Differentiation between 3,4- and 4,15-Epoxyeudesmanolides by Electrospray Ionization Tandem Mass Spectrometry

Dias, Herbert Júnior; Stefani, Ricardo; Tomaz, José Carlos; Vessecchi, Ricardo; Crotti, Antônio Eduardo Miller

doi:https://doi.org/10.1155/2017/7921867

Journal of Analytical Methods in Chemistry

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

Research Article | Open Access

Volume 2017 | Article ID 7921867 | https://doi.org/10.1155/2017/7921867

Differentiation between 3,4- and 4,15-Epoxyeudesmanolides by Electrospray Ionization Tandem Mass Spectrometry

Herbert Júnior Dias,¹Ricardo Stefani,²José Carlos Tomaz,³Ricardo Vessecchi,¹and Antônio Eduardo Miller Crotti¹

Academic Editor: Erwin Rosenberg

Received11 Jul 2017

Accepted03 Oct 2017

Published06 Nov 2017

Abstract

We investigated the fragmentation of the eudesmanolide-type sesquiterpene lactones 1α-(4-hydroxymethacryloyloxy)-3α,4α-epoxy-8α-hydroxyeudesm-11(13)-6α,12-olide (1) and 1α-(2,3-epoxyangeloyloxy)-4α,15-epoxy-8α-hydroxyeudesm-11(13)-6α,12-olide (2) by electrospray ionization tandem mass spectrometry (ESI-MS/MS). The elimination of the different ester substituent at C(1) directly from protonated 1 and 2 (A) led to the formation of two regioisomer product ions B (A − RCO₂H). Further fragmentation of B resulted from consecutive eliminations of H₂O and CO molecules. However, we identified four product ions that allowed for the differentiation between 3,4- and 4,15-epoxyeudesmanolides. The formation of these diagnostic ions was associated with the C(3)–O bond of compound 1, which propitiates the participation of the lone pair of the oxygen epoxide in the formation of B through a Grob-Wharton-type fragmentation, then resulting in an alternative fragmentation pathway. These data can be useful for the fast differentiation between epoxyeudesmanolide regioisomers directly from Dimerostemma extracts by liquid chromatography-tandem mass spectrometry (LC-MS/MS), as an alternative to NMR, or even for quantitation studies of these compounds using multiple reaction monitoring (MRM) scan.

1. Introduction

Eudesmanolides are sesquiterpene lactones (STL) biosynthetically derived from farnesyl pyrophosphate, whose occurrence has been widely reported in plants of the Asteraceae family [1]. These compounds display a wide spectrum of biological activities, such as antitumor [2], antiproliferative [3], anti-inflammatory [4], antifungal [5, 6], antimicrobial [7], insecticidal [8], and inhibitory activity of the protein PTP1B, responsible for type 2 diabetes and obesity [9].

Structurally, eudesmanolides exhibit a decalin system fused to a -lactone ring. Although trans-fused eudesmanolides are the most common forms, cis-fused eudesmanolides may also occur [1]. The structural diversity of these compounds emerges mainly from oxidations in the basic sesquiterpene skeleton [1, 10]. The enzymatic oxidation of the double bonds of eudesmanolides along the biosynthetic process results in the formation of epoxyeudesmanolide regioisomers, whose structural elucidation often requires a detailed (and sometimes exhaustive) analysis of the ¹H and ¹³C nuclear magnetic resonance (NMR) spectra [11].

Over the last two decades, electrospray ionization tandem mass spectrometry (ESI-MS/MS) has proved to be a powerful analytical technique for the fast identification of natural products [12, 13]. In some specific cases, the high sensitivity and selectivity, as well as the possibility of using nondeuterated solvents, have rendered ESI-MS/MS even more attractive than NMR [14]. Moreover, the coupling of liquid chromatography to electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) has allowed for the quantification of these compounds directly from crude extracts and complex matrices [14, 15]. It is noteworthy that the sensitivity and the selectivity of LC-MS/MS can be increased significantly by using the multiple reaction monitoring (MRM) scan mode, which is based on two or more transitions from the precursor ion to specific (and eventually diagnostic) product ions [16]. However, the fragmentation patterns of several classes of natural products under collision-induced dissociation (CID) conditions have not been well-established yet, which has made building spectral libraries difficult and limited the use of LC-ESI-MS/MS for qualitative and quantitative studies on these compounds [12].

