Vitamin C
Names | |
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Other names | l-ascorbic acid, ascorbic acid, ascorbate |
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Clinical data | |
Drug class | Vitamin |
Main uses | Scurvy[1] |
Side effects | Gastrointestinal discomfort, headache, trouble sleeping, flushing of the skin[2][3] |
Pregnancy category |
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Routes of use | By mouth, IM, IV, subQ |
Defined daily dose | 200 mg (by mouth or injection)[5] |
External links | |
AHFS/Drugs.com | Monograph |
MedlinePlus | a682583 |
Legal | |
License data | |
Legal status |
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Pharmacokinetics | |
Bioavailability | Rapid and complete |
Protein binding | Negligible |
Elimination half-life | Varies according to plasma concentration |
Excretion | Kidney |
Chemical and physical data | |
Formula | C6H8O6 |
Molar mass | 176.12 g·mol−1 |
3D model (JSmol) | |
Density | 1.694 g/cm3 |
Melting point | 190–192 °C (374–378 °F) (some decomposition)[6] |
Boiling point | 552.7 °C (1,026.9 °F) [7] |
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Vitamin C, also known as ascorbic acid and ascorbate, is a vitamin found in various foods and sold as a dietary supplement.[2] It is used to prevent and treat scurvy.[2] Vitamin C is an essential nutrient involved in the repair of tissue and the enzymatic production of certain neurotransmitters.[2][8] It is required for the functioning of several enzymes and is important for immune system function.[8][9] It also functions as an antioxidant.[10]
There is some evidence that regular use of supplements may reduce the duration of the common cold, but it does not appear to prevent infection.[10][3][11] It is unclear whether supplementation affects the risk of cancer, cardiovascular disease, or dementia.[12][13] It may be taken by mouth or by injection.[2]
Vitamin C is generally well tolerated.[2] Large doses may cause gastrointestinal discomfort, headache, trouble sleeping, and flushing of the skin.[2][3] Normal doses are safe during pregnancy.[4] The United States Institute of Medicine recommends against taking large doses.[8]
Vitamin C was discovered in 1912, isolated in 1928, and in 1933, was the first vitamin to be chemically produced.[14] It is on the World Health Organization's List of Essential Medicines.[15] Vitamin C is available as an inexpensive generic and over-the-counter medication.[2][16][17] Partly for its discovery, Albert Szent-Györgyi and Walter Norman Haworth were awarded the 1937 Nobel Prizes in Physiology and Medicine and Chemistry, respectively.[18][19] Foods containing vitamin C include citrus fruits, kiwifruit, guava, broccoli, Brussels sprouts, bell peppers and strawberries.[10] Prolonged storage or cooking may reduce vitamin C content in foods.[10]
Medical uses
Vitamin C has a definitive role in treating scurvy, which is a disease caused by vitamin C deficiency. Beyond that, a role for vitamin C as prevention or treatment for various diseases is disputed, with reviews reporting conflicting results. A 2012 Cochrane review reported no effect of vitamin C supplementation on overall mortality.[20] It is on the World Health Organization's List of Essential Medicines.[15]
Scurvy
The disease scurvy is caused by vitamin C deficiency and can be prevented and treated with vitamin C-containing foods or dietary supplements.[2][8] It takes at least a month of little to no vitamin C before symptoms occur.[21] Early symptoms are malaise and lethargy, progressing to shortness of breath, bone pain, bleeding gums, susceptibility to bruising, poor wound healing, and finally fever, convulsions and eventual death.[2] Until quite late in the disease the damage is reversible, as healthy collagen replaces the defective collagen with vitamin C repletion. Treatment can be orally or by intramuscular or intravenous injection.[2] Scurvy was known to Hippocrates in the classical era. The disease was shown to be prevented by citrus fruit in an early controlled trial by a Royal Navy surgeon, James Lind, in 1747, and from 1796 lemon juice was issued to all Royal Navy crewmen.[22][23]
Infection
Research in the common cold has been divided into effects on prevention, duration, and severity. A Cochrane review which looked at at least 200 mg/day concluded that vitamin C taken on a regular basis was not effective in prevention. Restricting analysis to trials that used at least 1000 mg/day also saw no prevention benefit. However, taking vitamin C on a regular basis did reduce the average duration by 8% in adults and 14% in children, and also reduced severity of colds.[11] A subsequent analysis in children found that vitamin C approached statistical significance for prevention and reduced the duration of upper respiratory tract infections.[24] A subset of trials in adults reported that supplementation reduced the incidence of colds by half in marathon runners, skiers, or soldiers in subarctic conditions.[11] Another subset of trials looked at therapeutic use, meaning that vitamin C was not started unless the people started to feel the beginnings of a cold. In these, vitamin C did not impact duration or severity.[11] An earlier review stated that vitamin C did not prevent colds, did reduce duration, did not reduce severity.[25] The authors of the Cochrane review concluded that:
The failure of vitamin C supplementation to reduce the incidence of colds in the general population indicates that routine vitamin C supplementation is not justified … Regular supplementation trials have shown that vitamin C reduces the duration of colds, but this was not replicated in the few therapeutic trials that have been carried out. Nevertheless, given the consistent effect of vitamin C on the duration and severity of colds in the regular supplementation studies, and the low cost and safety, it may be worthwhile for common cold patients to test on an individual basis whether therapeutic vitamin C is beneficial for them."[11]
Use of intravenous vitamin C has not been found to be useful in sepsis in 2022, with such use resulting in worse outcomes.[26]
Cancer
There are two questions of whether vitamin C has an impact on cancer. First, within the normal range of dietary intake without additional dietary supplementation, are people who consume more vitamin C at lower risk for developing cancer, and if so, does supplements have the same benefit? Second, for people diagnosed with cancer, will large amounts of vitamin C treat the cancer, reduce the side effects of other treatments, and so prolong survival and improve quality of life? A 2013 Cochrane review found no evidence that vitamin C supplementation reduces the risk of lung cancer in healthy people or those at high risk due to smoking or asbestos exposure.[27] A second meta-analysis found no effect on the risk of prostate cancer.[28] Two meta-analyses evaluated the effect of vitamin C supplementation on the risk of colorectal cancer. One found a weak association between vitamin C consumption and reduced risk, and the other found no effect from supplementation.[29][30] A 2011 meta-analysis failed to find support for the prevention of breast cancer with vitamin C supplementation,[31] but a second study concluded that vitamin C may be associated with increased survival in those already diagnosed.[32]
Under the rubric of orthomolecular medicine, "Intravenous vitamin C is a contentious adjunctive cancer therapy, widely used in naturopathic and integrative oncology settings." [33] With oral administration absorption efficiency decreases as amounts increase. Intravenous administration bypasses this.[34] Doing so makes it possible to achieve plasma concentrations of 5 to 10 millimoles/liter (mmol/L), which far exceed the approximately 0.2 mmol/L limit from oral consumption.[35] The theories of mechanism are contradictory. At high tissue concentrations ascorbic acid is described as acting as a pro-oxidant, generating hydrogen peroxide (H2O2) to kill tumor cells. The same literature claims that ascorbic acid acts as an antioxidant, thereby reducing the adverse effects of chemotherapy and radiation therapy.[33][34] Research continues in this field, but a 2014 review concluded: "Currently, the use of high-dose intravenous vitamin C [as an anticancer agent] cannot be recommended outside of a clinical trial."[36] A 2015 review added: "There is no high-quality evidence to suggest that ascorbate supplementation in cancer patients either enhances the antitumor effects of chemotherapy or reduces its toxicity. Evidence for ascorbate's anti-tumor effects was limited to case reports and observational and uncontrolled studies."[37]
Heart disease
There is no evidence as of 2017 that taking vitamin C decreases cardiovascular disease.[38] One 2013 review found no evidence that vitamin C supplementation reduces the risk of myocardial infarction, stroke, cardiovascular mortality, or all-cause mortality.[12] Another 2013 review found an association between higher circulating vitamin C levels or dietary vitamin C and a lower risk of stroke.[39]
