You should concentrate your sample volatile metabolome as much possible as you can since you will choose the scan acquisition mode at your MS instrument. For this, you can select a gas sampling technique combined with a static or dynamic headspace sample prep strategy. As dynamic headspace, you may prefer to apply purge and trap if your configuration is amenable. Otherwise, you can prefer static headspace sampling/extraction and use SPME fibers as the professor suggested. It is also possible to consider liquid sampling. You can choose the Bligh&dyer approach and perform liquid-liquid partitioning using chloroform and/or ether along with alcohol. But if your volatiles are at low concentrations this approach would not be reasonable...
thank you prof Noel .W Davies , i will keep your advice in mind. thank you for the article Elias Bou-Maroun. thank you for the suggestions and clarification İsmail Emir Akyildiz