UHPLC‐Q‐TOF‐MS/MS Dereplication to Identify Chemical Constituents of <i>Hedera helix</i> Leaves in Vietnam

Pham, Hong Ngoc; Tran, Chieu An; Trinh, Thi Diep; Nguyen Thi, Ngoc Lan; Tran Phan, Huynh Nhu; Le, Van Nhan; Le, Ngoc Hung; Phung, Van Trung

doi:https://doi.org/10.1155/2022/1167265

Journal of Analytical Methods in Chemistry

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Abstract Introduction Materials and Methods Results and Discussion Conclusions Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2022 | Article ID 1167265 | https://doi.org/10.1155/2022/1167265

UHPLC‐Q‐TOF‐MS/MS Dereplication to Identify Chemical Constituents of Hedera helix Leaves in Vietnam

Hong Ngoc Pham,¹Chieu An Tran,¹Thi Diep Trinh,²Ngoc Lan Nguyen Thi,³Huynh Nhu Tran Phan,¹Van Nhan Le,¹Ngoc Hung Le,¹and Van Trung Phung¹

Academic Editor: Mohamed Abdel-Rehim

Received18 Jan 2022

Revised01 Jun 2022

Accepted30 Jun 2022

Published08 Aug 2022

Abstract

Hedera helix has been reported to contain a wide range of metabolites and produce many pharmacological effects. This research demonstrates the determination and evaluation of the phytochemical profiling of H. helix grown in central Vietnam. Methanolic extract of ivy had been analyzed by ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC‐Q‐TOF‐MS/MS). MS, and MS/MS experiments were manipulated using both negative and positive ionization modes to provide molecular mass information and production spectra for the structural elucidation of compounds. A total of 46 compounds including 24 triterpene saponins and other compounds were successfully identified of which four established saponin structures have been reported for the first time. This study has provided a base for building a quality control of the raw materials according to the profile of triterpene saponins and assessment of pharmaceutical ingredients of H. helix planted in Vietnam.

1. Introduction

Hedera helix L., the common ivy, is one of the 15 species of the genus Hedera, Araliaceae family. As an evergreen dioecious woody liana [1], ivy has an intense vitality, even in the cold winter. The common ivy is a popular ornamental plant in many countries. The plant grows naturally in Western, Central, and Southern Europe, North America, and Asia [2]. Hedera helix is applied to treat overactive thyroid (hyperthyroidism), rheumatic diseases, and respiratory tract inflammation [2]. In Vietnam, ivy is grown in areas with cool climates such as Da Lat, Moc Chau, and Sapa and is mainly used for decoration. Therefore, it has been little published research on its chemical composition and pharmacological effects. Therefore, the identification of chemical constituents is significant in the phytochemistry study of H. helix grown in Vietnam.

Phytochemical compounds were detected in ivy leaves including flavonoids, coumarins, phenolic acids, sterols, alkaloids, anthocyanins [3–5], and, in particular, triterpene saponins [1]. Some of the triterpene saponins and derivatives isolated from the ivy plant were as follows: helixoside A, helixoside B, 3-O-β-glucosyl hederagenin, 3-O-β-glucosyl-(1⟶2)- β-glucosyl oleanolic acid, 3-O-β-glucosyl-(1⟶2)-β-glucosyl hederagenin, 3-O-β-glucosyl 28-O-β-glucosyl-(1⟶6)-β-glucosyl hederagenin, hederagenin, oleanolic acid, bayogenin, α-hederin, hederagenin 3-O-β-glucoside, and hederasaponins B, C, D, E, F, G, H, and I [6].

A triterpene saponin’s chemical structure is composed of an aglycone and sugar chain(s). In most cases, a series of saponins can be found in the same plant, with similar skeleton but slightly varied sugar chains. Due to the strong polarity and structural similarities, isolating a single saponin compound is frequently challenging. Furthermore, even with high-resolution nuclear magnetic resonance (NMR), structural elucidation of saponin is difficult, especially when the sugar chain contains more than three sugar residues [7]. As a result, a new method for quickly identifying and characterizing existing and novel structures is required.