Brain function
A 2017 systematic review found lower vitamin C concentrations in people with cognitive impairment, including Alzheimer's disease and dementia, compared to people with normal cognition.[40] The cognitive testing, however, relied on the Mini-Mental State Examination, which is only a general test of cognition, indicating an overall low quality of research assessing the potential importance of vitamin C on cognition in normal and impaired people.[40] A review of nutrient status in people with Alzheimer's disease reported low plasma vitamin C, but also low blood levels of folate, vitamin B12, and vitamin E.[41]
Studies examining the effects of vitamin C intake on the risk of Alzheimer's disease have reached conflicting conclusions.[42][43] Maintaining a healthy dietary intake is probably more important than supplementation for achieving any potential benefit.[44]
Other diseases
A 2010 review found no role for vitamin C supplementation in the treatment of rheumatoid arthritis.[45] Vitamin C supplementation does not prevent or slow the progression of age-related cataract.[46]
Dosage
The defined daily dose is 200 mg by mouth or injection.[5] For the treatment of scurvy in those 12 years and older 500 mg twice per day for at least two weeks is recommended.[1] For younger children 100 to 250 mg twice per day is recommended.[1] For prevention of scurvy the dose is 50 mg once per day.[1]
Side effects
Vitamin C is a water-soluble vitamin,[47] with dietary excesses not absorbed, and excesses in the blood rapidly excreted in the urine, so it exhibits remarkably low acute toxicity.[9] More than two to three grams may cause indigestion, particularly when taken on an empty stomach. However, taking vitamin C in the form of sodium ascorbate and calcium ascorbate may minimize this effect.[48] Other symptoms reported for large doses include nausea, abdominal cramps and diarrhea. These effects are attributed to the osmotic effect of unabsorbed vitamin C passing through the intestine.[8] In theory, high vitamin C intake may cause excessive absorption of iron. A summary of reviews of supplementation in healthy subjects did not report this problem, but left as untested the possibility that individuals with hereditary hemochromatosis might be adversely affected.[8]
There is a longstanding belief among the mainstream medical community that vitamin C increases risk of kidney stones.[49] "Reports of kidney stone formation associated with excess ascorbic acid intake are limited to individuals with renal disease".[8] Reviews state that "data from epidemiological studies do not support an association between excess ascorbic acid intake and kidney stone formation in apparently healthy individuals",[8][50] although one large, multi-year trial did report a nearly two-fold increase in kidney stones in men who regularly consumed a vitamin C supplement.[51]
Biology
Significance
Vitamin C is an essential nutrient for certain animals including humans. The term vitamin C encompasses several vitamers that have vitamin C activity in animals. Ascorbate salts such as sodium ascorbate and calcium ascorbate are used in some dietary supplements. These release ascorbate upon digestion. Ascorbate and ascorbic acid are both naturally present in the body, since the forms interconvert according to pH. Oxidized forms of the molecule such as dehydroascorbic acid are converted back to ascorbic acid by reducing agents.[8][52]
Vitamin C functions as a cofactor in many enzymatic reactions in animals (and humans) that mediate a variety of essential biological functions, including wound healing and collagen synthesis. In humans, vitamin C deficiency leads to impaired collagen synthesis, contributing to the more severe symptoms of scurvy.[8] Another biochemical role of vitamin C is to act as an antioxidant (a reducing agent) by donating electrons to various enzymatic and non-enzymatic reactions.[8] Doing so converts vitamin C to an oxidized state - either as semidehydroascorbic acid or dehydroascorbic acid. These compounds can be restored to a reduced state by glutathione and NADPH-dependent enzymatic mechanisms.[53][54][55]
In plants, vitamin C is a substrate for ascorbate peroxidase. This enzyme utilizes ascorbate to neutralize excess hydrogen peroxide (H2O2) by converting it to water (H2O) and oxygen.[9][52][56]
Vitamin C distributes readily in high concentrations into immune cells, has antimicrobial and natural killer cell activities, promotes lymphocyte proliferation, and is consumed quickly during infections, effects indicating a prominent role in immune system regulation.[57] The European Food Safety Authority found a cause and effect relationship exists between the dietary intake of vitamin C and functioning of a normal immune system in adults and in children under three years of age.[58][59]
Deficiency
Serum levels are considered saturated, achieved by consuming supplement amounts above the Recommended Dietary Allowance, at >65 μmol/L (1.1 mg/dL). Adequate defined as ≥50 μmol/L, hypovitaminosis at ≤23 μmol/L and deficient at ≤11.4 μmol/L.[60][61] For people ≥20 years old, data from the U.S. 2003-04 NHANES survey showed mean and median serum concentrations of 49.0 and 54.4 μmol/L, respectively. The percent of people reported as deficient was 7.1%.[61]
Scurvy is a disease resulting from a deficiency of vitamin C. Without this vitamin, collagen made by the body is too unstable to perform its function and several other enzymes in the body do not operate correctly.[9] Scurvy is characterized by spots on and bleeding under the skin, spongy gums, 'corkscrew' hair growth, and poor wound healing. The skin lesions are most abundant on the thighs and legs, and a person with the ailment looks pale, feels depressed, and is partially immobilized. In advanced scurvy there are open, suppurating wounds, loss of teeth, bone abnormalities and, eventually, death.[62] The human body can store only a certain amount of vitamin C,[47] and so the body stores are depleted if fresh supplies are not consumed.
Notable human dietary studies of experimentally induced scurvy were conducted on conscientious objectors during World War II in Britain and on Iowa state prisoners in the late 1960s to the 1980s. Men in the prison study developed the first signs of scurvy about four weeks after starting the vitamin C-free diet, whereas in the earlier British study, six to eight months were required, possibly due to the pre-loading of this group with a 70 mg/day supplement for six weeks before the scorbutic diet was fed. Men in both studies had blood levels of ascorbic acid too low to be accurately measured by the time they developed signs of scurvy. These studies both reported that all obvious symptoms of scurvy could be completely reversed by supplementation of only 10 mg a day.[21][63]
Diet
Recommended levels
US vitamin C recommendations (mg per day)[8] | |
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RDA (children ages 1–3 years) | 15 |
RDA (children ages 4–8 years) | 25 |
RDA (children ages 9–13 years) | 45 |
RDA (girls ages 14–18 years) | 65 |
RDA (boys ages 14–18 years) | 75 |
RDA (adult female) | 75 |
RDA (adult male) | 90 |
RDA (pregnancy) | 85 |
RDA (lactation) | 120 |
UL (adult female) | 2,000 |
UL (adult male) | 2,000 |
Recommendations for vitamin C intake by adults have been set by various national agencies:
- 40 milligrams per day: India National Institute of Nutrition, Hyderabad[64]
- 45 milligrams per day or 300 milligrams per week: the World Health Organization[65]
- 80 milligrams per day: the European Commission Council on nutrition labeling[66]
- 90 mg/day (males) and 75 mg/day (females): Health Canada 2007[67]
- 90 mg/day (males) and 75 mg/day (females): United States National Academy of Sciences.[8]
- 100 milligrams per day: Japan National Institute of Health and Nutrition.[68]
- 110 mg/day (males) and 95 mg/day (females): European Food Safety Authority[69]
In 2000 the North American Dietary Reference Intake chapter on vitamin C updated the Recommended Dietary Allowance (RDA) to 90 milligrams per day for adult men and 75 mg/day for adult women, and set a Tolerable upper intake level (UL) for adults of 2,000 mg/day.[8] The table shows RDAs for the United States and Canada for children, and for pregnant and lactating women.[8] For the European Union, the EFSA set higher recommendations for adults, and also for children: 20 mg/day for ages 1–3, 30 mg/day for ages 4–6, 45 mg/day for ages 7–10, 70 mg/day for ages 11–14, 100 mg/day for males ages 15–17, 90 mg/day for females ages 15–17. For pregnancy 100 mg/day; for lactation 155 mg/day.[69] India, on the other hand, has set recommendations much lower: 40 mg/day for ages 1 through adult, 60 mg/day for pregnancy, and 80 mg/day for lactation.[64] Clearly, there is not consensus among countries.
