Summary
Brinzolamide (trade name Azopt) is a carbonic anhydrase inhibitor used to lower intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
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| Pronunciation | brin ZOH la mide |
| Trade names | Azopt |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a601233 |
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| Routes of administration | Ophthalmic |
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| Bioavailability | Absorbed systemically, but below detectable levels (less than 10 ng/mL) |
| Protein binding | ~60% |
| Elimination half-life | 111 days |
| Excretion | Kidney (60%) |
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| ECHA InfoCard | 100.149.376 |
| Chemical and physical data | |
| Formula | C12H21N3O5S3 |
| Molar mass | 383.50 g·mol−1 |
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Brinzolamide was approved as a generic medication in the United States in November 2020.[2]
Chemistry edit
Brinzolamide is a carbonic anhydrase inhibitor (specifically, carbonic anhydrase II). Carbonic anhydrase is found primarily in erythrocytes (but also in other tissues including the eye). It exists as a number of isoenzymes, the most active of which is carbonic anhydrase II (CA-II).
Indications edit
Use for the treatment of open-angle glaucoma and raised intraocular pressure due to either excess aqueous humor production or inadequate drainage of the humor via the trabecular meshwork.
Pharmacodynamics edit
Inhibition of carbonic anhydrase in the ciliary processes of the eye decreases aqueous humor secretion and thus lowers the intraocular pressure in the anterior chamber, presumably by reducing the rate of formation of bicarbonate ions with subsequent reduction in sodium and fluid transport; this may alleviate the effects of open-angle glaucoma.
Pharmacokinetics edit
Absorption edit
The recommended frequency for topical application is two times per day. Following ocular instillation, the suspension is systemically absorbed to some degree; however the plasma concentrations are low and generally below the limits of detection (less than 10 ng/mL) due to extensive binding by tissues and erythrocytes. Oral administration is less-favored due to variable absorption from the stomach mucosa and an increased side-effect profile versus ophthalmic administration.
Distribution edit
The compound is fairly well protein-bound (60%), but adheres extensively to the carbonic anhydrase-containing erythrocytes. Due to the abundance of readily-bound erythrocytes and minimal known metabolism, Brinzolamide's whole blood half-life is very long (111 days).
Metabolism edit
While definitive sites of metabolism have not been firmly established, there are several metabolites worthy of note. N-Desethylbrinzolamide is an active metabolite of the parent compound, and thus exhibits carbonic anhydrase inhibitory activity (largely carbonic anhydrase-I, when in the presence of Brinzolamide) and also accumulates in the erythrocytes. However, Brinzolamide's other known metabolites (N-Desmethoxypropylbrinzolamide and O-Desmethylbrinzolamide) either have no activity or their activity is currently unknown.
Excretion edit
Brinzolamide is excreted primarily unchanged (60%) in the urine, although the renal clearance rate has not been definitively determined. N-Desethylbrinzolamide is also found in the urine along with lower concentrations of the inactive metabolites, N-Desmethoxypropylbrinzolamide and O-Desmethylbrinzolamide; exact levels have not been definitively determined.
Cautions edit
Side effects edit
- Common, but mild: blurred vision; bitter, sour, or unusual taste; itching, pain, watering, or dryness of the eyes; feeling that something is in the eye; headache; runny nose
- Rare, but serious: fast or irregular heartbeat; fainting; skin rash, hives, or itching; severe eye irritation, redness, or swelling; swelling in the face, lips, or throat; wheezing or trouble breathing
Precautions edit
- Hypersensitivity to other sulfonamides
- Acute angle-closure glaucoma
- Concomitant administration of oral carbonic anhydrase inhibitors
- Moderate-to-severe chronic kidney disease or liver disease
Combinations edit
With timolol edit
The combination of brinzolamide with timolol is marketed under the trade name Azarga. This combination may be more effective than either medication alone.[3]
With brimonidine edit
The combination of brinzolamide with brimonidine is marketed under the trade name Simbrinza.[4][5] This combination may be more effective than either medication alone.[4][5]
References edit
- ^ "Brinzolamide ophthalmic (Azopt) Use During Pregnancy". Drugs.com. 16 May 2019. Retrieved 17 August 2020.
- ^ "First Generic Drug Approvals". U.S. Food and Drug Administration (FDA). Retrieved 13 February 2021.
- ^ Croxtall JD, Scott LJ (2009). "Brinzolamide/timolol: in open-angle glaucoma and ocular hypertension". Drugs & Aging. 26 (5): 437–46. doi:10.2165/00002512-200926050-00007. PMID 19552495.
- ^ a b "Simbrinza EPAR". European Medicines Agency. Retrieved 11 June 2020.
- ^ a b "Simbrinza- brinzolamide/brimonidine tartrate suspension/ drops". DailyMed. 9 September 2019. Retrieved 11 June 2020.
Further reading edit
- Ermis S, Ozturk F, Inan U (2005). "Comparing the effects of travoprost and brinzolamide on intraocular pressure after phacoemulsification". Eye. 19 (3): 303–7. doi:10.1038/sj.eye.6701470. PMID 15258611. S2CID 7285009.
- Iester M, Altieri M, Michelson G, Vittone P, Traverso C, Calabria G (2004). "Retinal peripapillary blood flow before and after topical brinzolamide". Ophthalmologica. 218 (6): 390–6. doi:10.1159/000080942. PMID 15564757. S2CID 24843128.
- Kaup M, Plange N, Niegel M, Remky A, Arend O (2004). "Effects of brinzolamide on ocular haemodynamics in healthy volunteers". Br J Ophthalmol. 88 (2): 257–62. doi:10.1136/bjo.2003.021485. PMC 1771998. PMID 14736787.
- March WF, Ochsner KI (2000). "The long-term safety and efficacy of brinzolamide 1.0% (azopt) in patients with primary open-angle glaucoma or ocular hypertension". Am J Ophthalmol. 129 (2): 136–143. doi:10.1016/S0002-9394(99)00343-8. PMID 10682964.
- Sall KN, Greff LJ, Johnson-Pratt LR, DeLucca PT, Polis AB, Kolodny AH, et al. (March 2003). "Dorzolamide/timolol combination versus concomitant administration of brimonidine and timolol: six-month comparison of efficacy and tolerability". Ophthalmology. 110 (3): 615–624. doi:10.1016/S0161-6420(02)01900-0. PMID 12623832.
