drugs Flashcards

1
Q

digoxin

A

used to treat heart failure arythmia by Na/K pump

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2
Q

Drugs Class: Beta-Lactam and cephalosporin

A

Target= penicillin binding proteins
Mechanism= preventing peptidoglycan cross linking
Example= penicillin, Flucloxacillin

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3
Q

Drug Class: glycopeptide

A

target = C terminal, D-Ala -D-Ala
mechanism= prevents transglycolation and transpeptidation
example= vancomycin

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4
Q

drug class: cyclic peptide

A

mechanism = prevents the carriage of building blocks of peptidoglycan bacterial wall outside of the inner membrane.
Example = bacitracin

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5
Q

drugs class: phosphonic acid

A

target = murA protein
mechanism = inhibits the first stage of peptidoglycan synthesis
example = fosphomycin

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6
Q

drug class: lipopeptides

A

mechanism = calcium dependant membrane depolarisation
example = daptomycin

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7
Q

examples of B-lactamase resistant penicillins

A

methicillin
oxacillin
nafcillin
cloxacillin
dicloxacillin

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8
Q

examples of broad spectrum penicillins

A

ampicillin
amoxicillin

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9
Q

examples of extended spectrum penicillins

A

carbenicillin
ticaracillin
azlocillin
piperacillin

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10
Q

examples of cephalosporins

A

cephalexin

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11
Q

sulphonamides and trimethoprim

A

antibiotics that act through an inhibition of the folate pathway in bacteria - bacteria have to make their own supply but we don’t as we get it in out diet - selective toxicity
sulphonamides will inhibit - dihydropteroate synthetase
trimethoprim will inhibit = dihydrofolate reductase

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12
Q

aminoglycosides

A
  • forms ionic bonds with the cell
  • penetrates the cell wall by a transport mechanism across cell membrane
  • diffuse into the cytoplasm and then binds to the bacterial ribosomes to inhibit protein synthesis
    EG- streptomycin
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13
Q

tetracyclines

A
  • prevent attachment of the tRNA to the acceptor A site on mRNA
  • prevents the addition of amino acids to the peptide chain
    The difference in activity of tetracyclines are related to their solubility in the lipid membrane of bacteria
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14
Q

chloramphenicol, erythromycin, clindamycin

A

they prevent the addition of new amino acid to the growing peptide chain by binding to the ribosomes, this prevents the association of the peptide-transferase with the amino acid and no peptide bond will be formed.

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15
Q

fluoroquinolones

A
  • synthetic antibiotics
  • they act by inhibiting DNA topoisomerase II
  • this enzyme catalyses the introduction of negative supercoil in DNA permitting transcription and replication.
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16
Q

Lidocaine - acting and onset time?

A

Medium acting
Rapid onset

17
Q

Prilocaine

A

Medium acting
NO VASODILATION

18
Q

Bupivacaine?

A

Long acting
Slow onset

19
Q

Articaine

A

Short acting
Rapid onset

20
Q

3 ester containing local anaesthetics?

A

Tetracaine. - long acting, slow onset
Chloroprocaine - medium acting
Benzocaine- atypical mechanism of action

21
Q

Aspirin?

A

Irreversible COX-1 inhibitor.
Binds to the serine group next to the active site

Cox-1 catalyses the conversion of arachidonic acid into prostaglandins.