.
“rye bo FLAY vin”
.
C17H20N4O6
.
(also known as ‘vitamin B2’)
.
*’riboflavin’ is a vitamin found in food and used as a ‘dietary supplement’*
.
It is required by the body for cellular respiration
Food sources include eggs, green vegetables, milk and other dairy product, meat, mushrooms, and almonds
Some countries require its addition to grains
As a supplement it is used to prevent and treat riboflavin deficiency.
At amounts far in excess of what is needed to meet dietary needs as a nutrient, riboflavin may prevent migraines
Riboflavin may be given by mouth or injection
It is nearly always well tolerated
Normal doses are safe during pregnancy
Riboflavin was discovered in 1920, isolated in 1933, and first synthesized in 1935
It is on the World Health Organization’s List of Essential Medicines.[6]
Definition
Riboflavin, also known as vitamin B2, is a vitamin found in food, sold as a dietary supplement, and used in food fortification programs in countries where deficiency is common.[4][7][8][9][10]
Deficiency[edit]
Signs and symptoms[edit]
Mild riboflavin deficiencies can exceed 50% of the population in developing countries and in refugee situations. Deficiency is uncommon in the United States and in other countries that have wheat flour, bread, pasta, corn meal or rice enrichment regulations. In the U.S., starting in the 1940s, flour, corn meal and rice have been fortified with B vitamins as a means of restoring some of what is lost in milling, bleaching and other processing. For adults 20 and older, average intake from food and beverages is 1.8 mg/day for women and 2.5 mg/day for men. An estimated 23% consume a riboflavin-containing dietary supplement that provides on average 10 mg. The U.S. Department of Health and Human Services conducts National Health and Nutrition Examination Survey every two years and reports food results in a series of reports referred to as “What We Eat In America.” From NHANES 2011–2012, estimates were that 8% of women and 3% of men consumed less than the RDA. When compared to the lower Estimated Average Requirements, fewer than 3% did not achieve the EAR level.[citation needed]
Riboflavin deficiency (also called ariboflavinosis) results in stomatitis including painful red tongue with sore throat, chapped and fissured lips (cheilosis), and inflammation of the corners of the mouth (angular stomatitis). There can be oily scaly skin rashes on the scrotum, vulva, philtrum of the lip, or the nasolabial folds. The eyes can become itchy, watery, bloodshot and sensitive to light.[11] Due to interference with iron absorption, even mild to moderate riboflavin deficiency results in an anemia with normal cell size and normal hemoglobin content (i.e. normochromic normocytic anemia). This is distinct from anemia caused by deficiency of folic acid (B9) or cyanocobalamin (B12), which causes anemia with large blood cells (megaloblastic anemia).[12] Deficiency of riboflavin during pregnancy can result in birth defects including congenital heart defects[13] and limb deformities.[14] Prolonged riboflavin insufficiency is also known to cause degeneration of the liver and nervous system.[7]
The stomatitis symptoms are similar to those seen in pellagra, which is caused by niacin (B3) deficiency. Therefore, riboflavin deficiency is sometimes called “pellagra sine pellagra” (pellagra without pellagra), because it causes stomatitis but not widespread peripheral skin lesions characteristic of niacin deficiency.[11]
Riboflavin deficiency prolongs recovery from malaria,[15] despite preventing growth of plasmodium (the malaria parasite).[16]
Causes[edit]
Riboflavin is continuously excreted in the urine of healthy individuals,[17] making deficiency relatively common when dietary intake is insufficient.[17] Riboflavin deficiency is usually found together with other nutrient deficiencies, particularly of other water-soluble vitamins. A deficiency of riboflavin can be primary – poor vitamin sources in one’s daily diet – or secondary, which may be a result of conditions that affect absorption in the intestine, the body not being able to use the vitamin, or an increase in the excretion of the vitamin from the body.
Subclinical deficiency has also been observed in women taking oral contraceptives, in the elderly, in people with eating disorders, chronic alcoholism and in diseases such as HIV, inflammatory bowel disease, diabetes and chronic heart disease. The Celiac Disease Foundation points out that a gluten-free diet may be low in riboflavin (and other nutrients) as enriched wheat flour and wheat foods (bread, pasta, cereals, etc.) are a major dietary contribution to total riboflavin intake.[citation needed]
Diagnosis[edit]
Overt clinical signs are rarely seen among inhabitants of the developed countries. The assessment of riboflavin status is essential for confirming cases with unspecific symptoms where deficiency is suspected.
Glutathione reductase is a nicotinamide adenine dinucleotide phosphate (NADPH) and FAD-dependent enzyme, and the major flavoprotein in erythrocytes. The measurement of the activity coefficient of erythrocyte glutathione reductase (EGR) is the preferred method for assessing riboflavin status.[18] It provides a measure of tissue saturation and long-term riboflavin status. In vitro enzyme activity in terms of activity coefficients (AC) is determined both with and without the addition of FAD to the medium. ACs represent a ratio of the enzyme’s activity with FAD to the enzyme’s activity without FAD. An AC of 1.2 to 1.4, riboflavin status is considered low when FAD is added to stimulate enzyme activity. An AC > 1.4 suggests riboflavin deficiency. On the other hand, if FAD is added and AC is < 1.2, then riboflavin status is considered acceptable.[19] Tillotson and Bashor[20] reported that a decrease in the intakes of riboflavin was associated with increase in EGR AC. In the UK study of Norwich elderly,[21] initial EGR AC values for both males and females were significantly correlated with those measured 2 years later, suggesting that EGR AC may be a reliable measure of long-term biochemical riboflavin status of individuals. These findings are consistent with earlier studies.[22]
Experimental balance studies indicate that urinary riboflavin excretion rates increase slowly with increasing intakes, until intake level approach 1.0 mg/d, when tissue saturation occurs. At higher intakes, the rate of excretion increases dramatically.[18] Once intakes of 2.5 mg/d are reached, excretion becomes approximately equal to the rate of absorption[23] At such high intake a significant proportion of the riboflavin intake is not absorbed. If urinary riboflavin excretion is <19 µg/g creatinine (without recent riboflavin intake) or < 40 µg per day are indicative of deficiency.
Treatment[edit]
Multi-vitamin dietary supplements often contain 100% of the U.S. Daily Value (1.3 mg) for riboflavin, and can be used by persons concerned about an inadequate diet. Over-the-counter dietary supplements are available in the United States with doses as high as 100 mg, but there is no evidence that these high doses have any additional benefit for healthy people.[citation needed]
Medical uses[edit]
Corneal ectasia is a progressive thinning of the cornea; the most common form of this condition is keratoconus. Collagen cross-linking by applying riboflavin topically then shining UV light is a method to slow progression of corneal ectasia by strengthening corneal tissue.[24]
A 2017 review found that riboflavin taken daily in amounts roughly 200 to 400 times the Recommended Dietary Allowance (RDA) may be useful to prevent migraines in adults, but found that clinical trials in adolescents and children had mixed outcomes.[25] A hypothesis has been proposed that riboflavin improves mitochondrial energy production.[26]
Pharmacokinetics[edit]
The body absorbs little[specify] riboflavin from single doses beyond 27 mg.[4][27] When excess amounts are consumed, they are either not absorbed or the small[specify] amount that is absorbed is excreted in urine.[7]
After a single oral dose, biologic half-life is about 66 to 84 minutes in healthy people.[27]
Biosynthesis[edit]
The biosynthesis of one riboflavin molecule requires one molecule of GTP and two molecules of ribulose 5-phosphate as substrates. The imidazole ring of GTP is hydrolytically opened, yielding a 4, 5-diaminopyrimidine which is converted to 5-amino-6-ribitylamino-2, 4(1H,3H)-pyrimidinedione by a sequence of deamination, side chain reduction and dephosphorylation. Condensation of 5-amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione with 3, 4-dihydroxy-2-butanone 4-phosphate obtained from ribulose 5-phosphate affords 6,7-dimethyl-8-ribityllumazine. Dismutation of the lumazine derivative yields riboflavin and 5-amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione, which is recycled in the biosynthetic pathway. The structure of the biosynthetic enzyme, 6,7-dimethyl-8-ribityllumazine synthase, has been studied in considerable detail.
Side effects[edit]
In humans, there is no evidence for riboflavin toxicity produced by excessive intakes, in part because it has lower water solubility than other B vitamins, because absorption becomes less efficient as doses increase, and because what exceeds the absorption is excreted via the kidneys into urine.[19] Even when 400 mg of riboflavin per day was given orally to subjects in one study for three months to investigate the efficacy of riboflavin in the prevention of migraine headache, no short-term side effects were reported.[28] Any excess at nutritionally relevant doses is excreted in the urine,[29] imparting a bright yellow color when in large quantities. The limited data available on riboflavin’s adverse effects do not mean, however, that high intakes have no adverse effects, and the Food and Nutrition Board urges people to be cautious about consuming excessive amounts of riboflavin.[7]
Function[edit]
Flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) function as cofactors for a variety of flavoprotein enzyme reactions:
Flavoproteins of electron transport chain, including FMN in Complex I and FAD in Complex II
FAD is required for the production of pyridoxic acid from pyridoxal (vitamin B6) by pyridoxine 5′-phosphate oxidase
The primary coenzyme form of vitamin B6 (pyridoxal phosphate) is FMN dependent
Oxidation of pyruvate, α-ketoglutarate, and branched-chain amino acids requires FAD in the shared E3 portion of their respective dehydrogenase complexes
Fatty acyl CoA dehydrogenase requires FAD in fatty acid oxidation
FAD is required to convert retinol (vitamin A) to retinoic acid via cytosolic retinal dehydrogenase
Synthesis of an active form of folate (5-methyltetrahydrofolate) from 5,10-methylenetetrahydrofolate by methylenetetrahydrofolate reductase is FADH2 dependent
FAD is required by Kynurenine 3-monooxygenase to convert tryptophan to niacin (vitamin B3)
Reduction of the oxidized form of glutathione (GSSG) to its reduced form (GSH) by glutathione reductase is FAD dependent
For the molecular mechanism of action see main articles flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD)
Dietary recommendations[edit]
United States
Age group (years) RDA for riboflavin (mg/d)[7] Tolerable upper intake level[7]
Infants 0–6 months 0.3* ND
Infants 6–12 months 0.4*
1–3 0.5
4–8 0.6
9–13 0.9
Females 14–18 1.0
Males 14–18 1.3
Females 19+ 1.1
Males 19+ 1.3
Pregnant females 14–50 1.4
Lactating females 14–50 1.6
European Food Safety Authority
Age group (years) Adequate Intake of riboflavin (mg/d)[30] Tolerable upper limit[30]
7–11 months 0.4 ND
1–3 0.6
4–6 0.7
7–10 1.0
11–14 1.4
15–17 1.6
18+
Australia and New Zealand
Age group (years) Adequate Intake of riboflavin (mg/d)[31] Upper level of intake[31]
0–6 months 0.3* ND
7–12 months 0.4*
1–3 0.5
4–8 0.6
9–13 0.9
Females 14–70 1.1
Males 14–70 1.3
Females >70 1.3
Males >70 1.6
Pregnant females 14–50 1.4
Lactating females 14–50 1.6
- Adequate intake for infants, no RDA/RDI yet established[7]
The National Academy of Medicine (then the U.S. Institute of Medicine [IOM]) updated Estimated Average Requirements (EARs) and Recommended Dietary Allowances (RDAs) for riboflavin in 1998. The current EARs for riboflavin for women and men ages 14 and up are 0.9 mg/day and 1.1 mg/day, respectively; the RDAs are 1.1 and 1.3 mg/day, respectively. RDAs are higher than EARs so as to identify amounts that will cover people with higher than average requirements. RDA for pregnancy is 1.4 mg/day. RDA for lactation is 1.6 mg/day. For infants up to 12 months the Adequate Intake (AI) is 0.3–0.4 mg/day. and for children ages 1–13 years the RDA increases with age from 0.5 to 0.9 mg/day. As for safety, the IOM sets Tolerable upper intake levels (ULs) for vitamins and minerals when evidence is sufficient. In the case of riboflavin there is no UL, as there is no human data for adverse effects from high doses. Collectively the EARs, RDAs, AIs and ULs are referred to as Dietary Reference Intakes (DRIs).[19][7]
The European Food Safety Authority (EFSA) refers to the collective set of information as Dietary Reference Values, with Population Reference Intake (PRI) instead of RDA, and Average Requirement instead of EAR. AI and UL defined the same as in United States. For women and men ages 15 and older the PRI is set at 1.6 mg/day. PRI for pregnancy is 1.9 mg/day, for lactation 2.0 mg/day. For children ages 1–14 years the PRIs increase with age from 0.6 to 1.4 mg/day. These PRIs are higher than the U.S. RDAs.[32] The EFSA also reviewed the safety question and like the U.S., decided that there was not sufficient information to set an UL.[33]
For U.S. food and dietary supplement labeling purposes the amount in a serving is expressed as a percent of Daily Value (%DV). For riboflavin labeling purposes 100% of the Daily Value was 1.7 mg, but as of May 27, 2016, it was revised to 1.3 mg to bring it into agreement with the RDA.[34][35] Compliance with the updated labeling regulations was required by 1 January 2020 for manufacturers with US$10 million or more in annual food sales, and by 1 January 2021 for manufacturers with lower volume food sales.[36][37] A table of the old and new adult daily values is provided at Reference Daily Intake.