Cigarette smokers and people exposed to secondhand smoke have lower serum vitamin C levels than nonsmokers.[61] The thinking is that inhalation of smoke causes oxidative damage, depleting this antioxidant vitamin.[8][68] The U.S. Institute of Medicine estimated that smokers need 35 mg more vitamin C per day than nonsmokers, but did not formally establish a higher RDA for smokers.[8] One meta-analysis showed an inverse relationship between vitamin C intake and lung cancer, although it concluded that more research is needed to confirm this observation.[70]
The U.S. National Center for Health Statistics conducts biannual National Health and Nutrition Examination Survey (NHANES) to assess the health and nutritional status of adults and children in the United States. Some results are reported as What We Eat In America. The 2013-2014 survey reported that for adults ages 20 years and older, men consumed on average 83.3 mg/d and women 75.1 mg/d. This means that half the women and more than half the men are not consuming the RDA for vitamin C.[71] The same survey stated that about 30% of adults reported they consumed a vitamin C dietary supplement or a multi-vitamin/mineral supplement that included vitamin C, and that for these people total consumption was between 300 and 400 mg/d.[72]
In 2000 the Institute of Medicine of the U.S. National Academy of Sciences set a Tolerable upper intake level (UL) for adults of 2,000 mg/day. The amount was chosen because human trials had reported diarrhea and other gastrointestinal disturbances at intakes of greater than 3,000 mg/day. This was the Lowest-Observed-Adverse-Effect Level (LOAEL), meaning that other adverse effects were observed at higher intakes.[8] The European Food Safety Authority (EFSA) reviewed the safety question in 2006 and reached the conclusion that there was not sufficient evidence to set a UL for vitamin C.[73] The Japan National Institute of Health and Nutrition reviewed the same question in 2010 and also reached the conclusion that there was not sufficient evidence to set a UL.[68]
Food labeling
For U.S. food and dietary supplement labeling purposes, the amount in a serving is expressed as a percent of Daily Value (%DV). For vitamin C labeling purposes, 100% of the Daily Value was 60 mg, but as of May 27, 2016 it was revised to 90 mg to bring it into agreement with the RDA.[74][75] Compliance with the updated labeling regulations was required by 1 January 2020, for manufacturers with $10 million or more in annual food sales, and by 1 January 2021 for manufacturers with less than $10 million in annual food sales.[76][77][78] During the first six months following the 1 January 2020 compliance date, the FDA plans to work cooperatively with manufacturers to meet the new Nutrition Facts label requirements and will not focus on enforcement actions regarding these requirements during that time.[76] A table of the old and new adult Daily Values is provided at Reference Daily Intake.
European Union regulations require that labels declare energy, protein, fat, saturated fat, carbohydrates, sugars, and salt. Voluntary nutrients may be shown if present in significant amounts. Instead of Daily Values, amounts are shown as percent of Reference Intakes (RIs). For vitamin C, 100% RI was set at 80 mg in 2011.[79]
Sources
The richest natural sources of vitamin C are fruits and vegetables.[9] The vitamin is the most widely taken nutritional supplement and is available in a variety of forms,[9] including tablets, drink mixes, and in capsules.
Plant sources
While plant foods are generally a good source of vitamin C, the amount in foods of plant origin depends on the variety of the plant, soil condition, climate where it grew, length of time since it was picked, storage conditions, and method of preparation.[80][81] The following table is approximate and shows the relative abundance in different raw plant sources.[82][83] As some plants were analyzed fresh while others were dried (thus, artificially increasing concentration of individual constituents like vitamin C), the data are subject to potential variation and difficulties for comparison. The amount is given in milligrams per 100 grams of the edible portion of the fruit or vegetable:
Plant source[84] | Amount (mg / 100g) |
---|---|
Kakadu plum | 1000–5300[85] |
Camu camu | 2800[83][86] |
Acerola | 1677[87] |
Seabuckthorn | 695 |
Indian gooseberry | 445[88][89] |
Rose hip | 426 |
Guava | 228 |
Blackcurrant | 200 |
Yellow bell pepper/capsicum | 183 |
Red bell pepper/capsicum | 128 |
Kale | 120 |
Plant source[84] | Amount (mg / 100g) |
---|---|
Kiwifruit, broccoli | 90 |
Green bell pepper/capsicum | 80 |
Loganberry, redcurrant, Brussels sprouts | 80 |
Cloudberry, elderberry | 60 |
Papaya, strawberry | 60 |
Orange, lemon | 53 |
Pineapple, cauliflower | 48 |
Cantaloupe | 40 |
Grapefruit, raspberry | 30 |
Passion fruit, spinach | 30 |
Cabbage, lime | 30 |
Plant source[84] | Amount (mg / 100g) |
---|---|
Mango | 28 |
Blackberry | 21 |
Potato, honeydew melon | 20 |
Tomato | 14 |
Cranberry | 13 |
Blueberry, grape | 10 |
Apricot, plum, watermelon | 10 |
Avocado | 8.8 |
Onion | 7.4 |
Cherry, peach | 7 |
Carrot, apple, asparagus | 6 |
Animal sources
Animal-sourced foods do not provide much vitamin C, and what there is, is largely destroyed by the heat of cooking. For example, raw chicken liver contains 17.9 mg/100 g, but fried, the content is reduced to 2.7 mg/100 g. Chicken eggs contain no vitamin C, raw or cooked.[84] Vitamin C is present in human breast milk at 5.0 mg/100 g and 6.1 mg/100 g in one tested sample of infant formula, but cow's milk contains only 1.0 mg/ 100 g.[90]
Food preparation
Vitamin C chemically decomposes under certain conditions, many of which may occur during the cooking of food. Vitamin C concentrations in various food substances decrease with time in proportion to the temperature at which they are stored.[91] Cooking can reduce the vitamin C content of vegetables by around 60%, possibly due to increased enzymatic destruction.[92] Longer cooking times may add to this effect.[93]
Another cause of vitamin C loss from food is leaching, which transfers vitamin C to the cooking water, which is decanted and not consumed. Broccoli may retain vitamin C during cooking or storage more than most vegetables.[94]
Supplements
Vitamin C dietary supplements are available as tablets, capsules, drink mix packets, in multi-vitamin/mineral formulations, in antioxidant formulations, and as crystalline powder.[2] Vitamin C is also added to some fruit juices and juice drinks. Tablet and capsule content ranges from 25 mg to 1500 mg per serving. The most commonly used supplement compounds are ascorbic acid, sodium ascorbate and calcium ascorbate.[2] Vitamin C molecules can also be bound to the fatty acid palmitate, creating ascorbyl palmitate, or else incorporated into liposomes.[95]
Food fortification
In 2014, the Canadian Food Inspection Agency evaluated the effect of fortification of foods with ascorbate in the guidance document, Foods to Which Vitamins, Mineral Nutrients and Amino Acids May or Must be Added.[96] Voluntary and mandatory fortification was described for various classes of foods. Among foods classified for mandatory fortification with vitamin C were fruit-flavored drinks, mixes, and concentrates, foods for a low-energy diet, meal replacement products, and evaporated milk.[96]
Food additives
Ascorbic acid and some of its salts and esters are common additives added to various foods, such as canned fruits, mostly to retard oxidation and enzymatic browning.[97] The relevant European food additive E numbers are:
- E300 ascorbic acid (approved for use as a food additive in the EU,[98] U.S.[99] and Australia and New Zealand)[100]
- E301 sodium ascorbate (approved for use as a food additive in the EU,[98] U.S.[101] and Australia and New Zealand)[100]
- E302 calcium ascorbate (approved for use as a food additive in the EU,[98] U.S.[99] and Australia and New Zealand)[100]
- E303 potassium ascorbate (approved in Australia and New Zealand,[100] but not in U.S.)
- E304 fatty acid esters of ascorbic acid such as ascorbyl palmitate (approved for use as a food additive in the EU,[98] U.S.[99] and Australia and New Zealand)[100]
Pharmacology
Pharmacodynamics
Vitamin C – specifically, in the form of ascorbate – performs numerous physiological functions in the human body by serving as an enzyme substrate and/or cofactor and an electron donor. These functions include the synthesis of collagen, carnitine, and neurotransmitters; the synthesis and catabolism of tyrosine; and the metabolism of microsome.[55] During biosynthesis, ascorbate acts as a reducing agent, donating electrons and preventing oxidation to keep iron and copper atoms in their reduced states.
