Wikipedia

Lecithin

(Redirected from Soy lecithin)

Not to be confused with Lectin.

Lecithin (/ˈlɛsɪθɪn/ LESS-ith-in; from the Ancient Greek λέκιθος lékithos "yolk") is a generic term to designate any group of yellow-brownish fatty substances occurring in animal and plant tissues which are amphiphilic – they attract both water and fatty substances (and so are both hydrophilic and lipophilic), and are used for smoothing food textures, emulsifying, homogenizing liquid mixtures, and repelling sticking materials.[1][2]

An example of a phosphatidylcholine, a type of phospholipid in lecithin. Shown in red – choline residue and phosphate group; black – glycerol residue; green – monounsaturated fatty acid residue; blue – saturated fatty acid residue.
The different forms of lecithin – powder, two different concentration liquids, granular and powder lecithin

Lecithins are mixtures of glycerophospholipids including phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, phosphatidylserine, and phosphatidic acid.[3]

Lecithin was first isolated in 1845 by the French chemist and pharmacist Théodore Gobley.[4] In 1850, he named the phosphatidylcholine lécithine.[5] Gobley originally isolated lecithin from egg yolk and established the complete chemical formula of phosphatidylcholine in 1874;[6] in between, he demonstrated the presence of lecithin in a variety of biological materials, including venous blood, human lungs, bile, roe, and brains of humans, sheep and chicken.

Lecithin can easily be extracted chemically using solvents such as hexane, ethanol, acetone, petroleum ether or benzene; or extraction can be done mechanically. Common sources include egg yolk,[7] marine foods, soybeans,[7] milk, rapeseed, cottonseed, and sunflower oil. It has low solubility in water, but is an excellent emulsifier. In aqueous solution, its phospholipids can form either liposomes, bilayer sheets, micelles, or lamellar structures, depending on hydration and temperature. This results in a type of surfactant that usually is classified as amphipathic. Lecithin is sold as a food additive and dietary supplement. In cooking, it is sometimes used as an emulsifier and to prevent sticking, for example in non-stick cooking spray.

Production

edit

Commercial lecithin, as used by food manufacturers, is a mixture of phospholipids in oil. The lecithin can be obtained by water degumming the extracted oil of seeds. It is a mixture of various phospholipids, and the composition depends on the origin of the lecithin. A major source of lecithin is soybean oil. Because of the EU requirement to declare additions of allergens in foods, in addition to regulations regarding genetically modified crops, a gradual shift to other sources of lecithin (such as sunflower lecithin) is taking place.[8] The main phospholipids in lecithin from soy and sunflower are phosphatidylcholine, phosphatidylinositol, phosphatidylethanolamine, phosphatidylserine, and phosphatidic acid. They are often abbreviated to PC, PI, PE, PS and PA, respectively. Purified phospholipids are produced by companies commercially.

Hydrolysed lecithin

edit

To modify the performance of lecithin to make it suitable for the product to which it is added, it may be hydrolysed enzymatically. In hydrolysed lecithins, a portion of the phospholipids have one fatty acid removed by phospholipase. Such phospholipids are called lysophospholipids. The most commonly used phospholipase is phospholipase A2, which removes the fatty acid at the C2 position of glycerol. Lecithins may also be modified by a process called fractionation. During this process, lecithin is mixed with an alcohol, usually ethanol. Some phospholipids, such as phosphatidylcholine, have good solubility in ethanol, whereas most other phospholipids do not dissolve well in ethanol. The ethanol is separated from the lecithin sludge, after which the ethanol is removed by evaporation to obtain a phosphatidylcholine-enriched lecithin fraction.

Genetically modified crops as a source of lecithin

edit

As described above, lecithin is highly processed. Therefore, genetically modified (GM) protein or DNA from the original GM crop from which it is derived often is undetectable – in other words, it is not substantially different from lecithin derived from non-GM crops.[9] Nonetheless, consumer concerns about genetically modified food have extended to highly purified derivatives from GM food, such as lecithin.[10] This concern led to policy and regulatory changes in the EU in 2000, when Commission Regulation (EC) 50/2000 was passed[11] which required labelling of food containing additives derived from GMOs, including lecithin. Because it is nearly impossible to detect the origin of derivatives such as lecithin, the European regulations require those who wish to sell lecithin in Europe to use a meticulous, but essential system of identity preservation (IP).[9][12]

Properties and applications

edit
 
Soy lecithin for sale at a grocery store in Uruguay

Lecithins have emulsification and lubricant properties, and are a surfactant. They can be completely metabolized (see inositol) by humans, so are well tolerated by humans and nontoxic when ingested.