Sources[edit]
Food and beverages that provide riboflavin without fortification are milk, cheese, eggs, leaf vegetables, liver, kidneys, lean meats, legumes, mushrooms, and almonds.[7][8]
The milling of cereals results in considerable loss (up to 60%) of vitamin B2, so white flour is enriched in some countries by addition of the vitamin. The enrichment of bread and ready-to-eat breakfast cereals contributes significantly to the dietary supply of vitamin B2. Polished rice is not usually enriched, because the vitamin’s yellow color would make the rice visually unacceptable to the major rice-consuming populations. However, most of the flavin content of whole brown rice is retained if the rice is steamed (parboiled) prior to milling. This process drives the flavins in the germ and aleurone layers into the endosperm. Free riboflavin is naturally present in foods along with protein-bound FMN and FAD. Bovine milk contains mainly free riboflavin, with a minor contribution from FMN and FAD. In whole milk, 14% of the flavins are bound noncovalently to specific proteins.[38] Milk and yogurt contain some of the highest riboflavin content.[4] Egg white and egg yolk contain specialized riboflavin-binding proteins, which are required for storage of free riboflavin in the egg for use by the developing embryo.[citation needed]
Riboflavin is added to baby foods, breakfast cereals, pastas and vitamin-enriched meal replacement products. It is difficult to incorporate riboflavin into liquid products because it has poor solubility in water, hence the requirement for riboflavin-5′-phosphate (E101a), a more soluble form of riboflavin. Riboflavin is also used as a food coloring and as such is designated in Europe as the E number E101.[39]
Other animals[edit]
In other animals, riboflavin deficiency results in lack of growth,[40] failure to thrive, and eventual death. Experimental riboflavin deficiency in dogs results in growth failure, weakness, ataxia, and inability to stand. The animals collapse, become comatose, and die. During the deficiency state, dermatitis develops together with hair loss. Other signs include corneal opacity, lenticular cataracts, hemorrhagic adrenals, fatty degeneration of the kidney and liver, and inflammation of the mucous membrane of the gastrointestinal tract.[41] Post-mortem studies in rhesus monkeys fed a riboflavin-deficient diet revealed about one-third the normal amount of riboflavin was present in the liver, which is the main storage organ for riboflavin in mammals.[42] Riboflavin deficiency in birds results in low egg hatch rates.[43]
Chemistry[edit]
As a chemical compound, riboflavin is a yellow-orange solid substance with poor solubility in water compared to other B vitamins. Visually, it imparts color to vitamin supplements (and bright yellow color of urine in persons taking it).[3]
Industrial uses[edit]
Fluorescent spectra of riboflavin
Because riboflavin is fluorescent under UV light, dilute solutions (0.015–0.025% w/w) are often used to detect leaks or to demonstrate coverage in an industrial system such a chemical blend tank or bioreactor.[citation needed]
Industrial synthesis[edit]
Large cultures of Micrococcus luteus growing on pyridine (left) and succinic acid (right). The pyridine culture has turned yellow from produced riboflavin.
The industrial scale production of riboflavin using diverse microorganisms, including filamentous fungi such as Ashbya gossypii, Candida famata and Candida flaveri, as well as the bacteria Corynebacterium ammoniagenes and Bacillus subtilis.[44] The latter organism, genetically modified to both increase the production of riboflavin and to introduce an antibiotic (ampicillin) resistance marker, is employed at a commercial scale to produce riboflavin for feed and food fortification. The chemical company BASF has installed a plant in South Korea, which is specialized on riboflavin production using Ashbya gossypii. The concentrations of riboflavin in their modified strain are so high that the mycelium has a reddish/brownish color and accumulates riboflavin crystals in the vacuoles, which will eventually burst the mycelium. Riboflavin is sometimes overproduced, possibly as a protective mechanism, by some bacteria in the presence of high concentrations of hydrocarbons or aromatic compounds. One such organism is Micrococcus luteus (American Type Culture Collection strain number ATCC 49442), which develops a yellow color due to production of riboflavin while growing on pyridine, but not when grown on other substrates, such as succinic acid.[45]
History[edit]
The name “riboflavin” comes from “ribose” (the sugar whose reduced form, ribitol, forms part of its structure) and “flavin”, the ring-moiety which imparts the yellow color to the oxidized molecule (from Latin flavus, “yellow”).[46] The reduced form, which occurs in metabolism along with the oxidized form, is colorless.
“Vitamin B” was originally considered to have two components, a heat-labile vitamin B1 and a heat-stable vitamin B2.[2] In the 1920s, vitamin B2 was initially thought to be the factor necessary for preventing pellagra.[2] In 1923, Paul Gyorgy in Heidelberg was investigating egg-white injury in rats;[2] the curative factor for this condition was called vitamin H, which is now called biotin. Since both pellagra and vitamin H deficiency were associated with dermatitis, Gyorgy decided to test the effect of vitamin B2 on vitamin H deficiency in rats. He enlisted the service of Wagner-Jauregg in Kuhn’s laboratory.[2] In 1933, Kuhn, Gyorgy, and Wagner found that thiamin-free extracts of yeast, liver, or rice bran prevented the growth failure of rats fed a thiamin-supplemented diet.[2]
Further, the researchers noted that a yellow-green fluorescence in each extract promoted rat growth, and that the intensity of fluorescence was proportional to the effect on growth.[2] This observation enabled them to develop a rapid chemical and bioassay to isolate the factor from egg white in 1933.[2] The same group then isolated the same preparation (a growth-promoting compound with yellow-green fluorescence) from whey using the same procedure (lactoflavin). In 1934, Kuhn’s group identified the structure of so-called flavin and synthesized vitamin B2, leading to evidence in 1939 that riboflavin was essential for human health.[2]
Research[edit]
Donated whole blood can be treated with riboflavin and then with ultraviolet light as a pathogen reduction technology.[47]
See also[edit]
Flavin
Riboflavin kinase
Riboflavin synthase
References[edit]
^ “Riboflavin”. Drugs.com. 1 October 2020. Retrieved 12 October 2020.
^ Jump up to: a b c d e f g h i j Northrop-Clewes CA, Thurnham DI (2012). “The discovery and characterization of riboflavin”. Annals of Nutrition & Metabolism. 61 (3): 224–30. doi:10.1159/000343111. PMID 23183293. S2CID 7331172.
^ Jump up to: a b c d e f g h “Riboflavin”. Drugs.com, The American Society of Health-System Pharmacists. 1 August 2018. Archived from the original on 30 December 2016. Retrieved 7 November 2018.
^ Jump up to: a b c d e f g “Riboflavin: Fact Sheet for Health Professionals”. Office of Dietary Supplements, US National Institutes of Health. 20 August 2018. Retrieved 7 November 2018.
^ “Why fortify?”. Food Fortification Initiative. 2017. Archived from the original on 4 April 2017. Retrieved 4 April 2017.
^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
^ Jump up to: a b c d e f g h i Institute of Medicine (1998). “Riboflavin”. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC: The National Academies Press. pp. 87–122. ISBN 978-0-309-06554-2. Archived from the original on 17 July 2015. Retrieved 29 August 2017.
