Chemometric-assisted fingerprinting profiling of the Pagoda (Clerodendrum paniculatum L.) extract variation using proton nuclear magnetic resonance (1H NMR) method, compound isolation, and cytotoxic activity

Yasir, Budiman and Azwar Ar, Muh and Paluseri, Andi Hendra and Sukara, Muhammad Akmal and Saito, Yohei and Nakagawa-Goto, Kyoko and Raihan, Muhammad and Alam, Gemini and Rohman, Abdul F. (2025) Chemometric-assisted fingerprinting profiling of the Pagoda (Clerodendrum paniculatum L.) extract variation using proton nuclear magnetic resonance (1H NMR) method, compound isolation, and cytotoxic activity. Journal of Research in Pharmacy, 29 (3). 971 - 984.

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Abstract

One of the best solutions to understanding the chemical data of complex natural substances is to use chemometric techniques. This research aims to apply chemometric techniques, specifically principal component analysis (PCA) and cluster analysis (CA), to determine the fingerprint profiles of nine pagoda extracts (PCP) and their isolated compounds using<sup>1</sup>H NMR data and to conduct initial cytotoxicity tests on the extracts. PCP flowers were extracted using various solvents and extraction methods, resulting in 9 types of extracts. The methanol-extracted flower portion was subjected to maceration and the compounds were then isolated using various techniques, including silica gel, column chromatography, and preparative thin layer chromatography (PTLC), which yielded 3 types of compounds. The structures were identified using 1D and 2D NMR and mass spectrometry. Meanwhile, their cytotoxic activity was tested on MCF-7, A549, KB, KB-VIN, and MDA-MB-231 cancer cells using the sulforhodamine B (SRB) assay. The research results revealed that compounds (1) stigmasta-5,22,25-trien-3β-ol, (2) 6-nonadecenoic acid, and (3) 6,9-nonadecadienoic acid, methyl ester was discovered in this plant for the first time. The fingerprinting profile of the PCP extracts and compounds showed resonance at δ<inf>H</inf> 5.33 ppm (m, 1H) and δ<inf>H</inf> 5.24 ppm (m, 1H). PCA of the 12 samples with eigenvalues > 1 explained 91 of the data and exhibited a normal distribution. The score plot was influenced by PC1 (82.2) and PC2 (10.5). The loading plot and CA combined with the linearity of (1), (2), and (3) with respect to the variation in extracts had determination coefficients (R² = 0.7550-0.9288) and similarities (78.26-98.98). Cytotoxicity activity showed weak growth inhibition (> 89.6) in all tested cancer cell types. In conclusion,<sup>1</sup> H NMR spectrum and chemometrics detects the fingerprinting profile of Pagoda extract variations, clustering extracts, identifying marker compounds, and potential for cytotoxicity studies in cancer cells.

Item Type: Article
Additional Information: Cited by: 0; All Open Access; Gold Open Access
Uncontrolled Keywords: 6 nonadecenoic acid; 6,9 nonadecadienoic acid, methyl ester; clerodendrum paniculatum extract; flower extract; plant extract; stigmasta 5,22,25 trien 3beta ol; sulforhodamine B; unclassified drug; A-549 cell line; Article; carbon nuclear magnetic resonance; cell proliferation; chemical fingerprinting; chemometrics; Clerodendrum; Clerodendrum paniculatum; cluster analysis; controlled study; cytotoxicity; drug determination; drug isolation; flower; heteronuclear multiple bond correlation; heteronuclear multiple quantum coherence; human; human cell; KB cell line; limit of quantitation; MCF-7 cell line; MDA-MB-231 cell line; microwave assisted extraction; nonhuman; proton nuclear magnetic resonance; thin layer chromatography
Subjects: R Medicine > RM Therapeutics. Pharmacology
R Medicine > RS Pharmacy and materia medica
Divisions: Faculty of Pharmacy
Depositing User: Muh Aly Mubarok
Date Deposited: 27 Apr 2026 05:36
Last Modified: 27 Apr 2026 05:36
URI: https://ir.lib.ugm.ac.id/id/eprint/24283

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