Oxymetazoline Explained

Verifiedfields:changed
Watchedfields:changed
Verifiedrevid:462267467
Width:200
Tradename:Afrin, others
Dependency Liability:Moderate
Routes Of Administration:Intranasal, eye drop, topical
Atc Prefix:D11
Atc Suffix:AX27
Atc Supplemental:
, (combinations),
Legal Uk:GSL
Legal Us:OTC
Legal Us Comment:/ Rx-only
Metabolism:Kidney (30%), fecal (10%)
Elimination Half-Life:5–6 hours
Cas Number:1491-59-4
Pubchem:4636
Iuphar Ligand:124
Drugbank:DB00935
Chemspiderid:4475
Unii:8VLN5B44ZY
Kegg:D08322
Chebi:7862
Chembl:762
Iupac Name:3-(4,5-Dihydro-1H-imidazol-2-ylmethyl)-2,4-dimethyl-6-tert-butyl-phenol
C:16
H:24
N:2
O:1
Smiles:Oc1c(c(c(cc1C(C)(C)C)C)CC/2=N/CCN\2)C
Stdinchi:1S/C16H24N2O/c1-10-8-13(16(3,4)5)15(19)11(2)12(10)9-14-17-6-7-18-14/h8,19H,6-7,9H2,1-5H3,(H,17,18)
Stdinchikey:WYWIFABBXFUGLM-UHFFFAOYSA-N
Melting Point:301.5

Oxymetazoline, sold under the brand name Afrin among others, is a topical decongestant and vasoconstrictor medication. It is available over-the-counter as a nasal spray to treat nasal congestion and nosebleeds, as eye drops to treat eye redness due to minor irritation, and (in the United States) as a prescription topical cream to treat persistent facial redness due to rosacea in adults. Its effects begin within minutes and last for up to six hours. Intranasal use for longer than three days may cause congestion to recur or worsen, resulting in physical dependence.

Oxymetazoline is a derivative of imidazole.[1] It was developed from xylometazoline at Merck by Wolfgang Fruhstorfer and Helmut Müller-Calgan in 1961.[2] A direct sympathomimetic, oxymetazoline binds to and activates α1 adrenergic receptors and α2 adrenergic receptors, most notably.[1] One study classified it in the following order: α(2A) > α(1A) ≥ α(2B) > α(1D) ≥ α(2C) >> α(1B), but this is not universally agreed upon.[3]

Another study classified it with selectivity ratios in alpha 2 adrenergic receptors of 200 for a2A vs a2B, 7.1 a2A vs a2C, and 28.2 a2B vs a2C.[4]

In 2021, it was the 292nd most commonly prescribed medication in the United States, with more than 600,000 prescriptions.[5] [6]

Medical uses

Oxymetazoline is available over-the-counter as a topical decongestant in the form of oxymetazoline hydrochloride in nasal sprays.[7]

In the United States, oxymetazoline 1% cream is approved by the Food and Drug Administration for topical treatment of persistent facial erythema (redness) associated with rosacea in adults.[8]

Due to its vasoconstricting properties, oxymetazoline is also used to treat nose bleeds[9] [10] and eye redness due to minor irritation (marketed as Visine L.R. in the form of eye drops).

In July 2020, oxymetazoline received approval by the FDA for the treatment of acquired drooping eyelid.[11]

Side effects

Rebound congestion

Rebound congestion, or rhinitis medicamentosa, may occur. A 2006 review of the pathology of rhinitis medicamentosa concluded that use of oxymetazoline for more than three days may result in rhinitis medicamentosa and recommended limiting use to three days.[12]

Australian regulatory submission

Novartis recommended a five day maximum usage period, rather than three days, in a submission to the Therapeutic Goods Administration. Novartis suggested that "The justification [for 3 days] was not based on evidence" and cited an extensive body of evidence, and noting a range of recommended periods from five to ten days, which coincides with the typical duration of the common cold.[13]

Overdose

There is no specific antidote for oxymetazoline, although its pharmacological effects may be reversed by an adrenergic antagonists such as phentolamine.

Pharmacology

Pharmacodynamics

Oxymetazoline is a sympathomimetic that selectively agonizes α1 and, partially, α2 adrenergic receptors.[14] Since vascular beds widely express α1 receptors, the action of oxymetazoline results in vasoconstriction. In addition, the local application of the drug also results in vasoconstriction due to its action on endothelial postsynaptic α2 receptors; systemic application of α2 agonists, in contrast, causes vasodilation because of centrally-mediated inhibition of sympathetic tone via presynaptic α2 receptors.[15] Vasoconstriction of vessels results in relief of nasal congestion in two ways: first, it increases the diameter of the airway lumen; second, it reduces fluid exudation from postcapillary venules.[16] It can reduce nasal airway resistance (NAR) up to 35.7% and reduce nasal mucosal blood flow up to 50%.[17]

Pharmacokinetics

Since imidazolines are sympathomimetic agents, their primary effects appear on α adrenergic receptors, with little if any effect on β adrenergic receptors.[18] Like other imidazolines, Oxymetazoline is readily absorbed orally. Effects on α receptors from systemically absorbed oxymetazoline hydrochloride may persist for up to 7 hours after a single dose.[19] The elimination half-life in humans is 5–8 hours.[20] It is excreted unchanged both by the kidneys (30%) and in feces (10%).