Vitamin C functions as a cofactor for the following enzymes:
- Three groups of enzymes (prolyl-3-hydroxylases, prolyl-4-hydroxylases, and lysyl hydroxylases) that are required for the hydroxylation of proline and lysine in the synthesis of collagen.[102][103][104] These reactions add hydroxyl groups to the amino acids proline or lysine in the collagen molecule via prolyl hydroxylase and lysyl hydroxylase, both requiring vitamin C as a cofactor. The role of vitamin C as a cofactor is to oxidize prolyl hydroxylase and lysyl hydroxylase from Fe2+ to Fe3+ and to reduce it from Fe3+ to Fe2+. Hydroxylation allows the collagen molecule to assume its triple helix structure, and thus vitamin C is essential to the development and maintenance of scar tissue, blood vessels, and cartilage.[47]
- Two enzymes (ε-N-trimethyl-L-lysine hydroxylase and γ-butyrobetaine hydroxylase) that are necessary for synthesis of carnitine.[105] Carnitine is essential for the transport of fatty acids into mitochondria for ATP generation.
- Hypoxia-inducible factor-proline dioxygenase enzymes (isoforms: EGLN1, EGLN2, and EGLN3)[105][106]
- Dopamine beta-hydroxylase participates in the biosynthesis of norepinephrine from dopamine.[107][108]
- Peptidylglycine alpha-amidating monooxygenase amidates peptide hormones by removing the glyoxylate residue from their c-terminal glycine residues. This increases peptide hormone stability and activity.[109][110]
Pharmacokinetics
Absorption
From the U.S. National Institutes of Health: [In humans] "Approximately 70%–90% of vitamin C is absorbed at moderate intakes of 30–180 mg/day. However, at doses above 1,000 mg/day, absorption falls to less than 50%."[10] It is transported through the intestine via both glucose-sensitive and glucose-insensitive mechanisms, so the presence of large quantities of sugar in the intestine can slow absorption.[111]
Ascorbic acid is absorbed in the body by both active transport and simple diffusion. Sodium-Dependent Active Transport—Sodium-Ascorbate Co-Transporters (SVCTs) and Hexose transporters (GLUTs)—are the two transporter proteins required for active absorption. SVCT1 and SVCT2 import the reduced form of ascorbate across plasma membranes.[112] GLUT1 and GLUT3 are glucose transporters, and transfer only the dehydroascorbic acid (DHA) form of vitamin C.[113] Although dehydroascorbic acid is absorbed in higher rate than ascorbate, the amount of dehydroascorbic acid found in plasma and tissues under normal conditions is low, as cells rapidly reduce dehydroascorbic acid to ascorbate.[114]
Transport
SVCTs appear to be the predominant system for vitamin C transport in the body,[112] the notable exception being red blood cells, which lose SVCT proteins during maturation.[115] In both vitamin C synthesizers (example: rat) and non-synthesizers (example: human) cells with few exceptions maintain ascorbic acid concentrations much higher than the approximately 50 micromoles/liter (µmol/L) found in plasma. For example, the ascorbic acid content of pituitary and adrenal glands can exceed 2,000 µmol/L, and muscle is at 200-300 µmol/L.[116] The known coenzymatic functions of ascorbic acid do not require such high concentrations, so there may be other, as yet unknown functions. Consequences of all this organ content is that plasma vitamin C is not a good indicator of whole-body status, and people may vary in the amount of time needed to show symptoms of deficiency when consuming a diet very low in vitamin C.[116]
Excretion
Excretion can be as ascorbic acid, via urine. In humans, during times of low dietary intake, vitamin C is reabsorbed by the kidneys rather than excreted. Only when plasma concentrations are 1.4 mg/dL or higher does re-absorption decline and the excess amounts pass freely into the urine. This salvage process delays onset of deficiency.[117] Ascorbic acid also converts (reversibly) to dehydroascorbate (DHA) and from that compound non-reversibly to 2,3-diketogluonate and then oxalate. These three compounds are also excreted via urine. Humans are better than guinea pigs at converting DHA back to ascorbate, and thus take much longer to become vitamin C deficient.[118]
Chemistry
The name "vitamin C" always refers to the l-enantiomer of ascorbic acid and its oxidized forms, such as dehydroascorbate (DHA). Therefore, unless written otherwise, "ascorbate" and "ascorbic acid" refer in the nutritional literature to l-ascorbate and l-ascorbic acid respectively. Ascorbic acid is a weak sugar acid structurally related to glucose. In biological systems, ascorbic acid can be found only at low pH, but in solutions above pH 5 is predominantly found in the ionized form, ascorbate. All of these molecules have vitamin C activity and thus are used synonymously with vitamin C, unless otherwise specified.
Numerous analytical methods have been developed for ascorbic acid detection. For example, vitamin C content of a food sample such as fruit juice can be calculated by measuring the volume of the sample required to decolorize a solution of dichlorophenolindophenol (DCPIP) and then calibrating the results by comparison with a known concentration of vitamin C.[119][120]
Testing
Simple tests are available to measure the levels of vitamin C in urine and serum.[60][61] These better reflect recent dietary intake rather than total body content.[8] It has been observed that while serum concentrations follow a circadian rhythm or reflect short-term dietary impact, content within cells or tissues is more stable and can give a better view of the availability of ascorbate within the entire organism. However, very few hospital laboratories are adequately equipped and trained to carry out such detailed analyses.[121][122]
Biosynthesis
The vast majority of animals and plants are able to synthesize vitamin C, through a sequence of enzyme-driven steps, which convert monosaccharides to vitamin C. Yeasts do not make l-ascorbic acid but rather its stereoisomer, erythorbic acid.[123] In plants, this is accomplished through the conversion of mannose or galactose to ascorbic acid.[124][125] In animals, the starting material is glucose. In some species that synthesize ascorbate in the liver (including mammals and perching birds), the glucose is extracted from glycogen; ascorbate synthesis is a glycogenolysis-dependent process.[126] In humans and in animals that cannot synthesize vitamin C, the enzyme l-gulonolactone oxidase (GULO), that catalyses the last step in the biosynthesis, is highly mutated and non-functional.[127][128][129][130]
Synthesis in animals
There is some information on serum vitamin C concentrations maintained in animal species that are able to synthesize vitamin C. One study of several breeds of dogs reported an average of 35.9 μmol/L.[131] A report on goats, sheep and cattle reported ranges of 100–110, 265-270 and 160-350 μmol/L, respectively.[132]
The biosynthesis of ascorbic acid in vertebrates starts with the formation of UDP-glucuronic acid. UDP-glucuronic acid is formed when UDP-glucose undergoes two oxidations catalyzed by the enzyme UDP-glucose 6-dehydrogenase. UDP-glucose 6-dehydrogenase uses the co-factor NAD+ as the electron acceptor. The transferase UDP-glucuronate pyrophosphorylase removes a UMP and glucuronokinase, with the cofactor ADP, removes the final phosphate leading to d-glucuronic acid. The aldehyde group of this compound is reduced to a primary alcohol using the enzyme glucuronate reductase and the cofactor NADPH, yielding l-gulonic acid. This is followed by lactone formation—utilizing the hydrolase gluconolactonase—between the carbonyl on C1 and hydroxyl group on C4. l-Gulonolactone then reacts with oxygen, catalyzed by the enzyme l-gulonolactone oxidase (which is nonfunctional in humans and other Haplorrhini primates; see Unitary pseudogenes) and the cofactor FAD+. This reaction produces 2-oxogulonolactone (2-keto-gulonolactone), which spontaneously undergoes enolization to form ascorbic acid.[133][134] [118]
Some mammals have lost the ability to synthesize vitamin C, including simians and tarsiers, which together make up one of two major primate suborders, Haplorrhini. This group includes humans. The other more primitive primates (Strepsirrhini) have the ability to make vitamin C. Synthesis does not occur in most bats[127] nor in species in the rodent family Caviidae, that includes guinea pigs and capybaras, but does occur in other rodents, including rats and mice.[135]
