ethanol precipitation. While the fraction S-EA is very toxic to any cell line, the fraction P-EA is a promising candidate for studies against cancer due to its high toxicity to tumoral cells and low toxicity to normal cells.
Keyphrases
- oxidative stress
- induced apoptosis
- mass spectrometry
- nitric oxide
- ionic liquid
- gas chromatography
- high resolution
- endoplasmic reticulum stress
- risk assessment
- papillary thyroid
- signaling pathway
- climate change
- cell death
- tandem mass spectrometry
- drug induced
- living cells
- solid phase extraction
- high resolution mass spectrometry