Skip to main navigation Skip to search Skip to main content

Pharmacokinetics and absorption of paromomycin and gentamicin from topical creams used to treat cutaneous leishmaniasis

  • William R. Ravis
  • , Alejandro Llanos-Cuentas
  • , Nestor Sosa
  • , Mara Kreishman-Deitrick
  • , Karen M. Kopydlowski
  • , Carl Nielsen
  • , Kirsten S. Smith
  • , Philip L. Smith
  • , Janet H. Ransom
  • , Yuh Jing Lin
  • , Max Grogl
  • Auburn University
  • Instituto Conmemorativo Gorgas de Estudios de la Salud
  • US Army Medical Materiel Development Activity
  • Fast-Track Drugs and Biologics LLC
  • Walter Reed Army Institute of Research

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

This study evaluated the pharmacokinetics of topical creams containing 15% paromomycin ("paromomycin alone") and 15% paromomycin plus 0.5% gentamicin (WR 279,396) in patients with cutaneous leishmaniasis. The investigational creams were applied topically to all lesions once daily for 20 days. Plasma samples were analyzed for simultaneous quantitation of paromomycin and gentamicin isomers and total gentamicin. Pharmacokinetic parameters for gentamicin could not be calculated because detectable levels were rarely evident. After one application, the paromomycin area under the concentration-time curve from 0 to 24 h (AUC0-24) was 2,180±2,621 ng h/ml (mean±standard deviation [SD]) for the paromomycin-alone group and 975.6±1,078 ng h/ml for the WR 279,396 group. After 20 days of application, the paromomycin AUC0-24 and maximum concentration of drug (Cmax) were 5 to 6 times greater than those on day 1 for both treatment groups. For the paromomycin-alone group, the AUC0-24 was 8,575±7,268 ng h/ml and the Cmax was 1,000±750 ng/ml, compared with 6,037±3,956 ng h/ml and 660±486 ng/ml for the WR 279,396 group, respectively. Possibly due to large intersubject variability, no differences (P >0.05) in the AUC0-24 or Cmax were noted between treatment or between sites on day 1 or 20. The percentage of dose absorbed on day 20 was 12.0%±6.26% and 9.68%±6.05% for paromomycin alone and WR 279,396, respectively. Paromomycin concentrations in plasma after 20 days of application were 5 to 9% of those after intramuscular administration of 15 mg/kg of body weight/day to adults for the systemic treatment of visceral leishmaniasis. Effective topical treatment of cutaneous leishmaniasis appears to be possible with limited paromomycin and gentamicin systemic absorption, thus avoiding drug accumulation and toxicity. (The work described here has been registered at ClinicalTrials.gov under registration no. NCT01032382 and NCT01083576.)

Original languageEnglish
Pages (from-to)4809-4815
Number of pages7
JournalAntimicrobial Agents and Chemotherapy
Volume57
Issue number10
DOIs
StatePublished - Oct 2013

Fingerprint

Dive into the research topics of 'Pharmacokinetics and absorption of paromomycin and gentamicin from topical creams used to treat cutaneous leishmaniasis'. Together they form a unique fingerprint.

Cite this