Ticarcillin

Chemical formula: C₁₅H₁₆N₂O₆S₂  Molecular mass: 384.427 g/mol  PubChem compound: 36921

Pharmacodynamic properties

Ticarcillin disrupts bacterial cell wall development by inhibiting peptidoglycan synthesis and/or by interacting with penicillin-binding proteins. Ticarcillin is susceptible to degradation by β-lactamases, so the spectrum of activity does not normally include organisms which produce these enzymes.

Pharmacokinetic properties

Distribution

Ticarcillin has been found to be approximately 45% bound to human serum protein and clavulanic acid approximately 25% bound. Ticarcillin can be detected in tissues and interstitial fluid following parenteral administration.

Distribution of ticarcillin into bile and pleural fluid has been demonstrated. The results of experiments involving the administration of clavulanic acid to animals suggest that this compound, like ticarcillin, is well distributed in body tissues.

Renal Impairment

An inverse relationship exists between the serum half-life of ticarcillin and creatinine clearance. The half-life of ticarcillin in patients with renal failure is approximately 13 hours.

Ticarcillin may be removed from patients undergoing dialysis; the actual amount removed depends on the duration and type of dialysis.

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