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Antibiotics
Compounds naturally produced by molds and bacteria that inhibit the growth of or kill other microorganisms.
Selective Toxicity
The ability of antimicrobial drugs to cause greater harm to microorganisms than to the human host.
Spectrum of Activity
The range of bacteria species affected by an antibiotic, categorized as broad spectrum or narrow spectrum.
Half-life
The time required for half of the concentration of a drug to be eliminated from the body.
Antimicrobial Resistance
The ability of bacteria to resist the effects of antimicrobial drugs, categorized as innate/intrinsic or acquired resistance.
B-lactam drugs
Antibiotics that inhibit enzymes critical for peptidoglycan synthesis in bacterial cell walls.
Ribosome
Cellular structure targeted by antimicrobial drugs like aminoglycosides, tetracyclines, macrolides, and lincosamides to inhibit protein synthesis.
Fluoroquinolones
Synthetic drugs that inhibit bacterial DNA topoisomerases, affecting DNA replication and repair.Nucleic acid Synthesis
Sulfonamides
Antibiotics that competitively inhibit enzymes in the folate pathway of bacteria, essential for their growth.
Polymyxin B
An antimicrobial drug that binds to Gram-negative bacterial cell membranes, altering permeability and causing leakage.
synergistic
one drug adds to the activity of another
Antagonistic
one Drug interferes with the other
Additive
no effect
Bacteriostatic Drugs
inhibit bacterial growth, hosts defenses eliminate
Bacterial Drugs
kill bacteria
Drug inactivating enzymes
can inactivate drugs by modifing them
Alteration in Target Molecule
minor changes can prevent antimicrobial drugs from binding
Decreased uptore of Drug
change in porins of outer membrane in Gram Neg bacteria altering permeability and preventing drug uptake
Vancomycin
Cell wall synthesis (Peptidoglycan)
daptomycin
Cell membrane integrity
Trimethoprim
metabolic pathways (Folate Synthesis)
aminogycosides
protien synthesis
Rifamycin
Nucleic acid Synthesis
Tetracyclines
Protein Synthesis