History

The oxymetazoline brand Afrin was first sold as a prescription medication in 1966. After finding substantial early success as a prescription medication, it became available as an over-the-counter drug in 1975. Schering-Plough did not engage in heavy advertising until 1986.[21]

Society and culture

Brand names

Brand names include Afrin, ClariClear, Dristan, Drixine, Drixoral, Nasivin, Nasivion, Nezeril, Nostrilla, Logicin, Vicks Sinex, Visine L.R., Sudafed OM, Otrivin, Oxy, SinuFrin, Upneeq, and Mucinex Sinus-Max.

Notes and References

  1. Web site: PubChem . Bethesda (MD) . National Library of Medicine (US), National Center for Biotechnology Information . CID 4636 . Oxymetazoline .
  2. DE . 1117588 . 2-(2,6-dimethyl-3-hydroxy-4-tert-butyl-benzyl)-2-imidazoline,and acid addition salts thereof,and process for their manufacture . E Merck AG. Fruhstorfer W, Müller-Calgan H . 23 November 1961 . . .
  3. Haenisch B, Walstab J, Herberhold S, Bootz F, Tschaikin M, Ramseger R, Bönisch H . Alpha-adrenoceptor agonistic activity of oxymetazoline and xylometazoline . Fundamental & Clinical Pharmacology . 24 . 6 . 729–739 . December 2010 . 20030735 . 10.1111/j.1472-8206.2009.00805.x . 25064699 .
  4. Proudman RG, Akinaga J, Baker JG . The signaling and selectivity of α-adrenoceptor agonists for the human α2A, α2B and α2C-adrenoceptors and comparison with human α1 and β-adrenoceptors . Pharmacology Research & Perspectives . 10 . 5 . e01003 . October 2022 . 36101495 . 9471048 . 10.1002/prp2.1003 .
  5. Web site: The Top 300 of 2021 . ClinCalc . 14 January 2024 . 15 January 2024 . https://web.archive.org/web/20240115223848/https://clincalc.com/DrugStats/Top300Drugs.aspx . live .
  6. Web site: Oxymetazoline - Drug Usage Statistics . ClinCalc . 14 January 2024.
  7. Web site: Oxymetazoline . Lexi-Comp: Merck Manual Professional . Merck.com . 15 April 2013.
  8. Patel NU, Shukla S, Zaki J, Feldman SR . Oxymetazoline hydrochloride cream for facial erythema associated with rosacea . Expert Review of Clinical Pharmacology . 10 . 10 . 1049–1054 . October 2017 . 28837365 . 10.1080/17512433.2017.1370370 . 19930755 .
  9. Katz RI, Hovagim AR, Finkelstein HS, Grinberg Y, Boccio RV, Poppers PJ . A comparison of cocaine, lidocaine with epinephrine, and oxymetazoline for prevention of epistaxis on nasotracheal intubation . Journal of Clinical Anesthesia . 2 . 1 . 16–20 . 1990 . 2310576 . 10.1016/0952-8180(90)90043-3 .
  10. Krempl GA, Noorily AD . Use of oxymetazoline in the management of epistaxis . The Annals of Otology, Rhinology, and Laryngology . 104 . 9 Pt 1 . 704–706 . September 1995 . 7661519 . 10.1177/000348949510400906 . 37579139 .
  11. Web site: UPNEEQ Label . accessdata.fda.gov . 8 July 2020 .
  12. Ramey JT, Bailen E, Lockey RF . Rhinitis medicamentosa . Journal of Investigational Allergology & Clinical Immunology . 16 . 3 . 148–155 . 2006 . 16784007 .
  13. Web site: Novartis Consumer Health Australasia. Consultation submission: OTC nasal decongestant preparations for topical use: proposed advisory statements for medicines . Nguyen TM . 2014.
  14. Book: Westfall TC, Westfall DP . Chapter 6. Neurotransmission: The Autonomic and Somatic Motor Nervous Systems . Brunton LL, Lazo JS, Parker KL. Goodman & Gilman's The Pharmacological Basis of Therapeutics . 11th . http://www.accessmedicine.com/content.aspx?aID=954433 . AccessMedicine . Anatomy and General Functions of the Autonomic and Somatic Motor Nervous Systems . 24 January 2015 . dead . https://web.archive.org/web/20110930100924/http://www.accessmedicine.com/content.aspx?aID=954433 . 30 September 2011 . .
  15. Book: Biaggioni I, Robertson D . Chapter 9. Adrenoceptor Agonists & Sympathomimetic Drugs . Katzung BG . Basic & Clinical Pharmacology . 11th . 30 November 2011 . dead . https://web.archive.org/web/20110930100935/http://www.accessmedicine.com/content.aspx?aID=4520412 . 30 September 2011 .
  16. Widdicombe J . Microvascular anatomy of the nose . Allergy . 52 . 40 Suppl . 7–11 . 1997 . 9353554 . 10.1111/j.1398-9995.1997.tb04877.x . 46018611 .
  17. Bende M, Löth S . Vascular effects of topical oxymetazoline on human nasal mucosa . The Journal of Laryngology and Otology . 100 . 3 . 285–288 . March 1986 . 3950497 . 10.1017/S0022215100099151 . 37998936 .
  18. Book: Clinical veterinary toxicology . 2004 . Mosby . Plumlee KH . 978-0-323-01125-9 . St. Louis, Mo. . 460904351.
  19. Web site: Decongestants (Toxicity) - Toxicology . 3 April 2023 . Merck Veterinary Manual .
  20. Book: Dalefield R . Veterinary toxicology for Australia and New Zealand . 2017 . 978-0-12-799912-8 . Amsterdam, Netherlands . McGraw Hill LLC . 992119220.
  21. News: Dougherty PH . Advertising; Afrin Goes After Users Of Nasal Decongestants. The New York Times. 20 October 1986. 30 March 2015.