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Spme fibre 57326u

Manufactured by Merck Group
Sourced in Germany

The SPME fibre 57326U is a solid-phase microextraction (SPME) fibre designed for the extraction and concentration of analytes from various sample matrices. It is a versatile tool used in analytical chemistry and environmental monitoring applications. The fibre's core function is to facilitate the sampling and preconcentration of target compounds prior to their analysis by analytical techniques such as gas chromatography or liquid chromatography.

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2 protocols using spme fibre 57326u

1

Extraction and Analysis of Hornet Volatiles

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Seven hornets (4 queens and 3 workers) were kept one by one the same day of their capture in a pyramidal acrylic box (Figure 3a). The structure of this pyramid is useful to introduce the hornets to a glass vial. The pyramid was also darkened, except for its vertex, by placing a black cloth on it. Thereby, the hornets tended to exit the pyramid through the vertex. Each hornet was then transferred to a glass vial with aluminium foil placed on both sides of the container to limit air movement (Figure 3b). A 65 µm thick polydimethylsiloxane/divinylbenzene (PDMS/DVB) fibre (Supelco SPME fibre 57326U, Darmstadt, Germany) was fixed at the glass bottle, with the hollow SPME needle stuck through the aluminium foil, exposing the fibre, close to the hornet, to adsorb the volatile compounds present in the headspace. Before use, the SPME fibre was preconditioned and thermally cleaned. This was done thermally by exposing the fibre at a conditioning temperature of 250 °C for 30 min in the GC injection port. The chosen extraction mode was Headspace (HS) since the analytes of interest are highly volatile. Thus, the fibre was introduced into the glass vial with the hornet and exposed in dark for 30 min at 25 °C. After this period, the fibre was retracted and transferred to the gas phase chromatograph (GC) injector where the compounds were desorbed for 5 min.
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2

Volatile Extraction from Honey using SPME

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A 7.5 g honey sample was introduced into a 20 mL vial, before adding 7.5 mL of a 30% sodium chloride solution. After placing a magnetic stirrer, the vial was sealed. Then, the sample was stirring until homogenisation was achieved and placed into a thermostatic bath at 50 °C. A 65 µm thick polydimethylsiloxane/divinylbenzene (PDMS/ DVB) fiber (Supelco SPME fibre 57326U, Darmstadt, Germany) was used for the extraction and subsequent analysis of the volatile compounds by SPME. Before use, the SPME fiber was preconditioned and thermally cleaned. This was done thermally by exposing the fiber to a conditioning temperature of 250 °C for 50 min in the GC injection port. The chosen extraction mode was Headspace (HS), since the analytes of interest were highly volatile. Thus, the fiber was introduced into the vial and exposed to the headspace under the sample for 60 min. After this period, the fibre was retracted and transferred to the gas phase chromatograph (GC) injector, where the compounds were desorbed for 5 min.
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