Phentolamine

Revision as of 02:04, 25 July 2014 by GeraldChi (talk | contribs)
Jump to navigation Jump to search
Phentolamine
Clinical data
Trade namesRegitine
AHFS/Drugs.comMicromedex Detailed Consumer Information
Pregnancy
category
Routes of
administration
Usually IV or IM
ATC code
Pharmacokinetic data
MetabolismHepatic
Elimination half-life19 minutes
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaC17H19N3O
Molar mass281.352 g/mol
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)

WikiDoc Resources for Phentolamine

Articles

Most recent articles on Phentolamine

Most cited articles on Phentolamine

Review articles on Phentolamine

Articles on Phentolamine in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Phentolamine

Images of Phentolamine

Photos of Phentolamine

Podcasts & MP3s on Phentolamine

Videos on Phentolamine

Evidence Based Medicine

Cochrane Collaboration on Phentolamine

Bandolier on Phentolamine

TRIP on Phentolamine

Clinical Trials

Ongoing Trials on Phentolamine at Clinical Trials.gov

Trial results on Phentolamine

Clinical Trials on Phentolamine at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Phentolamine

NICE Guidance on Phentolamine

NHS PRODIGY Guidance

FDA on Phentolamine

CDC on Phentolamine

Books

Books on Phentolamine

News

Phentolamine in the news

Be alerted to news on Phentolamine

News trends on Phentolamine

Commentary

Blogs on Phentolamine

Definitions

Definitions of Phentolamine

Patient Resources / Community

Patient resources on Phentolamine

Discussion groups on Phentolamine

Patient Handouts on Phentolamine

Directions to Hospitals Treating Phentolamine

Risk calculators and risk factors for Phentolamine

Healthcare Provider Resources

Symptoms of Phentolamine

Causes & Risk Factors for Phentolamine

Diagnostic studies for Phentolamine

Treatment of Phentolamine

Continuing Medical Education (CME)

CME Programs on Phentolamine

International

Phentolamine en Espanol

Phentolamine en Francais

Business

Phentolamine in the Marketplace

Patents on Phentolamine

Experimental / Informatics

List of terms related to Phentolamine

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Phentolamine (Regitine) is a reversible[1] nonselective alpha-adrenergic antagonist.[2]

Mechanism

Its primary action is vasodilation due to α1 blockade.[3]

It also can lead to reflex tachycardia because of hypotension and α2 inhibition, which increases sympathetic tone.[4]

Uses

The primary application for phentolamine is for the control of hypertensive emergencies, most notably due to pheochromocytoma. [5]

It also has usefulness in the treatment of cocaine-induced cardiovascular complications, where one would generally avoid Beta-blockers (e.g. metoprolol), as they can cause unopposed alpha-adrenergic mediated coronary vasoconstriction, worsening myocardial ischemia and hypertension. It is important to note that phentolamine is not a first-line agent for this indication. Phentolamine should only be given to patients who do not fully respond to benzodiazepines, nitroglycerin, and calcium channel blockers. [6][7]

When given by injection it causes blood vessels to expand, thereby increasing blood flow. When injected into the penis (intracavernosal), it increases blood flow to the penis, which results in an erection.[8]

It may be stored in crash carts to counteract severe peripheral vasoconstriction secondary to extravasation of peripherally placed vasopressor infusions, typically of norepinephrine. Epinephrine infusions are less vasoconstrictive than norepinephrine as they primarily stimulate beta receptor more than alpha receptors, but the effect remains dose dependent.

Phentolamine also has diagnostic and therapeutic roles in complex regional pain syndrome (reflex sympathetic dystrophy).[9]

Phentolamine has recently been introduced in the dental field as a local anesthetic reversal agent. Distributed by Septodont, OraVerse is a Phentolamine Mesylate injection designed to reverse the local vasoconstrictor properties used in many local anesthetics to prolong anesthesia.[10] OraVerse has been shown to accelerate the reversal of the lingering soft-tissue numbness associated with the widely used anesthetic-vasoconstrictor combinations.[11]

Chemistry

Phentolamine can be synthesized by alkylation of 3-(4-methylanilino)phenol using 2-chloromethylimidazoline:[12][13]

References

  1. Jewell, John R.; Longworth, David L.; Stoller, James K.; Casey, David (2003). The Cleveland Clinic internal medicine case reviews. Hagerstown, MD: Lippincott Williams & Wilkins. p. 32. ISBN 0-7817-4266-8.
  2. Phentolamine at the US National Library of Medicine Medical Subject Headings (MeSH)
  3. Brock G. Oral phentolamine (Vasomax). Drugs Today (Barcelona). 2000 Feb-Mar;36(2-3):121-4.
  4. Shen, Howard (2008). Illustrated Pharmacology Memory Cards: PharMnemonics. Minireview. p. 14. ISBN 1-59541-101-1.
  5. Tuncel M, Ram VC. Hypertensive emergencies. Etiology and management. American Journal of Cardiovascular Drugs. 2003;3(1):21-31.
  6. Hollander JE, Henry TD. Evaluation and management of the patient who has cocaine-associated chest pain. Cardiology Clinics. 2006 Feb;24(1):103-14.
  7. Chan GM, Sharma R, Price D, Hoffman RS, Nelson LS. Phentolamine Therapy for Cocaine-Association Acute Coronary Syndrome (CAACS). Journal of Medical Toxicology. 2006 Sep;2(3):108-11.
  8. Bella AJ, Brock GB. Intracavernous pharmacotherapy for erectile dysfunction. Endocrine. 2004 Mar-Apr;23(2-3):149-55.
  9. Rowbotham MC. Pharmacologic management of complex regional pain syndrome. Clinical Journal of Pain. 2006 Jun;22(5):425-9.
  10. http://www.novalar.com/oraverse-dental-specialty-pharmaceutical
  11. Malamed S. What's new in local anaesthesia? Society For The Advancement Of Anaesthesia In Dentistry Digest. 2009 Jan;25:4-14.
  12. K. Miescher, A. Marxer, E. Urech, Template:US Patent (1950)
  13. E. Urech, A. Marxer, K. Miescher, Helv. Chim. Acta, 33, 1386 (1950)

Template:Peripheral vasodilators