The major components of commercial soybean-derived lecithin are:[13]

Lecithin is used for applications in human food, animal feed, pharmaceuticals, paints, and other industrial applications.

Applications include:

  • In the pharmaceutical industry, it acts as a wetting agent, stabilizing agent and a choline enrichment carrier, helps in emulsification and encapsulation, and is a good dispersing agent. It can be used in manufacture of intravenous fat infusions and for therapeutic use.
  • In animal feed, it enriches fat and protein and improves pelletization.
  • In the paint industry, it forms protective coatings for surfaces with painting and printing ink, helps as a rust inhibitor, is a colour intensifying agent, catalyst, conditioning aid modifier, and dispersing aid; it is a good stabilizing and suspending agent, emulsifier, and wetting agent, helps in maintaining uniform mixture of several pigments, helps in grinding of metal oxide pigments, is a spreading and mixing aid, prevents hard settling of pigments, eliminates foam in water-based paints, and helps in fast dispersion of latex-based paints.
  • Lecithin also may be used as a release agent for plastics, an anti-sludge additive in motor lubricants, an anti-gumming agent in gasoline, and an emulsifier, spreading agent, and antioxidant in textile, rubber, and other industries.

Food additive

edit

The nontoxicity of lecithin leads to its use with food, as a food additive or in food preparation. It is used commercially in foods requiring a natural emulsifier or lubricant.

In confectionery, it reduces viscosity, replaces more expensive ingredients, controls sugar crystallization and the flow properties of chocolate, helps in the homogeneous mixing of ingredients, improves shelf life for some products, and can be used as a coating. In emulsions and fat spreads, such as margarines with a high fat content of more than 75%, it stabilizes emulsions, reduces spattering (splashing and scattering of oil droplets) during frying, improves texture of spreads and flavor release.[14] In doughs and baking, it reduces fat and egg requirements, helps even out distribution of ingredients in dough, stabilizes fermentation, increases volume, protects yeast cells in dough when frozen, and acts as a releasing agent to prevent sticking and simplify cleaning. It improves wetting properties of hydrophilic powders (such as low-fat proteins) and lipophilic powders (such as cocoa powder), controls dust, and helps complete dispersion in water.[15] Lecithin keeps cocoa and cocoa butter in a candy bar from separating. It can be used as a component of cooking sprays to prevent sticking and as a releasing agent.

In the EU Lecithin is designated at food additive E322.[16]

Dietary supplement

edit

Lecithin contains dietary precursors to choline, an essential nutrient, which was formerly classified as a B vitamin (vitamin B4).[17][18] Lecithin is a mixture of fats that contains phospholipids, including phosphatidylcholine, and the human body can convert phosphatidylcholine into choline.[19][20][21] The choline content in lecithin can vary, but it's found that phosphatidylcholine makes up about 25 to 35 percent of lecithin. Furthermore, only about 12 percent of phosphatidylcholine is actually choline. This adds up to a choline content of approximately 4 percent for lecithin. For example, 10 grams of lecithin has 2,500mg of phosphatidylcholine.[21][19]

Phosphatidylcholine is approximately 13.7% choline; as such, about 342mg of choline is present per 10 grams of lecithin. Therefore, 10 grams of lecithin can be a source for the body to produce about the same amount of choline (342mg) as can be produced by the body from 2 egg yolks.[21][22][19] The recommended intake of choline varies depending on age, sex, and physiological conditions, and is roughly 500 mg per day for adults.[23][24]

Lecithin is generally recognized as safe (GRAS) by the FDA.[25][20]

