Analysis of antioxidative and antiviral biomarkers β-amyrin, β-sitosterol, lupeol, ursolic acid in Guiera senegalensis leaves extract by validated HPTLC methods

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Abstract

Guiera senegalensis J.F. Gmel is a broad-spectrum African folk- medicinal plant, having activities against fowlpox and herpes viruses. Very recently, we have shown the anti-hepatitis B vius (HBV) potential of G. senegalensis leaves extract (GSLE). Here, we report the antioxidative and hepatoprotective efficacy of GSLE, including HPTLC quantification of four biomarkers of known antioxidative and antiviral activities. In cultured liver cells (HuH7) GSLE attenuated DCFH-induced oxidative stress and cytotoxicity. This was supported by in vitro DPPH radical-scavenging and β-carotene-linoleic acid bleaching assays that showed strong antioxidant activity of GSLE. Further, two simple and sensitive HPTLC methods (I and II) were developed and validated to quantify β-amyrin, β- sitosterol, lupeol, ursolic acid in GSLE. While HPTLC-I (hexane: ethylacetate; 75:25; v/v) enabled quantification of β-amyrin (Rf = 0.39; 20.64 μg/mg) and β-sitosterol (Rf = 0.25; 18.56 μg/mg), HPTLC-II (chloroform: methanol; 97:3; v/v) allowed estimation of lupeol (Rf = 0.47; 6.72 μg/mg) and ursolic acid (Rf = 0.23; 5.81 μg/mg) in GSLE. Taken together, the identified biomarkers strongly supported the antioxidant and anti-HBV potential of GSLE, suggesting its activity via abating the oxidative stress. To our knowledge, this is the first report on HPTLC analysis of these biomarkers in G. senegalensis that could be adopted for standardization and quality-control of herbal-formulations.

Figures

  • Fig. 1. Chemical structures of antioxidant biomarkers analyzed in the prese
  • Fig. 3. MTT cell proliferation assay, showing in vitro hepatoprotective effect of GSLE on cultured HuH7 cells. Values (Y-axis): means of three determinations.
  • Fig. 2. In vitro antioxidant assays of G. senegalensis (leaves) ethanol-extract (GSLE). (A linoleic acid bleaching method showing inhibition of lipid peroxidation by different conc
  • Fig. 4. Pictograms of TLC plates for G. senegalensis (leaves) ethanol-extract (GSLE) derivatized with p-anisaldehyde in day light. (A) Method-I (b-amyrin and b-sitosterol): mobile phase- hexane: ethylacetate (7.5:2.5; v/v), (B) Method-II (lupeol and ursolic acid): mobile phase- chloroform: methanol (97:3; v/v).
  • Fig. 5. Chromatograms of antioxidant biomarkers analysis in GSLE. (A) Chromatogram of b-sitosterol (Rf = 0.25) and b-amyrin (Rf = 0.39) scanned at kmax = 540 nm; mobile phase (Method I) - hexane: ethylacetate (7.5: 2.5; v/v). (B) Chromatogram of ursolic acid (Rf = 0.23) and lupeol (Rf = 0.47) scanned at kmax = 630 nm; mobile phase (Method II) – chloroform: methanol (97:3; v/v). (C) Chromatogram of GSLE (b-sitosterol, spot 5, Rf = 0.25; b-amyrin, spot 7, Rf = 0.39) scanned at kmax = 540 nm; mobile phase (Method I) – hexane: ethylacetate (7.5: 2.5; v/v). (D) Chromatogram of GSLE (ursolic acid, spot 5, Rf = 0.23; lupeol, spot 8, Rf = 0.47) scanned at kmax = 630 nm; mobile phase (Method II) - chloroform: methanol (97:3; v/v).
  • Table 1 Rf, Linear regression data for the calibration curve of b-amyrin, b-sitosterol, lupeol and ur
  • Table 2 Recovery as accuracy studies of the proposed method of b-amyrin, b-sitosterol, lupeol and
  • Table 3 Precision of the proposed HPTLC Method-I & II (n = 6).

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APA

Parvez, M. K., Alam, P., Arbab, A. H., Al-Dosari, M. S., Alhowiriny, T. A., & Alqasoumi, S. I. (2018). Analysis of antioxidative and antiviral biomarkers β-amyrin, β-sitosterol, lupeol, ursolic acid in Guiera senegalensis leaves extract by validated HPTLC methods. Saudi Pharmaceutical Journal, 26(5), 685–693. https://doi.org/10.1016/j.jsps.2018.02.022

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