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Class of antibiotics | Antibiotics | Mechanism of action | References |
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Penicillin | Ampicillin, piperacillin, piperacillin-tazobactam, and cefepime | Disrupt the synthesis of the peptidoglycan layer of bacterial cell walls | [34] |
Penicillin combinations | Amoxicillin/clavulanate | The second component reduces the effectiveness of some forms of bacterial resistance to the first component | [35] |
Cephalosporins | Cefuroxime 2nd generation, cefoxitin 2nd generation, cefixime 3rd generation, ceftazidime 3rd generation, ceftriaxone 3rd generation, cefpodoxime 2nd generation | Disrupt the synthesis of the peptidoglycan layer of bacterial cell walls | [36] |
Carbapenems | Imipenem, meropenem | Inhibition of cell wall synthesis | [34] |
Aminoglycosides | Amikacin, gentamicin, netilmicin, tobramycin, streptomycin | It inhibits the translocation of the peptidyl-tRNA from the A-site to the P-site, leaving the bacterium unable to synthesize proteins vital to its growth | [37] |
Quinolones/fluoroquinolones | Ciprofloxacin, levofloxacin, norfloxacin | Inhibits the bacterial DNA gyrase or the topoisomerase IV enzyme, thereby inhibiting DNA replication and transcription | [34] |
Fosfomycin | Fosfomycin | Inactivates enol pyruvyl transferase, thereby blocking cell wall synthesis | [38] |
Nitrofurans | Nitrofurantoin | Reduced by bacterial flavoproteins to reactive intermediates that inhibit bacterial ribosomes and other macromolecules | [39] |
Sulfonamides | Trimethoprim-sulfamethoxazole | Folate synthesis inhibition | [40] |
Monobactams | Aztreonam | Disrupt the synthesis of the peptidoglycan layer of bacterial cell walls | [41] |
Tetracyclines | Tetracycline, doxycycline | Inhibits the binding of aminoacyl-tRNA to the mRNA-ribosome complex. They do so mainly by binding to the 30S ribosomal subunit in the mRNA translation complex | [34] |
Glycylcycline | Tigecycline | It has a similar structure and action to tetracycline, but it is stronger | [42] |
Polymyxin | Colistin | Blocks the peptidoglycan bacterial cell wall outside of the inner membrane | [43] |
Lincosamides | Clindamycin | Binds to the 50S subunit of bacterial ribosomal RNA thereby inhibiting protein synthesis | [44] |
Macrolides | Clarithromycin, erythromycin | Inhibition of bacterial protein biosynthesis by binding reversibly to the subunit 50S S of the bacterial ribosome, thereby inhibiting translocation of peptidyl-tRNA | [45] |
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