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Antimicrobial DrugsAntimicrobial Drugs
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Classification of AntibioticsClassification of Antibioticsby Mechanism of Actionby Mechanism of Action
1. Inhibition of cell wall synthesis– Beta-lactam drugs
• Penicillins• Cephalosporins• Carbapenems
– The others• Cycloserine• Vancomycin• bacitracin
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Classification of AntibioticsClassification of Antibioticsby Mechanism of Actionby Mechanism of Action
2. Disruption of cell membranes– Polymyxin– Polyenes (anti-
fungal agents)
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Classification of AntibioticsClassification of Antibioticsby Mechanism of Actionby Mechanism of Action
3. Inhibition of protein synthesis– Reversible inhibition (bacteristatic)
• Chloramphenicol• The tetracyclines• The macrolides (erythromycin)• Clindamycin• Streptogramins• Linezolid
– Irreversible – the bactericidal aminoglycosides
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4. inhibition of nucleic acid synthesis
1. rifamycins (RNA)
2. quinolones (DNA)
5. antimetabolites (folate metabolism)
1. trimethoprim
2. sulfonamides
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Susceptibility and ResistanceSusceptibility and Resistance
• In vitro values are guides, not rules
• In vivo, bug is resistant if cidal concentrations are toxic to the host
• Achievable serum concentrations are what determine susceptibility or resistance to drug– Low pH, high protein
concentrations, anoxia– Pharmacological parameters of
drugs (serum versus other bodily fluids) Kirby Bauer Plate
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Bacterial Mechanisms Bacterial Mechanisms of Resistanceof Resistance
1. Prevent antibiotic from reaching its target
2. Destroy or inactivate antibiotic before it reaches target
3. Alter target
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Choosing the right antibiotic – is it really Choosing the right antibiotic – is it really neededneeded??
• Nature of the illness – is it a bacterial infection or something else?
• Presumptive diagnosis (based on history and clinical symptoms) – Empiric therapy – broad spectrum drug– Specific therapy – narrow spectrum
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Choosing the right antibiotic – Choosing the right antibiotic – pharmacokinetic considerationspharmacokinetic considerations..
• Location of infection– Some antibiotics may or may not reach
therapeutic concentrations in certain bodily fluids (ex. CSF and urine)
• Degree to which antibiotic binds serum proteins– Excessive binding will affect passive diffusion
of antibiotic from serum to tissue
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Choosing the right antibiotic Choosing the right antibiotic – – host factors.host factors.
• Status of host immune system (cidal vs. static)
• Local environment of infected site (pus, foreign bodies, etc)
• Age (organ function in newborns and elderly)
• Inherited metabolic disorder
• Pregnancy (fetal or neonatal development)
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Choosing the right antibiotic Choosing the right antibiotic – host factors– host factors..
• drug allergies– Rashes– Anaphylaxis
• Co-morbid conditions are aggravated by some antibiotics– Seizures– Blood disorders
SJS Syndrome
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The ConsequencesThe Consequences
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General Outline for AntibioticsGeneral Outline for Antibiotics• Chemistry • Effect on microbes
– Spectrum of coverage– Mechanism(s) of action– Mechanism(s) of resistance
• Pharmacology of antibiotic class– Absorbance– Fate after absorption– Excretion
• Pharmacology of select agents• Therapeutic uses• Toxicity/contraindications
– Common (> 10%)– Uncommon (1-9%)– Rare (< 1%)
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SulfonamidesSulfonamides
• Analogues of para-aminobenzoic acid
• Broad spectrum
• Competitive inhibitors of dihydropteroate synthase – needed for folic acid synthesis
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SulfonamidesSulfonamides
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• Cidal in urine
• Mechanisms of resistance
– Altered affinity of enzyme for drug
– Decreased permeability or active efflux
– New pathway of folic acid synthesis
SulfonamidesSulfonamides
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SulfonamidesSulfonamides
• Mostly absorbed from GI tract• Binds variably to serum
albumin • Wide tissue distribution,
including transplacentally• Variably inactivated in liver by
acetylation and then excreted in urine