As part of our ongoing project on the gas-phase fragmentation reactions of natural products and their analytical applications [17], in this study, we will report the fragmentation of two 3,4- and 4,15-epoxyeudesmanolides using ESI-CID-MS/MS and its potential to distinguish these compounds.

2. Material and Methods

2.1. Mass Spectrometry Analysis

The epoxyeudesmanolides 1 (1-(4-hydroxymethacryloyloxy)-3,4-epoxy-8-hydroxyeudesm-11(13)-6,12-olide) and 2 (1-(2,3-epoxyangeloyloxy)-4,15-epoxy-8-hydroxyeudesm-11(13)-6,12-olide) (Figure 1) were previously isolated from Dimerostemma vestitum [11] and Dimerostemma rotundifolium [18].

Compounds 1 and 2 were dissolved in methanol/water 4 : 1 (v/v) and analyzed on a Quattro-LC instrument (Micromass, Manchester, UK), provided with an electrospray ion source operating in the positive ion mode and a triple quadrupole (QqQ) mass analyzer. Solutions of the compounds (0.3 mg·mL⁻¹) were infused into the ESI source at a flow rate of 5 μL·min⁻¹ using a Harvard Apparatus model 1746 (Holliston, MA) syringe pump. The desolvation and ionization source block temperatures were at 250 and 120°C, respectively. The capillary and the cone voltage were optimized to 3.0 kV and 15 V, respectively. Collision-induced dissociation (CID) was performed on the isolated protonated molecule using argon collision gas (7 psi) and nitrogen was used as desolvation and nebulizing gas (flow rates of 260 and 26 L·h⁻¹, resp.). The analytical mass range was 40–400 . In labeled hydrogen experiments, deuterium oxide (D₂O, 99.9 atom % D, Aldrich®) was added to the samples in a proportion of 10% v/v. The product ion spectra were obtained using collision energy ranging from 0 to 30 eV. Quasi-MS³ experiments were carried out by selecting the product ions generated by in-source dissociation and using them as precursor ions in CID experiments.

2.2. Computational Methods

The conformational analyses of the epoxyeudesmanolides 1-2 were obtained by estimation of most stable conformers and optimization of geometries applying MM2 force field. The lowest energy conformers were reoptimized on the basis of DFT calculations at mPW1PW91/6-31+G(d) level, employing Gaussian 03 software [19]. The stationary point was estimated through vibration frequencies calculation at the same model. The protonation sites of the epoxyeudesmanolides 1-2 were investigated employing the proton affinity (PA) as descriptor, as previously reported [20]. The enthalpy of the proton for the reaction M + H⁺ → MH⁺ was considered as 1.48 kcal·mol⁻¹ at 298 K [21]. Molecular electrostatic potential maps (MEP) were also plotted employing Molekel software [22].

3. Results and Discussion

3.1. Structure-Fragmentation Relationships

Previous reports have demonstrated the importance of structure-fragmentation relationships for the rationalization of the gas-phase fragmentation pathways of compounds that exhibit the same structure core [12, 23–25]. However, to achieve trustable structure-fragmentation relationships, the product ion spectra must be obtained using the same collision energies (). The optimum value must reduce the relative intensity of the precursor ion below 50% and maximize the intensity of other product ions without promoting extensive fragmentation [26]. In this work, the optimum for compounds 1 and 2 was found at 15 eV. The product ion spectra of protonated 1 and 2 at 15 eV are shown in Figure 2. The assignments of main product ions (relative intensity higher than 5%) of protonated 1 and 2 are given in Table 1.

(a)

(b)

The comparison between the product ion spectra of protonated 1 (3,4-epoxyeudesmanolide) and 2 (4,15-epoxyeudesmanolide), which differ in the acyloxy group at C(1), revealed a common product ion with 263 (B). This ion results from the elimination of the corresponding carboxylic acids (4′-hydroxymetacrylic acid for 1 and 2′,3′-epoxyangelic acid for 2) directly from the protonated molecule. Therefore, the product ion B of protonated 1 and 2 are regioisomers; consequently, differences between their fragmentations are expected to be due to the position of the epoxide ring in the basic structure of these eudesmanolides. A series of product ions derived from B by means of consecutive eliminations of H₂O (18 u) and CO (28 u) are also common to 1 and 2, such as C (B − H₂O), E (C − H₂O), F (C − CO), H (E − CO), J (H − H₂O), and K (H − CO). This fragmentation pattern is similar to those previously reported for other sesquiterpene lactones [26]. On the other hand, the product ions D ( 235), G ( 209), I ( 189), and L ( 145) were observed only in the product ion spectrum of 1. Thus, these diagnostic ions can be useful to differentiate a 3,4-epoxyeudesmanolide (1) from a 4,15-epoxyeudesmanolide (2) isomer exhibiting the same structural core. Indeed, data from quasi-MS³ experiments supported that the product ions F ( 217) and H ( 199) can be formed by two different pathways. The ion F can be resulting from the elimination of CO from C (for 1 and 2) or H₂O from D (only for 1), whereas H can be formed by elimination of CO from E or H₂O from F for both the compounds. An overview of the fragmentation pathways of protonated epoxyeudesmanolides 1 and 2 allowed for identifying some diagnostic ions as depicted in Scheme 1.

3.2. Search for the Protonation Site

The determination of the protonation site has been reported as an important step for the rationalization of the gas-phase fragmentation pathways [25]. In principle, protonation can take place in many basic sites of the structure; however, an excess of the species containing the proton attached to the most basic site of the structure is expected. Upon CID conditions, two main possibilities must be considered: (a) the proton could remain bounded to the most basic site of compounds after the collision activation, so that the kinetic energy is only converted into internal energy [27] and (b) the proton is initially attached to the most basic site of molecule, but it can migrate to less basic sites upon CID process, then initiating the fragmentation process, in accordance with the “proton mobile model” [28]. In this study, we first used molecular electrostatic maps (MEPs, Figure 3) to identify the possible sites of the structures of the epoxyeudesmanolides 1 and 2, in which the protonation can occur during the ionization process. The MEPs of these compounds (Figure 3) indicated the oxygen atoms as the most likely protonation sites, mainly the carbonyl oxygen [29, 30]. Next, the proton affinity (PA) values were estimated for all the protonation sites suggested by MEPs (Figure 3). The PA values indicated that the carbonyl oxygen of the -lactone ring of both epoxyeudesmanolides is the most susceptible sites to protonation.

In addition, the translational energy of the protonated epoxyeudesmanolides 1 ( 365) and 2 ( 379) converted into internal energy by the collision gas (argonium) at eV were calculated to 34.0 and 32.9 kcal·mol⁻¹, respectively [31]. These data revealed that the energy provided upon CID is higher than the difference between the energies of all the protonation sites, as estimated by computational methods.

3.3. Formation of the General Ions B, C, E, F, H, J, and K

The product ion B ( 263) is formed from protonated 1 and 2 by means of the elimination of the ester side chain at C(1) as its corresponding carboxylic acid, as previously mentioned in this paper. Data from the hydrogen labeled experiments (Table 1) revealed that the deuterium/hydrogen attached to the molecule during the ionization process is involved in this step. These data evidenced that the elimination of the carboxylic acid must be preceded by the proton migration from the -lactone oxygen (the most basic site of the structure of 1 and 2) to the carbonyl oxygen of the ester function at C(1). The energy difference needed to promote this migration is estimated to be 10.7 kcal·mol⁻¹ for 1 and 6.6 kcal·mol⁻¹ for 2, as indicated by the PA values, which is lower than the corresponding to eV. The elimination of side-chain group at C(1) by inductive cleavage results in the product ion B1 ( 26), as shown in Scheme 2 [32]. Considering that B1 is a secondary carbocation, its rearrangement to B2 (a tertiary carbocation) by means of a 1,2-alkyl shift is driven by the charge stabilization [33]. Alkyl migrations driven by increase in the stability due to hyperconjugative effects have been also reported for similar compounds, such as steroids [34]. Elimination of H₂O from B2 by means of a remote hydrogen rearrangement leads to the formation of C1 ( 245), which is the most intense product ion in the CID spectrum of the epoxyeudesmanolides 1 and 2 [35].

Further fragmentation of C1 is preceded by its conversion into C2, from which the opening of the -lactone ring occurs to produce the acylium ion C3, as previously reported for other -lactones (Scheme 2) [36]. The water elimination from C3 produces E ( 227), which has an extended conjugation as compared to C3. Elimination of CO elimination from E results in the vinylic carbocation H ( 199), which can easily rearrange to the aromatic cation H1 by means of a hydride shift from C(5) to C(11) [37]. On the other hand, the CO elimination from C3 can be assisted by a 1,2-hydride shift from C(7) to C(11) to result in the product ion F ( 217). Finally, dehydration of F1 also leads to H1, as confirmed by data from quasi-MS³ experiments (Scheme 2). The differences between the relative intensities of F in the product ion spectrum of 1 (62%) and 2 (19%) will be further discussed in this paper.