Reptiles and older orders of birds make ascorbic acid in their kidneys. Recent orders of birds and most mammals make ascorbic acid in their liver.[125] A number of species of passerine birds also do not synthesize, but not all of them, and those that do not are not clearly related; there is a theory that the ability was lost separately a number of times in birds.[136] In particular, the ability to synthesize vitamin C is presumed to have been lost and then later re-acquired in at least two cases.[137] The ability to synthesize vitamin C has also been lost in about 96% of fish (the teleosts).[136]
Most tested families of bats (order Chiroptera), including major insect and fruit-eating bat families, cannot synthesize vitamin C. A trace of gulonolactone oxidase was detected in only 1 of 34 bat species tested, across the range of 6 families of bats tested.[138] There are at least two species of bats, frugivorous bat (Rousettus leschenaultii) and insectivorous bat (Hipposideros armiger), that retain (or regained) their ability of vitamin C production.[139][140]
Some of these species (including humans) are able to make do with the lower amounts available from their diets by recycling oxidised vitamin C.[141]
On a milligram consumed per kilogram of body weight basis, most simian species consume the vitamin in amounts 10 to 20 times higher than what is recommended by governments for humans.[142] This discrepancy constitutes much of the basis of the controversy on current recommended dietary allowances. It is countered by arguments that humans are very good at conserving dietary vitamin C, and are able to maintain blood levels of vitamin C comparable with simians on a far smaller dietary intake, perhaps by recycling oxidized vitamin C.[141]
Plant pathways
There are many different biosynthesis pathways for ascorbic acid in plants. Most of these pathways are derived from products found in glycolysis and other pathways. For example, one pathway goes through the plant cell wall polymers.[127] The plant ascorbic acid biosynthesis pathway most principal seems to be l-galactose. l-Galactose reacts with the enzyme l-galactose dehydrogenase, whereby the lactone ring opens and forms again but with lactone between the carbonyl on C1 and hydroxyl group on C4, resulting in l-galactonolactone.[134] l-Galactonolactone then reacts with the mitochondrial flavoenzyme l-galactonolactone dehydrogenase.[143] to produce ascorbic acid.[134] l-Ascorbic acid has a negative feedback on l-galactose dehydrogenase in spinach.[144] Ascorbic acid efflux by embryo of dicots plants is a well-established mechanism of iron reduction, and a step obligatory for iron uptake.[lower-alpha 1]
All plants synthesize ascorbic acid. Ascorbic acid functions as a cofactor for enzymes involved in photosynthesis, synthesis of plant hormones, as an antioxidant and also regenerator of other antioxidants.[146] Plants use multiple pathways to synthesize vitamin C. The major pathway starts with glucose, fructose or mannose (all simple sugars) and proceeds to L-galactose, L-galactonolactone and ascorbic acid.[146][147] There is feedback regulation in place, in that the presence of ascorbic acid inhibits enzymes in the synthesis pathway.[148] This process follows a diurnal rhythm, so that enzyme expression peaks in the morning to support biosynthesis later on when mid-day sunlight intensity demands high ascorbic acid concentrations.[147] Minor pathways may be specific to certain parts of plants; these can be either identical to the vertebrate pathway (including the GLO enzyme), or start with inositol and get to ascorbic acid via L-galactonic acid to L-galactonolactone.[146]
Evolution
Ascorbic acid is a common enzymatic cofactor in mammals used in the synthesis of collagen, as well as a powerful reducing agent capable of rapidly scavenging a number of reactive oxygen species (ROS). Given that ascorbate has these important functions, it is surprising that the ability to synthesize this molecule has not always been conserved. In fact, anthropoid primates, Cavia porcellus (guinea pigs), teleost fishes, most bats, and some Passeriform birds have all independently lost the ability to internally synthesize Vitamin C in either the kidney or the liver.[149][137] In all of the cases where genomic analysis was done on an ascorbic acid auxotroph, the origin of the change was found to be a result of loss-of-function mutations in the gene that codes for L-Gulono-γ-lactone oxidase, the enzyme that catalyzes the last step of the ascorbic acid pathway outlined above.[150] One explanation for the repeated loss of the ability to synthesize vitamin C is that it was the result of genetic drift; assuming that the diet was rich in vitamin C, natural selection would not act to preserve it.[151][152]
In the case of the simians, it is thought that the loss of the ability to make vitamin C may have occurred much farther back in evolutionary history than the emergence of humans or even apes, since it evidently occurred soon after the appearance of the first primates, yet sometime after the split of early primates into the two major suborders Haplorrhini (which cannot make vitamin C) and its sister suborder of non-tarsier prosimians, the Strepsirrhini ("wet-nosed" primates), which retained the ability to make vitamin C.[153] According to molecular clock dating, these two suborder primate branches parted ways about 63 to 60 million years ago.[154] Approximately three to five million years later (58 million years ago), only a short time afterward from an evolutionary perspective, the infraorder Tarsiiformes, whose only remaining family is that of the tarsier (Tarsiidae), branched off from the other haplorrhines.[155][156] Since tarsiers also cannot make vitamin C, this implies the mutation had already occurred, and thus must have occurred between these two marker points (63 to 58 million years ago).[157]
It has also been noted that the loss of the ability to synthesize ascorbate strikingly parallels the inability to break down uric acid, also a characteristic of primates. Uric acid and ascorbate are both strong reducing agents. This has led to the suggestion that, in higher primates, uric acid has taken over some of the functions of ascorbate.[158]
History
Scurvy at sea
In the 1497 expedition of Vasco da Gama, the curative effects of citrus fruit were known.[159][160] Later, the Portuguese planted fruit trees and vegetables in Saint Helena, a stopping point for homebound voyages from Asia, which sustained passing ships.[161]
Authorities occasionally recommended plant food to prevent scurvy during long sea voyages. John Woodall, the first surgeon to the British East India Company, recommended the preventive and curative use of lemon juice in his 1617 book, The Surgeon's Mate.[162] In 1734, the Dutch writer Johann Bachstrom gave the firm opinion that "scurvy is solely owing to a total abstinence from fresh vegetable food, and greens."[163][164]
Scurvy had long been a principal killer of sailors during the long sea voyages.[165] According to Jonathan Lamb, "In 1499, Vasco da Gama lost 116 of his crew of 170; In 1520, Magellan lost 208 out of 230;...all mainly to scurvy."[166]
The first attempt to give scientific basis for the cause of this disease was by a ship's surgeon in the Royal Navy, James Lind. While at sea in May 1747, Lind provided some crew members with two oranges and one lemon per day, in addition to normal rations, while others continued on cider, vinegar, sulfuric acid or seawater, along with their normal rations, in one of the world's first controlled experiments.[23] The results showed that citrus fruits prevented the disease. Lind published his work in 1753 in his Treatise on the Scurvy.[22][167]
Fresh fruit was expensive to keep on board, whereas boiling it down to juice allowed easy storage but destroyed the vitamin (especially if boiled in copper kettles).[93] It was 1796 before the British navy adopted lemon juice as standard issue at sea. In 1845, ships in the West Indies were provided with lime juice instead, and in 1860 lime juice was used throughout the Royal Navy, giving rise to the American use of the nickname "limey" for the British.[23] Captain James Cook had previously demonstrated the advantages of carrying "Sour krout" on board, by taking his crews to the Hawaiian Islands without losing any of his men to scurvy.[168] For this, the British Admiralty awarded him a medal.
