Literature DB >> 4357182

Serum and urinary concentrations of cyclacillin in humans.

C G Hertz.   

Abstract

Cyclacillin is a semisynthetic penicillin produced from the penicillin nucleus (6-aminopenicillanic acid) by acylation with 1-aminohexanecarboxylic acid. The absorption and excretion characteristics of cyclacillin were defined in one completely randomized and three three-way crossover experiments. Mean peak serum cyclacillin levels appeared earlier and were fivefold higher than those obtained with equal doses of ampicillin. High serum cyclacillin concentrations were reached at 0.5 h and by 2 h were lower than ampicillin. Serum ampicillin concentrations peaked at 1.5 h, remaining slightly higher than those for cyclacillin for the next 4.5 h. The mean area for the cyclacillin curve was significantly superior to either of the ampicillin formulations. Mean serum concentrations of cyclacillin exhibited a smooth dose-response, approximately doubling in each instance as the dose was doubled from 250 to 500 and from 500 to 1,000 mg. High concentrations of cyclacillin were also demonstrated in urine. Neither ratio of drug to metabolite in the urine nor the percent of excretion was significantly affected by the dose level. Sixty-seven percent of the drug was excreted unchanged, and 17% was excreted as penicilloic acid, with most of the excretion occurring within 6 h of administration. In subjects given 500 mg of cyclacillin (four times daily) for 6 days, 2% of the drug was excreted as 1-aminocyclohexanecarboxylic acid, and approximately 55% (24 to 91%) was unchanged. Neither formation nor excretion of the former was sex dependent.

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Year:  1973        PMID: 4357182      PMCID: PMC444557          DOI: 10.1128/AAC.4.3.361

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  3 in total

1.  [Basic and clinical studies of aminocyclohexyl penicillin].

Authors:  H Okubo; Y Fujimoto; Y Okamoto; J Tsukada; J Makino
Journal:  Jpn J Antibiot       Date:  1970-02

2.  [Clinical use of aminocyclohexyl penicillin(AC-PC) in the field of surgery].

Authors:  K Shibata; T Kato; M Fujii; Y Okuda
Journal:  Jpn J Antibiot       Date:  1970-02

3.  Antimicrobial activity and pharmacological distribution of Wy-4508, an aminoalicyclic penicillin.

Authors:  S B Roseman; L S Weber; G Owen; G H Warren
Journal:  Antimicrob Agents Chemother (Bethesda)       Date:  1967
  3 in total
  7 in total

1.  Absorption of amino penicillins from everted rat intestine.

Authors:  C Dixon; L W Mizen
Journal:  J Physiol       Date:  1977-08       Impact factor: 5.182

2.  Double-blind clinical trials of oral cyclacillin and ampicillin.

Authors:  J A Gold; C P Hegarty; M W Deitch; B R Walker
Journal:  Antimicrob Agents Chemother       Date:  1979-01       Impact factor: 5.191

3.  Ampicillin and alternatives.

Authors:  A Dyas; R Wise
Journal:  Br Med J (Clin Res Ed)       Date:  1983-02-19

4.  Oral cyclacillin interacts with the absorption of oral ampicillin, amoxycillin, and bacampicillin.

Authors:  J Sjövall; G Alván; D Westerlund
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

5.  Comparative pharmacokinetics of cyclacillin and amoxicillin in infants and children.

Authors:  C M Ginsburg; G H McCracken; T C Zweighaft; J C Clahsen
Journal:  Antimicrob Agents Chemother       Date:  1981-06       Impact factor: 5.191

6.  Pharmacological and in vitro evaluation of cyclacillin: assessment as potential single-dose therapy for treatment of Neisseria gonorrhoeae infection.

Authors:  K F Wagner; A D Blair; G W Counts; K K Holmes
Journal:  Antimicrob Agents Chemother       Date:  1980-01       Impact factor: 5.191

Review 7.  The aminopenicillins: development and comparative properties.

Authors:  D S Reeves; D W Bullock
Journal:  Infection       Date:  1979       Impact factor: 3.553

  7 in total

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