Novel diffusion cell for in vitro transdermal permeation, compatible with automated dynamic sampling

I.J Bosman, A.L Lawant, S.R. Avegaart, K Ensing, R.A de Zeeuw

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Scopus)

Abstract

The development of a new diffusion cell for in vitro transdermal permeation is described. The so-called Kelder cells were used in combination with the ASPEC system (Automatic Sample Preparation with Extraction Columns), which is designed for the automation of solid-phase extractions (SPE). Instead of SPE columns, 20 Kelder cells were placed in the racks. This allowed automatic sampling of up to 20 cells for 24 h in a dynamic mode. The cells consist of an inlet compartment, a donor compartment and a receptor compartment. The size and the depth of the inlet compartment were important to avoid entrapment of air bubbles in the receptor compartment. The Kelder cells mimic blood flow beneath the skin by replacement of the permeating drug every 2 min. Hence sink conditions are more easily maintained than with the static Franz diffusion cell. The performance of the cells was tested with permeation experiments using atropine as a model drug permeating through an artificial membrane (Silastic). The use of this skin model minimized the variability in permeation of atropine as compared with human skin.

Original languageEnglish
Pages (from-to)1015 - 1023
Number of pages9
JournalJournal of Pharmaceutical and Biomedical Analysis
Volume14
Issue number8-10
Publication statusPublished - Jun-1996
Event5th International Symposium on Drug Analysis - , Belgium
Duration: 12-Sept-199515-Sept-1995

Keywords

  • ASPEC system
  • atropine
  • automated dynamic sampling
  • diffusion cell
  • in vitro
  • Kelder cell
  • silastic
  • FLOW-THROUGH
  • SKIN
  • PENETRATION
  • ABSORPTION
  • MODEL

Fingerprint

Dive into the research topics of 'Novel diffusion cell for in vitro transdermal permeation, compatible with automated dynamic sampling'. Together they form a unique fingerprint.

Cite this