Formation of the product ion J ( 181) for both 1 and 2 is preceded the cleavage of the C(3)–O of H1 and consequent opening of the epoxide ring by means of remote hydrogen rearrangements (Scheme 3). On the other hand, although the product ions K ( 171) are formed for both the protonated epoxyeudesmanolides 1 and 2, their formations depend on the position of the epoxide ring. For compound 1, the oxygen lone pair is involved in a Grob-Wharton-type fragmentation, which results in the cleavage of the C(2)–C(3) bond and consequent formation of the intermediate ion H4. Further heterolytic cleavage of the C(4)–O produces a terminal carbonyl group (i.e., an aldehyde), from which the CO is eliminated to form the product ion K1 ( 171). In contrast, formation of K for compound 2 is initiated by the conversion of H1 into the intermediate ion H6 by means of a rearrangement assisted by the oxygen lone pair of the epoxide ring. Cleavage of the C(4)–O produces H7, from which the CO elimination occurs to produce K2 ( 171) by a mechanism similar to that involved in the formation of K1 from H5 (Scheme 3).

3.4. Formation of the Diagnostic Ions D, G, I, and L

The formation of the product ions D ( 235), G ( 209), I ( 189), and L ( 145), which are diagnostic for compound 1, is associated with the C(3)–O bond. This bond places the oxygen of the epoxide ring at a particular position of the eudesmanolide skeleton that propitiates the direct participation of the oxygen lone pair in the elimination of the ester side chain at C(1). By means of the Grob-Wharton fragmentation depicted in Scheme 4, the 3,4-epoxide ring can play a key role in the formation of B through another pathway compared to that proposed in Scheme 2. The heterolytic cleavage of the C(4)–O bond of the resulting product ion B3 ( 263) produces the intermediate ion B4 (pathway a, Scheme 4). Elimination of CO from the aldehyde moiety of B4 produces D ( 235), which is diagnostic for the epoxide ring between C(3) and C(4). Further opening of the -lactone leads to the formation of the intermediate acylium ion D1, which decomposes into F2 ( 217). In the case of compound 1, the product ion F can be formed through two different pathways, as shown in Schemes 2 and 4. This could explain, at least in principle, the higher relative intensity of this ion in the CID spectrum of 1 as compared to 2. On the other hand, pathway b involves the elimination of H₂O from B3 and consequent formation of C4 ( 245). The elimination of 2-methyloxirene (C₃H₄O) by means of the heterolytic cleavage of the C(4)–C(5) and further 1,2-methyl shift from C(10) to C(5), which is driven by the charge stabilization, caused I1 ( 189). Further remote hydrogen rearrangement results in the opening of the -lactone ring and produces the intermediate ion I2, which has extended conjugation as compared to I1. Elimination of CO₂ from I2 (44 u) results in the product ion L ( 145), which is also diagnostic for the epoxide ring between C(3) and C(4).

Finally, the product ion G ( 209) from E can also be considered diagnostic for presence of epoxide ring at position 3,4. For compound 1, its formation involves opening of the epoxide ring by a remote hydrogen rearrangement and further elimination of H₂O (Scheme 5). A similar pathway could also lead to the formation of G for compound 2. However, the aromaticity of G1 makes it much more stable than G2, which displays an exocyclic double bond between C(4) and C (15). Therefore, the formation of G1 is much more favored energetically than the formation of G2, so that the product ion of 209 is observed only in the product ion spectrum of 1.

4. Conclusions

In summary, we have identified a series of diagnostic ions for compound 1 that could be useful for the fast differentiation of 3,4- and 4,15-epoxyeudesmanolides 1 and 2 by ESI-MS/MS, as an alternative to NMR. Moreover, these results could be also applied to the selective quantitation of these compounds directly from Dimerostemma extracts by liquid chromatography-tandem mass spectrometry (LC-MS/MS) using the transition of the precursor ion to these diagnostic ions in multiple reaction monitoring (MRM) methodologies. However, further studies with a wide range of epoxyeudesmanolides should be addressed to verify the potential of ESI-MS/MS to identify other epoxyeudesmanolides derivatives.

Conflicts of Interest

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

Acknowledgments

The authors acknowledge the Brazilian foundations FAPESP (Proc. 2013/20094-0 and Proc. 2014/23604-1) and CNPq (Proc. 141883/2014-6 and Proc. 442384/2014-9) for financial support.

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Copyright © 2017 Herbert Júnior Dias et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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