The name antiscorbutic was used in the eighteenth and nineteenth centuries for foods known to prevent scurvy. These foods included lemons, limes, oranges, sauerkraut, cabbage, malt, and portable soup.[169] In 1928, the Canadian Arctic anthropologist Vilhjalmur Stefansson showed that the Inuit avoid scurvy on a diet of largely raw meat. Later studies on traditional food diets of the Yukon First Nations, Dene, Inuit, and Métis of Northern Canada showed that their daily intake of vitamin C averaged between 52 and 62 mg/day,[170] comparable with the Estimated Average Requirement.[8]
Discovery
Vitamin C was discovered in 1912, isolated in 1928 and synthesized in 1933, making it the first vitamin to be synthesized.[14] Shortly thereafter Tadeus Reichstein succeeded in synthesizing the vitamin in bulk by what is now called the Reichstein process.[172] This made possible the inexpensive mass-production of vitamin C. In 1934 Hoffmann–La Roche trademarked synthetic vitamin C under the brand name Redoxon[173] and began to market it as a dietary supplement.[lower-alpha 2]
In 1907 a laboratory animal model which would help to identify the antiscorbutic factor was discovered by the Norwegian physicians Axel Holst and Theodor Frølich, who when studying shipboard beriberi, fed guinea pigs their test diet of grains and flour and were surprised when scurvy resulted instead of beriberi. By luck, this species did not make its own vitamin C, whereas mice and rats do.[175] In 1912, the Polish biochemist Casimir Funk developed the concept of vitamins. One of these was thought to be the anti-scorbutic factor. In 1928, this was referred to as "water-soluble C," although its chemical structure had not been determined.[176]
From 1928 to 1932, Albert Szent-Györgyi and Joseph L. Svirbely's Hungarian team, and Charles Glen King's American team, identified the anti-scorbutic factor. Szent-Györgyi isolated hexuronic acid from animal adrenal glands, and suspected it to be the antiscorbutic factor.[177] In late 1931, Szent-Györgyi gave Svirbely the last of his adrenal-derived hexuronic acid with the suggestion that it might be the anti-scorbutic factor. By the spring of 1932, King's laboratory had proven this, but published the result without giving Szent-Györgyi credit for it. This led to a bitter dispute over priority.[177] In 1933, Walter Norman Haworth chemically identified the vitamin as l-hexuronic acid, proving this by synthesis in 1933.[178][179][180][181] Haworth and Szent-Györgyi proposed that L-hexuronic acid be named a-scorbic acid, and chemically l-ascorbic acid, in honor of its activity against scurvy.[181][14] The term's etymology is from Latin, "a-" meaning away, or off from, while -scorbic is from Medieval Latin scorbuticus (pertaining to scurvy), cognate with Old Norse skyrbjugr, French scorbut, Dutch scheurbuik and Low German scharbock.[182] Partly for this discovery, Szent-Györgyi was awarded the 1937 Nobel Prize in Medicine,[183] and Haworth shared that year's Nobel Prize in Chemistry.[19]
In 1957, J.J. Burns showed that some mammals are susceptible to scurvy as their liver does not produce the enzyme l-gulonolactone oxidase, the last of the chain of four enzymes that synthesize vitamin C.[184][185] American biochemist Irwin Stone was the first to exploit vitamin C for its food preservative properties. He later developed the theory that humans possess a mutated form of the l-gulonolactone oxidase coding gene.[186]
In 2008, researchers at the University of Montpellier discovered that in humans and other primates the red blood cells have evolved a mechanism to more efficiently utilize the vitamin C present in the body by recycling oxidized l-dehydroascorbic acid (DHA) back into ascorbic acid for reuse by the body. The mechanism was not found to be present in mammals that synthesize their own vitamin C.[141]
Large doses
Vitamin C megadosage is a term describing the consumption or injection of vitamin C in doses comparable to or higher than the amounts produced by the livers of mammals which are able to synthesize vitamin C. The theory behind this, although not the actual term, was described in 1970 in an article by Linus Pauling. Briefly, his position was that for optimal health, humans should be consuming at least 2,300 mg/day to compensate for the inability to synthesize vitamin C. The recommendation also fell into the consumption range for gorillas - a non-synthesizing near-relative to humans.[187] A second argument for high intake is that serum ascorbic acid concentrations increase as intake increases until it plateaus at about 190 to 200 micromoles per liter (µmol/L) once consumption exceeds 1,250 milligrams.[188] As noted, government recommendations are a range of 40 to 110 mg/day and normal plasma is approximately 50 µmol/L, so 'normal' is about 25% of what can be achieved when oral consumption is in the proposed megadose range.
Pauling popularized the concept of high dose vitamin C as prevention and treatment of the common cold in 1970. A few years later he proposed that vitamin C would prevent cardiovascular disease, and that 10 grams/day, initially (10 days) administered intravenously and thereafter orally, would cure late-stage cancer.[189] Mega-dosing with ascorbic acid has other champions, among them chemist Irwin Stone and the controversial Matthias Rath and Patrick Holford, who both have been accused of making unsubstantiated treatment claims for treating cancer and HIV infection.
The mega-dosing theory is to a large degree discredited. Modest benefits are demonstrated for the common cold. Benefits are not superior when supplement intakes of more than 1,000 mg/day are compared to intakes between 200 and 1,000 mg/day, and so not limited to the mega-dose range.[190][191] The theory that large amounts of intravenous ascorbic acid can be used to treat late-stage cancer is - some forty years after Pauling's seminal paper - still considered unproven and still in need of high quality research.[36][37] However, a lack of conclusive evidence has not stopped individual physicians from prescribing intravenous ascorbic acid to thousands of people with cancer.[37]
Society and culture
In February 2011, the Swiss Post issued a postage stamp bearing a depiction of a model of a molecule of vitamin C to mark the International Year of Chemistry.[192]
Cost
In the U.S. the daily cost of vitamin C is about $1.71 for 50 ml.[193]
-
Costs (USA)
-
Prescriptions (USA)
Industrial production
Vitamin C is produced from glucose by two main routes. The Reichstein process, developed in the 1930s, uses a single pre-fermentation followed by a purely chemical route. The modern two-step fermentation process, originally developed in China in the 1960s, uses additional fermentation to replace part of the later chemical stages. The Reichstein process and the modern two-step fermentation processes use sorbitol as the starting material and convert it to sorbose using fermentation. The modern two-step fermentation process then converts sorbose to 2-keto-l-gulonic acid (KGA) through another fermentation step, avoiding an extra intermediate. Both processes yield approximately 60% vitamin C from the glucose feed.[194]
In 2017, China produced about 95% of the world supply of ascorbic acid (vitamin C),[195] which is China's most exported vitamin, having total revenue of US$880 million in 2017.[196] Due to pressure on Chinese industry to discontinue burning coal normally used for vitamin C manufacturing, the price of vitamin C rose three-fold in 2016 alone to US$12 per kg.[195]
Pharmacopoeias
Notes
- ↑ Dicot plants transport only ferrous iron (Fe2+), but if the iron circulates as ferric complexes (Fe3+), it has to undergo a reduction before it can be actively transported. Plant embryos efflux high amounts of ascorbate that chemically reduce iron(III) from ferric complexes.[145]
- ↑ "In 1934, Hoffman-La Roche, which bought the Reichstein process patent, became the first pharmaceutical company to mass produce and market synthetic vitamin C, under the brand name Redoxon."[174]
References
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- ↑ 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 2.12 "Ascorbic Acid". The American Society of Health-System Pharmacists. Archived from the original on December 30, 2016. Retrieved December 8, 2016.
- ↑ 3.0 3.1 3.2 World Health Organization (2009). Stuart MC, Kouimtzi M, Hill SR (eds.). WHO Model Formulary 2008. World Health Organization. hdl:10665/44053. ISBN 9789241547659.
- ↑ 4.0 4.1 "Ascorbic acid Use During Pregnancy". Drugs.com. Archived from the original on December 31, 2016. Retrieved December 30, 2016.
- ↑ 5.0 5.1 "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on July 28, 2020. Retrieved September 15, 2020.
- ↑ Merck Index, 14th ed.
- ↑ "Vitamin C". ChemSpider. Royal Society of Chemistry. Archived from the original on July 24, 2020. Retrieved July 25, 2020.
- ↑ 8.00 8.01 8.02 8.03 8.04 8.05 8.06 8.07 8.08 8.09 8.10 8.11 8.12 8.13 8.14 8.15 8.16 8.17 8.18 8.19 "Vitamin C". Dietary Reference Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington, DC: The National Academies Press. 2000. pp. 95–185. ISBN 978-0-309-06935-9. Archived from the original on September 2, 2017. Retrieved September 1, 2017.
- ↑ 9.0 9.1 9.2 9.3 9.4 9.5 "Vitamin C". Micronutrient Information Center, Linus Pauling Institute, Oregon State University, Corvallis, OR. July 1, 2018. Archived from the original on July 12, 2019. Retrieved June 19, 2019.
- ↑ 10.0 10.1 10.2 10.3 10.4 "Fact Sheet for Health Professionals – Vitamin C". Office of Dietary Supplements, US National Institutes of Health. February 11, 2016. Archived from the original on July 30, 2017.
- ↑ 11.0 11.1 11.2 11.3 11.4 Hemilä H, Chalker E (January 2013). "Vitamin C for preventing and treating the common cold". The Cochrane Database of Systematic Reviews (1): CD000980. doi:10.1002/14651858.CD000980.pub4. PMC 1160577. PMID 23440782.
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Antioxidant vitamin supplementation has no effect on the incidence of major cardiovascular events, myocardial infarction, stroke, total death, and cardiac death.
- ↑ 14.0 14.1 14.2 Squires, Victor R. (2011). The Role of Food, Agriculture, Forestry and Fisheries in Human Nutrition - Volume IV. EOLSS Publications. p. 121. ISBN 9781848261952. Archived from the original on December 25, 2020. Retrieved August 8, 2020.
- ↑ 15.0 15.1 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.
- ↑ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 1049. ISBN 9780857113382.
- ↑ "International Drug Price Indicator Guide. Vitamin C: Supplier Prices". Management Sciences for Health, Arlington, VA. 2016. Archived from the original on March 23, 2017. Retrieved March 22, 2017.
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- ↑ 19.0 19.1 19.2 Zetterström R (May 2009). "Nobel Prize 1937 to Albert von Szent-Györgyi: identification of vitamin C as the anti-scorbutic factor". Acta Paediatrica. 98 (5): 915–9. doi:10.1111/j.1651-2227.2009.01239.x. PMID 19239412.
- ↑ Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C (March 2012). "Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases". The Cochrane Database of Systematic Reviews. 3 (3): CD007176. doi:10.1002/14651858.CD007176.pub2. hdl:10138/136201. PMID 22419320.
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- ↑ 22.0 22.1 Lind J (1753). A Treatise of the Scurvy. London: A. Millar. In the 1757 edition of his work, Lind discusses his experiment starting on page 149. Archived March 20, 2016, at the Wayback Machine
- ↑ 23.0 23.1 23.2 23.3 Baron JH (June 2009). "Sailors' scurvy before and after James Lind--a reassessment" (PDF). Nutrition Reviews. 67 (6): 315–32. doi:10.1111/j.1753-4887.2009.00205.x. PMID 19519673. Archived from the original (PDF) on December 1, 2017. Retrieved August 8, 2020.
- ↑ Vorilhon P, Arpajou B, Vaillant Roussel H, Merlin É, Pereira B, Cabaillot A (March 2019). "Efficacy of vitamin C for the prevention and treatment of upper respiratory tract infection. A meta-analysis in children". Eur. J. Clin. Pharmacol. 75 (3): 303–11. doi:10.1007/s00228-018-2601-7. PMID 30465062. S2CID 53718830.
- ↑ Heimer KA, Hart AM, Martin LG, Rubio-Wallace S (May 2009). "Examining the evidence for the use of vitamin C in the prophylaxis and treatment of the common cold". Journal of the American Academy of Nurse Practitioners. 21 (5): 295–300. doi:10.1111/j.1745-7599.2009.00409.x. PMC 7166744. PMID 19432914.
- ↑ Lamontagne, F; Masse, MH; Menard, J; Sprague, S; Pinto, R; Heyland, DK; Cook, DJ; Battista, MC; Day, AG; Guyatt, GH; Kanji, S; Parke, R; McGuinness, SP; Tirupakuzhi Vijayaraghavan, BK; Annane, D; Cohen, D; Arabi, YM; Bolduc, B; Marinoff, N; Rochwerg, B; Millen, T; Meade, MO; Hand, L; Watpool, I; Porteous, R; Young, PJ; D'Aragon, F; Belley-Cote, EP; Carbonneau, E; Clarke, F; Maslove, DM; Hunt, M; Chassé, M; Lebrasseur, M; Lauzier, F; Mehta, S; Quiroz-Martinez, H; Rewa, OG; Charbonney, E; Seely, AJE; Kutsogiannis, DJ; LeBlanc, R; Mekontso-Dessap, A; Mele, TS; Turgeon, AF; Wood, G; Kohli, SS; Shahin, J; Twardowski, P; Adhikari, NKJ; LOVIT Investigators and the Canadian Critical Care Trials, Group. (June 23, 2022). "Intravenous Vitamin C in Adults with Sepsis in the Intensive Care Unit". The New England journal of medicine. 386 (25): 2387–2398. doi:10.1056/NEJMoa2200644. PMID 35704292.
- ↑ Cortés-Jofré, Marcela; Rueda, José-Ramón; Asenjo-Lobos, Claudia; Madrid, Eva; Bonfill Cosp, Xavier (March 4, 2020). "Drugs for preventing lung cancer in healthy people". The Cochrane Database of Systematic Reviews. 3: CD002141. doi:10.1002/14651858.CD002141.pub3. ISSN 1469-493X. PMC 7059884. PMID 32130738.
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- ↑ Xu X, Yu E, Liu L, Zhang W, Wei X, Gao X, Song N, Fu C (November 2013). "Dietary intake of vitamins A, C, and E and the risk of colorectal adenoma: a meta-analysis of observational studies". European Journal of Cancer Prevention. 22 (6): 529–39. doi:10.1097/CEJ.0b013e328364f1eb. PMID 24064545.
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- ↑ Fulan H, Changxing J, Baina WY, Wencui Z, Chunqing L, Fan W, Dandan L, Dianjun S, Tong W, Da P, Yashuang Z (October 2011). "Retinol, vitamins A, C, and E and breast cancer risk: a meta-analysis and meta-regression". Cancer Causes & Control. 22 (10): 1383–96. doi:10.1007/s10552-011-9811-y. PMID 21761132.
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- ↑ 37.0 37.1 37.2 Jacobs C, Hutton B, Ng T, Shorr R, Clemons M (February 2015). "Is there a role for oral or intravenous ascorbate (vitamin C) in treating patients with cancer? A systematic review". The Oncologist. 20 (2): 210–23. doi:10.1634/theoncologist.2014-0381. PMC 4319640. PMID 25601965.
- ↑ Al-Khudairy L, Flowers N, Wheelhouse R, Ghannam O, Hartley L, Stranges S, Rees K (March 2017). "Vitamin C supplementation for the primary prevention of cardiovascular disease". The Cochrane Database of Systematic Reviews. 3: CD011114. doi:10.1002/14651858.CD011114.pub2. PMC 6464316. PMID 28301692.
- ↑ Chen GC, Lu DB, Pang Z, Liu QF (November 2013). "Vitamin C intake, circulating vitamin C and risk of stroke: a meta-analysis of prospective studies". Journal of the American Heart Association. 2 (6): e000329. doi:10.1161/JAHA.113.000329. PMC 3886767. PMID 24284213.
- ↑ 40.0 40.1 Travica N, Ried K, Sali A, Scholey A, Hudson I, Pipingas A (August 30, 2017). "Vitamin C status and cognitive function: A systematic review". Nutrients. 9 (9): E960. doi:10.3390/nu9090960. PMC 5622720. PMID 28867798.
- ↑ Lopes da Silva S, Vellas B, Elemans S, Luchsinger J, Kamphuis P, Yaffe K, Sijben J, Groenendijk M, Stijnen T (2014). "Plasma nutrient status of patients with Alzheimer's disease: Systematic review and meta-analysis". Alzheimer's and Dementia. 10 (4): 485–502. doi:10.1016/j.jalz.2013.05.1771. PMID 24144963.
- ↑ Crichton GE, Bryan J, Murphy KJ (September 2013). "Dietary antioxidants, cognitive function and dementia--a systematic review". Plant Foods for Human Nutrition. 68 (3): 279–92. doi:10.1007/s11130-013-0370-0. PMID 23881465.
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- ↑ Koshizaka T, Nishikimi M, Ozawa T, Yagi K (February 1988). "Isolation and sequence analysis of a complementary DNA encoding rat liver L-gulono-gamma-lactone oxidase, a key enzyme for L-ascorbic acid biosynthesis". The Journal of Biological Chemistry. 263 (4): 1619–21. PMID 3338984.
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- ↑ Pollock, JI; Mullin, RJ (1986). "Vitamin C biosynthesis in prosimians: Evidence for the anthropoid affinity of Tarsius". American Journal of Physical Anthropology. 73 (1): 65–70. doi:10.1002/ajpa.1330730106. PMID 3113259. Archived from the original on June 28, 2012.