• Some agents can precipitate in acid urine
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Rapidly Absorbed and EliminatedRapidly Absorbed and Eliminated SulfonamidesSulfonamides
• Bind extensively to plasma proteins
• Highly concentrated in urine (cidal)
Sulfisoxazole, sulfamethoxazole, sulfadiazine
Sulfamethoxazole combined with trimethoprim (Bactrim) is widely used to treat a variety of infections (esp. UTI)
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Poorly AbsorbedPoorly Absorbed in GI tract in GI tract SulfonamidesSulfonamides
• Sulfasalazine
• Used to treat ulcerative colitis and irritable bowel syndrome
• Gut flora metabolize drug into 2 compounds, 1 toxic, 1 therapeutic (5-aminosalicylate)
Ulcerative Colitis
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Sulfonamides forSulfonamides for Topical UseTopical Use
• SulfacetamideSulfacetamide– Good penetration in eye– Non-irritating
• Silver sulfadiazineSilver sulfadiazine– Prevention and treatment
of burn wound infections
Bacterial corneal infection
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Long Acting Long Acting SulfonamideSulfonamide
SulfadoxineSulfadoxine
• Serum half-life is measured in days rather than minutes or hours
• Combined with Pyrimethamine to treat malaria
Plasmodium vivax
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Therapeutic Uses Therapeutic Uses of Sulfonamidesof Sulfonamides
• Urinary tract infections
• Nocardiosis: • Nocardia asteroides• Nocardia brasiliensis
• Toxoplasmosis (avoid using in pregnant women)
Nocardia asteroides
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Toxicity/Contraindications Toxicity/Contraindications of Sulfonamides - UTof Sulfonamides - UT
• Crystallization in acid urine– Common to uncommon depending on drug– Alkalize urine or increase hydration
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Toxicity/Contraindications Toxicity/Contraindications of Sulfonamides - of Sulfonamides - bloodblood
• Acute hemolytic anemia – Rare to extremely rare– Associated with glucose-6-phosphate
dehydrogenase activity in RBC
• Agranulocytosis (extremely rare)
• Aplastic anemia (extremely rare)
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Toxicity/Contraindications Toxicity/Contraindications of Sulfonamides - of Sulfonamides - immuneimmune
• Hypersensitivity reactions (common to uncommon)– Skin and mucous membrane manifestations
(rashes)– Serum sickness– Focal or diffuse necrosis of the liver (rare)
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Toxic Epidermal Necrolysis (TEN)Toxic Epidermal Necrolysis (TEN)
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Toxicity/Contraindications Toxicity/Contraindications of Sulfonamides - miscellaneousof Sulfonamides - miscellaneous
• Nausea, anorexia, vomiting (common)
• Kernicterus – Displacement of bilirubin from
plasma albumin to brain resulting in encephalopathy
– Never give sulfa drugs to a pregnant or lactating woman
• Potentiation of oral anticoagulants, sulfonylurea hypoglycemic drugs, and hydantoin anticonvulsantsBilirubin
deposits in neonatal
brain
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The QuinolonesThe Quinolones• Naladixic acid was a byproduct of chloroquine synthesis• Current drugs are fluorinated 4-quinolones• Broad coverage (some broader than others)• Targets DNA topoisomerase II (DNA gyrase) (G-) and
topoisomerase IV (G+)• Resistance due to efflux and mutations in targets
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QuinolonesQuinolones
• Favorable pharmacological attributes– Orally administered, quickly absorbed,
even with a full stomach– Excellent bioavailability in a wide range of
tissues and body fluids (including inside cells)
• Mostly cleared by the kidneys– Exceptions are pefloxacin and moxifloxacin
which are metabolized by liver
• Ciprofloxacin, ofloxacin, and pefloxacin are excreted in breast milk
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Therapeutic Uses of QuinolonesTherapeutic Uses of Quinolones
• Urinary tract infections• Prostatitis• STD’s
– Chlamydia– Chancroid– Not syphilis or gonorrhea
(due to increased resistance)
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Therapeutic Uses of QuinolonesTherapeutic Uses of Quinolones
• GI and abdominal – Travelers diarrhea– Shigellosis– Typhoid fever
•
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• Respiratory tract– All work well against atypical pneumonia agents (eg,
chlamydia, mycoplasma, and legionella), – New agents for strep. Pneumonia– Respiratory fluoroquinolones: Levofloxacin,
gatifloxacin, gemifloxacin, and moxifloxacin.– are effective and used increasingly for treatment of
upper and lower respiratory tract infections.
Therapeutic Uses of QuinolonesTherapeutic Uses of Quinolones
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Therapeutic Uses of QuinolonesTherapeutic Uses of Quinolones
• Bone, joint, soft tissue– Ideal for chronic
osteomylitis• Resistance developing
in S. aureus, P. aeruginosa, and S. marcesens
– Good against polymicrobial infections like diabetic foot ulcers
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Therapeutic Uses of QuinolonesTherapeutic Uses of Quinolones
• Ciprofloxacin for anthrax and tularemia (Francisella tularensis)
• Combined with other drugs, useful for atypical Mycobacterium sp. or for prophylaxis in neutropenic patients
Pulmonary Pulmonary AnthraxAnthrax
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Toxicity/Contraindications of QuinoloneToxicity/Contraindications of Quinolone
• Nausea, vomiting, abdominal discomfort (common)• Diarrhea and antibiotic-associated colitis (uncommon to
rare)• CNS side effects
– Mild headache and dizziness (common to rare)– Hallucinations, delirium, and seizures (rare)
• May damage growing cartilage and cause an arthropathy. Thus, these drugs are not routinely recommended for patients under 18 years of age (common)– Quinolones not given to children unless benefits
outweigh the risks • Leukopenia, eosinophila, heart arrhythmias (rare)
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The Beta-LactamsThe Beta-Lactams
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PenicillinsPenicillins
• Penicillium notatum produces the only naturally occuring agent – penicillin G or benzylpenicillin
• P. chrysogenum produces 6-aminopenicillanic acid, raw material for
semi-synthetics
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PenicillinsPenicillins
• Spectrum of activity based on R groups added to 6-aminopenicillanic acid core
• All are bactericidal and inhibit transpeptidases
• Mechanisms of resistance– Alter affinity of transpeptidase– Enzymatically cleave the beta-lactam ring– Efflux pumps– Poor penetration into cell
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PenicillinsPenicillins
• Administered orally, intramuscularly, or intravenously depending on agent
• After oral dose, widely distributed in tissues and secretions (except CNS, prostatic fluid, and the eye)
• Do not kill intracellular pathogens
• Food interferes with adsorption
• Rapid elimination through kidney, secreted in breast milk
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1.1. Penicillins G and VPenicillins G and V• Effective against aerobic G+ organisms except
Staphylococcus, Pen G active against Neisseria and anaerobes
• 2/3 of oral Pen G destroyed by stomach acid, Pen V is more resistant so more is delivered to serum
• Rapid elimination through kidney so probenecid is added to slow excretion.
• Procaine, or benzathine forms of Pen G (im)
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• Most drug is bound to serum albumin but significant amounts show up in liver, bile, kidney, semen, joint fluid, lymph, etc.
• Cautious use in neonates and infants because renal function is not fully established
• Patients with renal failure clear the drugs through liver although at a slow pace
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Penicillins G and V Therapeutic UsesPenicillins G and V Therapeutic Uses
• Streptococcus pneumoniae infections• S. pyogenes infections• Viridans strep endocarditis (also given
prophylactically)• Anaerobes except Bacteroides fragilis
group• Meningococcal infections• Syphilis and other diseases caused by
spirochetes
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2. Isoxazolyl Penicillins2. Isoxazolyl Penicillins
• Oxacillin, cloxacillin, dicloxacillin, nafcillin• Designed to resist staphylococcal beta-
lactamases• Like Pen V, stable in stomach acid but usually
given parentally for serious staph infections• MRSA not covered• Absorption and fate of drugs after absorption,
excretion similar to Pen G and Pen V
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3. Aminopenicillins3. Aminopenicillins
• Ampicillin and amoxicillin• Broad spectrum
– Not effective against beta-lactamase producers– Beta-lactamase inhibitors extend spectrum (clavulanic
acid, sulbactam, tazobactam)
• Both are acid resistant but amoxicillin is better absorbed, even with food
• Don’t bind plasma proteins as much as predecessors
• Secreted through the kidney
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AminopenicillinsAminopenicillinsTherapeutic UsesTherapeutic Uses
• Upper respiratory tract infections• Otitis media• Uncomplicated UTI• Acute bacterial meningitis in kids• Typhoid fever
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4. A Carboxypenicillin and 4. A Carboxypenicillin and a Ureidopenicillina Ureidopenicillin
• Ticarcillin and piperacillin– Ticarcillin is anti-Pseudomonas
drug– Piperacillin + tazobactam has the
broadest spectrum
• Given parentally• Used for serious infections
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Toxicity/Contraindications Toxicity/Contraindications of Penicillinsof Penicillins
1. Hypersensitivity reactions (uncommon)– Rash, fever, bronchospasm, vasculitis,
serum sickness, exfoliative dermatitis, SJS, anaphylaxis
– Drugs act as haptens when bound to serum proteins
– Rashes will disappear when drug is withdrawn or can treat with antihistamines
– For patients with allergies, switch to a different class of antibiotics
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Toxicity/Contraindications Toxicity/Contraindications of Penicillinsof Penicillins
• GI disturbances with oral penicillins.
