Trials for Gathering Information on an Unknown Peak in the GC-MS Spectra of Horse and Pony Hair Extracts

The volatile compounds from horse and pony hairs and skin were analyzed to determine bioactive molecules that are kairomones used for host location by blood-feeding diptera. In this study, horse and pony hair samples were extracted with organic solvents (pentane or hexane) and analyzed by gas chro-matography-mass spectrometry analysis (GC-MS) with closed electron ionization (CEI). Using the GC-MS analysis, we observed a compound peak, which could not be identified by comparison to mass spectra in the mass spectral library. This unknown compound was often the largest peak in the chromatogram and had a retention index and mass spectral fragmentation similar to nonanal. However, there were several differences in the fragmentation pattern. When compared to a nonanal reference standard, it was evident that this was a different compound. Hydrodistillation of pony hair was another extraction method to obtain the unknown component in higher concentrations. Analysis of this extract with GC-flame ionization detector (FID) with GC-MS confirmed the same unknown peak. Further experiments and analysis with the various mass spectroscopy tools gave the possible molecular ion with mass-to-charge ratio (m/z) 142, corresponding to the unknown component.


Introduction
Blood-feeding diptera such as stable flies, Stomoxys calcitrans (L.), horse flies, Tabanus spp. and Hybomitra spp., as well as deer flies, Chrysops spp., can cause irritation and distress in mammals [1]. Tabanid flies impact mammals via transmission of disease, reduced weight gains in animals and annoyance [2].
Mammalian sebum (secretions from the skin surface of mammals) contains an array of compounds possessing unusual unsaturation sites, chain lengths, and branching patterns [3]. The hydrolysis products on some mammalian (human, rat, rabbit, mouse, sheep, guinea pig etc.) skin surfaces include squalene, sterols, monohydric alcohols, alkane-1,2-diols, αand ω-hydroxy acids [4]- [9], and unhydrolyzed products: squalene, free sterols, sterol monoesters, monoester waxes, diester waxes (type I and II), glyceryl ether diesters, triglycerides and free fatty acids [10] [11] [12] [13]. Chatt and Katz [14] identified free fatty acids, monoglycerides, diglycerides, triglycerides, wax esters, hydrocarbons, and alcohols from the hair. A study of the chemical composition of 20 different mammalian species showed a uniqueness of the sebum composition for each species, although there were similarities within genera, e.g., intermediates of cholesterol biosynthetic pathway; variety of mono-and diesters, typically, containing unusual fatty acids [15] [16], identified anteiso-branched 18-methyl-eicosanoic acid (MEA), comprising approximately 40% of the total fatty acids in the integral lipid fraction in mammalian hair. Additionally, cholesterol sulphate and ceramides were identified. Chemical analyses of the mammalian pelage have focused on the even-toed ungulates (Cetartiodactyla), chiefly on bovids [17] [18]. Analyses of the pelage chemistry of odd-toed ungulates (Perissodactyla) are confined to the domestic horse (Equus caballus) and other equids. These studies revealed giant (C 28 -C 36 ) lactone rings of ω-hydroxy acids, known as equolides, among horses, asses, and zebras [19]. Scott and Miller [20] reported that freshly liberated sebum contains triglycerides and wax esters in the hair follicles which becomes contaminated with lipase-producing bacteria (Staphylococcus spp.), as well as linoleic, myristic, oleic and palmitic acids. The structure of sterols and fatty acids are speciesspecific, thus, the molecular composition can serve as a fingerprint for the species; e.g. only surface lipids for Equidae contain lactones (about 47% of the total), and sterol esters, cholesterol and wax diesters. Nicolaides, Fu and Rice [21] identified icosane and cholesteryl acetate on horse skin surface. In the skin surface lipids from the sides of male and female horses (E. caballus), Downing and Colton [22] identified cholesterol, cholesteryl esters and the lactones of ω-hydroxy acids, each including a methyl group in the n − 1 position, mostly mono-unsaturated (n − 8 or n − 10), but, also, with small amounts of saturated and dienoic species. Ferreira et al. [23] identified predominantly ethyl octanoate, ethyl deca-noate, and, as minor components, hexanal, heptanal, and (E)-2-decenal in horse extracts. According to Wertz [24] the ω-hydroxy acids that are products from the hydrolysis of horse lactones from the common horse (E. caballus) are mostly monounsaturated, iso-branched and have 33-, 35-and 37-carbons in the major compounds.
To identify components responsible for the attraction of flies and other insects to horses, we investigated horse hair volatiles/extracts. Gas chromatographymass spectroscopy (GC-MS) analysis led to the discovery of an unknown compound. It was the most abundant peak in the chromatogram. This compound was not detected in similar analyses of dog and donkey hair extracts; however, it was observed in the hair extract from a pony. To the best of our knowledge, the peak observed in our study has not been reported previously according to the existing literature. This report details our attempt to identify the unknown compound in horse and pony hairs.

