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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.

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