UHPLC‐Q‐TOF‐MS/MS has been an increasingly powerful and important technique for elucidating chemical structures [8]. UHPLC-QTOF-MS/MS is capable of accurately measuring molecular mass by giving the elemental composition of obtained ions. The technique has been widely used in analyzing complex samples due to its high resolution and sensitivity. In some previously published research, UHPLC-QTOF-MS/MS was applied to characterize chemical constituents and metabolites in medicinal herbs, and obtained considerable results. Small metabolites profiling of the Eurycoma longifolia aqueous extracts were performed using LC-MS/MS [9]. An integrated approach using UHPLC-QTOF-MS/MS was developed for the systematic analysis of 46 physalins from the crude extracts of Physalis alkekengi calyx [10]. Sun et al. identified 31 saponins in Shizhu ginseng applying UPLC‐MS/MS [11]. UPLC‐Q‐TOF‐MS/MS‐guided dereplication of Pulsatilla chinensis was conducted, which resulted in the identification of 22 triterpenoid saponins (11 pairs of isomers) with four aglycone skeletons [12].

In addition, ivy leaves extracts were noted to exhibit antimicrobial, anthelmintic, antimutagenic, antitumor, antileishmanial, antithrombin, antioxidant, antispasmodic, and anti-inflammatory activities [13–21]. Triterpene saponins are the bioactive compounds responsible for the medicinal use of ivy [1]. Hederagenin has potential antitumor activity [22]. Hederasaponin B has antiviral activity against Enterovirus 71 subgenotypes C3 and C4a, via inhibiting the viral VP2 protein expression and blocking viral capsid protein synthesis [23]. α-hederin has a potent inhibitory effect on breast cancer cell development and promotes apoptosis in these cells [24]. Hederacoside C was reported to have anti-inflammatory effect against induced acute lung inflammation by Staphylococcus aureus both in vivo and in vitro [25].

To the best of our knowledge, the UHPLC‐Q‐TOF‐MS/MS study of phytochemicals in the H. helix leaves extract has not been announced. The present study aims to characterize the chemical constituents, especially triterpene saponins presented in the ivy leaves planted in Vietnam. The results of this work can assist in clarifying the metabolic profile of H. helix. Acceleration of finding the new compounds and assessment of the potential ingredients from this valuable species are concerned for pharmaceutical application.

2. Materials and Methods

2.1. Chemicals and Reagents

Deionized water for HPLC and HPLC grade acetonitrile, methanol, and analytical grade formic acid (≥98%) were obtained from Scharlau (Barcelona, Spain).

Two reference standards including α‐hederin and hederacoside C were obtained from Sigma-Aldrich Chemical Co. (Singapore). The purity of each compound was no less than 98%. The standards were stored at 4°C before being used for analysis.

2.2. Sample Preparation

Hedera helix was collected from Da Lat province, Vietnam, and identified by botanist Tran Huu Dang MSc, Southern Institute of Ecology, Vietnam Academy of Science and Technology. A voucher specimen (Code: NaPro.33.1019) was deposited in the Center for Research and Technology Transfer, Vietnam Academy of Science and Technology. The leaves were gently washed, allowed to air dry, and cut into fine pieces. 100.0 mg of leaves pieces was accurately weighed into a tube with a cover, and 2.0 mL of methanol-water (8 : 2, v/v) solvent was added. The sample was ultrasonicated for 10 min and then heated to 50°C for 5 min. After being centrifuged, the extract was pipetted to a 10.0 mL volumetric flask. The residue was continued on the extraction step. After five times of extraction, the solution was exactly scaled up to 10.0 mL using the solvent solution. The sample was filtrated through a 0.45-μm filter membrane before injecting it for UHPLC‐Q‐TOF‐MS/MS analysis. Standard solutions of α‐hederin and hederacoside C were prepared in methanol at a concentration of 1000 (ppm).

