Journal of Cystic Fibrosis
Volume 7, Issue 1 , Pages 79-84, January 2008

Pharmacokinetics and sputum penetration of azithromycin during once weekly dosing in cystic fibrosis patients

  • E.B. Wilms

      Affiliations

    • Central Hospital Pharmacy, Escamplaan 900, 2547EX The Hague, The Netherlands
    • Corresponding Author InformationCorresponding author. Fax: +31 0031703217156.
  • ,
  • D.J. Touw

      Affiliations

    • Central Hospital Pharmacy, Escamplaan 900, 2547EX The Hague, The Netherlands
  • ,
  • H.G.M. Heijerman

      Affiliations

    • Adult Cystic Fibrosis Centre, Department of Pulmonology, Haga Teaching Hospital Leyenburg , Leyweg 275, 2545CH The Hague, The Netherlands

Received 14 January 2007; received in revised form 4 May 2007; accepted 15 May 2007.

Abstract 

In this study we examined pharmacokinetics, systemic exposure and sputum penetration of azithromycin (AZM) in CF patients on chronic daily AZM therapy after changing to a once weekly dosing scheme.

Eight adult CF patients using AZM 500 mg/day were changed to a once weekly dose of 1000 mg during 3 months. Once per month sputum and blood samples were collected. AZM was quantified in blood plasma and polymorphonuclear neutrophils.

The cumulative weekly dose was reduced with a factor of 3.5 (7×500 mg vs. 1×1000 mg weekly).This led to a reduction in area under the curve (AUC±S.D.) with a factor of 2.5±0.8 in plasma, 2.8±0.9 in blood, 2.2±1.1 in PMNNs and to a reduction in average sputum concentration with a factor of 3.0 (±1.5).

At 1000 mg once weekly reduced but still substantial concentrations were achieved in PMNNs and in sputum. Although not significant, a tendency towards less than linear reduction was found. In order to calculate and propose an optimal dosing scheme we need to establish a relation between exposure levels and clinical efficacy.

Keywords: Azithromycin, Pharmacokinetics, Sputum, Penetration, Polymorphonuclear neutrophil, Once weekly dosing

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PII: S1569-1993(07)00064-1

doi:10.1016/j.jcf.2007.05.005

Journal of Cystic Fibrosis
Volume 7, Issue 1 , Pages 79-84, January 2008