Anti Microbal Flashcards
(38 cards)
kill either Gram-positive or Gram-negative bacteria
Narrow-spectrum antibiotics:
kill both Gram positives and Gram negatives.
Broad-spectrum antibiotics:
referred to as B-lactam drugs
PENICILLINS
molecular structure includes a four sided ring structure known as a
B-lactam ring
they are produced and can be purified directly from cultures of Penicillium moulds
• Penicillin G and Penicillin V.
NATURAL PENICILLINS
also B-lactam antibiotics and, like penicillin, are
produced by moulds.
• interfere with cell wall synthesis
• are bactericidal
CEPHALOSPORINS
agents are active primarily against Gram-positive bacteria.
First-generation
have increased activity against Gram- negative
bacteria
Second-generation cephalosporins
have even greater activity against Gram negatives
Third-generation cephalosporins
active against both Gram positives and Grams negatives, including P . Aeruginosa. e.g., Cefepime
Fourth-generation
expanded activity against aerobic Gram-positive cocci, including methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus epidermidis MRSE e g., Ceftaroline
Fifth-generation
powerful antibacterial
• e.g,imipenem &. meropenem
• target the cell envelope
- have excellent activity against a broad spectrum of
bacteria, including many aerobic Gram-positive bacteria, most aerobic Gram-negative bacteria, and most anaerobes.
CARBAPENEMS
• target the cell envelope.
• e.g.,vancomyci
• have excellent activity against most aerobic and
anaerobic Gram-positive bacteria.
• enterococci, are becoming resistant to these drugs
• have a number of toxic side effects.
GLYCOPEPTIDES
major factor that limits their use is their toxicity
Aminoglycosides
• E.g., T obramycin, Gentamicin &. Amikacin
AMIKACIN
• inhibit protein synthesis
• bacteriostatic at lower doses and bactericidal at higher doses include erythromycin, clarithromycin, and azithromycin
• effective against: chlamydias, mycoplasmas, T . pallidum, and Legionella spp.
Azithromycin and Erythromycin
MACROLIDES
• bactericidal drugs inhibit DNA synthesis
The most commonly used, Ciprofloxacin and Levofloxacin effective against members of the tamiye Enterobacteriaceae and aeruginosa.
fluoroquinolone
• drugs inhibit production of folic acid (a vitamin) in those bacteria that require p-aminobenzoic acid (PABA) to synthesize folic acid*
Sulfamethoxazole + Trimethoprim
Sulfonamide
a single antimicrobial agent is not sufficient to destroy all the pathogens that develop during the course of a disease
• two or more drugs may be used simultaneously to kill all the pathogens to prevent resistant mutant pathogens from emerging
MULTIDRUG THERAPY
which multidrug-resistant strains of Mycobacterium tuberculosis are frequently encountered four drugs
isoniazid,
rifampin,
pyrazinamide, and
ethambutol
a parenteral antibiotic, was the first drug® used to treat TB.
Streptomycin
discovered in 1952, was the first oral drug preparation effective against the tubercle bacillus.
Isoniazid
is a bactericidal drug that inhibits tubercle cell wall synthesis and blocks pyridoxine (vitamin B6), which is used for intracellular enzyme production
soniazid
is taken alone, bacterial resistance occurs quickly
Rifampin