^ Jump up to: a b Higdon J, Drake VJ (2007). “Riboflavin”. Micronutrient Information Center. Linus Pauling Institute at Oregon State University. Archived from the original on 11 February 2010. Retrieved 3 December 2009.
^ Merrill AH, McCormick DB (2020). “Riboflavin”. In BP Marriott, DF Birt, VA Stallings, AA Yates (eds.). Present Knowledge in Nutrition, Eleventh Edition. London, United Kingdom: Academic Press (Elsevier). pp. 189–208. ISBN 978-0-323-66162-1.
^ “Map: Count of Nutrients In Fortification Standards”. Global Fortification Data Exchange. Retrieved 1 August 2020.
^ Jump up to: a b Sebrell WH, Butler RE (1939). “Riboflavin Deficiency in Man (Ariboflavinosis)”. Public Health Reports. 54 (48): 2121–2131. doi:10.2307/4583104. JSTOR 4583104.
^ Lane M, Alfrey CP (April 1965). “The Anemia of Human Riboflavin Deficiency”. Blood. 25 (4): 432–442. doi:10.1182/blood.V25.4.432.432. PMID 14284333.
^ Smedts HP, Rakhshandehroo M, Verkleij-Hagoort AC, de Vries JH, Ottenkamp J, Steegers EA, Steegers-Theunissen RP (October 2008). “Maternal intake of fat, riboflavin and nicotinamide and the risk of having offspring with congenital heart defects”. European Journal of Nutrition. 47 (7): 357–365. doi:10.1007/s00394-008-0735-6. PMID 18779918. S2CID 25548935.
^ Robitaille J, Carmichael SL, Shaw GM, Olney RS (September 2009). “Maternal nutrient intake and risks for transverse and longitudinal limb deficiencies: data from the National Birth Defects Prevention Study, 1997–2003”. Birth Defects Research. Part A, Clinical and Molecular Teratology. 85 (9): 773–779. doi:10.1002/bdra.20587. PMID 19350655.
^ Das BS, Das DB, Satpathy RN, Patnaik JK, Bose TK (April 1988). “Riboflavin deficiency and severity of malaria”. European Journal of Clinical Nutrition. 42 (4): 277–83. PMID 3293996.
^ Dutta P, Pinto J, Rivlin R (November 1985). “Antimalarial effects of riboflavin deficiency”. Lancet. 2 (8463): 1040–3. doi:10.1016/S0140-6736(85)90909-2. PMID 2865519. S2CID 35542771.
^ Jump up to: a b Brody T (1999). Nutritional Biochemistry. San Diego: Academic Press. ISBN 978-0-12-134836-6. OCLC 162571066.
^ Jump up to: a b Rosalind, Gibson S. (2005) “Riboflavin” in Principles of Nutritional Assessment, 2nd ed. Oxford University Press.
^ Jump up to: a b c Gropper SS, Smith JL, Groff JL (2009). “Ch. 9: Riboflavin”. Advanced Nutrition and Human Metabolism (5th ed.). Wadsworth: CENGAG Learning. pp. 329–33. ISBN 9780495116578.
^ Tillotson JA, Baker EM (April 1972). “An enzymatic measurement of the riboflavin status in man”. The American Journal of Clinical Nutrition. 25 (4): 425–31. doi:10.1093/ajcn/25.4.425. PMID 4400882.
^ Bailey AL, Maisey S, Southon S, Wright AJ, Finglas PM, Fulcher RA (February 1997). “Relationships between micronutrient intake and biochemical indicators of nutrient adequacy in a “free-living’ elderly UK population”. The British Journal of Nutrition. 77 (2): 225–42. doi:10.1079/BJN19970026. PMID 9135369.
^ Rutishauser IH, Bates CJ, Paul AA, Black AE, Mandal AR, Patnaik BK (July 1979). “Long-term vitamin status and dietary intake of healthy elderly subjects. 1. Riboflavin”. The British Journal of Nutrition. 42 (1): 33–42. doi:10.1079/BJN19790087. PMID 486392.
^ Horwitt MK, Harvey CC, Hills OW, Liebert E (June 1950). “Correlation of urinary excretion of riboflavin with dietary intake and symptoms of ariboflavinosis”. The Journal of Nutrition. 41 (2): 247–64. doi:10.1093/jn/41.2.247. PMID 15422413.
^ Mastropasqua L (2015). “Collagen cross-linking: when and how? A review of the state of the art of the technique and new perspectives”. Eye and Vision. 2: 19. doi:10.1186/s40662-015-0030-6. PMC 4675057. PMID 26665102.
^ Thompson DF, Saluja HS (August 2017). “Prophylaxis of migraine headaches with riboflavin: A systematic review”. Journal of Clinical Pharmacy and Therapeutics. 42 (4): 394–403. doi:10.1111/jcpt.12548. PMID 28485121.
^ McCormick, DB (2012). “Riboflavin”. In JW Erdman Jr; IA MacDonald; SH Zeisel (eds.). Present Knowledge in Nutrition (Tenth ed.). Hoboken, NJ: Wiley-Blackwell. pp. 280–92. ISBN 978-0-470-95917-6.
^ Jump up to: a b “Riboflavin (Vitamin B2)”.
^ Boehnke C, Reuter U, Flach U, Schuh-Hofer S, Einhäupl KM, Arnold G (July 2004). “High-dose riboflavin treatment is efficacious in migraine prophylaxis: an open study in a tertiary care centre”. European Journal of Neurology. 11 (7): 475–7. doi:10.1111/j.1468-1331.2004.00813.x. PMID 15257686. S2CID 46147839.
^ Zempleni J, Galloway JR, McCormick DB (January 1996). “Pharmacokinetics of orally and intravenously administered riboflavin in healthy humans”. The American Journal of Clinical Nutrition. 63 (1): 54–66. doi:10.1093/ajcn/63.1.54. PMID 8604671.
^ Jump up to: a b European Food Safety Authority (February 2006). “Tolerable Upper Intake Levels for Vitamins and Minerals” (PDF). EFSA. Retrieved 18 June 2018.
^ Jump up to: a b “Nutrient reference values for Australia and New Zealand” (PDF). National Health and Medical Research Council. 9 September 2005. Retrieved 19 June 2018.
^ “Overview on Dietary Reference Values for the EU population as derived by the EFSA Panel on Dietetic Products, Nutrition and Allergies” (PDF). 2017. Archived (PDF) from the original on 28 August 2017.
^ “Tolerable Upper Intake Levels For Vitamins And Minerals” (PDF). European Food Safety Authority. 2006. Archived (PDF) from the original on 16 March 2016.
^ “Federal Register May 27, 2016 Food Labeling: Revision of the Nutrition and Supplement Facts Labels. FR page 33982” (PDF). Archived (PDF) from the original on 8 August 2016.
^ “Daily Value Reference of the Dietary Supplement Label Database (DSLD)”. Dietary Supplement Label Database (DSLD). Retrieved 16 May 2020.
^ “Changes to the Nutrition Facts Label”. U.S. Food and Drug Administration (FDA). 27 May 2016. Retrieved 16 May 2020. This article incorporates text from this source, which is in the public domain.
^ “Industry Resources on the Changes to the Nutrition Facts Label”. U.S. Food and Drug Administration (FDA). 21 December 2018. Retrieved 16 May 2020. This article incorporates text from this source, which is in the public domain.
^ Kanno C, Kanehara N, Shirafuji K, Tanji R, Imai T (February 1991). “Binding form of vitamin B2 in bovine milk: its concentration, distribution and binding linkage”. Journal of Nutritional Science and Vitaminology. 37 (1): 15–27. doi:10.3177/jnsv.37.15. PMID 1880629.
^ “Current EU approved additives and their E Numbers”. UK Food Standards Agency. 27 July 2007. Archived from the original on 7 October 2010. Retrieved 3 December 2009.
^ Patterson BE, Bates CJ (May 1989). “Riboflavin deficiency, metabolic rate and brown adipose tissue function in sucking and weanling rats”. The British Journal of Nutrition. 61 (3): 475–483. doi:10.1079/bjn19890137. PMID 2547428.
^ Sebrell WH, Onstott RH (1938). “Riboflavin Deficiency in Dogs”. Public Health Reports. 53 (3): 83–94. doi:10.2307/4582435. JSTOR 4582435.
^ Waisman HA (1944). “Production of Riboflavin Deficiency in the Monkey”. Experimental Biology and Medicine. 55 (1): 69–71. doi:10.3181/00379727-55-14462. S2CID 83970561.
^ Romanoff AL, Bauernfeind JC (1942). “Influence of riboflavin-deficiency in eggs on embryonic development (Gallus domesticus)”. The Anatomical Record. 82 (1): 11–23. doi:10.1002/ar.1090820103. S2CID 84855935.
^ Stahmann KP, Revuelta JL, Seulberger H (May 2000). “Three biotechnical processes using Ashbya gossypii, Candida famata, or Bacillus subtilis compete with chemical riboflavin production”. Applied Microbiology and Biotechnology. 53 (5): 509–516. doi:10.1007/s002530051649. PMID 10855708. S2CID 2471994.
^ Sims GK, O’loughlin EJ (October 1992). “Riboflavin Production during Growth of Micrococcus luteus on Pyridine”. Applied and Environmental Microbiology. 58 (10): 3423–3425. doi:10.1128/AEM.58.10.3423-3425.1992. PMC 183117. PMID 16348793.
^ “Riboflavin”. Online Etymology Dictionary, Douglas Harper. 2018. Retrieved 7 November 2018.
^ Yonemura S, Doane S, Keil S, Goodrich R, Pidcoke H, Cardoso M (July 2017). “Improving the safety of whole blood-derived transfusion products with a riboflavin-based pathogen reduction technology”. Blood Transfusion = Trasfusione del Sangue. 15 (4): 357–364. doi:10.2450/2017.0320-16. PMC 5490732. PMID 28665269Note: Authored by Terumo employees
External links[edit]
Higdon, Jane, “Riboflavin”, Micronutrient Information Center, Linus Pauling Institute, Oregon State University
“Riboflavin”. Drug Information Portal.
U.S. National Library of Medicine.
en.wikipedia.org /wiki/Riboflavin
Riboflavin
Contributors to Wikimedia projects
29-37 minutes
Riboflavin
Riboflavin.svg
Riboflavin-3d-balls.png
Chemical structure
Clinical data
Trade names Many[1]
Other names vactochrome, lactoflavin, vitamin G[2]
AHFS/Drugs.com Monograph
License data
US DailyMed: Riboflavin
Routes of
administration By mouth, intramuscular, intravenous
ATC code
A11HA04 (WHO) S01XA26 (WHO)
Legal status
Legal status
US: Dietary supplement
Pharmacokinetic data
Elimination half-life 66 to 84 minutes
Excretion Urine
Identifiers
IUPAC name[show]
CAS Number
83-88-5 check
PubChem CID
493570
IUPHAR/BPS
6578
DrugBank
DB00140
ChemSpider
431981
UNII
TLM2976OFR
KEGG
D00050
ChEBI
CHEBI:17015
ChEMBL
ChEMBL1534
E number E101, E101(iii) (colours) Edit this at Wikidata
CompTox Dashboard (EPA)
DTXSID8021777 Edit this at Wikidata
ECHA InfoCard 100.001.370 Edit this at Wikidata
Chemical and physical data
Formula C17H20N4O6
Molar mass 376.369 g·mol−1
3D model (JSmol)
Interactive image
SMILES[show]
InChI
riboflavin (vitamin B2) is part of the vitamin B group
the name “riboflavin” comes from
“ribose” (the sugar whose reduced form, ribitol, forms part of its structure)
“flavin”, the ring-moiety which imparts the yellow color to the oxidized molecule (from Latin flavus, “yellow”).
The reduced form, which occurs in metabolism along with the oxidized form, is colorless
.
.
*👨🔬🕵️♀️🙇♀️*SKETCHES*🙇♂️👩🔬🕵️♂️*
.
.
.
.
.
💕💝💖💓🖤💙🖤💙🖤💙🖤❤️💚💛🧡❣️💞💔💘❣️🧡💛💚❤️🖤💜🖤💙🖤💙🖤💗💖💝💘
.
.
*🌈✨ *TABLE OF CONTENTS* ✨🌷*
.
.
🔥🔥🔥🔥🔥🔥🔥*we won the war* 🔥🔥🔥🔥🔥🔥🔥