dc.contributor.author | Flaten, Gøril Eide | |
dc.contributor.author | Awoyemi, Opeyemi Linda Ronke | |
dc.contributor.author | Luthman, Kristina | |
dc.contributor.author | Brandl, Martin | |
dc.contributor.author | Massing, Ulrich | |
dc.date.accessioned | 2016-02-16T09:30:49Z | |
dc.date.available | 2016-02-16T09:30:49Z | |
dc.date.issued | 2009-02 | |
dc.description.abstract | In-vitro screening for oral absorption has become an essential part of drug discovery and
development. Recently, a new phospholipid vesicle-based permeation assay was
developed which has shown to satisfyingly predict passive absorption of drugs in
humans. The purpose of the current study was to investigate whether the assay may be
further developed into a high-throughput tool by automating its most time consuming
steps. The following challenges were addressed: (i) to design, build and test a heatsealing
machine for mounting of the desired type of filter support onto both single wells
and 24-well titre plate inserts, and (ii) to transfer the permeability assay to a robotic work
station with attached UV-reader. The workstation is able to pipette and transport both
plates and filter inserts and perform on-line photometric quantification of the amount of
drug permeated. In order to enable the robot to move single (Standard-Transwell®) filter
inserts, an extension of the gripping arm was designed, built and tested. Furthermore, in
an alternative approach 24-well filter plates (Millicell®) were used instead of single filter
inserts. The latter turned out to be more suitable in terms of error-free high-throughput
robotic handling. The permeability values of drugs gained by the two automated
procedures were compared with those measured by manual handling of the assay. Only
neglectable differences in permeability values were seen.
In conclusion, the most time-consuming steps of the assay were shown to be eligible for
automation. This represents an interesting addition to the tool-box of in-vitro
permeability screening assays running in a medium- to high-throughput format due to its
easiness, its transferability to other laboratories and its good correlation with in vivo data
on fraction absorbed of drugs in humans. | en_US |
dc.description | This is the accepted manuscript version. Published version available at <a href=http://dx.doi.org/10.1016/j.jala.2008.04.002>http://dx.doi.org/10.1016/j.jala.2008.04.002</a> | |
dc.identifier.citation | Journal of the Association for Laboratory Automation 14(2009) nr. 1 s. 12-21 | en_US |
dc.identifier.cristinID | FRIDAID 337155 | |
dc.identifier.doi | 10.1016/j.jala.2008.04.002 | |
dc.identifier.issn | 1535-5535 | |
dc.identifier.uri | https://hdl.handle.net/10037/8498 | |
dc.identifier.urn | URN:NBN:no-uit_munin_8066 | |
dc.language.iso | eng | en_US |
dc.publisher | SAGE Publications | en_US |
dc.rights.accessRights | openAccess | |
dc.subject | Automation | en_US |
dc.subject | high throughput | en_US |
dc.subject | drug permeability | en_US |
dc.subject | liposomes | en_US |
dc.subject | artificial membrane | en_US |
dc.subject | VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Pharmacology: 728 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Farmakologi: 728 | en_US |
dc.title | The Phospholipid Vesicle-Based Drug Permeability Assay: 5. Development Toward an Automated Procedure for High-Throughput Permeability Screening | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |