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IUPAC name α-Hydro-ω-{-3,4-dihydro-2H-1-benzopyran-6-yl}oxy)butanoyl]oxy}poly(oxyethylene) | |
Other names Tocofersolan; Vitamin E PEG succinate; α-Tocopherol polyethylene glycol succinate (TPGS); Liqui-E | |
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ECHA InfoCard | 100.123.651 |
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Properties | |
Chemical formula | (C2H4O)nC33H54O5 |
Molar mass | Variable |
Pharmacology | |
ATC code | A11HA08 (WHO) |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Clinical data | |
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Trade names | Vedrop |
Other names | Tocophersolan (USAN US) |
AHFS/Drugs.com | UK Drug Information |
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ECHA InfoCard | 100.123.651 |
Tocofersolan (INN; also known as tocophersolan, tocopherol polyethylene glycol succinate, or TPGS) is a synthetic water-soluble version of vitamin E. Natural forms of vitamin E are fat soluble, but not water-soluble. Tocofersolan is polyethylene glycol derivative of α-tocopherol that enables water solubility.
Tocofersolan is used as a vitamin E supplement or to treat vitamin E deficiency in individuals who cannot absorb fats due to disease. On 24 July 2009 the European Medicines Agency approved tocofersolan under the trade name Vedrop 50 mg/ml oral solution for the treatment of vitamin E deficiency due to digestive malabsorption in paediatric patients with congenital or hereditary chronic cholestasis, from birth (in term newborns) to 16 or 18 years of age (depending on the region).
Tocofersolan is also used in cosmetics and pharmaceuticals as an antioxidant.
References
- "Vedrop 50 mg/ml oral solution - Summary of Product Characteristics (SmPC)". (emc). 19 June 2019. Retrieved 24 July 2020.
- "Vedrop EPAR". European Medicines Agency (EMA). Archived from the original on 24 July 2020. Retrieved 24 July 2020.
- "Tocophersolan Oral". WebMD.
- "Vedrop Summary of Product Characteristics" (PDF). European Medicines Agency.
- Ash M, Ash I (2004). Handbook of Preservatives. Synapse Info Resources. p. 568. ISBN 1-890595-66-7.
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Fat soluble |
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Water soluble |
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