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Db 23 capillary column

Manufactured by Merck Group
Sourced in United States

The DB-23 capillary column is a laboratory equipment product designed for chromatographic analysis. It is a long, narrow tube filled with a stationary phase material that is used to separate and analyze the components of a mixture. The column's core function is to facilitate the separation and identification of chemical substances within a sample.

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3 protocols using db 23 capillary column

1

Soxhlet Extraction and GC Analysis of Fatty Acids

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An automated Soxhlet apparatus (Soctec Avanti 2055, Foss, Sweden) was used to extract the fat from MNM as described by the Association of Official Analytical Chemists (AOAC, 2006 , method number 920.39). The methyl ethers were analyzed using gas chromatography as described by Christopherson and Glass, (1969) . Briefly, the fat extracts were trans-methylated with 2 M methanol-sodium hydroxide. Heptane was used to extract the fatty acid methyl esters which were then filtered and dried under nitrogen. The fatty acids were separated by a temperature gradient over 45 min on gas chromatography with nitrogen as carrier gas on a DB-23 capillary column (90  cm  ×  250 μm   ×   0.25 μm) (Supelco, Sigma-Aldrich). The chromatograph consisted of an HP6890 gas chromatograph (Hewlett Packard, Bristol, United Kingdom) with a flame ionization detector (FID). Both the detector and injector temperatures were set at 300 °C. A PC equipped with Chemstation software was used for quantification. Nonadecanoic acid (C19:0) was used as an internal standard.
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2

Fatty Acid Profiling by GC-FID

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The Fölch method was used to extract the lipids and subsequently derivatize them using a concentrated solution of HCl in methanol (5% v/v). The tubes were sealed, shaken vigorously, and then placed in boiling water for 10 min. Then, they were cooled, 2 mL of milli-Q distilled water and 1 mL of hexane were added. The tubes were capped, shaken and centrifuged (1333× g, 15 min) until both layers were clear. The upper phase containing the methyl esters was filtered (0.45 um). Finally, the methyl esters were injected and analyzed in an Agilent Technologies 7890A gas chromatograph (Agilent Technologies; Santa Clara, CA, USA), equipped with a Supelco DB 23 capillary column (30 m, 250 lm i.d., 0.25 mm) and with a flame ionization detector (FID). The fatty acids were identified by comparing with the retention times of Supelco 37-Component FAME Mix fatty acid methyl ester standards (Sigma-Aldrich, St. Louis, MO, USA). The area of the different peaks was analyzed using PeakFit software (version 4.12 for Windows, SPSS Inc., Chicago, IL, USA) and results were expressed as g of fatty acid per 100 g of lipid. Assays were performed by duplicate.
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3

Fatty Acid Profiling of Meat Extracts

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The Soxhlet Apparatus was used to extract the oil from the breast muscle sample as described by the Association of Analytical Chemists (AOAC, 2006 ; method number: 920.39). The fatty acid profiles of the oil extracted from the meat were determined as described by Christopherson & Glass, (1969) . Briefly, the oil extracts were trans-methylated with 2 mol/L methanol sodium hydroxide. The resulting fatty acid methyl esters were extracted in heptane, filtered (Nylon syringe filters, pore size: 0.45 µm, diameter: 13 mm with a glass fibre prefilter, Membrane Solutions) and dried under nitrogen after which they were separated by a temperature gradient over 45 min on a gas chromatograph with nitrogen as carrier gas on a DB-23 capillary column (90  cm  ×  250 μm  ×  0.25 μm; Supelco, Sigma-Aldrich). The gas chromatograph consisted of an HP6890 GC (Hewlett Packard, Bristol, UK) with a flame ionisation detector. Both the detector and injector temperatures were set at 300 °C. A personal computer equipped with Chemstation software (Agilent Technologies Inc., Santa Clara, CA, USA) was used for quantification. Nonadecanoic acid (C19:0) was used as an internal standard.
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