There is no robust, scientifically validated clinical research investigating the safety and effectiveness of high-dose lecithin supplementation in lactating women and their infants. A meta-analysis found no evidence that high doses of lecithin improved milk flow in breast-feeding mothers or infants, though concluded that "higher maternal choline intake was likely to be associated with better child neurocognition and neurodevelopment."[25][20]

Soy lecithin does not contain enough allergenic proteins for most people allergic to soy, although the US FDA only exempts a few soy lecithin products from its mandatory requirements for allergenic source labeling.[26] An alternative source of lecithin, derived from sunflowers, is available as a dietary supplement for those with concerns about soy-based foods.[27]

A 2003 review of randomized trials found no benefit of lecithin in people with dementia.[28]

Religious restrictions

edit

Soy-derived lecithin is considered by some to be kitniyot and prohibited on Passover for Ashkenazi Jews when many grain-based foods are forbidden, but not at other times. This does not necessarily affect Sephardi Jews, who do not have the same restrictions on rice and kitniyot during Passover.[29]

Muslims are not forbidden to eat lecithin per se; however, since it may be derived from animal as well as plant sources, care must be taken to ensure this source is halal. Lecithin derived from plants and egg yolks is permissible, as is that derived from animals slaughtered according to the rules of dhabihah.[30]

Sunflower lecithin, sourced from the seeds of sunflowers, is entirely plant-based and may be an option for those with religious or cultural concerns regarding food intake.

