Tocofersolan
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IUPAC name
α-Hydro-ω-{[4-oxo-4-({(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-yl}oxy)butanoyl]oxy}poly(oxyethylene)
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Other names
Tocofersolan; Vitamin E PEG succinate; α-Tocopherol polyethylene glycol succinate (TPGS); Liqui-E
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Identifiers | |
3D model (JSmol)
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DrugBank | |
ECHA InfoCard | 100.123.651 |
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Properties | |
(C2H4O)nC33H54O5 | |
Molar mass | Variable |
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Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
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Clinical data | |
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Trade names | Vedrop |
Other names | Tocophersolan (USANUS) |
AHFS/Drugs.com | UK Drug Information |
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ECHA InfoCard | 100.123.651 |
Tocofersolan(INN) ortocophersolan,also referred to asTPGS(fortocopherolpolyethylene glycol succinate), is a synthetic water-soluble version ofvitamin E.Natural forms of vitamin E are fat soluble, but not water-soluble. Tocofersolan ispolyethylene glycolderivative ofα-tocopherolthat 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.[3] On 24 July 2009 theEuropean Medicines Agencyapproved tocofersolan under the trade nameVedrop50 mg/ml oral solution for the treatment of vitamin E deficiency due to digestivemalabsorptioninpaediatricpatients withcongenitalor hereditary chroniccholestasis,from birth (in term newborns) to 16 or 18 years of age (depending on the region).[4]
Tocofersolan is also used in cosmetics and pharmaceuticals as anantioxidant.[5]
References[edit]
- ^"Vedrop 50 mg/ml oral solution - Summary of Product Characteristics (SmPC)".(emc).19 June 2019.Retrieved24 July2020.
- ^"Vedrop EPAR".European Medicines Agency(EMA).Retrieved24 July2020.
- ^"Tocophersolan Oral".WebMD.
- ^"Vedrop Summary of Product Characteristics "(PDF).European Medicines Agency.[permanent dead link]
- ^Ash M, Ash I (2004).Handbook of Preservatives.Synapse Info Resources. p. 568.ISBN1-890595-66-7.