2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
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Chem. Listy, 102, s265–s1311 (2008) Environmental Chemistry & Technology<br />
is presented in bold; where no compliance existed, “n.i.” is<br />
stated, which stands for “not identified”. Concerning results,<br />
it is evident that not all the content substances were present<br />
in all extracts. Mostly, they were detected in the ethanolic<br />
extract and in the first petroleum extract and their presence in<br />
these two extracts was influenced by the chemical nature of<br />
these substances.<br />
Table I<br />
Identification of volatile compounds in sweet pepper<br />
extracts<br />
RF Ethanol RF Petroleum RF Petroleum Identified<br />
ether I ether II compound<br />
– 0.17 – pinene<br />
0.23 0.22 – cymene<br />
0.28 – – terpinene<br />
0.38 0.41 0.39 n.i.<br />
0.52 0.65 0.67 n.i.<br />
0.69 0.68 – n.i.<br />
0.93 – – n.i.<br />
0.96 – – n.i.<br />
0.99 – – n.i.<br />
As the second method of essential oils components<br />
analysis, SPME in connection with GC/MS was used. The<br />
method was optimalized and measurements were performed<br />
under conditions mentioned above. Also by this method, not<br />
the concentration of substances, but their identification was<br />
the matter of concern. In contrast to TLC, the isolation/preconcentration<br />
of target compounds was performed via headspace<br />
method. To confirm the presence of a given substance<br />
nIST spectral library search was used. The Fig. 1. shows<br />
chromatogram of sweet pepper spice. In Table II is a summary<br />
of substances identified via spectral library search in<br />
this spice.<br />
Fig. 1. Chromatogram of sweet pepper<br />
By comparison of Tables I and II it is obvious, that more<br />
single volatile substances and their isomers can be recognised<br />
s438<br />
Table II<br />
Retention times and identification of compounds present in<br />
sweet pepper<br />
Peak number Retention Time Identification<br />
1. 7.97 α-pinene<br />
<strong>2.</strong> 9.24 β-pinene<br />
3. 9.71 β-myrcene<br />
4. 10.09 α-felandrene<br />
5. 10.26 3-karene<br />
6. 10.46 α-terpinene<br />
7. 10.71 p-cymene<br />
8. 10.84 limonene<br />
9. 11.76 γ-terpinene<br />
10. 1<strong>2.</strong>66 4-karene<br />
by means of SPME in connection with GC/MS. Similar comparison<br />
could be made at all spices used.<br />
Conclusion<br />
Analytical separation-based methods were used for the<br />
identification of content substances present in essential oils of<br />
seven spice species. Following results were obtained:<br />
The isolation of essential oils content substances can be<br />
performed by the means of either appropriate solvent<br />
extraction, or passive sampling via SPME.<br />
Screening chromatography method on the thin layer<br />
(TLC) is appropriate for the quick identification of content<br />
substances in essential oils. This method is also<br />
recommended by the Pharmaceutical Codex6 •<br />
•<br />
.<br />
• Decisive GC/MS method enabled the identification of<br />
more content substances, including some isomers, at all<br />
spice and herbal tea samples analysed.<br />
This work was supported by the Ministry of Education<br />
of the Czech Republic under research project MSM 621<br />
71242<strong>2.</strong><br />
REFEREnCES<br />
1. Marsili, R.: Techniques for Analyzing Food Aroma. CRC<br />
1996.<br />
<strong>2.</strong> Podlech, D.: Kapesní atlas léčivé rostliny, Slovart<br />
2007.<br />
3. Wager, H., Bladt, S., Zgainski, E. M.: Plant drug analysis.<br />
Springer – Verlag 1984.<br />
4. Pawliszyn, J.: Solid Phase Microextraction: Theory and<br />
Practice. Wiley-VCH 1997.<br />
5. Sides, S., Robards, K., Helliwell, S.: Trend.Anal.Chem.,<br />
19, 322 (2000).<br />
6. Český farmaceutický kodex. X-EGEM 1993.