<i>Pelargonium sidoides</i> Root Extract: Simultaneous HPLC Separation, Determination, and Validation of Selected Biomolecules and Evaluation of SARS-CoV-2 Inhibitory Activity

This study aimed to establish a validated HPLC-UV analytical method for the determination of gallic acid, catechin, scopoletin, and umckalin in phytoformulations containing <i>P. sidoides</i>. Also, to assess the anti-SARS-CoV-2 effect of <i>P. sidoides</i> and these biomolec...

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Bibliographic Details
Main Authors: Manal A. Alossaimi (Author), May A. Alzeer (Author), Fatma M. Abdel Bar (Author), Mai H. ElNaggar (Author)
Format: Book
Published: MDPI AG, 2022-09-01T00:00:00Z.
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Summary:This study aimed to establish a validated HPLC-UV analytical method for the determination of gallic acid, catechin, scopoletin, and umckalin in phytoformulations containing <i>P. sidoides</i>. Also, to assess the anti-SARS-CoV-2 effect of <i>P. sidoides</i> and these biomolecules in vitro. An HPLC-UV method was developed and verified by testing the commercial forms, Kalobin<sup>®</sup> and Umca<sup>®</sup>. It revealed low detectable scopoletin and high umckalin levels. <i>Pelargonium sidoides</i> exhibited a significant reduction of SARS-CoV-2-induced cytopathic effect in Vero E6 cells (IC<sub>50</sub> 13.79 μg/mL and selectivity index, SI 6.3), whereas scopoletin showed a remarkable anti-SARS-CoV-2 activity with better selectivity (IC<sub>50</sub> 17.79 μg/mL and SI 14.22). An in-silico prediction of the drugability indicated that the studied biomolecules are under the acceptable norms of Lipinski's rule, water-soluble, and showed high GIT absorption and bioavailability. Docking study towards the essential molecular targets for viral replication and entry of SARS-CoV-2 indicated good binding affinity of scopoletin (−6.4 Kcal/mol) towards the interface region between the SARS-CoV-2 spike protein RBD and the ACE2 surface receptor indicating the probability of interference with the viral entry to the human cells and showed H-bonding with His-41 in the active site of the main protease which may explain its high antiviral activity.
Item Description:10.3390/ph15101184
1424-8247