Advances in Herbal Research | online ISSN 2209-1890
RESEARCH ARTICLE   (Open Access)

Antioxidant and Pharmacognostic Evaluation of Achyranthes Aspera: Therapeutic Potential and Analytical Validation of Secondary Metabolites

Muhammad Rashad1,*, Muhammad Athar Adil2, Muhammad Bilal Siddique3, Sohaib Peerzadah2, Malik Saadullah1

+ Author Affiliations

Australian Herbal Insight 7 (1) 1-14 https://doi.org/10.25163/ahi.719692

Submitted: 18 January 2024 Revised: 13 March 2024  Published: 15 March 2024 


Abstract

The therapeutic potential of plants in human health has been recognized since ancient times, with Achyranthes aspera (A. aspera) being historically used to treat various ailments. This study aimed to standardize A. aspera by evaluating multiple pharmacognostic parameters, including microscopic analysis, organoleptic assessment, and forthcoming analytical techniques. Dry powdered plant material was extracted using methanol, followed by liquid-liquid extraction with dichloromethane. The extracts were screened for different phytoconstituents, and their total phenolic and flavonoid contents were assessed using gallic acid and quercetin standards, respectively. The antioxidant activity of the methanolic and dichloromethane extracts was tested in vitro against the free radical DPPH. The methanolic extract exhibited maximum antioxidant efficacy, with an IC50 value of 7.61 μg/ml, while the dichloromethane extract showed an IC50 of 14.25 μg/ml, compared to standard ascorbic acid. Scanning electron microscopy (SEM) analyzed the surface morphology of the dried powder, and atomic absorption spectroscopy (AAS) confirmed the absence of toxic metals in both extracts. High-performance liquid chromatography (HPLC) revealed 55.965% quercetin content, indicating a high concentration of flavonoids. Fourier transform infrared spectroscopy (FTIR) identified functional groups like ethyl amines, alkenes, alkanes, primary nitro groups, and esters, contributing to the plant's enhanced stability. These findings highlight A. aspera's potential as a source of bioactive compounds with antioxidant properties, confirming its historical use and paving the way for future pharmacological applications.

Keywords: Achyranthes aspera, Pharmacognostic evaluation, Secondary metabolites, Analytical techniques, Herbal medicine

References


Andrade-Cetto, A., & Heinrich, M. (2005). Mexican plants with hypoglycaemic effect used in the treatment of diabetes. Journal of Ethnopharmacology, 99(3), 325-348.

Balunas, M. J., & Kinghorn, A. D. (2005). Drug discovery from medicinal plants. Life Sciences, 78(5), 431-441.

Brown, P., & Hartwick, R. A. (1988). High-performance liquid chromatography.

Edwin, S., et al. (2008). Wound healing and antioxidant activity of A. aspera. Pharmaceutical Biology, 46(12), 824-828.

Eid, A., Elmarzugi, N., & El-Enshasy, H. (2013). On the phytopharmacological effect of Swietenia macrophylla.

Fakhar-E-Alam, M., Amjad, I., Saadullah, M., et al. (2024). Antitumor activity of zinc oxide nanoparticles fused with green extract of Nigella sativa. Journal of Saudi Chemical Society, 28(2), 101814.

Garrido, G., et al. (2016). Journal of Pharmacy & Pharmacognosy Research Volume 4, Issue 1. Journal of Pharmacy & Pharmacognosy Research, 4, 1-48.

Giancarlo, S., et al. (2006). Hypoglycaemic activity of two spices extracts: Rhus coriaria L. and Bunium persicum Boiss. Natural Product Research, 20, 882-886.

Gilani, A. H. (2005). Trends in ethnopharmacology. Journal of Ethnopharmacology, 100(1-2), 43-49.

Kumar, V. K., & Lalitha, K. (2017). Pharmacognostical and phytochemical studies of Helleborus niger L. root. Ancient Science of Life, 36(3), 151.

Lindsay, S., & Barnes, J. (1992). High-performance liquid chromatography. John Wiley & Sons.

