Data interpretation from sample inhomogeneity

In order to avoid problems with sample inhomogeneity, the entire oil sample from each sample of shale was dissolved in 1.5 to 2.5 mL of CS2 (about 1 g oil to 1.5 mL solvent). One pL of this solution was injected into a Hewlett-Packard Model 5880 Gas Chromatograph equipped with capillary inlet and a 50 m x 0.25 mm Quadrex "007" methyl silicone column. Injection on the column is made with a split ratio of approximately 1 to 100. The column temperature started at 60°C and increased at 4°C/min to 280°C where it remained for a total run time of 90 min. The carrier gas was helium at a pressure of 0.27 MPa flowing at a rate of 1 cm /min. The injector temperature was 325°C and the flame ionization detector (FID) temperature was 350°C. Data reduction was done using a Hewlett-Packard Model 3354 Laboratory Automation System with a standard loop interface. Identification of various components was based on GC/MS interpretation described previously (4). For multiple runs on the same shale, the relative standard deviations of the biomarker ratios were about 10%. 

In summary, the presence of sample inhomogeneity at different levels may complicate the interpretation of lipidomics data. Recognizing these complications as well as any unique features resulted from the complications should help us interpreting lipidomics data better. 

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