Evaluation and method development for quantification of Piperine in Balchaturbhadra Churna by RP- HPLC

Authors

  • Adithya Kumar C Department of Pharmaceutical Analysis, Santhiram College of Pharmacy, Nerawada, Nandyal, Andhra Pradesh. India.
  • Bhavya Sree P Department of Industrial Pharmacy, Santhiram College of Pharmacy, Nerawada, Nandyal 518112. Andhra Pradesh. India.
  • Suresh Kumar SV Department of Pharmacognosy, Santhiram College of Pharmacy, Nerawada, Nandyal, Andhra Pradesh. India.
  • Nageswara Rao L Department of Pharmaceutical Analysis, Santhiram College of Pharmacy, Nerawada, Nandyal, Andhra Pradesh. India.
  • Siva Sanker Reddy L Department of Pharmaceutical Analysis, Santhiram College of Pharmacy, Nerawada, Nandyal, Andhra Pradesh. India.
  • Ragamala KC Department of Kaumarabhritya, SV Ayurvedic College & Hospital, Tirupathi, Andhra Pradesh. India.

DOI:

https://doi.org/10.47552/ijam.v16i1.5969

Keywords:

Balchaturbhadra Churna, Total phenolic content, Total flavonoid content, Preliminary phytochemical screening, Marker compound, RP-HPLC

Abstract

Aim and Objective: This study aimed to prepare Balchaturbhadra Churna in the laboratory and evaluate its Pharmacognostic, physicochemical, and phytochemical properties, including developing an RP-HPLC method for estimating Piperine as a marker compound. Methods: The prepared Balchaturbhadra Churna was analysed using WHO guidelines for macroscopic, physical, and chemical parameters. The methanolic extract was used for Piperine estimation through RP-HPLC. Results: The macroscopic characteristics, such as colour, odour, and taste were recorded. Physical parameters were determined, including loss on drying, ash value, extractive value, swelling index, foaming index, and powder properties (angle of repose, bulk density, tapped density, and compressibility index). Additionally, total phenolic, flavonoid and preliminary phytochemical screening were performed. The results were compared with a marketed formulation of Balchaturbhadra Churna. The retention time of standard Piperine was 4.50 minutes, while the Piperine in the laboratory and marketed formulations was detected at 4.478 and 4.480 minutes, respectively. The Piperine concentration in the laboratory and marketed formulations was 0.19% w/w and 0.21% w/w, respectively. The developed HPLC method was successfully validated. Conclusion: The laboratory-prepared and marketed formulations of Balchaturbhadra Churna were systematically evaluated and compared. The findings contribute to the standardization of Balchaturbhadra Churna, an Ayurvedic formulation.

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Published

2025-04-09

How to Cite

C, A. K., P, B. S., SV, S. K., L, N. R., L, S. S. R., & KC, R. (2025). Evaluation and method development for quantification of Piperine in Balchaturbhadra Churna by RP- HPLC. International Journal of Ayurvedic Medicine, 16(1), 184–190. https://doi.org/10.47552/ijam.v16i1.5969

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Section

Research Articles