1. Site of Action of Antibiotics

2. Cell Wall Synthesis Inhibitors
Some antimicrobial drugs selectively interfere with synthesis of the bacterial cell wall—a structure that mammalian cells do not possess.
The cell wall is composed of a polymer called peptidoglycan that consists of glycan units joined to each other by peptide cross-links.

3. To be maximally effective, inhibitors of cell wall synthesis require actively proliferating microorganisms.
They have little or no effect on bacteria that are not growing and dividing.
The most important members of this group of drugs are the β-lactam antibiotics (named after the β-lactam ring that is essential to their activity).

4. β-Lactam Antibiotics

6. Penicillins
Most widely effective and the least toxic drugs but increased resistance has limited their use.
Family differ from one another in:
the R substituent attached to the 6- aminopenicillanic acid residue, The nature of this side chain affects:
Antimicrobial spectrum.
Stability to stomach acid.
Crosshypersensitivity.
Susceptibility to bacterial degradative enzymes (β-lactamases)

8. Mechanism of Action
The penicillins interfere with the last step of bacterial cell wall synthesis (transpeptidation or cross-linkage)
Resulting in exposure of the osmotically less stable membrane.
Cell lysis can then occur
through osmotic pressure
through the activation of autolysins.
Bactericidal
Penicillins are only effective against rapidly growing organisms that synthesize a peptidoglycan cell wall.
Inactive against organisms devoid of this structure, such as mycobacteria, protozoa, fungi, and viruses.

9. Mechanism of Action Inactivation of Penicillin-binding proteins:
bacterial enzymes involved in the synthesis of the cell wall and in the maintenance of the morphologic features of the bacterium.
proteins on the bacterial cell membrane.

10. Inhibition of transpeptidase:
Penicillins inhibit this transpeptidase-catalyzed reaction.
cell wall integrity.

11. Inhibition of transpeptidase:

12. Production of autolysins:
Degradative enzymes that participate in the normal remodeling of the bacterial cell wall.
In the presence of a penicillin, the degradative action of the autolysins proceeds in the absence of cell wall synthesis.
penicillins inhibit:
cell wall synthesis.
destruction of the existing cell wall by autolysins.

13. Antibacterial spectrum
Penicillins antibacterial spectrum is determined by
Ability to cross the bacterial peptidoglycan cell wall to reach the PBPs in the periplasmic space.
Factors that determine the susceptibility of PBPs to these antibiotics include the size, charge, and hydrophobicity of the particular β-lactam antibiotic.
In general, gram-positive microorganisms have cell walls that are easily traversed by penicillins, and absence of resistance they are susceptible to these drugs.

14. Gram-negative microorganisms have an outer lipopolysaccharide membrane surrounding the cell wall that presents a barrier to the water-soluble penicillins.
Gram-negative bacteria have proteins inserted in the lipopolysaccharide layer that act as water-filled channels (called porins) to permit transmembrane entrance.

15. Natural penicillins
Penicillin G
Penicillin V
Obtained from fermentations of the fungus Penicillium chrysogenum.
Semisynthetic penicillins
Amoxicillin
Ampicillin
Attaching different R groups to the 6-aminopenicillanic acid nucleus.
Penicillin V is more acid stable than penicillin G.
Similar spectrum

16. Pencillin inactivation by β-lactamases (penicillinases) that are produced by the resistant bacteria.
Despite widespread use and increase in resistance.
Penicillin remains the drug of choice:
Gas gangrene (Clostridium perfringens) and
Syphilis (Treponema pallidum).

17. Antistaphylococcal penicillins:
Methicillin
Nafcillin
Oxacillin
Dicloxacillin
β-lactamase (penicillinase)-resistant penicillins.
Their use is restricted to the treatment of infections caused by penicillinase-producing staphylococci, including methicillinsensitive Staphylococcus aureus (MSSA).
Methicillin is not used clinically in the United States except in laboratory tests to identify resistant strains of S. aureus. Because of its toxicity (interstitial nephritis)
MRSA is currently a source of serious community and nosocomial (hospital-acquired) infections and is resistant to most commercially available β-lactam antibiotics.
The penicillinase-resistant penicillins have minimal to no activity against gram-negative infections.

18. Extended-spectrum penicillins
Ampicillin
Amoxicillin
Antibacterial spectrum similar to penicillin G but are more effective against gram negative bacilli.
Widely used in the treatment of respiratory infections
Amoxicillin is employed prophylactically by dentists in high-risk patients for the prevention of bacterial endocarditis.
Resistance to these antibiotics is now a major clinical problem because of inactivation by plasmid-mediated penicillinases.

19. Formulation with a β-lactamase inhibitors:
Amoxicillin/ clavulanic acid
Ampicillin/sulbactam
Without the β-lactamase inhibitor, MSSA is resistant to ampicillin and amoxicillin.

20. Antipseudomonal penicillins:
Piperacillin
Ticarcillin
Activity against Pseudomonas aeruginosa
Parenteral formulations only.
Piperacillin is the most potent.
They are effective against many gram-negative bacilli, but not against Klebsiella because of its constitutive penicillinase.
Ticarcillin /clavulanic acid
Piperacillin /tazobactam
Extends the antimicrobial spectrum of these antibiotics to include penicillinase-producing organisms.

21. Resistance β-Lactamase activity Decreased permeability to the drug
Altered PBPs

22. Route of Administration

23. Depot forms Procaine penicillin G benzathine penicillin G
IM and serve as depot forms.
They are slowly absorbed into the circulation and persist at low levels over a long time period.

24. Pharmacokineics Absorption:
Food decreases the absorption of all the penicillinase-resistant penicillins because as gastric emptying time increases, the drugs are destroyed by stomach acid.
Should be taken on an empty stomach.
Distribution:
The β-lactam antibiotics distribute well throughout the body.
All the penicillins cross the placental barrier
No teratogenic effects.
Penetration into bone or cerebrospinal fluid (CSF) is insufficient for therapy unless these sites are inflamed.
Penicillin levels in the prostate are insufficient to be effective against infections.

25. Metabolism: Host metabolism of the β-lactam antibiotics is usually insignificant.
Excretion: The primary route of excretion is through kidney
Patients with impaired renal function must have dosage regimens adjusted.
Probenecid inhibits the secretion of penicillins by competing for active tubular secretion via the organic acid transporter increase blood levels.
The penicillins are also excreted in breast milk.

26. Adverse reactions Hypersensitivity: Approximately 5% percent
Cross-allergic reactions occur among the β-lactam antibiotics.
Patient history

27. Hematologic toxicities:
Nephritis:
Acute interstitial nephritis ( Methicillin )
Neurotoxicity:
Seizures if injected intrathecally
GABAergic inhibition.
Hematologic toxicities:
Decreased coagulation