See also

edit

References

edit
  1. ^ "Lecithin". Merriam Webster Dictionary Online. Archived from the original on 2018-06-12. Retrieved 2015-11-18.
  2. ^ Szuha BF (1989). "Chapter 7". Lecithins: Sources, Manufacture & Uses. The American Oil Chemist's Society. p. 109. ISBN 0-935315-27-6.
  3. ^ Smith J, Hong-Shum L, eds. (2011). Food Additives Data Book (2nd ed.). Chichester, West Sussex: Wiley-Blackwell. p. 334. ISBN 978-1-4443-9773-4. Complex mixture of phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, phosphatidic acid, glycolipids, etc.
  4. ^ Gobley T (1846). "Recherches chimiques sur le jaune d'œuf" [Chemical researches on egg yolk]. Journal de Pharmacie et de Chemie. 3rd series (in French). 9: 81–91.81-91&rft.date=1846&rft.aulast=Gobley&rft.aufirst=Théodore&rft_id=https://books.google.com/books?id=DC04AAAAMAAJ&pg=PA84&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  5. ^ Gobley T (1850). "Recherches chemiques sur les œufs de carpe" [Chemical researches on carp eggs]. Journal de Pharmacie et de Chemie. 3rd series (in French). 17: 401–430. Je propose de donner au premier le nom de Lécithine (de λεκιθος, jaune d'œuf), parce qu'on le rencontre en grande quantité dans le jaune d'œuf ... (I propose to give to the former the name of lecithin (from λεκιθος, egg yolk), because it is encountered in great quantity in egg yolk ... )401-430&rft.date=1850&rft.aulast=Gobley&rft.aufirst=Théodore&rft_id=https://books.google.com/books?id=vQVCAAAAcAAJ&pg=PA411&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  6. ^ Gobley T (1874). "Sur la lécithine et la cérébrine" [On lecithin and cerebrin]. Journal de Pharmacie et de Chimie. 4th series (in French). 19: 346–353.346-353&rft.date=1874&rft.aulast=Gobley&rft.aufirst=Théodore&rft_id=https://books.google.com/books?id=ypdGAQAAMAAJ&pg=PA346&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  7. ^ a b "Lecithin: Uses, Side Effects, Interactions, Dosage, and Warning". WebMD. 2019-01-30. Archived from the original on 2019-06-18. Retrieved 2019-06-18.
  8. ^ Efting M (August 3, 2021). "Emulsifier alternative: sunflower lecithin". Food & Beverage Insider. Archived from the original on July 24, 2023. Retrieved July 24, 2023. Sunflower lecithin is a promising alternative to the more common soybean lecithin, and could face increased demand from suppliers as a non-GMO product.
  9. ^ a b Marx GM (December 2010). Monitoring of genetically modified food products in South Africa (PDF) (PhD). University of the Free State. Archived from the original (PDF) on 2015-01-09.
  10. ^ "Danisco emulsifier to substitute non-GM soy lecithin as demand outstrips supply". FoodNavigator. July 1, 2005. Archived from the original on October 21, 2013. Retrieved January 15, 2013.
  11. ^ "Regulation (EC) 50/2000". europa.eu. Archived from the original on 2013-10-16. Retrieved 2013-01-15.
  12. ^ Davison J, Bertheau Y (2007). "EU regulations on the traceability and detection of GMOs: difficulties in interpretation, implementation, and compliance". CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources. 2 (77): 77. doi:10.1079/PAVSNNR20072077. Archived from the original on 2024-04-06. Retrieved 2017-11-01.
  13. ^ Scholfield CR (October 1981). "Composition of Soybean Lecithin". Journal of the American Oil Chemists' Society. 58 (10): 889–892. doi:10.1007/bf02659652. S2CID 9876375. Archived from the original on 2014-10-14. Retrieved 2014-08-21 – via USDA.889-892&rft.date=1981-10&rft_id=info:doi/10.1007/bf02659652&rft_id=https://api.semanticscholar.org/CorpusID:9876375#id-name=S2CID&rft.aulast=Scholfield&rft.aufirst=C. R.&rft_id=http://naldc.nal.usda.gov/download/26685/PDF&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  14. ^ Gunstone FD, Harwood JL, Dijkstra AJ, eds. (2007). "Food Uses of Oils and Fats". The Lipid Handbook. CRC Press. p. 340. ISBN 978-0-8493-9688-5. Archived from the original on 2024-04-06. Retrieved 2019-08-19.
  15. ^ Riehm DA, Rokke DJ, Paul PG, Lee HS, Vizanko BS, McCormick AV (2017-02-01). "Dispersion of oil into water using lecithin-Tween 80 blends: The role of spontaneous emulsification". Journal of Colloid and Interface Science. 487: 52–59. Bibcode:2017JCIS..487...52R. doi:10.1016/j.jcis.2016.10.010. ISSN 0021-9797. PMID 27744169.52-59&rft.date=2017-02-01&rft_id=info:doi/10.1016/j.jcis.2016.10.010&rft.issn=0021-9797&rft_id=info:pmid/27744169&rft_id=info:bibcode/2017JCIS..487...52R&rft.aulast=Riehm&rft.aufirst=David A.&rft.au=Rokke, David J.&rft.au=Paul, Prakash G.&rft.au=Lee, Han Seung&rft.au=Vizanko, Brent S.&rft.au=McCormick, Alon V.&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  16. ^ "Current EU approved additives and their E Numbers". UK Food Standards Agency. Archived from the original on 7 October 2010. Retrieved 26 November 2010.
  17. ^ Kansakar U, Trimarco V, Mone P, Varzideh F, Lombardi A, Santulli G (2023). "Choline supplements: An update". Front Endocrinol (Lausanne). 14: 1148166. doi:10.3389/fendo.2023.1148166. PMC 10025538. PMID 36950691.
  18. ^ Zeisel SH, da Costa KA (November 2009). "Choline: an essential nutrient for public health". Nutrition Reviews. 67 (11): 615–623. doi:10.1111/j.1753-4887.2009.00246.x. PMC 2782876. PMID 19906248.615-623&rft.date=2009-11&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782876#id-name=PMC&rft_id=info:pmid/19906248&rft_id=info:doi/10.1111/j.1753-4887.2009.00246.x&rft.aulast=Zeisel&rft.aufirst=S. H.&rft.au=da Costa, K. A.&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782876&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  19. ^ a b c Hirsch MJ, Growdon JH, Wurtman RJ (August 1978). "Relations between dietary choline or lecithin intake, serum choline levels, and various metabolic indices". Metabolism. 27 (8): 953–60. doi:10.1016/0026-0495(78)90139-7. PMID 672614.953-60&rft.date=1978-08&rft_id=info:doi/10.1016/0026-0495(78)90139-7&rft_id=info:pmid/672614&rft.aulast=Hirsch&rft.aufirst=MJ&rft.au=Growdon, JH&rft.au=Wurtman, RJ&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  20. ^ a b c "Lecithin use while Breastfeeding". Archived from the original on 2022-07-04. Retrieved 2024-04-06.
  21. ^ a b c Canty DJ, Zeisel SH (2009). "Lecithin and Choline in Human Health and Disease". Nutrition Reviews. 52 (10): 327–339. doi:10.1111/j.1753-4887.1994.tb01357.x. PMID 7816350.327-339&rft.date=2009&rft_id=info:doi/10.1111/j.1753-4887.1994.tb01357.x&rft_id=info:pmid/7816350&rft.aulast=Canty&rft.aufirst=David J.&rft.au=Zeisel, Steven H.&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  22. ^ D. L. Miller (2002). "Health benefits of lecithin and choline". Cereal Foods World. 47: 178–184. S2CID 88884706.178-184&rft.date=2002&rft_id=https://api.semanticscholar.org/CorpusID:88884706#id-name=S2CID&rft.au=D. L. Miller&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  23. ^ "Office of Dietary Supplements - Choline". Archived from the original on 2021-09-23. Retrieved 2024-04-06.
  24. ^ "Choline". 11 August 2020. Archived from the original on 6 April 2024. Retrieved 6 April 2024.
  25. ^ a b "Lecithin". Drugs and Lactation Database, National Library of Medicine, US National Institutes of Health. 20 September 2021. PMID 30000831. Archived from the original on 19 May 2022. Retrieved 19 May 2022.
  26. ^ "Soybeans and soy lecithin". Food Allergy Research and Resource Program. University of Nebraska–Lincoln. 7 August 2018. Archived from the original on 6 April 2024. Retrieved 14 December 2018.
  27. ^ Rondanelli M, Riva A, Allegrini P, Faliva MA, Naso M, Peroni G, Nichetti M, Gasparri C, Spadaccini D, Iannello G, Infantino V, Fazia T, Bernardinelli L, Perna S (2020). "The Use of a New Food-Grade Lecithin Formulation of Highly Standardized Ginger (Zingiber officinale) and Acmella oleracea Extracts for the Treatment of Pain and Inflammation in a Group of Subjects with Moderate Knee Osteoarthritis". J Pain Res. 13: 761–770. doi:10.2147/JPR.S214488. PMC 7183537. PMID 32368129.761-770&rft.date=2020&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183537#id-name=PMC&rft_id=info:pmid/32368129&rft_id=info:doi/10.2147/JPR.S214488&rft.aulast=Rondanelli&rft.aufirst=M&rft.au=Riva, A&rft.au=Allegrini, P&rft.au=Faliva, MA&rft.au=Naso, M&rft.au=Peroni, G&rft.au=Nichetti, M&rft.au=Gasparri, C&rft.au=Spadaccini, D&rft.au=Iannello, G&rft.au=Infantino, V&rft.au=Fazia, T&rft.au=Bernardinelli, L&rft.au=Perna, S&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7183537&rfr_id=info:sid/en.wikipedia.org:Lecithin" class="Z3988">
  28. ^ Higgins JP, Flicker L (2003). "Lecithin for dementia and cognitive impairment". Cochrane Database of Systematic Reviews. 3 (3): CD001015. doi:10.1002/14651858.CD001015. PMID 12917896.
  29. ^ (Reb Yehonatan Levy, Shomer Kashrut Mashgiach - based upon halachic rulings of CRC - Chicago Rabbinic Council, and from shiurim/lessons by Rabbi D. Raccah on "Pesach Preparations" following commentary from former Rishon-LeTzion Rav Ovadia Yosef). OK Kosher Certification, Keeping Kosher for Pesach. Archived 2012-03-15 at the Wayback Machine Retrieved on September 10, 2008.
  30. ^ Islamic Food and Nutrition Council of America FAQ, IFANCA: Consumer FAQ. Archived 2011-11-23 at the Wayback Machine. Retrieved on July 7, 2010. The practice of consuming Halal products is not widespread among Muslims, the practice is common with Muslims who follow Sharia laws.
edit
Retrieved from "https://en.wikipedia.org/w/index.php?title=Lecithin&oldid=1262265557"