Lecture notes from Imperial College London, Medical Biosciences BSc, 2nd year, Pharmacology module
PHAR 7 on antimicrobials: we will consider drugs that are used in the treatment of microbial infection, exploiting key differences in biochemistry that permit treatments with varying degrees of sel...
- prokaryotic life => Archaea & Bacteria
- unicellular with no membrane-bound nucleus/ organelles
- bacterial ribosomes => synthesise oligopeptides, proteins
- can symbiose w/ animal cells (ex: in gut) => commensal
relationship (only 1 benefits from interaction ≠ mutualistic )
-
no harm to host sometimes)
, - can be pathogenic (but membranes, fluid compo, pH, innate immune system try to prevent it)
- human body = 30 trillion human cells + 40 trillion bacterial cells
- shape diversity:
- diversity in cell walls: ≠ layers of petidoglycan (see after) => different responses to antibacterials
- evolution over time: many environmental niches colonised by bacteria (found everywhere)
=> 1st one: archaebacteria 4000 million years ago (still exist)
Magic bullets
- Paul Ehrlich found that arsenic-containing compounds cure syphilis (caused by treponema pallidum)
=> synthesised the organoarsenic salvarsan
- “Magic Bullet” = ideal therapeutic agent that affect the target organism selectively (no side-effects)
- antibacterials target (look at previous table)
=> genetic material replication
=> nucleic acid synthesis
=> structural integrity: cell wall synthesis
=> membrane needed for growth synthesis
=> protein synthesis
Introduction to antibacterial agents
- class I: target production of precursors using glucose
Istructural integrity
derived ATP => restrict downstream processes
- class II: target production of small molecules
from class I precursors
Ex: trimethoprim...
- class III: target production of macromolecules
from small molecule substrates
Ex: penicillin, ciprofloxacin...
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