Screening for triterpenoid saponins in plants using hyphenated analytical platforms

Recently the number of studies investigating triterpenoid saponins has drastically increased due to their diverse and potentially attractive biological activities. Currently the literature contains chemical structures of few hundreds of triterpenoid saponins of plant and animal origin. Triterpenoid saponins consist of a triterpene aglycone with one or more sugar moieties attached to it. However, due to similar physico-chemical properties, isolation and identification of a large diversity of triterpenoid saponins remain challenging. This study demonstrates a methodology to screen saponins using hyphenated analytical platforms, GC-MS, LC-MS/MS, and LC-SPE-NMR/MS, in the example of two different phenotypes of the model plant Barbarea vulgaris (winter cress), glabrous (G) and pubescent (P) type that are known to differ by their insect resistance. The proposed methodology allows for detailed comparison of saponin profiles from intact plant extracts as well as saponin aglycone profiles from hydrolysed samples. Continuously measured 1D proton NMR data during LC separation along with mass spectrometry data revealed significant differences, including contents of saponins, types of aglycones and numbers of sugar moieties attached to the aglycone. A total of 49 peaks were tentatively identified as saponins from both plants; they are derived from eight types of aglycones and with 2–5 sugar moieties. Identification of two previously known insect-deterrent saponins, hederagenin cellobioside and oleanolic acid cellobioside, demonstrated the applicability of the methodology for relatively rapid screening of bioactive compounds

Industrial scale isolation, structural and spectroscopic characterization of epiisopiloturine from Pilocarpus microphyllus stapf leaves: a promising alkaloid against schistosomiasis

This paper presents an industrial scale process for extraction, purification, and isolation of epiisopiloturine (EPI) (2(3H)- Furanone,dihydro-3-(hydroxyphenylmethyl)-4-[(1-methyl-1H-imidazol-4-yl)methyl]-, [3S-[3a(R*),4b]]), which is an alkaloid from jaborandi leaves (Pilocarpus microphyllus Stapf). Additionally for the first time a set of structural and spectroscopic techniques were used to characterize this alkaloid. EPI has shown schistomicidal activity against adults and young forms, as well as the reduction of the egg laying adult worms and low toxicity to mammalian cells (in vitro). At first, the extraction of EPI was done with toluene and methylene chloride to obtain a solution that was alkalinized with ammonium carbonate. The remaining solution was treated in sequence by acidification, filtration and alkalinization. These industrial procedures are necessary in order to remove impurities and subsequent application of the high performance liquid chromatography (HPLC). The HPLC was employed also to remove other alkaloids, to obtain EPI purity higher than 98%. The viability of the method was confirmed through HPLC and electrospray mass spectrometry, that yielded a pseudo molecular ion of m/z equal to 287.1 Da. EPI structure was characterized by single crystal X-ray diffraction (XRD), 1H and 13C nuclear magnetic resonance (NMR) in deuterated methanol/chloroform solution, vibrational spectroscopy and mass coupled thermal analyses. EPI molecule presents a parallel alignment of the benzene and the methyl imidazol ring separated by an interplanar spacing of 3.758 Å indicating a π-π bond interaction. The imidazole alkaloid melts at 225°C and decomposes above 230°C under air. EPI structure was used in theoretical Density Functional Theory calculations, considering the single crystal XRD data in order to simulate the NMR, infrared and Raman spectra of the molecule, and performs the signals attribution

Portable infrared laser spectroscopy for on-site mycotoxin analysis

Mycotoxins are toxic secondary metabolites of fungi that spoil food, and severely impact human health (e.g., causing cancer). Therefore, the rapid determination of mycotoxin contamination includingdeoxynivalenolandaflatoxinB1infoodandfeedsamplesisofprimeinterestforcommodity importers and processors. While chromatography-based techniques are well established in laboratory environments, only very few (i.e., mostly immunochemical) techniques exist enabling direct on-site analysis for traders and manufacturers. In this study, we present MYCOSPEC - an innovative approach for spectroscopic mycotoxin contamination analysis at EU regulatory limits for the first time utilizing mid-infrared tunable quantum cascade laser (QCL) spectroscopy. This analysis technique facilitates on-site mycotoxin analysis by combining QCL technology with GaAs/AlGaAs thin-film waveguides. Multivariate data mining strategies (i.e., principal component analysis) enabled the classification of deoxynivalenol-contaminated maize and wheat samples, and of aflatoxin B1 affected peanuts at EU regulatory limits of 1250 μg kg−1 and 8 μg kg−1, respectively

Sensing chlorinated hydrocarbons via miniaturized GaAs/AlGaAs thin-film waveguide flow cells coupled to quantum cascade lasers

Mid-infrared (MIR) sensors based on attenuated total reflection (ATR) spectroscopy provide robust, rapid and sensitive platforms for the detection of low levels of organic molecules and pollutants. Nowadays, MIR (3–15 μm) spectroscopy has evolved into a versatile sensing technique providing inherent molecular selectivity for the detection of organic and inorganic molecules. The excitation of vibrational and rotational transitions enables the qualitative and quantitative analysis of molecular constituents in solid, liquid, and vapor phases, which facilitates the application of MIR chem/bio sensors for on-site environmental analysis in scenarios such as trace pollutant monitoring or spill detection. This report presents the first integration of thin-film gallium arsenide/aluminum gallium arsenide (GaAs/AlGaAs) into a miniaturized liquid flow cell designed for continuous trace analysis of chlorinated hydrocarbons (CHCs) in water coupled to a broadly tunable quantum cascade laser (QCL), which facilitates in-field deployment of QCL-based sensing devices ensuring water quality and water safety

Characterization of Asphaltenes Precipitated at Different Solvent Power Conditions Using Atmospheric Pressure Photoionization (APPI) and Laser Desorption Ionization (LDI) Coupled to Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS)

In the present work, asphaltenes obtained using different <i>n</i>-heptane/crude oil ratios (HCORs) were analyzed using atmospheric pressure photoionization (APPI) and laser desorption ionization (LDI) coupled to Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The main objective was to improve the understanding of the components of the crude oil that precipitate under different solvent power conditions. Analysis of the compositional distribution of the asphaltenes reveals that the decrease in solvent power produces an increase in double bond equivalent (DBE) and the number of heteroatoms per molecule, while the carbon number remains almost unaltered. This finding seems to indicate that one of the main drivers for precipitation is aromaticity as HCOR increases and, consequently, the solvent power decreases. Both APPI and LDI FT-ICR MS produce average values that describe the general tendencies obtained using other techniques. Additionally, APPI FT-ICR MS closely matches bulk data of the most aromatic asphaltenes obtained in this study