Literature DB >> 12709348

Pharmacokinetics of intramuscularly administered ertapenem.

Donald G Musson1, Anup Majumdar, Kimberly Birk, Sherry Holland, Peter Wickersham, Susan X Li, Goutam Mistry, Alison Fisher, Scott Waldman, Howard Greenberg, Paul Deutsch, J Douglas Rogers.   

Abstract

Ertapenem (INVANZ) is a new once-a-day parental beta-lactam antimicrobial agent that has been shown to be highly effective as a single agent for treatment of various community-acquired and mixed infections. The plasma pharmacokinetics of a 1-g intramuscular (i.m.) dose was compared with those of a 1-g intravenous (i.v.) dose infused over 30 min, the recommended rate of i.v. infusion for comparison, and over 120 min, which more closely mimicked the time course for absorption of the i.m. form. In a three-period crossover study (Part A), 26 healthy subjects received single doses of ertapenem administered i.m., i.v. infused over 30 min, and i.v. infused over 120 min. Blood for ertapenem analysis was collected over 24 h postdose for each treatment. In Part B, these fasted subjects received a 1-g i.m. dose of ertapenem once daily for 7 days. Following a 1-g i.m. dose and a 1-g i.v. dose infused over 120 min, the geometric mean area under the concentration curve from hour 0 to infinity (AUC(0- infinity )) was 541.8 micro g. hr/ml following i.m. administration and 591.4 micro g. hr/ml following a 120-min infusion; the geometric mean ratio was 0.92 with a 90% confidence interval of 0.88 to 0.95. The geometric mean AUC(0- infinity ) was nearly identical when 1-g doses were infused over 30 or 120 min. Although the maximum concentration of drug in serum was somewhat lower following i.m. administration than following i.v. administration, the shape of the plasma concentration profiles was roughly comparable at later time points. Ertapenem did not accumulate after multiple 1-g i.m. daily doses over 7 days. The geometric mean ratio for AUC(0-24) (day 7/day 1) was 0.98 with a 90% confidence interval of 0.94 to 1.02. Thus, the relative bioavailability of the 1-g i.m. dose was 92%. Ertapenem does not accumulate following multiple daily 1-g i.m. doses over 7 days.

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Year:  2003        PMID: 12709348      PMCID: PMC153313          DOI: 10.1128/AAC.47.5.1732-1735.2003

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


  7 in total

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Journal:  Clin Infect Dis       Date:  2002-03-18       Impact factor: 9.079

2.  Pharmacokinetics of L-749,345, a long-acting carbapenem antibiotic, in primates.

Authors:  J G Sundelof; R Hajdu; C J Gill; R Thompson; H Rosen; H Kropp
Journal:  Antimicrob Agents Chemother       Date:  1997-08       Impact factor: 5.191

3.  High-performance liquid chromatographic methods for the determination of a new carbapenem antibiotic, L-749,345, in human plasma and urine.

Authors:  D G Musson; K L Birk; A M Cairns; A K Majumdar; J D Rogers
Journal:  J Chromatogr B Biomed Sci Appl       Date:  1998-12-11

4.  Estimation of variance for harmonic mean half-lives.

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Journal:  J Pharm Sci       Date:  1985-02       Impact factor: 3.534

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Authors:  Donald R Graham; Christopher Lucasti; Osvaldo Malafaia; Ronald L Nichols; Paul Holtom; Nora Quintero Perez; Andrea McAdams; Gail L Woods; T Paulette Ceesay; Richard Gesser
Journal:  Clin Infect Dis       Date:  2002-05-09       Impact factor: 9.079

6.  In vivo activity and pharmacokinetic evaluation of a novel long-acting carbapenem antibiotic, MK-826 (L-749,345).

Authors:  C J Gill; J J Jackson; L S Gerckens; B A Pelak; R K Thompson; J G Sundelof; H Kropp; H Rosen
Journal:  Antimicrob Agents Chemother       Date:  1998-08       Impact factor: 5.191

7.  Dose-dependent plasma clearance of MK-826, a carbapenem antibiotic, arising from concentration-dependent plasma protein binding in rats and monkeys.

Authors:  B K Wong; P J Bruhin; J H Lin
Journal:  J Pharm Sci       Date:  1999-02       Impact factor: 3.534

  7 in total
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Authors:  M A Zuur; S Ghimire; M S Bolhuis; A M A Wessels; R van Altena; W C M de Lange; J G W Kosterink; D J Touw; T S van der Werf; O W Akkerman; J W C Alffenaar
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Authors:  Gillian M Keating; Caroline M Perry
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4.  Model for Evaluating Antimicrobial Therapy To Prevent Life-Threatening Bacterial Infections following Exposure to a Medically Significant Radiation Dose.

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Review 5.  Ertapenem: a review of its use in the management of bacterial infections.

Authors:  Monique Curran; Dene Simpson; Caroline Perry
Journal:  Drugs       Date:  2003       Impact factor: 9.546

6.  Efficacy and safety of de-escalation therapy to ertapenem for treatment of infections caused by extended-spectrum-β-lactamase-producing Enterobacteriaceae: an open-label randomized controlled trial.

Authors:  Pinyo Rattanaumpawan; Peerawong Werarak; Anupop Jitmuang; Pattarachai Kiratisin; Visanu Thamlikitkul
Journal:  BMC Infect Dis       Date:  2017-03-01       Impact factor: 3.090

7.  Model-Informed Drug Development, Pharmacokinetic/Pharmacodynamic Cutoff Value Determination, and Antibacterial Efficacy of Benapenem against Enterobacteriaceae.

Authors:  Xi-Wei Ji; Feng Xue; Zi-Sheng Kang; Wei Zhong; Isabelle Hui-San Kuan; Xi-Ping Yang; Xiao Zhu; Yun Li; Yuan Lv
Journal:  Antimicrob Agents Chemother       Date:  2020-02-21       Impact factor: 5.191

  7 in total

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