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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1993-2-19
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pubmed:abstractText |
Pharmacologic considerations suggest that third-generation cephalosporins might penetrate the vitreous humor better after periocular injection and might be eliminated less readily after intravitreous injection than older agents. We studied the sodium salts of ceftizoxime, ceftriaxone, and ceftazidime, and of an investigational cephalosporin, cefepime, in rabbits. After a single subconjunctival injection in animals with normal eyes, vitreous levels ranged from 3 to 13 mg/L. After five subconjunctival injections in rabbits with infected eyes, vitreous concentrations ranged from 12 to 34 mg/L. These concentrations are not appreciably greater than those found with older beta-lactams. The vitreous half-life of the four drugs after intravitreous injection varied from 5.7 to 20 hours in rabbits with uninflamed eyes and from 9.4 to 21.5 hours in rabbits with infected eyes. Except for ceftizoxime, the half-lives were substantially longer than those for older beta-lactams and suggest predominantly anterior route elimination. Vitreous penetration of these new agents after subconjunctival injection does not appear to be sufficient to overcome the need for intravitreous injections in the treatment of endophthalmitis. However, the longer vitreous half-lives of some of the newer agents may be useful if the drugs are to be given intravitreally.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ceftazidime,
http://linkedlifedata.com/resource/pubmed/chemical/Ceftizoxime,
http://linkedlifedata.com/resource/pubmed/chemical/Ceftriaxone,
http://linkedlifedata.com/resource/pubmed/chemical/Cephalosporins,
http://linkedlifedata.com/resource/pubmed/chemical/cefepime
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0003-9950
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
121-5
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8424709-Animals,
pubmed-meshheading:8424709-Ceftazidime,
pubmed-meshheading:8424709-Ceftizoxime,
pubmed-meshheading:8424709-Ceftriaxone,
pubmed-meshheading:8424709-Cephalosporins,
pubmed-meshheading:8424709-Colony Count, Microbial,
pubmed-meshheading:8424709-Conjunctiva,
pubmed-meshheading:8424709-Disease Models, Animal,
pubmed-meshheading:8424709-Endophthalmitis,
pubmed-meshheading:8424709-Eye Infections, Bacterial,
pubmed-meshheading:8424709-Half-Life,
pubmed-meshheading:8424709-Rabbits,
pubmed-meshheading:8424709-Staphylococcal Infections,
pubmed-meshheading:8424709-Vitreous Body
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pubmed:year |
1993
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pubmed:articleTitle |
Pharmacokinetics of newer cephalosporins after subconjunctival and intravitreal injection in rabbits.
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pubmed:affiliation |
Department of Medicine, New England Medical Center, Boston, Mass.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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