Literature DB >> 10430551

Reproducible fentanyl doses delivered intermittently at different time intervals from an electrotransport system.

S K Gupta1, G Sathyan, B Phipps, M Klausner, M Southam.   

Abstract

The electrotransport transdermal fentanyl system (ET [fentanyl]), uses a small electrical current to enhance delivery of fentanyl to systemic circulation. Intermittent doses can be administered by periodic application of the current. The purpose of this study was to compare the effects of the frequency of intermittent drug delivery by ET (fentanyl) and compare the drug delivery to systemic circulation by ET (fentanyl) with intravenous administration. The topical safety was also determined for the ET (fentanyl) system. Nine adult male volunteers completed this three-treatment, randomized, 24-h, crossover study. ET (fentanyl) treatments with 200 microA direct current applied for 30 min at frequent (hourly) or infrequent (4-hourly) intervals over a 24-h period were compared. Also, the drug delivery to systemic circulation from ET (fentanyl) was compared with intravenous fentanyl 75 microg infused over 30 min every 4 h over a 24-hour period. The mean serum fentanyl concentration achieved with the hourly ET (fentanyl) regimen was higher than that for the 4-hourly ET (fentanyl) regimen as expected from the higher frequency of drug doses. The amount of fentanyl delivered estimated per dose from the ET (fentanyl) system using the iv fentanyl treatment as the reference was similar for the two ET regimens throughout the dosing period. This indicates consistent drug delivery regardless of the frequency of ET dosing. The majority of subjects reported either no, or barely perceptible, erythema 24 h after removal of the system.

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Year:  1999        PMID: 10430551     DOI: 10.1021/js980258b

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

1.  The effect of dosing frequency on the pharmacokinetics of a fentanyl HCl patient-controlled transdermal system (PCTS).

Authors:  Gayatri Sathyan; Katayoun Zomorodi; Shalini Gidwani; Suneel Gupta
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

2.  Characterisation of the pharmacokinetics of the fentanyl HCl patient-controlled transdermal system (PCTS): effect of current magnitude and multiple-day dosing and comparison with IV fentanyl administration.

Authors:  Gayatri Sathyan; Jennifer Jaskowiak; Mark Evashenk; Suneel Gupta
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

3.  Pharmacokinetics and tolerability of different doses of fentanyl following sublingual administration of a rapidly dissolving tablet to cancer patients: a new approach to treatment of incident pain.

Authors:  B Lennernäs; T Hedner; M Holmberg; S Bredenberg; C Nyström; H Lennernäs
Journal:  Br J Clin Pharmacol       Date:  2005-02       Impact factor: 4.335

4.  Acute postoperative pain management: focus on iontophoretic transdermal fentanyl.

Authors:  Consalvo Mattia; Flaminia Coluzzi
Journal:  Ther Clin Risk Manag       Date:  2007-03       Impact factor: 2.423

  4 in total

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