Mafenide

Chemical compound
  • D06BA03 (WHO)
Legal statusLegal status
  • In general: ℞ (Prescription only)
Identifiers
  • 4-(Aminomethyl)benzenesulfonamide
CAS Number
  • 138-39-6 ☒N
PubChem CID
  • 3998
ChemSpider
  • 3858 checkY
UNII
  • 58447S8P4L
KEGG
  • D02351 checkY
ChEMBL
  • ChEMBL419 checkY
CompTox Dashboard (EPA)
  • DTXSID6047860 Edit this at Wikidata
ECHA InfoCard100.004.843 Edit this at WikidataChemical and physical dataFormulaC7H10N2O2SMolar mass186.23 g·mol−13D model (JSmol)
  • Interactive image
  • O=S(=O)(c1ccc(cc1)CN)N
InChI
  • InChI=1S/C7H10N2O2S/c8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,5,8H2,(H2,9,10,11) checkY
  • Key:TYMRLRRVMHJFTF-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Mafenide (INN; usually as mafenide acetate, trade name Sulfamylon) is a sulfonamide-type medication used as an antibiotic. It was approved by the FDA in 1948.[citation needed]

Uses

Mafenide is used to treat severe burns.[1][2] It is used topically as an adjunctive therapy for second- and third-degree burns. It is bacteriostatic against many gram-positive and gram-negative organisms, including Pseudomonas aeruginosa. Some sources state that mafenide is more appropriate for non-facial burns, while chloramphenicol/prednisolone or bacitracin are more appropriate for facial burns.[3]

Mechanism of action

Mafenide works by reducing the bacterial population present in the avascular tissues of burns and permits spontaneous healing of deep partial-thickness burns. [citation needed]

Adverse reactions

Adverse reactions can include superinfection, pain or burning upon application, rash, pruritus, tachypnea, or hyperventilation. Mafenide is metabolized to a carbonic anhydrase inhibitor, which could potentially result in metabolic acidosis.[4]

Drug interactions

There are no significant interactions.[citation needed]

Contraindications

Mafenide is contraindicated in those with sulfonamide hypersensitivity or renal impairment.

Dosage

For use as adjunctive therapy for second- and third-degree burns to prevent infection, adults and children should apply topically to a thickness of approximately 1.6 mm to cleaned and debrided wound once or twice per day with a sterile gloved hand. The burned area should be covered with cream at all times.[citation needed]

References

  1. ^ Siuda JF, Cihonski CD (November 1972). "New compounds: carbamate derivatives of mafenide (homosulfanilamide)". Journal of Pharmaceutical Sciences. 61 (11): 1856–1857. doi:10.1002/jps.2600611143. PMID 4652670.
  2. ^ Haynes BW (June 1971). "Mafenide acetate in burn treatment". The New England Journal of Medicine. 284 (23): 1324. doi:10.1056/NEJM197106102842310. PMID 5576444.
  3. ^ Haik J, Ashkenazy O, Sinai S, Tessone A, Barda Y, Winkler E, et al. (November 2005). "Burn care standards in Israel: lack of consensus". Burns. 31 (7): 845–849. doi:10.1016/j.burns.2005.04.012. PMID 15967581.
  4. ^ "Sulfamylon (Mafenide Acetate)". RxList. Retrieved 22 December 2022.

External links

  • Mafenide information on RxList
  • v
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Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/or DNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
Nitrofuran derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins