Download Topical Antibiotics

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Probiotic wikipedia , lookup

Unique properties of hyperthermophilic archaea wikipedia , lookup

Pseudomonas aeruginosa wikipedia , lookup

Clostridium difficile infection wikipedia , lookup

Biofilm wikipedia , lookup

Phage therapy wikipedia , lookup

Carbapenem-resistant enterobacteriaceae wikipedia , lookup

Staphylococcus aureus wikipedia , lookup

Neisseria meningitidis wikipedia , lookup

Bacteriophage wikipedia , lookup

Human microbiota wikipedia , lookup

Skin flora wikipedia , lookup

Bacteria wikipedia , lookup

Small intestinal bacterial overgrowth wikipedia , lookup

Bacterial taxonomy wikipedia , lookup

Bacterial cell structure wikipedia , lookup

Bacterial morphological plasticity wikipedia , lookup

Transcript
Topical Antibiotics
• Topical antibiotics help prevent infections caused by
bacteria that get into minor cuts, scrapes, and burns.
• Treating minor wounds with antibiotics allows quicker
healing.
• If the wounds are left untreated, the bacteria will
multiply, causing pain, redness, swelling, itching, and
oozing.
• Untreated infections can eventually spread and
become much more serious.
Which bacteria?
• Most topical antibiotics are directed
against Staphylococcus aureus and
Streptococcus pyogenes.
• The anaerobic Gram-positive bacterial
species Propionibacterium acnes has
been linked to acne.
Which topical antibiotics are
common?
• Some widely used topical antibiotics are
bacitracin, neomycin, mupirocin, and
polymyxin B.
• Among the products that contain one or
more of these ingredients are Bactroban
(a prescription item), Neosporin,
Polysporin, and Triple Antibiotic
Ointment or Cream.
Classes of topical antibiotics
•
•
•
•
•
Cell wall synthesis inhibitors
Ribosome function inhibitors
Sulfa drugs
Burn treatment agents
Miscellaneous
Mupirocin (90% Pseudomonic acid A)
• Isolated from Pseudomonas fluorescens
– Antibacterial activity of substance from P. fluorescens
noted in 1887
– Purified in the 1960’s.
• Mupirocin works against Gram-positive bacteria
only
• Can be used to treat MRSA (although resistance is
rising)
• Ester linkage is rapidly hydrolyzed
hepatically, thus precluding utility as an
oral or intravenous antibiotic
• Mupirocin inhibits bacterial isoleucyl-tRNA
synthetase.
Products containing Mupirocin
Polymyxin B
Polymixin B
Daptomycin
Polymixin B
• Member of the lipopeptide class of
antibiotics, similar to daptomycin
Polymyxin: Antibacterial activity
• However, the polymyxins are only active
against gram negative bacteria (P.
aeruginosa, E. coli, K. pneumoniae),
while daptomycin is used to treat gram
positive bacteria
• The polymyxins are highly nephrotoxic
and are thus only used topically
Polymyxins: Mechanism of action
• Bind to the cytoplasmic membrane (to the
phosphatidylethanolamine) and make the
membrane more permeable.
Products containing polymyxin B
Bacitracin A
Bacitracin: History
• Isolated by John T. Goorley in 1943
• Found in the infected wound of the
patient Margaret Tracy
Bacitracin: Antibacterial
Activity
• Primarily used against gram positive
bacteria S. aureus and Streptococci
spp.
• Most gram negative organisms are
resistant
Bacitracin: Mechanism
• Bacitracin interferes with bacterial cell wall
synthesis
• Acts by blocking a step in the process
whereby the key subunits are transferred
from the cytoplasm
• Specifically bacitracin tightly binds
undecaprenyl pyrophosphate, preventing the
hydrolysis into undecaprenyl phosphate
• This step is essential for recycling of the
carrier
• Link
Products containing Bacitracin
Gramicidin
Gramicidin S
Gramicidins
• The Gramicidins are small peptides (15
amino acids)
• Some, such as gramicidin S, are cyclic
• Others, including Gramicidin A, B, C,
and D, are linear
• Commercial gramicidin is a mixture of
compounds, with gramicidin A being
major
Gramicidins: Mechanism of action
A gramicidin channel
• The gramicidins behave as ionophoric
substances
• The gramicidins self associate, thus
forming small pores that cause leakage
of essential cations from the cytoplasm
Gramicidin is an unusual peptide,
with alternating D & L amino acids.
In lipid bilayer membranes,
gramicidin dimerizes & folds as a
right-handed b-helix.
The dimer just spans the bilayer.
Gramicidin dimer
(PDB file 1MAG)
Primary structure of gramicidin
(A):
HCO-L-Val-Gly-L-Ala-D-Leu-L-Ala-D-Val-L-Val-D-ValL-Trp-D-Leu-L-Trp-D-Leu-L-Trp-D-Leu-L-TrpNHCH2CH2OH
Note: The amino acids are all
hydrophobic; both peptide ends are modified (blocked).
The outer surface of the
gramicidin dimer, which
interacts with the core of the
lipid bilayer, is hydrophobic.
Ions pass through the more
polar lumen of the helix.
Ion flow through individual
gramicidin channels can be
observed if a small number of
gramicidin molecules is
present in a lipid bilayer
separating 2 compartments
containing salt solutions.
Gramicidin dimer
(PDB file 1MAG)
Neomycin
Historical: Aminoglycosides
• Waksman and Schatz demonstrated the
antibacterial activity of Streptomyces
griseus in 1943
• Streptomycin isolated in 1944
• Neomycin isolated from Streptomyces
fradiae in 1949
Neomycin
• Neomycin is extremely nephrotoxic,
thus limiting its use to a topical antibiotic
• Neomycin has excellent activity against
gram negative bacteria and partial
activity against gram positive strains
• Some people have allergies to
neomycin
Mechanism of action
• Like other aminoglycosides, neomycin
works by binding to the bacterial 30S
ribosomal subunit, thus inhibiting protein
synthesis.
Silver sulfadiazine
Mechanism of action
• Sulfa drug works by normal mechanism
of interfering with the biosynthesis of
folic acid
• Heavy metals, like silver, seem to be
toxic to bacteria, probably due to their
ability to denature proteins through
reaction with disulfide bonds
Uses
• Used to treat burn patients