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. 2023 Oct 9:2023:6689271.
doi: 10.1155/2023/6689271. eCollection 2023.

Phytochemistry, Biological, and Toxicity Study on Aqueous and Methanol Extracts of Chromolaena odorata

Affiliations

Phytochemistry, Biological, and Toxicity Study on Aqueous and Methanol Extracts of Chromolaena odorata

Akash Budha Magar et al. ScientificWorldJournal. .

Abstract

The medicinal plant Chromolaena odorata is traditionally used by people living in different communities of Nepal and the globe against diabetes, soft tissue wounds, skin infections, diarrhea, malaria, and several other infectious diseases. The present study focuses on the qualitative and quantitative phytochemical analyses and antioxidant, antidiabetic, antibacterial, and toxicity of the plant for assessing its pharmacological potential. The extracts of flowers, leaves, and stems were prepared using methanol and distilled water as the extracting solvents. Total phenolic content (TPC) and total flavonoid content (TFC) were estimated by using the Folin-Ciocalteu phenol reagent method and the aluminum chloride colorimetric method. Antioxidant and antidiabetic activities were assessed using the DPPH assay and α-glucosidase inhibition assay. A brine shrimp assay was performed to study the toxicity, and the antibacterial activity test was performed by the agar well diffusion method. Phytochemical analysis revealed the presence of phenols, flavonoids, quinones, terpenoids, and coumarins as secondary metabolites. The methanol extract of leaves and flowers displayed the highest phenolic and flavonoid content with 182.26 ± 1.99 mg GAE/g, 128.57 ± 7.62 mg QE/g and 172.65 ± 0.48 mg GAE/g, 121.74 ± 7.06 mg QE/g, respectively. The crude extracts showed the highest DPPH free radical scavenging activity with half maximal inhibitory concentration (IC50) of 32.81 ± 5.26 µg/mL and 41.00 ± 1.10 µg/mL, respectively. The methanol extract of the leaves was found to be effective against bacterial strains such as K. pneumoniae (ZOI = 9.67 ± 0.32 mm), B. subtilis (ZOI = 15.00 ± 0 mm), and E. coli (7.3 ± 0.32 mm). The methanol extract of the flowers showed the most α-glucosidase inhibitory activity (IC50 227.63 ± 11.38 µg/mL), followed by the methanol extract of leaves (IC50 249.50 ± 0.97 µg/mL). The aqueous extract of the flowers showed the toxic effect with LC50 107.31 ± 49.04 µg/mL against the brine shrimp nauplii. In conclusion, C. odorata was found to be a rich source of plant secondary metabolites such as phenolics and flavonoids with potential effects against bacterial infection, diabetes, and oxidative stress in humans. The toxicity study showed that the aqueous extract of flowers possesses pharmacological activities. This study supports the traditional use of the plant against infectious diseases and diabetes and provides some scientific validation.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Photographs of plant samples collected from the study area.
Figure 2
Figure 2
Plot of percentage radical scavenging against concentrations (µg/mL) of plant extracts and standard (values are significantly different from their respective controls at p < 0.0001).
Figure 3
Figure 3
Correlation between (a) TPC and antioxidant, (b) TFC and antioxidant, and (c) antidiabetic and antioxidant activities as IC50 (all correlations are significant at p < 0.05).
Figure 4
Figure 4
Plot of percentage enzyme inhibition against concentrations (µg/mL) of plant extracts (values are significantly different from their respective controls at p < 0.001).
Figure 5
Figure 5
Antibacterial activity (ZOI) of plant extracts against the bacterial strains ((a) against Klebsiella pneumoniae, (b) against Staphylococcus aureus, (c) against Bacillus subtilis, and (d) against Escherichia coli); PC, positive control; NC, negative control.
Figure 6
Figure 6
Plot of percentage mortality against concentrations (µg/mL) of the plant extract (values are significantly different from their respective controls at p < 0.0001).

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References

    1. Ogurtsova K., Guariguata L., Barengo N. C., et al. IDF Diabetes Atlas: global estimates of undiagnosed diabetes in adults for 2021. Diabetes Research and Clinical Practice . 2022;183 doi: 10.1016/j.diabres.2021.109118.109118 - DOI - PubMed
    1. Ferreira R. C., Simons H. Z., Thompson W. S., et al. IL-21 production by CD4+ effector T cells and frequency of circulating follicular helper T cells are increased in type 1 diabetes patients. Diabetologia . 2015;58(4):781–790. doi: 10.1007/s00125-015-3509-8. - DOI - PMC - PubMed
    1. Morrish N. J., Wang S.-L., Stevens L. K., Fuller J. H., Keen H. Mortality and causes of death in the WHO multinational study of vascular disease in diabetes. Diabetologia . 2001;44(2) - PubMed
    1. Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature . 2001;414(6865):813–820. doi: 10.1038/414813a. - DOI - PubMed
    1. Szkudelski T., Szkudelska K. Anti-diabetic effects of resveratrol. Annals of the New York Academy of Sciences . 2011;1215(1):34–39. doi: 10.1111/j.1749-6632.2010.05844.x. - DOI - PubMed