antibiotics Flashcards

1
Q

what is pharmacokinetics?

A

what body does to drug (L, A,D, M,E)

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2
Q

What is pharmacodynamics?

A

what drug does to body

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3
Q

what is MIC ( minimum inhibitory concentration) & MBC (minimum drug- concentration)?

A

minimum inhibitory concentration :
- minimum drug concentration INHIBITING MICROBIAL GROWTH in virtro

minimum bacteriocidal conc
- Minimum drug concentration that KILLS MICROBES IN VITRO

MBC is 2-4 fold of mIC

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4
Q

concentration to MIC (Cmax : MIC)

A

every dose’s concentration spikes and goes down.

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5
Q

area under curve to MIC

A

drug effectiveness is affected by AMOUNT OF TIME SPENT IN MICR RANGE …. NOT DOSE

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6
Q

bioavailibility

A

drug that reaches circulation (%)

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7
Q

clearence

A

vol of fluid removed per unit of time

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8
Q

volume of distribution

A

high protein binding drugs have LOWER VD . The more lipophilic, the HIGHER THE VD

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9
Q

steady state

A

imp for MIC to AUC ratio & fraction of time

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10
Q

therapeutic index

A

range between minimum effective conc to mimumum toxic conc

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11
Q

factors effecting host

A

age (extremeties)
renal/liver function
co-morbidities
polypharmacy
allergy
conditions (Myasthesia gravis, G6PD)

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12
Q

drugs to avoid in myasthesia gravis

A

drugs impair Neuromuscular junction transmission

result: increase of weakness

Aminoglycosides
fluroquininolones
tetracyclines
clindamycin
sulfonamides
macrolides
ampicillin

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13
Q

antimicrobial drugs have adverse reactions, name them

A
  • allergic reactions
  • toxic effects - at high
    dose
  • bioflor suppression - allowing growth ex: clostridium difficile
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14
Q

staining techniques

A

provide contrast by using dyes

smear –> air dye –> heat fix

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15
Q

types of dye used in staining techniques

A
  • basic - cationic chromaphore
  • acidic - anionic chromophore - negative staining
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16
Q

3 types of staining techniques

A
  1. simple
  2. differencial
  3. special
17
Q

acid fast stain - test for microbacterial cell walls

A

cells retaining basic stain in acid-alcohol

18
Q

What are the characteristic factors of an antibiotic

A

selective toxicity -
- target bacteria while causing NO OR MINIMAL HARM to patient

Therapeutic index -
- ratio between TOXIC and therapeutic

antimicrobial action -
Bacteriostatic: prevents further bacterial growth
- bacteriocidal - kills bacteria

activity spectrum
- broad - target gram +ve & -ve
- narrow - gram -ve or gram +ve ONLY

ADME -
- BBB - blood brain barrier antibiotics (cephalosporins, doxycycline)

  • unstable in acid
  • half life duration
19
Q

explain selective toxicity in antibiotics

A

they target bacteria

BUT
cause NO or minimal harm to patient

20
Q

types of antibiotic

A

broad - gram +ve/-ve
narrow - only gram +ve OR -ve
bacteriocidal - kills
bacreriostatic - suppress growth
gram postitive
- thick peptidoglycan
- porous (lets in easy)
- CRYSTAL VIOLET gram stain absorbed into peptidoglycan

gram negative
- THIN peptidoglycan
- have 2nd outer membrane
- outer layer not allow crystal violet to reach peptiodglycan - Pink counterstain

21
Q

Gram +ve vs Gram -ve

A

-ve –> outer membrane makes it harder for antibiotics to cross

+ve –> greater access to antibiotics –> more easy penetration + interaction with peptidoglycan

22
Q

Bactericidal antibiotics

A

kill the bacteria

23
Q

what do antibiotics target to kill bacteria?

A
  • cell wall synthesis (structure & arrangment of peptidoglycan)
  • protein synthesis
  • nucleic acid synthesis
  • metabolic reactions
  • membrane function
24
Q

what is peptidoglycan

A

backbone of carbohydrate units with sets of amino acid residues attached

25
IMP Class 1 - Beta lactam antibiotics. how do they interfere with bacteria ? Can you name some examples?
interfere with or prevent formation of peptidoglycan cross- links by enzyme inhibition (antibiotics bind to penecillin-binding proteins) ex: - penecillin - cephalosporin - monobactamas - carabpenms - cillin, -sporin, - bactams, -penems
26
mechanism of action of beta lactam antibiotics
Beta lactam ring joins to the PHB (penecillin binding protein)'s amino terminus. structural change opens up beta lactam ring bind irreversibly to PBP inhibits transpeptidase activity = no cross linking of peptidoglycan chains in cell wall --> weak wall cell lysis by lack of osmotic control = bursting
27
how do beta lactam targeted bacteria gain antibiotic resistance
they disrupt interaction between beta lactam antibiotics and penecillin bindung protein = resistance penecillinase/β-lactamase is an enzyme secreted that DESTROYS NATURAL PENECILLINS --> released as DEFENSE MECHANISM AGAINST PENECILLIN
28
Are there any other antibiotic classes that inhibit cell wall synthesis ?
glycopeptides like vancomycin and teicopanin BUT BY DIFFERENT MECHANISM = SAME OUTCOME
29
What are extended-spectrum penecillins? Can you name an example?
have broader spectrum of activity against many bacteria. EX: AMOXICILLIN
30
Carboxypenecillins (carbenicillin, titracillin) & Ureidopenecillins (piperacillin, azlocillin, mezlocillin)
WIDER range and are effective against PSEUDOMONAS AERUGINOSA
31
how do we reduce probability of antibiotic resistance in treatment regimens? Can you provide examples
combining penicillin + beta lactamase INHIBITOR (prevent destruction of penecillin) Ex: Piperacillin-tazobactam & amoxicillin-clavulanic acid
32
Clinical pharmacokinetics of Penciillins - what are the characteristics that influence the way they work in body? (are they hydrophobic/hydrophilic and what organ processes the drug?)
- hydrophilic - do not cross blood brain barrier unless meninges inflammed --> effective in meningitis - excreted by kidneys uncharged - dose reduced in renal failure
33
examples of penecililins
flucolaxcillin (acid stable, oral or non oral) BETA LACTAMASE RESISTANCE narrow spectrum for MSSA infections (staphylococcus aureus)
34