HPTLC Fingerprinting Profile of Root of Punarnava (Boerhaavia diffusa Linn.)

Authors

  • Divya Raj PG Scholar, Department of Dravyagunavijnanam Government Ayurveda College, Tripunithura, Ernakulam, Kerala, India. Author
  • P Y Ansary Professor and HOD, Department of Dravyagunavijnanam Government Ayurveda College, Tripunithura, Ernakulam, Kerala, India. Author
  • Sara Moncy Ommen Professor and HOD, Department of Dravyagunavijnanam Government Ayurveda College, Kannur, Pariyaram, Kerala, India. Author
  • V V Shincymol Associate Professor, Department of Dravyagunavijnanam Government Ayurveda College, Tripunithura, Ernakulam, Kerala, India. Author

DOI:

https://doi.org/10.48165/IRJAY.2023.61102

Keywords:

Boerhaavia diffusa Linn, HPTLC Fingerprinting Profile, Punarnava, Root

Abstract

Introduction: The root of Punarnava (Boerhaavia diffusa Linn.) possesses high therapeutic value and is used in many  conditions such as Gulma (abdominal tumor), Pandu (anemia), Yakrit roga (liver disorders), Pleeha roga (splenic disorders),  and Hridroga (cardiac disorders). But, before internal administration, it is essential to confirm the drug’s authenticity and  quality. Obtaining authentic chromatographic fingerprints that accurately reflect the pharmacologically active and chemically  distinctive components of the drugs is essential. High-performance thin-layer chromatography (HPTLC) fingerprinting helps to  know the authenticity and identity of the drug. It is highly useful to avoid the unnecessary usage of adulterated drugs. Detection  of the marker compound is essential to know the mechanism of action a drug in particular diseases and systems of the body. Materials and Methods: In the present study, methanolic extract of root powder of B. diffusa Linn. was selected.  Solvent system used was toluene, ethyl acetate, and formic acid (5:4:0.5). After development, the plate was examined  under ultraviolet light 254 nm, 366 nm, and after derivatization in white light. Results and Discussion: While analyzing the HPTLC fingerprinting profile of Punarnava (B. diffusa Linn.), at  254 nm, it showed six peaks and at 366 nm, it showed ten peaks. At 254 nm, highest peak was obtained at Rf 0.03  with a total area of 4390.5 (AU). At 366 nm, highest peak obtained at Rf 0.02 with a total area of 7211.2 (AU). Conclusion:  For identification of medicinal plants, the HPTLC fingerprinting profile is a crucial component of the  standardization of herbal drugs. At 254 nm, it shows 6 peaks and at 366 nm, it shows 10 peaks.

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References

Chunekar KC, Bhavamisra. Bhavaprakasha Nighantu. Sloka 232-233 Varanasi: Chaukambha Bharati Academy; 2010. p. 406-8.

Tripati I, RajaNighantu. Sloka 117-120. Varanasi: Chaukambha Krishnadas Academy; 2009. p. 128.

Sharma PV. Kaiyyadeva Nighantu. Sloka 752-754 Varanasi: Chaukambha Orientalia; 2013. p. 139.

Ministry of Health and Family Welfare. Ayurveda Pharmacopoeia of India. 1st ed., Vol. 9., Part 1. New Delhi: Government of India; 2016. p. 65.

Khalid M, Siddiqui HH, Freed S. Pharmacognostical evaluation and qualitative analysis of Boerhavia diffusa L. roots. Int J Pharma Bio Sci 2012;3:P16-23.

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Published

2023-11-30

How to Cite

Raj, D., Ansary, P. Y., Ommen, S. M., & Shincymol, V. V. (2023). HPTLC Fingerprinting Profile of Root of Punarnava (Boerhaavia diffusa Linn.). International Research Journal of Ayurveda & Yoga, 6(11), 8-12. https://doi.org/10.48165/IRJAY.2023.61102