11/29/18

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Omega 3 triglyceride vs ethyl ester

Omega 3 triglyceride vs ethyl ester

Fish oil omega-3s are composed of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and are available to consumers as either triglycerides or ethyl esters. One of the most commonly discussed quality issues related to fish oil is which form is the best triglyceride (TG) or ethyl ester (EE). In what form are the long-chain omega-3 fatty acids (EPA and DHA) when ingested from fish? The answer is the triglyceride form. In fact, over 98% of all food-derived fats are in the triglyceride form.


Cost vs. absorption

Ethyl ester forms of omega-3 fatty acid supplements are the most prevalent form in the market today as they are cheaper to produce than their triglyceride counterparts. The industry has actually made ethyl esters because they form a moldable form as triglycerides. This EE form has a much higher boiling point and is easier to process when processed for supplement distribution. The main purpose of molecular distillation is to remove the industrial contaminants (eg heavy metal dioxins and PCBs) found in most fishfish oils of most supplement manufacturers and to concentrate EPA and DHA. This model focuses on sterility. Studies have shown that ethyl esters are the least bioavailable forms of omega-3 fatty acids compared to TG and / or whole fish.1 After purification by the distillation process, manufacturers leave them in an EE form for cost reasons , The process of converting fish oil EEs into TGs is costly. The cost of oil for TG concentrates is usually 30 to 40% higher than that of EE concentrates.


micro distillation

Ethyl esters are prepared by reacting crude fish oil in the form of a free fatty acid with ethanol (an industrial alcohol) to form a synthetic substrate. Under vacuum, the mixture is then distilled by heat and the resulting condensate is a concentrated omega-3 ethyl ester solution. Once this molecular distillation process is complete, however, it is possible to allow the fatty acids to bind in free form to an ethyl alcohol backbone or to re-attach them to a glycerol backbone (triglyceride).

metabolism

The EE form lacks the glycerol backbone. Therefore, the fatty acids will find an available triglyceride backbone or take one from an existing molecule. When the latter occurs, the molecule that lacks the backbone seeks another backbone, creating a domino effect. The free fatty acids are taken up by the enterocytes (intestinal epithelium) and must be converted back to TG for transport in the blood.3

Fats are stored and transported in the body in triglyceride form. Studies show that after ingestion of an omega-3 fatty acid molecule in triglyceride form, the fatty acids are cut from the glycerol backbone. The digested EE produce free fatty acids plus ethanol. This is a less efficient absorption process compared to the direct intake of a triglyceride in natural form, as the EE form in the body has to be converted back to a TG form. The delay in TG resynthesis suggests that the transport to blood in natural TG fish oils is more efficient than in EE.245. In addition, this retardation of TG resynthesis in EE fish oils causes release of ethyl alcohol and may subsequently be oxidative. Stress due to release of free radicals in addition to release of ethanol. 6

Only science

The bioavailability of various omega-3 formulations has been described by Dyerberg, the father of fish oil. In his study, 72 subjects received an esterified TG EE-free fatty acid fish oil or cod liver oil supplement for two weeks. The EPA and DHA levels were highest in the transesterified TG group and lowest in the cod liver oil.

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