2.3. UHPLC-Q-TOF Analysis

Sample analysis was performed on an ExionLC™ UHPLC system (AB SCIEX, USA) consisting of an ExionLC degasser, AC pumps, AC autosampler, controller, and AC column oven. Samples were analyzed on a Hypersil GOLD C18 column (150 × 2.1 mm, 3 µ) (Thermo Fisher Scientific, USA). The mobile phase, water containing 0.1% formic acid (A) and acetonitrile containing 0.1% formic acid (B), was run at a flow rate of 0.4 mL/min at 25°C. The gradient programming was as follows: 0–4 min, 2–20% B; 4–30 min, 20–68% B; 30–32 min, 68–98% B; 32–40 min, 98% B. Sample injection volume was 5.0 μL.

An AB SCIEX X500R QTOF mass spectrometer (AB SCIEX, USA) with a Turbo V ion source was coupled with the UHPLC system. Mass data were acquired in both negative and positive electrospray ionization (ESI) modes. The MS conditions were set as follows: the ion source temperature, 500°C; curtain gas, 30 psi; nebulizer gas (GS 1), 45 psi; heater gas (GS 2), 45 psi. For the TOF MS scan, the mass range was set at m/z 70–2000. For the TOF MS/MS scan, the mass range was set at m/z 50–1500. For the negative mode, ion spray voltage was set at −4.5 kV, the declustering potential (DP) was −70 V, the collision energy (CE) was performed at −20 eV, and the collision energy spread (CES) was 10 eV. For the positive mode, the ion spray voltage was set at 5.5 kV, the DP was 80 V, the CE was 20 eV, and the CES was 10 eV.

All the obtained data were processed by SCIEX OS software version 1.2.0.4122 (AB SCIEX, USA). The total ion chromatograms (TICs) of the Hedera helix extract in both positive and negative modes are shown in Figure 1.

(a)

(b)

3. Results and Discussion

3.1. Triterpene Saponins

3.1.1. Aglycones

Hedera helix aglycones include hederagenin and oleanolic acid. A relatively abundant series of dehydrated ions and/or a small aglycone ion can readily distinguish the parent skeleton for the aglycone. In the positive mode, the diagnostic fragment ions of these two aglycones can be easily detected.

For the hederagenin‐type aglycone, the precursor ion [M+H]⁺ at m/z 473.3631 could produce two specific fragment ions at m/z 455.3525 and 437.3419 by the elimination of H₂O. In many cases, the product ions at m/z 427.3576, 409.3470, and 391.3365 were observed by the losses of HCOOH from the three precursor ions mentioned earlier.

For the oleanolic‐type aglycone, the precursor ion [M+H]⁺ at m/z 457.3682 and the characteristic fragment ions at m/z 439.3576 by the neutral loss of H₂O were observed. In addition, the product ions at m/z 411.3629 and 393.3522 were presented by the losses of HCOOH from the two predominant ions.

The chemical structures and fragmentation pathways of the hederagenin and oleanolic acid aglycones are illustrated in Figures 2 and 3, respectively.

3.1.2. Sugar Chains

The sugar chains of triterpenoid saponins generally substitute at C‐3 and/or C‐28 position(s) of an aglycone. The common monosaccharide moieties of the sugar chains were glucopyranosyl (Glc), rhamnopyranosyl (Rha), arabinopyranosyl (Ara), and glucuronopyranosyl (Glu).

The composition of sugar chains can be inferred in the positive ion mode using the characteristic fragment ions, specifically as follows: the loss of Glc is 162 Da, Rha is 146 Da, Ara is 132 Da, and Glu is 176 Da. The sugar moieties at C‐3 and C‐28 were eliminated successively from C‐3 to C‐28 and from end to inner [12].

In the negative ion mode, the typical solvent adducts ion [M+HCOO]⁻ and deprotonated ion [M‐H]− can be usually observed, which provides the molecular mass and chemical formula of a compound. Typically, the sugar chain at C‐28 tends to be completely eliminated; then, the positions and composition of oligosaccharides chains can be readily differentiated and followed by an abundant fragment ion as a base peak [12].

