Carlo Bicchi

Influence of fibre coating in headspace solid-phase microextraction-gas chromatographic analysis of aromatic and medicinal plants.

Solid-phase microextraction (SPME) is a solvent-free technique, which is well established in headspace analysis since it is sensitive, because of the concentration factor achieved by the fibres, and selective, because of different coating materials which can be used. The performance of eight commercially available SPME fibres was compared to evaluate the recoveries of some characteristic components with different polarities and structures present in the headspace of four aromatic and medicinal plants: rosemary (Rosmarinus officinalis L.), sage (Salvia officinalis L.), thyme (Thymus vulgaris L.) and valerian (Valeriana officinalis L.). The relative concentration capacity of each fibre on the same components of each plant was also determined by comparing their abundance with that obtained by classical static-headspace GC. The partition coefficient, K1, between the headspace gaseous phase and SPME polymeric coating, and the relative concentration factors, of some of the characteristic components of the plant investigated dissolved in dibutyl phtalate, were also determined, under rigorously standardised analysis conditions. The results showed that the most effective fibres were those consisting of two components, i.e., a liquid phase (polydimethylsiloxane) and a porous solid (carboxen or divinylbenzene, or both).

Cyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields

This article reviews papers published over the period 1995-1998 dealing with the application of cyclodextrin derivatives (CDs) as chiral selector for direct enantiomer GC separation of volatile optically active components in the essential oil, extract, flavour and aroma fields. For each application, the racemate analysed, the CD employed as chiral selector and the matrix investigated are reported. The applications are grouped by analytical technique employed: capillary gas chromatography and capillary gas chromatography-mass spectrometry (GC and GC-MS); two-dimensional gas chromatography (GC x GC); capillary gas chromatography-isotope ratio-mass spectrometry (GC-IRMS); liquid chromatography-capillary gas chromatography (LC-GC).

Comparative analysis of pyrrolizidine alkaloids from natural sources by gas chromatography-mass spectrometry

Abstract Underivatized pyrrolizidine alkaloids (PAs) from natural sources (plants and insects) were analysed by capillary gas chromatography-mass spectrometry. GC-MS data (retention indices and [M]+) of ca 100 PAs separated on different fused-silica columns in two laboratories are presented and compared. The results suggest that polydimethylsiloxane coated columns (OV-1, DB-1) are well suited for comparative studies in different laboratories. Separation of PAs using either OV-1 or DB-1 in different laboratories even under slightly different conditions revealed almost identical RIs. Application of these columns and the combination of RI, [M]+ and group-specific MS fragmentation allows in many cases the unequivocal assignment of PAs from complex mixtures even in the presence of different geometrical isomers. Furthermore, it encourages a reliable comparison and exchange of data between laboratories.

Headspace Sorptive Extraction (HSSE) in the Headspace Analysis of Aromatic and Medicinal Plants

A new sampling technique, Headspace Sorptive Extraction (HSSE), is here applied for the first time to the headspace sampling of medicinal and aromatic plants. The analyte partition coefficient between HSSE-PDMS stir bar and sample headspace (K1), the concentration factor (CF), the reproducibility, and the minimum recoverable amount were determined by analyzing standard solution of high volatility C5–C7 compounds with different polarities and structures (cyclohexane, propyl acetate, hexanal, 1-hexen-3-ol, isoamyl acetate, and 2-heptanol). Four aromatic and medicinal plants, viz. rosemary (Rosmarinus officinalis L.), sage (Salvia officinalis L.), thyme (Thymus vulgaris L.), and valerian (Valeriana officinalis L.) were analyzed by HSSE-GC with PDMS stir bars, and their concentration capacity was compared with those of S-HS and HS-SPME with different fibers. HSSE showed very high concentration capability with both standard and real sample components.

ReviewCyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields

This article reviews papers published over the period 1995-1998 dealing with the application of cyclodextrin derivatives (CDs) as chiral selector for direct enantiomer GC separation of volatile optically active components in the essential oil, extract, flavour and aroma fields. For each application, the racemate analysed, the CD employed as chiral selector and the matrix investigated are reported. The applications are grouped by analytical technique employed: capillary gas chromatography and capillary gas chromatography-mass spectrometry (GC and GC-MS); two-dimensional gas chromatography (GC x GC); capillary gas chromatography-isotope ratio-mass spectrometry (GC-IRMS); liquid chromatography-capillary gas chromatography (LC-GC).

