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Analysis of Omega 3 and Omega 6 FAMEs in Fish Oil and Animal Fat Using an Agilent J&W DB-FATWAX Ultra Inert GC Column

Applications | 2017 | Agilent TechnologiesInstrumentation
GC, GC columns, Consumables
Industries
Food & Agriculture
Manufacturer
Agilent Technologies

Summary

Significance of the Topic


Analysis of Omega-3 and Omega-6 fatty acid methyl esters (FAMEs) is essential for nutritional labeling, quality control, and regulatory compliance in food and supplement industries. Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) are key markers of fish oil quality, while linoleic acid (LA) and arachidonic acid (ARA) reflect the composition of animal fats. High-resolution, reproducible chromatography methods are needed to distinguish structurally similar FAMEs and cis/trans isomers.

Aims and Overview of the Study


This application note evaluates the performance of the Agilent J&W DB-FATWAX Ultra Inert GC column for FAME analysis in fish oil and animal fat samples. Goals include:
  • Assessing chromatographic resolution of critical Omega-3 and Omega-6 FAMEs, especially DHA versus long-chain interferences (C24:0, C24:1)
  • Comparing performance against two competing WAX-type GC columns
  • Evaluating column inertness and thermal stability under maximum allowable operating temperature (MAOT) over extended conditioning periods

Methodology


Samples comprised a certified 37-component FAME standard, animal-source fat (PUFA No. 2), and Menhaden fish oil (PUFA No. 3). Standards were diluted in acetone and analyzed by GC with flame ionization detection. Key parameters for the method included helium carrier gas (constant flow), split/splitless injection, and a multi-step oven temperature program to optimize separation of saturated, monounsaturated, and polyunsaturated FAMEs.

Used Instrumentation


  • GC System: Agilent 7890B with flame ionization detector
  • Column: Agilent J&W DB-FATWAX Ultra Inert, 30 m × 0.25 mm, 0.25 μm film thickness
  • Autosampler: Agilent 7683B with 5 μL syringe
  • Consumables: Amber screw-top vials, BTO septa, Vespel/graphite ferrules, Ultra Inert glass wool liners, gold-plated inlet seals

Main Results and Discussion


The DB-FATWAX UI column achieved baseline separation for DHA (C22:6n3) from C24:0 and C24:1—challenging interferences in traditional WAX phases—and resolved cis/trans isomers of LA (C18:2n6). In contrast, competitor columns showed coelution or selectivity shifts after conditioning at MAOT for 20–40 hours. The Ultra Inert phase maintained consistent retention times and selectivity under prolonged high-temperature operation, indicating superior phase stability and minimal bleeding.

Chromatograms of PUFA No. 2 (animal fat) and PUFA No. 3 (Menhaden oil) demonstrated clean baselines and strong resolution of key Omega-6 (LA, ARA) and Omega-3 (ALA, EPA, DHA, DPA) components, enabling accurate quantification in complex matrices.

Benefits and Practical Applications


  • Enhanced resolution of critical FAMEs improves accuracy of nutritional labeling and QA/QC
  • Ultra Inert technology ensures reliable peak shape, lower detection limits, and long-term reproducibility
  • Extended column lifetime and consistent performance reduce maintenance and recalibration frequency
  • Applicability to a range of food and supplement matrices for routine and regulatory analyses

Future Trends and Potential Applications


Advancements may include integrating DB-FATWAX UI technology with automated sample prep and high-throughput workflows. Development of predictive retention models using machine learning could streamline method development. Expanding to hyphenated techniques (e.g., GC–MS) will support identification of novel fatty acids and lipid oxidation products. Sustainable carrier gases and column materials could address environmental concerns in analytical laboratories.

Conclusion


The Agilent J&W DB-FATWAX Ultra Inert GC column delivers superior resolution, inertness, and thermal stability for FAME analysis in fish oil and animal fat. Its robust performance under MAOT conditions and ability to separate DHA from long-chain interferences ensure accurate, reproducible quantification of Omega-3 and Omega-6 fatty acids, making it an ideal choice for food industry quality control and nutritional studies.

Reference


  1. Petrovic M, Kezic N, Bolanca V. Optimization of the GC method for routine analysis of the fatty acid profile in several food samples. Food Chemistry. 2010;122(1):285–291.
  2. Vickers AK. High efficiency FAMEs analyses using capillary GC. Agilent Technologies. Article Reprint 5989-6588EN. 2007.
  3. Dang NA, Vickers AK. A new PEG GC Column with improved inertness, reliability, and column lifetime. Agilent Technologies Competitor Comparison 5991-6683EN. 2016.

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