3.2. Characterization of Authentic Compounds

To clarify MS fragmentation patterns of triterpene saponins, two authentic compounds including α-hederin and hederacoside C were studied by UHPLC-Q-TOF-MS/MS.

α-hederin (T_R = 20.41) showed a deprotonated molecular ion [M‐H]− at m/z 749.4473 in the negative mode and a pseudomolecular ion [M+H]⁺ at m/z 751.4633 in the positive mode.

At T_R = 12.49, hederacoside C yielded [M+H]⁺ ion at m/z 1221.6313 and [M‐H]⁻ ion at m/z 1219.6110 in the positive and negative modes, respectively.

The major fragment ions observed in the mass spectra of the two triterpene saponins are summarized in Table 1. The typical MS and MS/MS spectra of α-hederin and hederacoside C are shown in Figure 4.

(a)

(b)

3.3. Structural Characterization of Triterpene Saponins

Based on the earlier strategy, 24 triterpene saponins were tentatively identified and characterized from the H. helix extract. The chemical structures are illustrated in Figure 5, and the MS data are listed in Table 2.

At T_R = 11.11, in the negative mode, compound 14 yielded an [M+HCOO]⁻ ion at m/z 1295.6279 and provided fragment ions at m/z 779 and 469 corresponding to the loss of 2 Glc and 1 Rha at C-28, and a Rha-Glc sugar chain at C-3 of the hederagenin aglycone. Hence, compound 14 was hederagenin 3-O-[α-L-rhamnopyranosyl-(1⟶2)-β-D-glucopyranoside], 28-O-[α-L-rhamnopyranosyl-(1⟶4)-β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl] ester.

Compound 16 (T_R = 11.31 min) yielded an [M+HCOO]⁻ ion at m/z 1149.5707 in the negative mode, primarily fragmented into ions at m/z 633 and 469, indicating hederagenin aglycone lost a Rha-Glc-Glc sugar chain at C-28, and a Glc at C-3. Thus, compound 16 was conditionally characterized as hederagenin 3-O-β-D-glucopyranoside, 28-O-[α-L-rhamnopyranosyl-(1⟶4)-β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl] ester.

In the positive mode, the MS/MS spectra of compounds 17 (T_R = 12.43 min) and 20 (T_R = 13.05 min) exhibited identical pseudomolecular ions [M+H]⁺ at m/z 1075.5687 and 1075.5680, respectively, and produced identical aglycone ions at m/z 391, 409, 437, 455, and 473, which corresponded to hederagenin. The fragmentation of compound 17 primarily yielded daughter ions at m/z 781, 619, and 473 because of the successive loss of Ara-Glc, Glc, and Rha. In addition, compound 17 produced a parent ion [M+HCOO]⁻ at m/z 1119.5508 in the negative mode, and fragmented into 603 and 469, indicating that the C‐28 position was substituted with 2 Glc and 1 Rha sugar chain. Consequently, compound 17 was characterized as hederagenin 3-O-α-L-arabinopyranoside, 28-O-[β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl-(1⟶4)-α-L-rhamnopyranosyl] ester or hederagenin 3-O-α-L-arabinopyranoside, 28-O-[β-D-glucopyranosyl-(1⟶2)-(β-D-glucopyranosyl-(1⟶4))-α-L-rhamnopyranosyl] ester. These were explored as two new structures, and the MS/MS fragmentation pathways of compound 17 are illustrated in Figures 6 and 7. However, fragmentation of [M+H]⁺ from compound 20 formed daughter ions at m/z 943, 797, 635, and 473, which corresponded to the sequential elimination of Ara, Rha, and 2 Glc, respectively. In the negative mode, [M-H]− ion at m/z 1073.5454 was fragmented to 749, indicating that the C‐28 position was substituted with the 2 Glc sugar chain. Hence, compound 20 was hederagenin 3-O-[α-L-arabinopyranosyl-(1⟶2)-α-L-rhamnopyranoside], 28-[β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl] ester.

