Surface biofunctionalization and production of miniaturized sensor structures using aerosol printing technologies

被引:56
作者
Grunwald, Ingo [1 ]
Groth, Esther [1 ]
Wirth, Ingo [1 ]
Schumacher, Julian [1 ]
Maiwald, Marcus [1 ]
Zoellmer, Volker [1 ]
Busse, Matthias [1 ]
机构
[1] Fraunhofer Inst Mfg Technol & Appl Mat Res IFAM, D-28359 Bremen, Germany
关键词
ELECTROCHEMICAL DNA BIOSENSORS; PROTEIN MICROARRAYS; GENE-EXPRESSION; FABRICATION; ARRAYS; SYSTEMS; TNF;
D O I
10.1088/1758-5082/2/1/014106
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The work described in this paper demonstrates that very small protein and DNA structures can be applied to various substrates without denaturation using aerosol printing technology. This technology allows high-resolution deposition of various nanoscaled metal and biological suspensions. Before printing, metal and biological suspensions were formulated and then nebulized to form an aerosol which is aerodynamically focused on the printing module of the system in order to achieve precise structuring of the nanoscale material on a substrate. In this way, it is possible to focus the aerosol stream at a distance of about 5 mm from the printhead to the surface. This technology is useful for printing fluorescence-marked proteins and printing enzymes without affecting their biological activity. Furthermore, higher molecular weight DNA can be printed without shearing. The advantages, such as printing on complex, non-planar 3D structured surfaces, and disadvantages of the aerosol printing technology are also discussed and are compared with other printing technologies. In addition, miniaturized sensor structures with line thicknesses in the range of a few micrometers are fabricated by applying a silver sensor structure to glass. After sintering using an integrated laser or in an oven process, electrical conductivity is achieved within the sensor structure. Finally, we printed BSA in small micrometre-sized areas within the sensor structure using the same deposition system. The aerosol printing technology combined with material development offers great advantages for future-oriented applications involving biological surface functionalization on small areas. This is important for innovative biomedical micro-device development and for production solutions which bridge the disciplines of biology and electronics.
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页数:11
相关论文
共 54 条
[1]   Electrical biochip technology - a tool for microarrays and continuous monitoring [J].
Albers, J ;
Grunwald, T ;
Nebling, E ;
Piechotta, G ;
Hintsche, R .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2003, 377 (03) :521-527
[2]   Investigation of microfabrication of biological sample arrays using piezoelectric and bubble-jet printing technologies [J].
Allain, LR ;
Stratis-Cullum, DN ;
Vo-Dinh, T .
ANALYTICA CHIMICA ACTA, 2004, 518 (1-2) :77-85
[3]   Microarray sampling-platform fabrication using bubble-jet technology for a biochip system [J].
Allain, LR ;
Askari, M ;
Stokes, DL ;
Vo-Dinh, T .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 371 (02) :146-150
[4]   3D protein microarrays:: Performing multiplex immunoassays on a single chip [J].
Angenendt, P ;
Glökler, J ;
Konthur, Z ;
Lehrach, H ;
Cahill, DJ .
ANALYTICAL CHEMISTRY, 2003, 75 (17) :4368-4372
[5]   Bio-microarray fabrication techniques - A review [J].
Barbulovic-Nad, Irena ;
Lucente, Michael ;
Sun, Yu ;
Zhang, Mingjun ;
Wheeler, Aaron R. ;
Bussmann, Markus .
CRITICAL REVIEWS IN BIOTECHNOLOGY, 2006, 26 (04) :237-259
[6]   Biological laser printing as an alternative to traditional protein arrayers [J].
Barron, JA ;
Young, HD ;
Ringeisen, BR ;
Dlott, DD ;
Krizman, DB .
Imaging, Manipulation, and Analysis of Biomolecules and Cells: Fundamentals and Applications III, 2005, 5699 :517-525
[7]   Printing of protein microarrays via a capillary-free fluid jetting mechanism [J].
Barron, JA ;
Young, HD ;
Dlott, DD ;
Darfler, MM ;
Krizman, DB ;
Ringeisen, BR .
PROTEOMICS, 2005, 5 (16) :4138-4144
[8]  
Barron JA, 2003, ABSTR PAP AM CHEM S, V226, pU481
[9]   Biological laser printing: A novel technique for creating heterogeneous 3-dimensional cell patterns [J].
Barron, JA ;
Wu, P ;
Ladouceur, HD ;
Ringeisen, BR .
BIOMEDICAL MICRODEVICES, 2004, 6 (02) :139-147
[10]   Protein patterning [J].
Blawas, AS ;
Reichert, WM .
BIOMATERIALS, 1998, 19 (7-9) :595-609