Oxacephem: Difference between revisions

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'''Oxacephem''' is a type of [[antibiotic]] that belongs to the [[cephalosporin]] class. It is a broad-spectrum antibiotic that is used to treat a variety of bacterial infections. Oxacephem is not commonly used in the United States, but it is available in some other countries.
{{Short description|A class of beta-lactam antibiotics}}
{{Use dmy dates|date=October 2023}}


== Mechanism of Action ==
'''Oxacephems''' are a class of [[beta-lactam antibiotics]] that are structurally related to the [[cephalosporins]]. They are characterized by the presence of an oxygen atom in place of the sulfur atom found in the cephalosporin core structure. This modification imparts unique properties to oxacephems, influencing their antibacterial activity and pharmacokinetic profiles.
Oxacephem works by inhibiting the synthesis of the bacterial cell wall. This causes the bacteria to become unstable and eventually die. The exact mechanism of action is not fully understood, but it is believed to involve the binding of the antibiotic to penicillin-binding proteins (PBPs) in the bacterial cell wall.


== Uses ==
==Structure and Mechanism of Action==
Oxacephem is used to treat a variety of bacterial infections, including those caused by [[Staphylococcus aureus]], [[Streptococcus pneumoniae]], and [[Escherichia coli]]. It is also used to treat infections caused by [[Klebsiella]] species and [[Proteus mirabilis]].
Oxacephems, like other beta-lactam antibiotics, exert their antibacterial effects by inhibiting bacterial [[cell wall]] synthesis. They achieve this by binding to and inactivating [[penicillin-binding proteins]] (PBPs), which are essential for the cross-linking of the [[peptidoglycan]] layer of bacterial cell walls. The disruption of cell wall synthesis leads to cell lysis and death, particularly in actively dividing bacteria.


== Side Effects ==
The unique feature of oxacephems is the replacement of the sulfur atom in the cephalosporin nucleus with an oxygen atom. This structural change can affect the spectrum of activity and resistance to beta-lactamases, enzymes produced by some bacteria that confer resistance to beta-lactam antibiotics.
Like all antibiotics, oxacephem can cause side effects. These may include nausea, vomiting, diarrhea, and allergic reactions. In rare cases, it can cause serious side effects such as [[Clostridium difficile]] infection and [[anaphylaxis]].


== Drug Interactions ==
==Clinical Uses==
Oxacephem can interact with other medications, including other antibiotics, blood thinners, and certain types of cancer medications. It is important to tell your doctor about all the medications you are taking before starting treatment with oxacephem.
Oxacephems are used to treat a variety of bacterial infections, particularly those caused by Gram-positive and some Gram-negative bacteria. They are often reserved for infections where other beta-lactams may not be effective due to resistance or patient allergies.


== See Also ==
===Common Indications===
* [[Cephalosporin]]
* [[Respiratory tract infections]]
* [[Urinary tract infections]]
* [[Skin and soft tissue infections]]
* [[Intra-abdominal infections]]
 
==Pharmacokinetics==
The pharmacokinetic properties of oxacephems can vary depending on the specific agent within this class. Generally, they are well absorbed after oral administration, although some may require parenteral administration for optimal efficacy. Oxacephems are distributed widely in body tissues and fluids, and they are primarily excreted unchanged in the urine.
 
==Side Effects==
As with other beta-lactam antibiotics, oxacephems can cause a range of side effects. Common adverse effects include:
* [[Allergic reactions]], ranging from mild rashes to severe [[anaphylaxis]]
* [[Gastrointestinal disturbances]], such as [[nausea]], [[vomiting]], and [[diarrhea]]
* [[Hematological effects]], including [[neutropenia]] and [[thrombocytopenia]]
 
==Resistance==
Bacterial resistance to oxacephems, as with other beta-lactams, can occur through several mechanisms:
* Production of beta-lactamases that hydrolyze the beta-lactam ring
* Alteration of PBPs, reducing the binding affinity of the antibiotic
* Efflux pumps that expel the antibiotic from the bacterial cell
 
==Related Pages==
* [[Beta-lactam antibiotics]]
* [[Cephalosporins]]
* [[Penicillin-binding proteins]]
* [[Antibiotic resistance]]
* [[Antibiotic resistance]]


[[Category:Beta-lactam antibiotics]]
[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Cephalosporin antibiotics]]
<gallery caption="Oxacephem">
 
File:Latamoxef.svg|Latamoxef
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File:Flomoxef.png|Flomoxef
 
== Oxacephem ==
<gallery>
File:Oxacephem Latamoxef.svg|Description of Oxacephem Latamoxef
File:Flomoxef.png|Description of Flomoxef
</gallery>
</gallery>

Latest revision as of 01:24, 20 February 2025

A class of beta-lactam antibiotics



Oxacephems are a class of beta-lactam antibiotics that are structurally related to the cephalosporins. They are characterized by the presence of an oxygen atom in place of the sulfur atom found in the cephalosporin core structure. This modification imparts unique properties to oxacephems, influencing their antibacterial activity and pharmacokinetic profiles.

Structure and Mechanism of Action[edit]

Oxacephems, like other beta-lactam antibiotics, exert their antibacterial effects by inhibiting bacterial cell wall synthesis. They achieve this by binding to and inactivating penicillin-binding proteins (PBPs), which are essential for the cross-linking of the peptidoglycan layer of bacterial cell walls. The disruption of cell wall synthesis leads to cell lysis and death, particularly in actively dividing bacteria.

The unique feature of oxacephems is the replacement of the sulfur atom in the cephalosporin nucleus with an oxygen atom. This structural change can affect the spectrum of activity and resistance to beta-lactamases, enzymes produced by some bacteria that confer resistance to beta-lactam antibiotics.

Clinical Uses[edit]

Oxacephems are used to treat a variety of bacterial infections, particularly those caused by Gram-positive and some Gram-negative bacteria. They are often reserved for infections where other beta-lactams may not be effective due to resistance or patient allergies.

Common Indications[edit]

Pharmacokinetics[edit]

The pharmacokinetic properties of oxacephems can vary depending on the specific agent within this class. Generally, they are well absorbed after oral administration, although some may require parenteral administration for optimal efficacy. Oxacephems are distributed widely in body tissues and fluids, and they are primarily excreted unchanged in the urine.

Side Effects[edit]

As with other beta-lactam antibiotics, oxacephems can cause a range of side effects. Common adverse effects include:

Resistance[edit]

Bacterial resistance to oxacephems, as with other beta-lactams, can occur through several mechanisms:

  • Production of beta-lactamases that hydrolyze the beta-lactam ring
  • Alteration of PBPs, reducing the binding affinity of the antibiotic
  • Efflux pumps that expel the antibiotic from the bacterial cell

Related Pages[edit]