what type of drug is vancomycin? how many of this type of drug are there?
non-ribosomal glycopeptide
-only 2 (this and teicoplanin)
vancomycin MOA
inhibits G(+) cell wall synthesis by covering D-Ala-D-Ala terminus, so PG can’t react w/ neighboring PG
what dose of vancomycin is bacteriocidal
1-5 ug/mL
resistance to vancomycin associated with what?
VRE connected to avoparcin use (livestock feed additive), but reversible (decreased resistance when stopped avoparcin use)
mechanism of vancomycin resistance?
D-Ala-D-Ala replaced by D-Ala-D-Lac (1000x reduced affinity)
toxicity/side effects of vancomycin
- rare: nephrotoxicity/ototoxicity (associated with high [circulating drug])
macrolide structure
macrocyclic lactone, 14-member ring, polyketide
how are polyketides produced? what pattern does it produce?
sequential addition of propionate groups to growing chain -> results in methyl groups on alternating C’s
where does erythromycin A come from?
most from Streptomyces fermentation -> erythronolide intermediate
how can you make erythromycin more soluble?
pka is 8.8, so can form more soluble salts:
macrolide MOA
bacteriostatic or bacteriocidal?
bacteriostatic mostly, but can be bacteriocidal in high concentration
where do macrolides accumulate and why is this important?
in leukocytes -> transported directly to infection
4 mechanisms of macrolide resistance
what hypothesis did the discovery of methylation of A2058 as a macrolide resistance mechanism provide?
resistance may originate in the producing organism and then transfer to other bacteria
resistance to what other bug is associated with macrolide use?
S. pneumoniae
what two bugs have inherent macrolide resistance? what is the mechanism of their resistance?
Pseudomonas and Enterobacter
-don’t allow entry of drug
describe acid inactivation of macrolides - how does this affect oral administration of macrolides?
intramolecular acid-catalyzed ketal formation at 6-OH -> causes GI cramping
-oral erythromycin must be enteric coated or as a stable salt/ester
2 ways in which acid inactivation is overcome?
describe macrolide metabolism
mainly demethylation in liver by CYP3A4
half life of erythromycin
1.5h
elimination of macrolides
mostly bile, small bit in urine
DDIs with each of the following macrolides:
erythro, clarithro inhibit CYP3A4 -> probs w/:
no reported cases with azithromycin
others: ergotamine, digoxin, methylprednisone
macrolide side effects: