Finafloxacin
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| Trade names | Xtoro |
| Routes of administration | otic, oral, intavenous |
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| Elimination half-life | 10 hours |
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| Formula | C20H19FN4O4 |
| Molar mass | 398.394 g·mol−1 |
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Finafloxacin (Xtoro) is a fluoroquinolone antibiotic. In the United States, it is approved by the Food and Drug Administration to treat acute otitis externa (swimmer's ear) caused by the bacteria Pseudomonas aeruginosa and Staphylococcus aureus.[2]
Medical uses[edit]
Finafloxacin is used to treat a type of ear infection called acute otitis externa caused by Pseudomonas aeruginosa and Staphylococcus aureus bacteria.[3] In the clinical trial that led to the drug's approval, finafloxacin shortened the time to cessation of ear pain from an average of 6.8 days in patients taking a placebo to 3.5 days.[3]
Finafloxacin cannot be purchased over-the-counter, and is available by prescription only.[4]
Available forms[edit]
Finafloxacin is commercially available as a 0.3% otic (meaning "for the ear") suspension for topical administration in the United States.[3] The suspension should be warmed gently in the hands for 1–2 minutes before administration to prevent dizziness, and shaken before use.[3] It is necessary to remain still for 1 minute, with the affected ear facing up while lying on one's side, after administration to allow finafloxacin to penetrate the ear canal and reach the site of infection.[3]
Specific populations[edit]
Pregnancy[edit]
Finafloxacin is classified as pregnancy category C, meaning that the risk for harming a developing fetus has not been ruled out.[5]
Pediatrics[edit]
The efficacy and safety profile of finafloxacin ear drops are unknown in children younger than the age of 1 years old.[4]
Geriatrics[edit]
There are no limitations against using finafloxacin ear drops in the elderly.[4]
Adverse effects[edit]
The spectrum of adverse effects caused by finafloxacin vary by the method of administration. People that have administered finafloxacin into their ears in the form of drops have experienced ear itching and nausea (<1% for both).[6] People that have administered finafloxacin by mouth or intravenously (IV) have experienced gastrointestinal side effects (including diarrhea, flatulence, and nausea), fatigue, headaches, musculoskeletal problems, and injection site reactions (if IV).[6] Respiratory disorders, including rhinitis and nasopharyngitis, have also been associated with the use of finafloxacin.[7]
People that are allergic to other quinolones may be allergic to finafloxacin as well, and use may result in an allergic reaction in that population.[3] Adverse effects consistent with an allergic reaction to finafloxacin may include swelling of the lips, tongue, or throat, difficulty swallowing, and shortness of breath.[4]
Overdose[edit]
It is not thought that an overdose of the otic suspension is likely to cause severe or life-threatening symptoms.[8]
Interactions[edit]
Owing to the local effect of administering finafloxacin into the ears, it is unlikely that it will affect or be affected by other medications that are administered into the systemic circulation (e.g. drugs taken by mouth, or by injection).[8]
Pharmacology[edit]
Mechanism of action[edit]
Finafloxacin is a fluoroquinolone class antibiotic of the 8-cyano subclass (referring to the CN substituent at the 8th position).[6] Like other fluoroquinolones, its antibiotic activity is derived from its pharmacological mechanism of action as a type II topoisomerase poison, preventing bacteria from replicating and performing other vital, cellular functions.[6] However, unlike other fluoroquinolones, finafloxacin is highly active under acidic (pH 5.0–6.0) conditions, where certain bacteria (like Helicobacter pylori, a bacterium that is known to infect the human stomach, despite the harsh acidity)[9] thrive.[6] Other acidic conditions found on the human body include the vagina, urinary tract, and skin, though finafloxacin is currently not used to treat infections in these areas either.[7]
Finafloxacin has demonstrated bactericidal activity against a range of bacterial pathogens, especially at acidic pH, with a post-antibiotic effect.[6] Owing to its activity against both Gram-positive and Gram-negative bacteria, finafloxacin is classified as a broad-spectrum antibiotic.[6]
Pharmacokinetics[edit]
Finafloxacin has good oral bioavailability, meaning that a substantial portion of a dose taken by mouth reaches a person's systemic circulation.[6] Some people have experienced unintentional, quantifiable absorption of finafloxacin into systemic circulation after administering the drug via the ear.[6]
The elimination half-life of finafloxacin is approximately 10 hours in humans.[7]
Chemistry[edit]
The chemical structure of finafloxacin has been described as a "fluorinated quinolone derivative with 8-cyano-substituent and 7-pyrrolo-oxazinyl moiety."[7] Its low isoelectric point (pH 6.7) is lower than the isoelectric point of another fluoroquinolone class antibiotic called ciprofloxacin (pH 7.4), which accounts for finafloxacin's superior activity at low pH (5.0–6.0).[7]
There are some notable differences between the chemistry of finafloxacin and related fluoroquinolones. For example, the 8-cyano-substituent is not found in ciprofloxacin, and moxifloxacin has an 8-methoxy-substituent instead. The oxygen atom in the ring structure of finafloxacin makes the molecule more hydrophilic than ciprofloxacin.[10]
The chemical structure of finafloxacin is nearly identical to that of pradofloxacin.
Synthesis[edit]
The synthesis of finafloxacin has been described in detail in its patents.[11] An example of its synthesis is provided below:[11]
History[edit]
Finafloxacin is the first FDA approved medication in the United States that was first developed by a Singaporean drug company.[12] Finafloxacin was officially approved by the FDA on December 17, 2014.[13] The company, MerLion Pharmaceuticals, partnered with the North American company Alcon to produce the drug commercially in the United States.[14]
Research[edit]
Owing to its high bactericidal activity in acidic environments, Bartoletti et al have speculated that finafloxacin may be useful in the treatment of urinary tract infections in the future.[15] Finafloxacin's manufacturer, MerLion, has invested money in studying the use of finafloxacin for this indication.[14]
References[edit]
- ^ "Health Canada New Drug Authorizations: 2016 Highlights". Health Canada. 14 March 2017. Retrieved 7 April 2024.
- ^ "FDA approves Xtoro to treat swimmer's ear". Food and Drug Administration. December 17, 2014.
- ^ a b c d e f "Finafloxacin: New fluoroquinolone for acute otitis externa". pharmacist.com. American Pharmacists Association. February 1, 2015. Retrieved 14 August 2017.
- ^ a b c d "finafloxacin (Otic route)". drugs.com. Retrieved 15 August 2017.
- ^ "Rx Update: Xtoro (Finafloxacin Otic Suspension)". contemporaryclinic.pharmacytimes.com. Contemporary Clinic 2017 Pharmacy & Healthcare Communications, LLC. Retrieved 14 August 2017.
- ^ a b c d e f g h i McKeage K (April 2015). "Finafloxacin: first global approval". Drugs. 75 (6): 687–93. doi:10.1007/s40265-015-0384-z. PMID 25808831. S2CID 207488603.
- ^ a b c d e Kocsis B, Domokos J, Szabo D (May 2016). "Chemical structure and pharmacokinetics of novel quinolone agents represented by avarofloxacin, delafloxacin, finafloxacin, zabofloxacin and nemonoxacin". Annals of Clinical Microbiology and Antimicrobials. 15 (1): 34. doi:10.1186/s12941-016-0150-4. PMC 4878067. PMID 27215369.
- ^ a b "Xtoro". drugs.com. Retrieved 15 August 2017.
- ^ Blaser MJ (October 2006). "Who are we? Indigenous microbes and the ecology of human diseases". EMBO Reports. 7 (10): 956–60. doi:10.1038/sj.embor.7400812. PMC 1618379. PMID 17016449.
- ^ Lemaire S, Van Bambeke F, Tulkens PM (July 2011). "Activity of finafloxacin, a novel fluoroquinolone with increased activity at acid pH, towards extracellular and intracellular Staphylococcus aureus, Listeria monocytogenes and Legionella pneumophila" (PDF). International Journal of Antimicrobial Agents. 38 (1): 52–9. doi:10.1016/j.ijantimicag.2011.03.002. PMID 21596526.
- ^ a b "Finafloxacin". pharmacodia.com. Retrieved 14 August 2017.
- ^ Poh LC (July 29, 2017). "Biotech sector poised to deliver more health and wealth". SPH Digital News. The Straits Times. Retrieved 15 August 2017.
- ^ "Xtoro Approval History". drugs.com. Retrieved 15 August 2017.
- ^ a b Lane EJ (January 27, 2015). "Singapore's MerLion eyes partner for Phase III of Finafloxacin urinary infection trials". Questex LLC. FierceBiotech. Retrieved 15 August 2017.
- ^ Bartoletti R, Cai T, Perletti G, Wagenlehner FM, Bjerklund Johansen TE (2015). "Finafloxacin for the treatment of urinary tract infections". Expert Opinion on Investigational Drugs. 24 (7): 957–63. doi:10.1517/13543784.2015.1052401. PMID 26068714. S2CID 27148906.