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Research Article

Identification of Chlorogenic Acid from Morus alba Leaves by UV-Vis Spectroscopy, FTIR, UPLC-QTOF-MS and Quantification by HPTLC

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Pages 706-722 | Received 03 May 2021, Accepted 23 Aug 2022, Published online: 04 Sep 2022
 

ABSTRACT

The present study aims to characterize chlorogenic acid extracted from Morus alba leaves by using suitable methods such as UV-Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) and further quantification by high-performance thin layer chromatography (HPTLC). Sonication method and methanol solvent (50:50%, v/v) is found more effective for the extraction of chlorogenic acid from leaf extract. UV-Vis spectra has shown maximum absorbance at λmax 330 nm, and found overlapping with standard chlorogenic acid. The functional groups of chlorogenic acid were identified by FTIR which indicated the presence of hydroxyl, carboxyl and carbonyl groups. In UPLC-QTOF-MS study, the mass spectra and total ion chromatogram analysis revealed the presence of structural isomers for chlorogenic acid at same m/z of parent ion 353. Mass fragments of daughter ions indicated base peak at m/z 191, m/z 173 and 179 were assigned as 5-O-caffeoylquinic acid, 4-O-caffeoylquinic acid and 3-O-caffeoylquinic acid. Quantitative analysis of chlorogenic acid was performed by HPLTC, overlapping absorption spectra of plant extract revealed great consistency with standard, confirms the specificity of HPTLC method. Similar retention factor (Rf) at 0.14 confirms the presence of chlorogenic acid in leaf extract. The standard plot shows good linear relationship from 200 to 1000 ng/spot (R2 = 0.9986). The detection limit was 15.45 ng/spot while limit of quantification was 46.84 ng/spot, with good average recovery rate between 97.96–99.03%. The amount of chlorogenic acid was quantified 10.8 mg/g dried weight extract.

Acknowledgments

The author expresses gratitude to Medicinal Plants Nursery-Botanical Garden Sarangpur (UT) Chandigarh for providing medicinal plant. In addition author would be highly thankful to Sophisticated Analytical Instruments Facility at Punjab University Chandigarh for conducting UPLC-QTOF-MS study and Dr Anshu Bansal at Sophisticated Instrumentation Centre Punjabi University for providing HPTLC facility, Gurpreet Singh in Department of Chemistry for FTIR study, Ashish Kumar Singh and Taranjeet Singh, Punjabi University Patiala for providing assistance.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Additional information

Funding

No funding was received for conducting this study.

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