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Betamethasone dipropionate

From Wikipedia, the free encyclopedia
Glucocorticoid steroid (chemical compound)
Pharmaceutical compound
Betamethasone dipropionate
Clinical data
Trade namesDiprolene, Sernivo, Diprosone, others
Other namesBetamethasone-17,21-dipropionate
AHFS/Drugs.comMonograph
MedlinePlusa682799
License data
Pregnancy
category
Routes of
administration
Topical
ATC code
Legal status
Legal status
Identifiers
  • [(8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-(2-propanoyloxyacetyl)-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.024.551Edit this at Wikidata
Chemical and physical data
FormulaC28H37FO7
Molar mass504.595 g·mol−1
3D model (JSmol)
  • O=C(OCC(=O)[C@]3(OC(=O)CC)[C@]2(C[C@H](O)[C@]4(F)[C@@]/1(\C(=C/C(=O)\C=C\1)CC[C@H]4[C@@H]2C[C@@H]3C)C)C)CC
  • InChI=1S/C28H37FO7/c1-6-23(33)35-15-22(32)28(36-24(34)7-2)16(3)12-20-19-9-8-17-13-18(30)10-11-25(17,4)27(19,29)21(31)14-26(20,28)5/h10-11,13,16,19-21,31H,6-9,12,14-15H2,1-5H3/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1 checkY
  • Key:CIWBQSYVNNPZIQ-XYWKZLDCSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Betamethasone dipropionate is aglucocorticoidsteroid withanti-inflammatory andimmunosuppressive properties. It is applied as atopical cream, ointment, lotion or gel (Diprolene) to treatitching and other skin conditions such aseczema. Minor side effects include dry skin and mild, temporary stinging when applied.[2] Betamethasone dipropionate is a "super high potency" corticosteroid used to treat inflammatory skin conditions such asdermatitis,eczema andpsoriasis. It is a synthetic analog of the adrenal corticosteroids. Although its exact mechanism of action is not known, it is effective when applied topically to cortico-responsive inflammatory dermatoses.[3] It is available as ageneric medication.[4]

Adverse effects

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Although the absorption of betamethasone dipropionate is small, when used for prolonged periods of time (periods exceeding two weeks), or across a large surface area (total use greater than 50 grams per week), it can have adverse effects. One such effect is the ability of the corticosteroid to suppress thehypothalamic–pituitary–adrenal axis.[3][5] This can lead to a depression in the release of adrenal hormones such ascortisol andadrenocorticotropic hormone, or ACTH. Symptoms of HPA axis suppression are often subtle and variable, but can often be detected using simple blood or urine tests such at ACTH stimulation test or urinary free cortisol.[5] Those at increased risk for HPA axis suppression are those who are more likely to absorb more of the steroid through the skin. These groups include:

  • Those who have used topical corticosteroids over a prolonged period of time
  • Those who have used corticosteroids to cover a large surface area
  • Those with broken skin barrier or extensive abrasions
  • Those who have recently undergone stress (such as illness, trauma, surgery)
  • Children under the age of 12

HPA axis suppression is preventable by supplementation with glucocorticosteroids. If HPA axis suppression occurs, it is often reversed shortly after discontinuation of treatment.[6]

Pharmacology

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Mechanism of action

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Further information:Glucocorticoid § Mechanism of action

Pharmacokinetics

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Absorption of topical corticosteroids depends on several factors such as the vehicle, or delivery system used by the drug, the integrity of the epidermal barrier, and whether or not an occlusive bandage is used in combination with the drug.[3]

The absorption of topical betamethasone dipropionate is theoretically minuscule; however, if absorbed it follows the same pharmacokinetic profile as is typical of systemic corticosteroids. It is metabolized primarily by the liver by hydrolysis to its metabolitesbetamethasone 17-monopropionate (primary) andbetamethasone and the 6β-hydroxy derivatives of those metabolites, and it is excreted primarily by the kidneys.[3][7]

