Betaxolol is a selective beta1 receptor blocker used in the treatment of hypertension and angina.[1] It is also a adrenergic blocker with no partial agonist action and minimal membrane stabilizing activity.[2] Being selective for beta1 receptors, it typically has fewer systemic side effects than non-selective beta-blockers, for example, not causing bronchospasm (mediated by beta2 receptors) as timolol may. Betaxolol also shows greater affinity for beta1 receptors than metoprolol. In addition to its effect on the heart, betaxolol reduces the pressure within the eye (intraocular pressure). This effect is thought to be caused by reducing the production of the liquid (which is called the aqueous humor) within the eye. The precise mechanism of this effect is not known. The reduction in intraocular pressure reduces the risk of damage to the optic nerve and loss of vision in patients with elevated intraocular pressure due to glaucoma.
Clinical data | |
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Trade names | Kerlone |
AHFS/Drugs.com | Monograph |
MedlinePlus | a609023 |
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Routes of administration | By mouth, ocular |
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Pharmacokinetic data | |
Bioavailability | 89% |
Metabolism | Liver |
Elimination half-life | 14–22 hours |
Excretion | Kidney (20%) |
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ECHA InfoCard | 100.113.058 |
Chemical and physical data | |
Formula | C18H29NO3 |
Molar mass | 307.434 g·mol−1 |
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Chirality | Racemic mixture |
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It was patented in 1975 and approved for medical use in 1983.[3]
Medical uses
editHypertension
editBetaxolol is most commonly ingested orally alone or with other medications for the management of essential hypertension.[4] It is a cardioselective beta blocker, targeting beta-1 adrenergic receptors found in the cardiac muscle. Blood pressure is decreased by the mechanism of blood vessels relaxing and improving the flow of blood.[5][6]
Glaucoma
editOphthalmic betaxolol is an available treatment for primary open angle glaucoma (POAG) and optical hypertension. Betaxolol effectively prevents the increase of intracellular calcium, which leads to increased production of the aqueous humor. In the context of open angle glaucoma, increased aqueous humor produced by ciliary bodies increases intraocular pressure, causing degeneration of retinal ganglion cells and the optic nerve.[7]
Furthermore, betaxolol is additionally able to protect retinal neurones following topical application from excitotoxicity or ischemia-reperfusion, providing a neuroprotective effect. This is thought to be attributed to its capacity to attenuate neuronal calcium and sodium influx.[8] Betaxolol is also an effective treatment for Intraocular pressure[9]
Paronychia
editOne study showed that topical betaxolol can be used in treating relapsed paronychia.[10]
Contraindications
edit- Hypersensitivity to the drug
- Patients with sinus bradycardia, heart block greater than first degree, cardiogenic shock, and overt cardiac failure
Side effects
editThis section needs expansion. You can help by adding to it. (January 2019) |
The adverse side-effects of betaxolol can be categorized into local and systemic effects.[7] The local effects include:
- transient irritation (20-40% of patients)
- burning
- pruritus, or general itching
- punctate keratitis
- blurry vision[11]
Systemically, patients taking betaxolol might experience:
- bradycardia
- hypotension
- fatigue
- sexual impotence
- hair loss
- confusion
- headache
- dizziness
- bronchospasm at higher doses
- cardiac problems such as arrhythmia, bundle branch block, myocardial infarction, sinus arrest, and congestive heart failure
- mental effects such as depression, disorientation, vertigo, sleepwalking, rhinitis
- dysuria
- metabolic side effects such as an increase in LDL cholesterol levels
- can mask the symptoms of hypoglycemia diabetic patients
History
editBetaxolol was approved by the U.S. Food and Drug Administration (FDA) for ocular use as a 0.5% solution (Betoptic) in 1985 and as a 0.25% solution (Betoptic S) in 1989.
Society and culture
editBrand names
editBrand names include Betoptic, Betoptic S, Lokren, Kerlone.
See also
editReferences
edit- ^ Buckley MM, Goa KL, Clissold SP (July 1990). "Ocular betaxolol. A review of its pharmacological properties, and therapeutic efficacy in glaucoma and ocular hypertension". Drugs. 40 (1): 75–90. doi:10.2165/00003495-199040010-00005. PMID 2202584. S2CID 46962082.
- ^ "Google Scholar". scholar.google.com. Retrieved 2023-12-26.
- ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 461. ISBN 9783527607495.
- ^ Tajran J, Goyal A (2023). "Betaxolol". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 32491793. Retrieved 2023-12-26.
- ^ "Betaxolol". MedlinePlus Drug Information. U.S. National Library of Medicine. Retrieved 2023-01-12.
- ^ "Betaxolol: MedlinePlus Drug Information". medlineplus.gov. Retrieved 2023-12-26.
- ^ a b Tajran J, Goyal A (2022). "Betaxolol". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 32491793. Retrieved 2023-01-12.
- ^ Wood JP, Schmidt KG, Melena J, Chidlow G, Allmeier H, Osborne NN (April 2003). "The beta-adrenoceptor antagonists metipranolol and timolol are retinal neuroprotectants: comparison with betaxolol". Experimental Eye Research. 76 (4): 505–516. doi:10.1016/s0014-4835(02)00335-4. PMID 12634114.
- ^ Goldberg I, Goldberg H (February 1995). "Betaxolol eye drops. A clinical trial of safety and efficacy". Australian and New Zealand Journal of Ophthalmology. 23 (1): 17–24. doi:10.1111/j.1442-9071.1995.tb01640.x. PMID 7619450.
- ^ Yen CF, Hsu CK, Lu CW (June 2018). "Topical betaxolol for treating relapsing paronychia with pyogenic granuloma-like lesions induced by epidermal growth factor receptor inhibitors". Journal of the American Academy of Dermatology. 78 (6): e143–e144. doi:10.1016/j.jaad.2018.01.015. PMID 29339238. S2CID 39861588.
- ^ Buckley MM, Goa KL, Clissold SP (July 1990). "Ocular betaxolol. A review of its pharmacological properties, and therapeutic efficacy in glaucoma and ocular hypertension". Drugs. 40 (1): 75–90. doi:10.2165/00003495-199040010-00005. PMID 2202584. S2CID 46962082.