• Large doses given to patients with renal failure can cause lethargy, confusion twitching and seizures
• Sudden release of procaine can cause dizziness, tinnitus, headache and hallucinations
Pseudomembranous colitis (Ampicillin).
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CephalosporinsCephalosporins
• Base molecule is 7-aminocephalosporanic acid produced by a Sardinian sewer mold
• R groups determine spectrum of activity and pharmacological properties
• Mechanism of action/resistance and class pharmacology essentially the same as penicillins
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First GenerationFirst GenerationCephalosporinsCephalosporins
• Cefazolin, cephalexin, cephadroxil• Excellent against susceptible staph and strep• Modest activity against G-• Cefazolin given parentally, others orally• More than half of the drug is bound to plasma proteins• Excreted by kidneys unmetabolized• Good for staph and strep skin and soft tissue infections
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Second GenerationSecond GenerationCephalosporinsCephalosporins
• Cefaclor, cefuroxime, cefprozil, cefotetan, cefoxitine, cefamandole
• Modest activity against G+, increased activity against G-, works against anaerobes
• Cefaclor and cefprozil given orally• Absorption and excretion same as first gen.• Good for treating
– respiratory tract infections – intra-abdominal infections – pelvic inflammatory disease– diabetic foot ulcers
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Third GenerationThird GenerationCephalosporinsCephalosporins
• Cefotaxime, ceftriaxone, cefoperazone, cefpodoxime, cefixime• Broad spectrum killers• Drugs of choice for serious infections• No effect against Listeria and beta-lactamase producing
pneumococci• Cefpodoxime and cefixime are given orally, others parentally• Most excreted by kidney
• Therapeutic uses – Bacterial meningitis (2 exceptions cefoperazone, cefixime)– Lyme disease– Life-threatening G- sepsis
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Fourth GenerationFourth GenerationCephalosporinCephalosporin
Cefepime– Same antimicrobial spectrum as third
generation but resists more beta-lactamases
– Given parentally, excellent penetration into CSF
– Good for nosocomial infections
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Toxicity/Contraindications Toxicity/Contraindications of Cephalosporinsof Cephalosporins
• Hypersensitivity reactions (uncommon) essentially same as for penicillins
• Cross-reaction between 2 classes
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• Other adverse effects:– Pain at injection site– Phlebitis after iv– When given with aminoglycosides, may
increase nephrotoxicity– Drugs containing methylthiotetrazole (eg
cefamandole, cefaperazone, cefotetan) may cause hypoprothrombinemia and disulfiram-like reaction.
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CarbapenemsCarbapenemsImipenem, Meropenem, ErtapenemBeta-lactam ring is fused to a 5 member ring system
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CarbapenemsCarbapenems• Effect on microbes and pharmacology of
carbapenems similar to penicillins– Wider G+ activity, G- and anaerobes
• For pseudomonal infections: given with aminoglycosides
• Parenteral administration
• Drugs of choice for infections caused by Enterobacter.
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Imipenem -Rapidly inactivated by renal dehydropeptidase I.
Should be given in combination with an inhibitor (Cilastatin)
• Adverse effects of imipenem-cilastatin: GI distress, CNS toxicity, partial cross-allerginicity with penicillins.
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Meropenem: - not metabolized by dehydropeptidases - less likely to cause seizures.
Ertapenem: has longer half-lifeLess effective against pseudomonasCauses pain at site of injection
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Aztreonam – a monobactamAztreonam – a monobactam
• Works only on G-, including Pseudomonas aeruginosa
• Useful for treating G- infections that require a beta-lactam because it does not elicit hypersensitivity reactions
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Toxicity/Contraindications Toxicity/Contraindications of Carbapenemsof Carbapenems
• Nausea and vomiting (common)
• Hypersensitivity reactions (uncommon)– Essentially the same as for penicillins,
exception is the monobactam– Cross-reactivity is possible, exception is the
monobactam
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The The End?End?
Nope.Nope.