Chemistry

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Betamethasone dipropionate is a white to almost white crystalline powder.[medical citation needed]

Regulation

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Betamethasone dipropionate was patented byMerck in 1987, as an augmented cream/lotion, Diprolene in the U.S., and Disprosone in Europe.[8] These patents expired in 2003 and 2007 respectively leading to generic production of betamethasone dipropionate. During this time other topical corticosteroids such astriamcinolone acetonide andclobetasol propionate also became available as generic creams. Merck filed for "pediatric exclusivity" in 2001 launching a clinical trial to prove betamethasone dipropionate's safety and efficacy for use in pediatrics.[9]

Betamethasone has also been used in the formulation ofcombination products such asLuxiq,Lotrisone andTaclonex.

  • Prestium Pharma: Luxiq (betamethasone valerate) Foam, 0.12%[10] is a mid-strength corticosteroid foam used primarily to treat psoriasis or other inflammatory conditions of the scalp.
  • Merck: Lotrisone (containing betamethasone dipropionate,clotrimazole)[11] contains both a corticosteroid (betamethasone) and anti-fungal agent (clotrimazole) and is used to treat fungal infections that are also inflamed
  • Leo Pharma: Taclonex (containing betamethasone dipropionate,calcipotriol)[12] is a combination of corticosteroid (betamethasone) and a vitamin D analogue (calcipotriene) and is used to treat frequent and persistent dermatatoses by reducing inflammation and promoting healing of the skin barrier.

Names

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Brand names include Alphatrex, Beta-Val, Diprolene, Diprolene AF, Diprosalic (withsalicylic acid)[13] Diprosone, Dovobet (LEO Pharma A/S),[14] Eleuphrat and Luxiq.[citation needed]

A tube of Diprosalic ointment

See also

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References

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  1. ^"Diprosone Cream - Summary of Product Characteristics (SmPC)".Electronic Medicines Compendium (EMC). Datapharm Ltd. 19 September 2019. Retrieved14 April 2020.
  2. ^"Betamethasone Dipropionate Side Effects".drugs.com.
  3. ^abcd"Diprolene".Drugs.com. 1 June 2021.
  4. ^"Betamethasone Monograph for Professionals".Drugs.com. 26 December 2019. Retrieved15 August 2020.
  5. ^ab"Diprolene Ointment".RxList. 29 June 2021.
  6. ^Ault A (25 March 2005)."Adrenal Suppression From Topical Corticosteroids Surprisingly High".MedPage Today. Archived fromthe original on 1 March 2016.
  7. ^"Enstilar (calcipotriene and betamethasone dipropionate) Foam, 0.005%/0.064% for topical use. Full Prescribing Information"(PDF). Parsippany, New Jersey: LEO Pharma Inc. 2015. Archived fromthe original(PDF) on 2018-09-20. Retrieved2015-11-21.
  8. ^"Profile for Tradename: Diprolene AF".DrugPatentWatch.com.
  9. ^"Diprolene Pediatric Exclusivity"(PDF).fda.gov. US:Center for Drug Evaluation and Research,Food and Drug Administration. Archived fromthe original(PDF) on December 28, 2014.
  10. ^"Luxíq".luxiq.com. Connetics Corporation. Archived fromthe original on 3 March 2007.
  11. ^"Lotrisone — clotrimazole and betamethasone dipropionate cream".DailyMed. U.S. National Library of Medicine. 14 June 2019. Retrieved13 April 2020.
  12. ^"TACLONEX Highlights of Prescribing Information".taclonex.com. LEO Laboratories Ltd.
  13. ^Weller RB, Hunter HJ, Mann MW (27 January 2015)."Formulary 1: Topical Treatments".Clinical Dermatology. John Wiley & Sons. p. 402.ISBN 978-0-470-65952-6. Retrieved2 December 2022 – via Google Books.
  14. ^"Dovobet Ointment - Summary of Product Characteristics".Electronic Medicines Compendium (EMC). Datapharm Ltd. – via medicines.org.uk.

External links

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