Article

Diffusion-driven device for a high-resolution dose-response profiling of combination chemotherapy.

Department of Biochemistry, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Analytical Chemistry (impact factor: 5.86). 06/2009; 81(13):5233-40. DOI:10.1021/ac900415s pp.5233-40
Source: PubMed

ABSTRACT Combination therapies have proven vital in the fight against HIV and cancer. However, the identification and optimization of such combination therapies is largely experience driven and an activity of clinicians rather than of systematic screening efforts. Here we present a diffusion device, compatible with the format of a 12-well microtiter plate, to create and test all possible mixtures of two substances with only two pipetting steps. Applications to the testing of different drug combinations and the parallel screening of different leukemia cell lines as well as primary patient cells are presented. The diffusion device yields qualitatively and quantitatively comparable results to an MTT viability assay conducted in a standard 96-well format albeit with a tremendous reduction of processing steps. In addition, a fluorescence-based annexin V binding assay of cell death was implemented. Next to the reduction of processing steps, the diffusion device constitutes a considerable assay miniaturization that overcomes the problems typically associated with miniaturization as a consequence of small sample volumes. Given its ease of handling, the device will greatly advance the development and optimization of combination drugs and the identification of optimum drug combinations in personalized medicine.

0 0
 · 
0 Bookmarks
 · 
30 Views

Keywords

12-well microtiter plate
 
binding assay
 
combination drugs
 
combination therapies
 
considerable assay miniaturization
 
different drug combinations
 
different leukemia cell lines
 
diffusion device
 
diffusion device yields qualitatively
 
fluorescence-based annexin
 
MTT viability assay
 
optimum drug combinations
 
possible mixtures
 
primary patient cells
 
processing steps
 
quantitatively comparable results
 
small sample volumes
 
standard 96-well format
 
systematic screening efforts
 
two pipetting steps