Materials and Methods
Horse and pony hairs were obtained on 03/17/2016 from the University of Florida's Institute of Food and Agricultural Sciences (UF/IFAS) Horse Teaching Unit, Gainesville, FL, USA. After the horse and pony had been groomed, hairs were sealed in glass bottles and stored in a freezer. For the extraction, pentane, n-hexane, dichloromethane (CH 2 Cl 2 ), acetone, ethyl acetate (EtOAc), ethanol were used. All solvents and neat nonanal as a reference standard (CAS # 124-19-6) were purchased from Sigma-Aldrich, St. Louis Corp., MO, USA.

Hydrodistillation of Pony Hair (Sample 2)
A sample of pony hair (150 g) was hydrodistilled for 3 h in a Clevenger-type apparatus (Fisher Scientific, Hampton, NH, USA). After 3 h, the hydrosol was collected and extracted three times with 100 mL of n-hexane at room temperature. The organic layer was dried over anhydrous sodium sulfate, evaporated using a rotary evaporator producing 12 mg of extract and stored in a dark glass bottle at 4˚C for subsequent analysis. The hydrodistillate was used for derivati-zation, as well.

Gas Chromatography-Mass Spectrometry Analysis (GC-MS) with
Closed Electron Ionization (CEI), Negative Ion Chemical Ionization (NICI), and Positive Ion Chemical Ionization (PICI) A 1 μL aliquot from each extract was analyzed along with the pentane blanks using a ThermoFinnigan DSQ (Thermo Fisher Scientific; Austin, TX) gas chromatograph (GC) equipped with a DB-5 (Agilent; Santa Clara, CA) column (30 m × 0.25 mm ID; 0.25 μm film thickness). The GC oven temperature program was set at an initial temperature of 50˚C and held at that temperature for 5 min post injection ramped at 3˚C/min to 240˚C and held 5 min at the same temperature.
The mass analyzer was scanned at a rate of 0.5 sec over a mass range of m/z 35 to m/z 650. The programmed temperature vaporizing (PTV) injection port was operated from 50˚C to 240˚C with a rate of 14.5˚C/sec, in splitless mode, the transfer line temperature was set to 200˚C, and the carrier gas was set to a constant flow of 1.5 mL/min. CEI-MS Spectra were recorded at 70 eV electron energy. Reagent gas flow was set at 0.3 mL/min for CEI and 2.5 mL/min for NICI and PICI. Tune files were used accordingly for CEI, NICI and PICI.
Derivatization with the acetic anhydride: Pony hair hydrodistillate (sample 2, 12 mg) was dissolved in chloroform (10 mL). Acetic anhydride (1 mL) and acetic acid (2 mL) were added and heated at 50˚C for 16 h [25]. Then mixture was washed with water (10 mL) and brine (10 mL). The mixture was concentrated under vacuum to dryness and redissolved in chloroform for analysis by CEI-GC-MS.
Identification: The analysis was carried out by comparison of the chromatographic peak retention indices to those of possible candidates, against standard compounds when available and by comparison with literature data. Comparisons of MS fragmentation patterns with those of standards and mass spectrum database search were performed using the Wiley GC-MS library (Wiley, New York, NY, USA), the NIST library (US National Institute of Standards and Technology, Gaithersburg, MD, USA) and the Adams Library [26]. Reference points to calculate the arithmetic retention indices (AI) [26] at CEI tune were generated by n-alkanes.

Gas Chromatography-Flame Ionization Detector (FID) and Gas
Chromatography-Mass Spectrometry Analysis (GC-MS) with Electron Impact (EI) Ion Source GC Analysis: The GC analysis was carried out using an Agilent 6890N GC system. The FID detector temperature was 300˚C. To obtain the same elution order with GC-MS, simultaneous auto-injection was done as a duplicate on the same column applying the same operational conditions. Relative percentage amounts of the separated compounds were calculated from FID chromatograms.
GC-MS Analysis: An Agilent 5975 GC-MSD system was used, where Innowax FSC column (60 m × 0.25 mm, 0.25 µm film thickness) was used with he-lium as carrier gas (0.8 mL/min). The GC oven temperature was kept at 60˚C for 10 min and programmed to 220˚C at a rate of 4˚C/min, and kept constant at 220˚C for 10 min and then programmed to 240˚C at a rate of 1˚C/min. The split ratio was adjusted at 40:1. The injector temperature was set to 250˚C. Mass spectra were recorded at 70 eV, where the mass range was from m/z 35 to 450.
Identification: The analysis of the unknown peak (sample 2) was accomplished by comparison of the relative retention time (RRT) with those of authentic samples or by comparison of their relative retention index (RRI) to series of n-alkanes [27]. Computer matching against commercial (Wiley GC/MS Library, MassFinder Software 4.0) [28] [29] [30] and in-house "Baser Library of Essential Oil Constituents" built up by genuine compounds and components of known oils was used for the identification.

