Guest guest Posted August 9, 2005 Report Share Posted August 9, 2005 Hold the phone, somethings odd here. Apparantly Bicillin, which IS used for lyme, is not benzylpenicillin but is metabolized to benzylpenicillin in the body. So perhaps the in vitro data I cited below have been disconfirmed, or perhaps the Bicillin prodrug is itself active against Bb, or something else. Arguably I should take care of my chemistry finals before diggin into the issue. > You asked if the chief syphilis drug, penicillin G (benzylpenicillin), > has been used for lyme. This brings up important observations. > > The syphilis agent Tp is equally - and highly - suceptible to both > benzylpenicillin and ceftriaxone in vitro. Bb is just as sensitive to > ceftriaxone - but evidently is 100x less sensitive to benzylpenicillin: > > http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=174684 > > Differences in suceptibility to different B-lactam drugs are usually > ascribed to the fat- or water-solubility of the drugs affecting their > penetration of the cell envelope. Apparantly fat-soluble drugs are > much less active against typical gram-negative organisms because they > have difficulty passing the water-soluble LPS coat of the outer > membrane. FOr one thing I'm not sure that theory is 100% theoretically > sound in itself, and for another, both Bb and Tp lack LPS. The fitness > of these drugs as substrates for bacterial efflux pumps may be of > significance in these observations, which constitute an intriguing > difference between these not-terribly-closely-related organisms. Quote Link to comment Share on other sites More sharing options...
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