Arbekacin: Difference between revisions
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{{Short description| | {{Short description|An aminoglycoside antibiotic used in the treatment of bacterial infections}} | ||
''' | ==Arbekacin== | ||
[[File:Arbekacin_structure.svg|thumb|right|Chemical structure of Arbekacin]] | |||
'''Arbekacin''' is an [[aminoglycoside]] [[antibiotic]] that is used primarily in the treatment of infections caused by [[Gram-positive bacteria]], including [[methicillin-resistant Staphylococcus aureus]] (MRSA). It is a semi-synthetic derivative of [[kanamycin]], which is another aminoglycoside antibiotic. | |||
== | ==Mechanism of action== | ||
Arbekacin works by binding to the bacterial [[ribosome]], specifically the 30S subunit, and inhibiting protein synthesis. This action is bactericidal, meaning it kills the bacteria rather than merely inhibiting its growth. The binding of arbekacin to the ribosome interferes with the initiation complex of protein synthesis and causes misreading of mRNA, leading to the production of nonfunctional or toxic peptides. | |||
==Clinical use== | |||
Arbekacin is primarily used in the treatment of infections caused by resistant strains of bacteria, such as MRSA. It is often reserved for cases where other antibiotics are ineffective due to resistance. Arbekacin is administered intravenously, and its use is typically limited to hospital settings. | |||
== | ==Side effects== | ||
As with other aminoglycosides, arbekacin can cause [[nephrotoxicity]] and [[ototoxicity]]. Nephrotoxicity refers to kidney damage, while ototoxicity refers to damage to the ear, which can result in hearing loss or balance issues. Monitoring of drug levels and kidney function is important during treatment to minimize these risks. | |||
== | ==Pharmacokinetics== | ||
The | Arbekacin is not absorbed from the gastrointestinal tract, so it must be administered parenterally. It is distributed widely in the body and is excreted primarily by the kidneys. The half-life of arbekacin can be prolonged in patients with renal impairment, necessitating dose adjustments. | ||
* | ==Related pages== | ||
* | * [[Aminoglycoside]] | ||
* | * [[Antibiotic resistance]] | ||
* | * [[Methicillin-resistant Staphylococcus aureus]] | ||
* [[Kanamycin]] | |||
[[Category:Aminoglycoside antibiotics]] | |||
[[Category:Antibiotics]] | |||
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[[Category: | |||
Latest revision as of 11:03, 15 February 2025
An aminoglycoside antibiotic used in the treatment of bacterial infections
Arbekacin[edit]

Arbekacin is an aminoglycoside antibiotic that is used primarily in the treatment of infections caused by Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). It is a semi-synthetic derivative of kanamycin, which is another aminoglycoside antibiotic.
Mechanism of action[edit]
Arbekacin works by binding to the bacterial ribosome, specifically the 30S subunit, and inhibiting protein synthesis. This action is bactericidal, meaning it kills the bacteria rather than merely inhibiting its growth. The binding of arbekacin to the ribosome interferes with the initiation complex of protein synthesis and causes misreading of mRNA, leading to the production of nonfunctional or toxic peptides.
Clinical use[edit]
Arbekacin is primarily used in the treatment of infections caused by resistant strains of bacteria, such as MRSA. It is often reserved for cases where other antibiotics are ineffective due to resistance. Arbekacin is administered intravenously, and its use is typically limited to hospital settings.
Side effects[edit]
As with other aminoglycosides, arbekacin can cause nephrotoxicity and ototoxicity. Nephrotoxicity refers to kidney damage, while ototoxicity refers to damage to the ear, which can result in hearing loss or balance issues. Monitoring of drug levels and kidney function is important during treatment to minimize these risks.
Pharmacokinetics[edit]
Arbekacin is not absorbed from the gastrointestinal tract, so it must be administered parenterally. It is distributed widely in the body and is excreted primarily by the kidneys. The half-life of arbekacin can be prolonged in patients with renal impairment, necessitating dose adjustments.