Mahajan, R. P., Mahire, R. R., & More, D. H. (2014). Phytochemical screening of aqueous and ethanol extracts of some medicinal plants and in-vitro study of inhibition of α-amylase. International Journal of Pharmacy, 1, 501-506.

Mari, K., Vadivu, R., & Radha, R. (2016). Phytochemical screening on the successive extracts of bark of Sterculia foetida Linn. Imperial Journal of Interdisciplinary Research, 2(4), 288-294.

Michalak, A. (2006). Phenolic compounds and their antioxidant activity in plants growing under heavy metal stress. Polish Journal of Environmental Studies, 15, 523-530.

Muthukrishnan, S., & Sivakkumar, T. (2018). Physicochemical evaluation, preliminary phytochemical investigation, fluorescence, and TLC analysis of leaves of Schleichera oleosa (Lour.) Oken. Indian Journal of Pharmaceutical Sciences, 80(3), 525-532.

Patel, D., et al. (2012). An overview on antidiabetic medicinal plants having insulin mimetic property. Asian Pacific Journal of Tropical Biomedicine, 2(4), 320-330.

Priya, C., et al. (2010). Antioxidant activity of A. aspera Linn stem extracts. Pharmacologyonline, 2, 228-237.

Rashad, M., & Saadullah, M. Euphorbia cotinifolia.

Rashad, M., Sampò, S., Cataldi, A., et al. (2023). Biological activities of gastropods secretions: Snail and slug slime. Natural Products and Bioprospecting, 13(1), 42.

Saadullah, M., Asif, M., Uzair, M., et al. (2022). Pharmacological evaluation of the hypoglycemic and anti-Alzheimer’s activities of aerial parts of Breynia distachia (Phyllanthaceae). Tropical Journal of Pharmaceutical Research, 21(3), 579-587.

Saadullah, M., Fakhar-E-Alam, M., Muzammil, S., et al. (2023). Evaluation of molecular mechanisms responsible for in vivo anti-Alzheimer’s property of Euphorbia cotinifolia methanol extract. Journal of King Saud University - Science, 35(6), 102785.

Saadullah, M., Farid, A., Ali, A., et al. (2022). Molecular modeling study of novel lancifolamide bioactive molecule as an inhibitor of acetylcholinesterase (AChE), herpes simplex virus (HSV-1), and anti-proliferative proteins. Molecules, 27(17), 5480.

Saadullah, M., Rashad, M., Asif, M., et al. (2023). Chapter 4 - Biosynthesis of phytonutrients. In Khan, H., Aschner, M., & Mirzaei, H. (Eds.), Phytonutrients and Neurological Disorders (pp. 57-105). Academic Press.

Santhiya, N., et al. (2016). Phytochemical analysis, anti-inflammatory activity, in vitro antidiabetic activity, and GC-MS profile of Erythrina variegata L. bark. Journal of Applied Pharmaceutical Science, 6(07), 147-155.

Saxena, A. K., et al. (1993). Impaired antioxidant status in diabetic rat liver. Effect of vanadate. Biochemical Pharmacology, 45(3), 539-542.

Sosa, A. A., Bagi, S. H., & Hameed, I. H. (2016). Analysis of bioactive chemical compounds of Euphorbia lathyrus using gas chromatography-mass spectrometry and Fourier-transform infrared spectroscopy. Journal of Pharmacognosy and Phytotherapy, 8(5), 109-126.

Telagari, M., & Hullatti, K. (2015). In-vitro α-amylase and α-glucosidase inhibitory activity of Adiantum caudatum Linn. and Celosia argentea Linn. extracts and fractions. Indian Journal of Pharmacology, 47(4), 425.

Vaghasiya, Y., Dave, R., & Chanda, S. (2011). Phytochemical analysis of some medicinal plants from Western region of India. Research Journal of Medicinal Plant, 5, 567-576.

Veeresham, C. (2012). Natural products derived from plants as a source of drugs. Journal of Advanced Pharmaceutical Technology & Research, 3(4), 200-201.

Yao, L. H., et al. (2004). Flavonoids in food and their health benefits. Plant Foods for Human Nutrition, 59(3), 113-122.

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