- ↑ Proctor P (1970). "Similar functions of uric acid and ascorbate in man?". Nature. 228 (5274): 868. Bibcode:1970Natur.228..868P. doi:10.1038/228868a0. PMID 5477017. S2CID 4146946.
- ↑ Cegłowski, Maciej (March 7, 2010). "Scott and Scurvy". Archived from the original on March 10, 2010.
- ↑ As they sailed farther up the east coast of Africa, they met local traders, who traded them fresh oranges. Within six days of eating the oranges, da Gama's crew recovered fully and he noted, "It pleased God in his mercy that ... all our sick recovered their health for the air of the place is very good." Infantile Scurvy: A Historical Perspective Archived September 4, 2015, at the Wayback Machine, Kumaravel Rajakumar
- ↑ On returning, Lopes' ship had left him on St Helena, where with admirable sagacity and industry he planted vegetables and nurseries with which passing ships were marvellously sustained. [...] There were 'wild groves' of oranges, lemons and other fruits that ripened all the year round, large pomegranates and figs. Santa Helena, A Forgotten Portuguese Discovery Archived May 29, 2011, at the Wayback Machine, Harold Livermore - Estudos em Homenagem a Luis Antonio de Oliveira Ramos, Faculdade de Letras da Universidade do Porto, 2004, pp. 630-631
- ↑ John Woodall, The Surgions Mate … (London, England : Edward Griffin, 1617), p. 89. From page 89: Archived April 11, 2016, at the Wayback Machine "Succus Limonum, or juice of Lemons … [is] the most precious help that ever was discovered against the Scurvy[;] to be drunk at all times; … "
- ↑ Armstrong A (1858). "Observation on Naval Hygiene and Scurvy, more particularly as the later appeared during the Polar Voyage". British and Foreign Medico-chirurgical Review: Or, Quarterly Journal of Practical Medicine and Surgery. 22: 295–305. Archived from the original on August 27, 2021. Retrieved August 8, 2020.
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- ↑ Lamb J (February 17, 2011). "Captain Cook and the Scourge of Scurvy". British History in depth. BBC. Archived from the original on February 21, 2011.
- ↑ Lamb J (2001). Preserving the self in the south seas, 1680–1840. University of Chicago Press. p. 117. ISBN 978-0-226-46849-5. Archived from the original on April 30, 2016.
- ↑ Singh S, Ernst E (2008). Trick or Treatment: The Undeniable Facts about Alternative Medicine. WW Norton & Company. pp. 15–18. ISBN 978-0-393-06661-6.
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ignored (help) - ↑ Kuhnlein HV, Receveur O, Soueida R, Egeland GM (June 2004). "Arctic indigenous peoples experience the nutrition transition with changing dietary patterns and obesity". The Journal of Nutrition. 134 (6): 1447–53. doi:10.1093/jn/134.6.1447. PMID 15173410.
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{{cite journal}}
: CS1 maint: unrecognized language (link) - ↑ Rosenfeld L (April 1997). "Vitamine--vitamin. The early years of discovery". Clinical Chemistry. 43 (4): 680–5. doi:10.1093/clinchem/43.4.680. PMID 9105273.
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{{cite journal}}
: CS1 maint: unrecognized language (link) - ↑ Kenéz J (December 1973). "[Eventful life of a scientist. 80th birthday of Nobel prize winner Albert Szent-Györgyi]". Munchener Medizinische Wochenschrift (in German). 115 (51): 2324–6. PMID 4589872.
{{cite journal}}
: CS1 maint: unrecognized language (link) - ↑ Szállási A (December 1974). "[2 interesting early articles by Albert Szent-Györgyi]". Orvosi Hetilap (in Hungarian). 115 (52): 3118–9. PMID 4612454.
{{cite journal}}
: CS1 maint: unrecognized language (link) - ↑ 181.0 181.1 "The Albert Szent-Gyorgyi Papers: Szeged, 1931-1947: Vitamin C, Muscles, and WWII". Profiles in Science. United States National Library of Medicine. Archived from the original on May 5, 2009.
- ↑ "Scurvy". Online Entymology Dictionary. Archived from the original on December 15, 2020. Retrieved November 19, 2017.
- ↑ "The Nobel Prize in Physiology or Medicine 1937". Nobel Media AB. Archived from the original on November 5, 2014. Retrieved November 20, 2014.
- ↑ Burns JJ, Evans C (December 1956). "The synthesis of L-ascorbic acid in the rat from D-glucuronolactone and L-gulonolactone". The Journal of Biological Chemistry. 223 (2): 897–905. PMID 13385237.
{{cite journal}}
: CS1 maint: url-status (link) - ↑ Burns JJ, Moltz A, Peyser P (December 1956). "Missing step in guinea pigs required for the biosynthesis of L-ascorbic acid". Science. 124 (3232): 1148–9. Bibcode:1956Sci...124.1148B. doi:10.1126/science.124.3232.1148-a. PMID 13380431.
- ↑ Henson DE, Block G, Levine M (April 1991). "Ascorbic acid: biologic functions and relation to cancer". Journal of the National Cancer Institute. 83 (8): 547–50. doi:10.1093/jnci/83.8.547. PMID 1672383. Archived from the original on December 25, 2020. Retrieved August 8, 2020.
- ↑ Pauling L (December 1970). "Evolution and the need for ascorbic acid". Proceedings of the National Academy of Sciences of the United States of America. 67 (4): 1643–8. Bibcode:1970PNAS...67.1643P. doi:10.1073/pnas.67.4.1643. PMC 283405. PMID 5275366.
- ↑ Mandl J, Szarka A, Bánhegyi G (August 2009). "Vitamin C: update on physiology and pharmacology". British Journal of Pharmacology. 157 (7): 1097–110. doi:10.1111/j.1476-5381.2009.00282.x. PMC 2743829. PMID 19508394.
- ↑ Cameron E, Pauling L (October 1976). "Supplemental ascorbate in the supportive treatment of cancer: Prolongation of survival times in terminal human cancer". Proceedings of the National Academy of Sciences of the United States of America. 73 (10): 3685–9. Bibcode:1976PNAS...73.3685C. doi:10.1073/pnas.73.10.3685. PMC 431183. PMID 1068480.
- ↑ "Vitamin C: Common cold". Corvallis, OR: Micronutrient Information Center, Linus Pauling Institute, Oregon State University. January 14, 2014. Archived from the original on July 12, 2019. Retrieved May 3, 2017.
- ↑ Hemilä, Harri (2009). "Vitamins and minerals". Commond Cold. pp. 275–307. doi:10.1007/978-3-7643-9912-2_13. hdl:10138/228060. ISBN 978-3-7643-9894-1.
- ↑ Stephens T (February 17, 2011). "Let the chemical games begin!". Swiss Info. Swiss Broadcasting Corporation. Archived from the original on August 31, 2011. Retrieved February 23, 2011.
- ↑ "Ascorbic acid Prices, Coupons & Patient Assistance Programs". Drugs.com. Archived from the original on January 16, 2021. Retrieved February 7, 2021.
- ↑ "The production of vitamin C" (PDF). Competition Commission. 2001. Archived from the original (PDF) on January 19, 2012. Retrieved February 20, 2007.
- ↑ 195.0 195.1 Jeff Gelski (November 6, 2017). "Vitamin C prices triple in a year's time". FoodBusiness News. Archived from the original on January 10, 2021. Retrieved August 15, 2019.
- ↑ Tingmin Koe (August 28, 2018). "'China-free' vitamin C: Industry defends standards against 'marketing claims'". NutraIngredients-Asia.com, William Reed Business Media, Ltd. Archived from the original on December 25, 2020. Retrieved August 15, 2019.
- ↑ British Pharmacopoeia Commission Secretariat (2009). "Index, BP 2009" (PDF). Archived from the original (PDF) on April 11, 2009. Retrieved February 4, 2010.
- ↑ "Japanese Pharmacopoeia, Fifteenth Edition" (PDF). 2006. Archived from the original (PDF) on July 22, 2011. Retrieved February 4, 2010.
External links
- "Vitamin C Fact Sheet". U.S. National Institutes of Health. Archived from the original on July 30, 2017. Retrieved August 8, 2020.
- "Ascorbic acid". Drug Information Portal. U.S. National Library of Medicine. Archived from the original on July 27, 2020. Retrieved August 8, 2020.
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