Extraction
During our search for new natural products with attractant or repellent activity against blood-feeding arthropods, we observed a peak consisting of an unknown compound in horse hair extract. Solvent extraction (sample 1) using pentane was conducted for both horse and pony hair samples. Extracts using n-hexane, CH 2 Cl 2 , acetone, EtOAc, ethanol were conducted using horse hair, however, pentane or hexane were selected the best extraction solvents since the peak of interest was most abundant compared to other solvent extracts. For further investigation, the hydrodistillation method (sample 2) was conducted only for the pony hair sample, because there was sufficient material for the hydrodistillation.
During distillation, volatile compounds dissolved in the hydrosol. After the distillation process, the hydrosol was collected, extracted with n-hexane and, subsequently, this n-hexane extract was used for analysis. Both methods gave the peak of interest. The peak intensity decreased over time (one year) by from 60% -70% to approximately 2% despite being stored in a freezer at −20˚C. The following data detail the efforts made to identify this unknown compound present in samples 1 and 2 using the various mass spectroscopy techniques.

Analysis by GC-MS
CEI-GC-MS Spectroscopy of the extracts (samples 1 and 2) using a polar GC column showed the unknown peak at retention time (RT ~ 15.76 min, AI = 1067). From the mass spectral library, this peak matched nonanal with a match score of 820 (out of 1000) and high probability (>80%). When compared with the authentic nonanal standard, the fragmentation pattern and the retention time were close, but not identical to that of nonanal (RT ~ 17.61 min) (Figure 1). The AI for nonanal is 1100 compared to 1067 for the unknown peak. The mixed injection of the horse/pony hair extract and nonanal, also, showed that the unknown peak does not correspond to nonanal. GC-MS analysis with NICI and PICI modes gave the mass-to-charge ratios (m/z) of 141 (M − 1) and 143 (M + 1), correspondingly ( Figure 2). Accordingly, we assumed that the mass of the molecular ion for the unknown component should be 142. To verify our assumption, the hydrodistillate (sample 2) was derivatized with acetic anhydride and analyzed by CEI-GC-MS method. At 26.86 min, a new peak was detected with m/z = 184 [~M + COCH 2 ], which could correspond to the sum of the mass ratios for the unknown component (m/z = 142) and ketene (m/z = 42) ( Figure 3).

Analysis by GC-FID and GC-MS
GC-FID And GC-MS using a polar column was also used to investigate the unknown peak. The compound of interest was present in both samples (1 and 2) with the RRI = 1550, and % calculated from FID data: EIMS, 70 eV, m/z (rel.  (Figure 4). However, the compound cannot be identified by commercially available mass spectral libraries, and in house "Baser Library of Essential Oil Constituents" library.

Analysis by ESI-MS and LC-MS
To further investigate the unknown peak, the extracts were analyzed by high resolution ESI-MS and LC-MS. By accurate ESI-MS spectra (without prior HPLC separation for apparative reasons) the masses related to the molecular ion of unknown were observed ( Figure 5). There were several species with a nominal mass of 142 -143 and they differ slightly in their exact mass, but 142.1595 was the most intense of them, followed by 143.1510.  To generate the possible molecular formulas from the monoisotopic mass [M + H] + ChemFinder software and virtual programs [29] [31] [32] were used. Generated for 142.1595, the first few formulas with the highest precision rates were: C 9 H 20 N + (−0.53 ppm), 8 8 2 C H N + (+87.95 ppm), . We assume [M + H] + = C 9 H 20 N + should correspond to the peak of interest; it might be related to or identical to the protonated imine of nonanal and has a matching precision rate within the acceptable 5 ppm window, and could generate similar ion fragments as nonanal itself. We were not able to separate this unknown compound from the extract, as during the isolation attempts the component would degrade. We assume that this component could be an unstable intermediate produced by a

Conclusion
In summary, while investigating the volatiles of the horse and pony hairs, we