The identified compounds 18 (T_R = 12.37 min) and 29 (T_R = 17.74 min) exhibited pseudomolecular ions [M+H]⁺ at m/z 1221.6233 and 1221.6303 in the positive mode, respectively, which fragmented in different manners. The fragmentation of these two saponins exhibited aglycone ions at m/z 473, 455, and 437, which corresponded to hederagenin. Comparing the MS/MS spectra and retention time information with the reference standards, compound 18 was undoubtedly determined as hederacoside C. Besides, under the negative mode, the parent ion of compound 29 was observed at m/z 1219.5990 and produced distinctive product ions at m/z 1073, 911, 749, 603, and 471 by the loss of sugar chain (Rha, Rha-Glc, Rha-Glc-Glc, Rha‐Glc-Glc‐Rha, and Rha‐Glc-Glc‐Rha-Ara) at C-3 of the aglycone. Consequently, compound 29 could be characterized as hederagenin 3-O-[α-L-rhamnopyranosyl-(1⟶4)-β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl-(1⟶4)-α-L-rhamnopyranosyl-(1⟶2)-α-L-arabinopyranoside].

At T_R = 12.63, in the negative mode, compound 19 yielded an [M+HCOO]⁻ ion at m/z 1119.5482 and provided fragment ions at m/z 749, 603, and 469 corresponding to the loss of 2 Glc at C-28 and a Rha-Ara sugar chain at C-3 of the hederagenin aglycone. Therefore, compound 19 was tentatively identified as hederagenin 3-O-[α-L-rhamnopyranosyl-(1⟶2)-α-L-arabinopyranoside], 28-O-[β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl] ester.

Compound 21 (T_R = 13.93 min) yielded an [M+HCOO]⁻ ion at m/z 1307.6264 in the negative mode, primarily fragmented into ions at m/z 791, 749, and 469, indicating that hederagenin aglycone C-28 lost an acetyl group in the Rha-Glc-Glc sugar chain, and C-3 lost a Rha-Ara sugar chain. Therefore, compound 21 was conditionally characterized as hederagenin 3-O-[α-L-Rhamnopyranosyl-(1⟶2)-α-L-arabinopyranoside], 28-O-[α-L-rhamnopyranosyl-(1⟶4)-6-O-acetyl-β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl] ester.

At T_R = 14.72, in the negative mode, compound 22 showed the formula of C₅₉H₉₆O₂₅ ([M-H]⁻ at m/z 1203.6189) and provided fragment ions at m/z 733 and 455, corresponding to the loss of 2 Glc and 1 Rha at C-28, and a Rha-Ara sugar chain at C-3 of the oleanolic acid aglycone. Hence, compound 22 was identified as hederacoside B.

The MS spectra of compound 23 (T_R = 14.77 min) yielded a parent ion [M+HCOO]⁻ at m/z 987.5210 in the negative mode, primarily fragmented into an ion at m/z 471, indicating that the C-28 sugar chain contained a Rha and 2 Glc, and the aglycone corresponded to hederagenin. Thus, compound 23 was determined as hederagenin 28-O-[α-L-rhamnopyranosyl-(1⟶4)-β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranoside].

Compound 24 (T_R = 15.42 min) yielded an [M+HCOO]⁻ ion at m/z 957.5047 in the negative mode, primarily fragmented into ions at m/z 749, 603, and 471, indicating the loss of Glc-Rha-Ara sugar chain at C-3 of hederagenin. Therefore, compound 24 was conditionally identified as hederagenin 3-O-[α-L-rhamnopyranosyl-(1⟶2)-(β-D-glucopyranosyl-(1⟶4))-α-L-arabinopyranoside] (hederacolchiside A).

Compound 25 showed the formula of C₄₂H₆₈O₁₄ ([M+HCOO]⁻ at m/z 841.4599) and provided fragment ion at m/z 471, corresponding to the loss of 2 Glc at C-28 of the hederagenin aglycone. Hence, compound 25 was tentatively characterized as hederagenin 28-O-[β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranoside].