Determination of phenolic diterpene antioxidants in rosemary (Rosmarinus officinalis L.) with different methods of extraction and analysis

The extraction from rosemary (Rosmarinus officinalis L.) of the phenolic diterpene antioxidants (PDAs), carnosic acid and carnosol, by sonication or Soxhlet extraction with acetone (with or without active charcoal bleaching) are compared with fractionated SFE extraction obtained by varying the dissolving power of supercritical carbon dioxide through the addition of methanol. For the further analysis of the PDAs, the results obtained by reversed-phase HPLC linked to a UV detector are compared with those produced when an evaporative light scattering detector or a particle beam interface linked to an MS were employed. Copyright

Fast supercritical fluid extraction and high-resolution gas chromatography with electron-capture and flame photometric detection for multiresidue screening of organochlorine and organophosphorus pesticides in Brazil’s medicinal plants

A description is given of a rapid and environmentally friendly method to determine organochlorine and organophosphorus pesticide multiresidues--malathion, methidathion, fenitrothion, fenthion, parathion-ethyl, parathion-methyl, lindane, hexachlorobenzene, chlorothalonil, tetradifon, alpha-endosulfan, beta-endosulfan and dieldrin-in Passiflora alata Dryander and pasiflora edulis Sims. f. flavicarpa Deg. leaves by supercritical fluid extraction and high-resolution gas chromatography with electron-capture and flame photometric detection (HRGC-ECD/FPD). The mild extraction conditions [pure CO2; 100 bar (1 bar = 10(5) Pa) and 40 degrees C (p = 0.62 g/ml); 5 min static+10 min dynamic extraction time; ODS trap and elution with 1 ml n-hexane at 2 ml/min] allow for direct analysis by HRGC-ECD/FPD with no prior cleaning procedure. The method provides. in accordance with the validation criteria of the European Pharmacopoeia, analytical results that are similar or even better than the official procedures, and is simpler, faster and cheaper. Mean recoveries of 69.8-107.1% were obtained, with 1.4-14.7% reproducibility (RSD). The method was applied to analyse commercial samples of Passiflora L. from Brazil. Twenty-three percent of the samples showed the presence of the organochlorine or organophosphorus pesticide residue investigated.

Analysis of environmental endocrine disrupting chemicals using the E-screen method and stir bar sorptive extraction in wastewater treatment plant effluents

Endocrine disrupting chemicals (EDCs) have become a major issue in the field of environmental science due to their ability to interfere with the endocrine system. Recent studies show that surface water is contaminated with EDCs, many released from wastewater treatment plants (WWTP). This pilot study used biological (E-screen assay) and chemical (stir bar sorptive extraction-GC-MS) analyses to quantify estrogenic activity in effluent water samples from a municipal WWTP and in water samples of the recipient river, upstream and downstream of the plant. The E-screen assay was performed on samples after solid phase extraction (SPE) to determine total estrogenic activity; the presence of estrogenic substances can be evaluated by measuring the 17-beta-estradiol equivalency quantity (EEQ). Untreated samples were also assayed with an acute toxicity test (Vibrio fischeri) to study the correlation between toxicity and estrogenic disruption activity. Mean EEQs were 4.7 ng/L (+/-2.7 ng/L) upstream and 4.4 ng/L (+/-3.7 ng/L) downstream of the plant, and 11.1 ng/L (+/-11.7 ng/L) in the effluent. In general the WWTP effluent had little impact on estrogenicity nor on the concentration of EDCs in the river water. The samples upstream and downstream of the plant were non-toxic or weakly toxic (0<TU<0.9) while the effluent was weakly toxic or toxic (0.4<TU<7.6). Toxicity and estrogenic activity were not correlated. At most sites, industrial mimics, such as the alkylphenols and phthalates, were present in higher concentrations than natural hormones. Although the concentrations of the detected xenoestrogens were generally higher than those of the steroids, they accounted for only a small fraction of the EEQ because of their low estrogenic potency. The EEQs resulting from the E-screen assay and those calculated from the results of chemical analyses using estradiol equivalency factors were comparable for all samples and closely correlated.

High throughput qualitative analysis of polyphenols in tea samples by ultra-high pressure liquid chromatography coupled to UV and mass spectrometry detectors

The analysis of polyphenols in tea extracts is important due to their potential health benefits. Therefore, efficient and high throughput analytical methods have been developed for the separation of seven predominant polyphenols, also known as catechin derivatives, present in tea extracts. Columns packed with sub-2-μm particles operating at elevated pressure (UHPLC strategy) were selected to improve chromatographic performance. The potential of UHPLC-UV was demonstrated with baseline resolution of all standard catechins in only 30 s using a 50-mm column packed with 1.7-μm particles. When dealing with real samples such as tea extracts, however, longer columns of up to 150 mm in length were employed to enhance the separation of catechin derivatives and other constituents within the tea samples while maintaining an acceptable analysis time. Two strategies based on 2-D experiments were proposed to clearly identify catechins. Firstly, a liquid-liquid extraction procedure was added prior to the UHPLC-UV analysis to decrease the complexity of the sample. Secondly, UHPLC was coupled to ESI-MS/MS to attain sufficient sensitivity and selectivity between catechin derivatives and other constituents of tea extract. These two strategies were found extremely promising as a clear discrimination of catechins from the matrix could be attained.

Improved method for the analysis of small amounts of essential oils by microdistillation followed by capillary gas chromatography

Abstract A method for the analysis of small amounts of essential oils by distillation in a microversion of a modified Marcusson apparatus followed by capillary gas chromatography is described. The analysis requires only very small amounts of plant material (0.2–3 g) and takes no more than 2 h, including sample preparation, distillation and capillary gas chromatography. The results of macroscale analysis by classical techniques were identical with those obtained with the microapparatus described in this paper. Some applications are given to illustrate this technique.