Preprint / Version 1

1H nuclear magnetic resonance-based metabolite profiling of guava leaf extract: an attempt to develop a prototype for standardization of plant extracts

Authors

  • Manasi Gholkar Department of Medicinal Plants, The Foundation for Medical Research, Dr. Kantilal J. Sheth Memorial Building, 84-A, R.G, Thadani Marg, Worli, Mumbai - 400018, MAHARASHTRA India
  • Jia Li Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK
  • Poonam Daswani Department of Medicinal Plants, The Foundation for Medical Research, Dr. Kantilal J. Sheth Memorial Building, 84-A, R.G, Thadani Marg, Worli, Mumbai - 400018, MAHARASHTRA India
  • P Tetali Presently Freelance Consultant & Formerly Scientist at Naoroji Godrej Centre for Plant Research (NGCPR), Shirwal, Maharashtra India
  • Tannaz Birdi Department of Medicinal Plants, The Foundation for Medical Research, Dr. Kantilal J. Sheth Memorial Building, 84-A, R.G, Thadani Marg, Worli, Mumbai - 400018, MAHARASHTRA India

Keywords:

1H NMR, Metabolomics, Psidium guajava, India

Abstract

Herbal medicines are fast gaining popularity. However, their acceptability by modern practitioners is low which is often due to lack of standardization. Several approaches towards standardization of herbals have been employed. The current study attempted to recognize key peaks from 1H NMR spectra which together would comprise of a spectral fingerprint relating to efficacy of Psidium guajava (guava) leaf extract as an antidiarrhoeal when a number of unidentified active principles are involved. Methods Ninety samples of guava leaves were collected from three locations over three seasons. Hydroalcoholic (water and ethanol, 50:50) extracts of these samples were prepared and their 1H NMR spectra were acquired. Spectra were also obtained for quercetin, ferulic acid and gallic acid as standards. Eight bioassays reflecting different stages of diarrhoeal pathogenesis were undertaken and based on pre-decided cut-offs, the extracts were classified as ‘good’ or ‘poor’ extracts. The bioactivity data was then correlated with the 1H NMR profiles using Regression or Orthogonal Partial Least Square-Discriminant Analysis (OPLS-DA). Results OPLS-DA showed seasonal and regional segregation of extracts. Significant models were established for seven bioassays, namely those for anti-bacterial activity against Shigella flexneri and Vibrio cholerae, adherence of E. coli, invasion of E. coli and S. flexneri and production and binding of toxin produced by V. cholerae. It was observed that none of the extracts were good or bad across all the bioassays. The spectral analysis showed multiple peaks correlating with a particular activity. Based on NMR and LC-MS/MS, it was noted that the extracts contained quercetin, ferulic acid and gallic acid. However, they did not correlate with the peaks that segregated extracts with good and poor activity. Conclusions The current study identified key peaks in 1H NMR spectra contributing to the anti-diarrhoeal activity of guava leaf extracts. The approach of using spectral fingerprinting employed in the present study can thus be used as a prototype towards standardization of plant extracts with respect to efficacy. Supplementary Information The online version contains supplementary material available at 10.1186/s12906-021-03221-5. Keywords: 1H NMR, Metabolomics, Psidium guajava, India

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