The MS spectra of compound 26 (T_R = 15.78 min) yielded a parent ion [M+HCOO]⁻ at m/z 811.448, primarily fragmented into ions at m/z 603 and 471, indicating that the C-3 sugar chain contained a Glc and an Ara, and the aglycone corresponded to hederagenin. Thus, compound 26 was conditionally identified as hederagenin 3-O-[β-D-glucopyranosyl-(1⟶2)-α-L-arabinopyranoside].

In the positive mode, the MS/MS spectra of compounds 28 (T_R = 17.68 min) exhibited pseudomolecular ions [M+H]⁺ at m/z 1089.5828, and produced aglycone ions at m/z 391, 409, 437, 455, and 473, which corresponded to hederagenin. The fragmentation of compound 28 primarily yielded daughter ions at m/z 927, 765, 619, and 473 because of the successive loss of Glc-Glc-Rha-Rha. By assembling all the fragmentation information compound 28, this compound was determined to be hederagenin 3-O-[β-D-glucopyranosyl-(1⟶6)-β-D-glucopyranosyl-(1⟶4)-α-L-rhamnopyranosyl-(1⟶2)-α-L-rhamnopyranoside] or hederagenin 3-O-[β-D-glucopyranosyl-(1⟶2)-(β-D-glucopyranosyl-(1⟶4))-α-L-rhamnopyranosyl-(1⟶2)-α-L-rhamnopyranoside]. They were investigated as two new saponin structures. The MS/MS fragmentation pathways of the structures of compound 28 are illustrated in Figures 8 and 9.

At T_R = 18.40, compound 30 showed the formula of C₃₆H₅₈O₉ ([M+HCOO]⁻ at m/z 679.4052) and fragmented into ions at m/z 471, indicating that the C-28 or C-3 sugar chain contained a Glc, and the aglycone was hederagenin. Thus, compound 30 was determined as hederagenin 28-O-β-D-glucopyranoside or hederagenin 3-O-β-D-glucopyranoside (hederacoside B).

The MS spectra of compound 31 (T_R = 18.62 min) yielded a parent ion [M-H]⁻ at m/z 779.4586, primarily fragmented into ions at m/z 633 and 471, indicating the loss of a Rha-Glc sugar chain at C-3 of hederagenin. Hence, compound 31 was conditionally identified as hederagenin 3-O-[α-L-rhamnopyranosyl-(1⟶2)-β-D-glucopyranoside].

Compound 32 showed a deprotonated molecular ion [M‐H]⁻ at m/z 647.3793 at T_R = 19.50. The MS/MS spectra showed an ion peak at m/z 471, which indicated that at C-28 or C-3 of hederagenin contained a Glu. Therefore, compound 32 was predicted to be hederagenin 28-O-β-D-glucuronopyranoside or hederagenin 3-O-β-D-glucuronopyranoside.

Compound 33 (T_R = 20.30 min) yielded [M+H]⁺ ion at m/z 751.4609 [M‐H]⁻ ion at m/z 749.4489 in the positive and negative modes, respectively. Comparing the MS/MS information and retention time with the reference standard, compound 33 was unambiguously identified as α-hederin.

At T_R = 20.38, compound 34 showed the formula of C₃₆H₅₈O₈ ([M+H]⁺ at m/z 619.4197). The fragment ions at m/z 391, 437, and 473 indicated the loss of a Rha at C-3 or C-28 of hederagenin aglycone. Thus, compound 34 was characterized as hederagenin 3-O-α-L-rhamnopyranoside or hederagenin 28-O-α-L-rhamnopyranoside.

The MS spectra of compound 36 (T_R = 21.16 min) yielded a parent ion [M+HCOO]⁻ at m/z 649.4963 and fragmented into 471, indicating the loss of an Ara at C-3 or C-28 of hederagenin. Consequently, compound 36 was identified as hederagenin 3-O-α-L-arabinopyranoside or hederagenin 28-O-α-L-arabinopyranoside.

