Aztreonam | |
---|---|
Drug class | |
Class identifiers | |
Use | Bacterial infection |
ATC code | J01DF |
External links | |
MeSH | D008997 |
Legal status | |
In Wikidata |
Monobactams are bacterially-produced monocyclic β-lactam antibiotics. The β-lactam ring is not fused to another ring, in contrast to most other β-lactams. [1]
Monobactams are narrow-spectrum antibiotics [2] effective only against (strictly or facultatively [3]) aerobic Gram-negative bacilli, [4] [5] [3] exhibiting a high level of resistance to beta-lactamases of these organisms. [3] Due to their narrow spectrum, monobactams can be used to treat infections by susceptible bacteria without disrupting the patient's microbiota. [2] Monobactams are nevertheless seldom used. [2]
Aztreonam is the principal [4] and sole commercially available member of monobactams. [6] Other monobactams include tigemonam, [7] nocardicin A, and tabtoxin.[ citation needed]
Monobactams exert their antibacterial effects by binding to penicillin-binding proteins (PBPs), thereby inhibiting bacterial wall synthesis. [5] Monobactams exhibit poor affinity for PBPs of Gram-positive bactera as well as of strictly anaerobic bacteria, resulting in a lack of significant antimicrobial activity against these kinds of organisms. [3] Monobactams are synergetic with aminoglycosides, and piperacillin. [5]
Bacterial resistance to monobactams have been observed, and is mediated by bacterial beta-lactamases. [5]
Adverse effects to monobactams can include skin rash and occasional abnormal liver functions.[ citation needed]
Monobactam antibiotics exhibit no IgE cross-reactivity reactions with penicillin but have shown some cross reactivity with cephalosporins, most notably ceftazidime, which contains an identical side chain as aztreonam. [8] Monobactams can trigger seizures in patients with history of seizures, although the risk is lower than with penicillins.[ citation needed]
Siderophore-conjugated monobactams show promise for the treatment of multi drug-resistant pathogens. [9]
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cite book}}
: CS1 maint: location missing publisher (
link)
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cite book}}
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Aztreonam | |
---|---|
Drug class | |
Class identifiers | |
Use | Bacterial infection |
ATC code | J01DF |
External links | |
MeSH | D008997 |
Legal status | |
In Wikidata |
Monobactams are bacterially-produced monocyclic β-lactam antibiotics. The β-lactam ring is not fused to another ring, in contrast to most other β-lactams. [1]
Monobactams are narrow-spectrum antibiotics [2] effective only against (strictly or facultatively [3]) aerobic Gram-negative bacilli, [4] [5] [3] exhibiting a high level of resistance to beta-lactamases of these organisms. [3] Due to their narrow spectrum, monobactams can be used to treat infections by susceptible bacteria without disrupting the patient's microbiota. [2] Monobactams are nevertheless seldom used. [2]
Aztreonam is the principal [4] and sole commercially available member of monobactams. [6] Other monobactams include tigemonam, [7] nocardicin A, and tabtoxin.[ citation needed]
Monobactams exert their antibacterial effects by binding to penicillin-binding proteins (PBPs), thereby inhibiting bacterial wall synthesis. [5] Monobactams exhibit poor affinity for PBPs of Gram-positive bactera as well as of strictly anaerobic bacteria, resulting in a lack of significant antimicrobial activity against these kinds of organisms. [3] Monobactams are synergetic with aminoglycosides, and piperacillin. [5]
Bacterial resistance to monobactams have been observed, and is mediated by bacterial beta-lactamases. [5]
Adverse effects to monobactams can include skin rash and occasional abnormal liver functions.[ citation needed]
Monobactam antibiotics exhibit no IgE cross-reactivity reactions with penicillin but have shown some cross reactivity with cephalosporins, most notably ceftazidime, which contains an identical side chain as aztreonam. [8] Monobactams can trigger seizures in patients with history of seizures, although the risk is lower than with penicillins.[ citation needed]
Siderophore-conjugated monobactams show promise for the treatment of multi drug-resistant pathogens. [9]
{{
cite book}}
: CS1 maint: location missing publisher (
link)
{{
cite book}}
: |editor4-first=
has generic name (
help); |journal=
ignored (
help)