Controlled antibody release from gelatin for on-chip sample preparation

被引:4
作者
Zhang, Xichen [1 ]
Wasserberg, Dorothee [1 ]
Breukers, Christian [1 ]
Terstappen, Leon W. M. M. [1 ]
Beck, Markus [1 ]
机构
[1] Fac Sci & Technol, MIRA Inst Biomed Technol & Tech Med, Med Cell Biophys, POB 217, NL-7500 AE Enschede, Netherlands
基金
欧洲研究理事会;
关键词
SOLUTE DIFFUSION; HYDROGELS; MICROFLUIDICS; MEMBRANES; REAGENTS; GELS; MOLECULES; POLYMERS; STORAGE; POINT;
D O I
10.1039/c5an02090e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A practical way to realize on-chip sample preparation for point-of-care diagnostics is to store the required reagents on a microfluidic device and release them in a controlled manner upon contact with the sample. For the development of such diagnostic devices, a fundamental understanding of the release kinetics of reagents from suitable materials in microfluidic chips is therefore essential. Here, we study the release kinetics of fluorophore-conjugated antibodies from (sub-) mu m thick gelatin layers and several ways to control the release time. The observed antibody release is well-described by a diffusion model. Release times ranging from similar to 20 s to similar to 650 s were determined for layers with thicknesses (in the dry state) between 0.25 mu m and 1.5 mu m, corresponding to a diffusivity of 0.65 mu m(2) s(-1) (in the swollen state) for our standard layer preparation conditions. By modifying the preparation conditions, we can influence the properties of gelatin to realize faster or slower release. Faster drying at increased temperatures leads to shorter release times, whereas slower drying at increased humidity yields slower release. As expected in a diffusive process, the release time increases with the size of the antibody. Moreover, the ionic strength of the release medium has a significant impact on the release kinetics. Applying these findings to cell counting chambers with on-chip sample preparation, we can tune the release to control the antibody distribution after inflow of blood in order to achieve homogeneous cell staining.
引用
收藏
页码:3068 / 3076
页数:9
相关论文
共 47 条
[21]   Point of Care Diagnostics: Status and Future [J].
Gubala, Vladimir ;
Harris, Leanne F. ;
Ricco, Antonio J. ;
Tan, Ming X. ;
Williams, David E. .
ANALYTICAL CHEMISTRY, 2012, 84 (02) :487-515
[22]   Size-dependent release of fluorescent macromolecules and nanoparticles from radically cross-linked hydrogels [J].
Henke, Matthias ;
Brandl, Ferdinand ;
Goepferich, Achim M. ;
Tessmar, Joerg K. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2010, 74 (02) :184-192
[24]   Reagents in microfluidics: an 'in' and 'out' challenge [J].
Hitzbleck, Martina ;
Delamarche, Emmanuel .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (21) :8494-8516
[25]   Controlled release of reagents in capillary-driven microfluidics using reagent integrators [J].
Hitzbleck, Martina ;
Gervais, Luc ;
Delamarche, Emmanuel .
LAB ON A CHIP, 2011, 11 (16) :2680-2685
[26]   Pre-storage of liquid reagents in glass ampoules for DNA extraction on a fully integrated lab-on-a-chip cartridge [J].
Hoffmann, Jochen ;
Mark, Daniel ;
Lutz, Sascha ;
Zengerle, Roland ;
von Stetten, Felix .
LAB ON A CHIP, 2010, 10 (11) :1480-1484
[27]   Development of a capillary flow microfluidic Escherichia coli biosensor with on-chip reagent delivery using water-soluble nanofibers [J].
Jin, Shengquan ;
Dai, Minhui ;
Ye, Bang-ce ;
Nugen, Sam R. .
MICROSYSTEM TECHNOLOGIES-MICRO-AND NANOSYSTEMS-INFORMATION STORAGE AND PROCESSING SYSTEMS, 2013, 19 (12) :2011-2015
[28]   Measurement of Biomolecular Diffusion in Extracellular Matrix Condensed by Fibroblasts Using Fluorescence Correlation Spectroscopy [J].
Kihara, Takanori ;
Ito, Junri ;
Miyake, Jun .
PLOS ONE, 2013, 8 (11)
[29]   A disposable, self-contained PCR chip [J].
Kim, Jitae ;
Byun, Doyoung ;
Mauk, Michael G. ;
Bau, Haim H. .
LAB ON A CHIP, 2009, 9 (04) :606-612
[30]   THE STRUCTURE AND PROPERTIES OF SOLID GELATIN AND THE PRINCIPLES OF THEIR MODIFICATION [J].
KOZLOV, PV ;
BURDYGINA, GI .
POLYMER, 1983, 24 (06) :651-666