Under the negative mode, compound 37 (T_R = 22.95 min) showed the diagnostic ion [M‐H]⁻ at m/z 631.3869 and a fragment ion at m/z 455, indicating that the C‐28 or C-3 position of oleanolic acid aglycone was substituted with a Glu. Thus, compound 37 was tentatively determined as oleanolic acid 28-O-β-D-glucuronopyranoside or oleanolic acid 3-O-β-D-glucuronopyranoside.

Compound 38 (T_R = 23.33 min) yielded an [M+HCOO]⁻ ion at m/z 663.4114 in the negative mode, primarily fragmented into an ion at m/z 455, meaning that the C-28 or C-3 sugar chain contained a Glc, and the aglycone corresponded to oleanolic acid. Hence, compound 38 was characterized as oleanolic acid 28-O-β-D-glucopyranoside or oleanolic acid 3-O-β-D-glucopyranoside (hederacoside A2).

The MS spectra of compound 40 (T_R = 24.03 min) yielded a pseudomolecular ion [M‐H]⁻ at m/z 733.4518. Under the negative mode, the diagnostic ions at m/z 587 and 455 indicated that in compound 40, the C‐28 position of oleanolic acid was substituted with a Rha, and the C-3 position of the aglycone contained an Ara, or the product ion represented for the loss of sugar chain Rha‐Ara at C-3 position only. Therefore, compound 40 was predicted to be oleanolic acid 3-O-α-L-rhamnopyranosyl-(1⟶2)-α-L-arabinopyranoside (β-hederin).

At T_R = 25.24, compound 42 showed the formula of C₃₀H₄₈O₄ ([M-H]⁻ at m/z 471.3488) and fragmented into ion at m/z 393. Comparing the MS/MS spectrum and data with the result of Hai-Long et al. [26], compound 42 was characterized as hederagenin.

3.4. Structural Characterization of Flavonoids and Flavonoid Glycosides

In the positive mode, compounds 4, 5, 7, and 8 were identified as rutin (m/z 611.1623), quercetin (m/z 303.0504), kaempferol-3-O-rutinoside (m/z 595.1670), and kaempferol (m/z 287.0557), respectively, confirmed by MS and MS/MS data comparison with the results of Renu and Brijesh [27].

In the negative mode, at T_R = 6.46, compound 3 exhibited an [M-H]^- ion at m/z 739.2050, and fragmented into 593 and 285, due to the elimination of a rhamnosyl group and a rutinosyl group, respectively. Therefore, compound 3 was identified as kaempferol 3-O-rutinoside-7-O-rhamnoside. Compound 6 yielded [M-H]^- ion at m/z 463.0897. Comparing the MS/MS data with Linling et al.’s publication [28], compound 6 was characterized as isoquercitrin. At T_R = 7.98, compound 10 showed deprotonated molecular ion [M-H]^- at m/z 447.0946 and produced a characteristic fragment ion at m/z 285, corresponding to the characteristic loss of a glucosyl group. Hence, compound 10 was determined as astragalin. All of the chemical structures of identified flavonoids are presented in Figure 10.

4. Conclusions

In the present work, by applying UHPLC‐Q‐TOF‐MS/MS in both positive and negative electrospray ionization modes as an efficient analytical method, the chemical constituents of H. helix could be rapidly discovered and identified in a single sample injection. As a result, 46 phytochemicals including 24 triterpene saponins were characterized, and four of which have yet been published before. UHPLC‐Q‐TOF‐MS/MS serves as a powerful analytical method for finding and instructing new phytochemical structures. Furthermore, the phytochemical profile result provides a base for quality control of H. helix raw materials. It also propels the medicinal application of this plant base on the metabolomic profiling of triterpene saponins.

Data Availability

The data used to support the results of this study are included within the article. Any further information is available from authors upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

This research was funded by the Vietnam National Foundation for Science and Technology Development (NAFOSTED) under grant no. 104.01–2019.28.

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