Biosensors and Bioelectronics 26 (2011) 2085–2089
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Biosensors and Bioelectronics
journal homepage: www.elsevier.com/locate/bios
Size-controllable quartz nanostructure for signal enhancement of DNA chip
Jung Suk Kim
a,1
, Jae Bum Cho
b,1
, Bo Gi Park
c
, Wonbae Lee
d
, Kyu Back Lee
c,d,∗
, Min-Kyu Oh
b,∗∗
a
Department of Biomedical Engineering, College of Medicine, Korea University, Anam-dong 5-1, Seoul 136-705, Republic of Korea
b
Department of Chemical and Biological Engineering, Korea University, Anam-dong 5-1, Seoul 136-713, Republic of Korea
c
Department of Interdisciplinary Bio/Micro System Technology, College of Engineering, Korea University, Anam-dong 5-1, Seoul 136-713, Republic of Korea
d
Department of Biomedical Engineering, College of Health Science, Korea University, San-1, Jeongneung-3-dong, Seoul 136-703, Republic of Korea
article info
Article history:
Received 16 June 2010
Received in revised form 5 September 2010
Accepted 6 September 2010
Available online 16 September 2010
Keywords:
Nanostructured quartz
Nanopillar
DNA chip
DNA sensor
abstract
A mask-free, cost-effective dry-etching method for the fabrication of height- and spacing-controlled,
pillar-like nanostructures was established in order to detect DNA molecules. The height and spacing of
the quartz nanostructure were regulated by successive O
2
and CF
4
reactive ion etching times. The height
and spacing of the nanostructures were tuned between 118 and 269 nm and between 107 and 161 nm,
respectively. Probe DNA was immobilized on the structure and hybridized with fluorescently-labeled
target DNA. Increases in the height and spacing of the nanopillar structure positively correlated with the
fluorescence intensity of bound DNA. Usage of the nanostructure increased the DNA detection limit by
up to 100-fold.
© 2010 Elsevier B.V. All rights reserved.
1. Introduction
Recently, numerous studies on fabrication of nanostructures
and their applications to biotechnology have been reported (Kaji
et al., 2003; Ogawa et al., 2007; Oillic et al., 2007b; Rosi and Mirkin,
2005; Anandan et al., 2006). A nanopattern of well-defined height
and spacing generally offers several advantages for improving the
sensing ability of a biosensor with several reasons. The first is
increased surface area with high aspect ratio for the immobiliza-
tion of more sensing probes. Second, appropriate spacing between
the immobilized probes on the nanostructure enhances the acces-
sibility of target materials (Oillic et al., 2007b). Finally, in an optical
sensing system, a patterned surface can reduce the quenching effect
of fluorescent signal materials by controlling immobilization and
spacing. The fabrication of silicon-based high-aspect-ratio nanos-
tructures is performed either by nanolithography followed by deep
RIE (Reactive Ion Etching) or nanomolding (Choi et al., 2009; Fu et
al., 2009). However, such methods still remain costly and problem-
atic in the point that those methods still require expensive masks or
master molds, and the cost for fabricating a mask or a master mold
increases exponentially as the required resolution gets smaller and
smaller in nanometer scale. Therefore, production of a nanopattern
with well-defined height and spacing via a simple low-cost method
∗
Corresponding author. Tel.: +82 2 940 2882; fax: +82 2 929 8044.
∗∗
Corresponding author. Tel.: +82 2 3290 3308; fax: +82 2 926 6102.
E-mail addresses: kblee@korea.ac.kr (K.B. Lee), mkoh@korea.ac.kr (M.-K. Oh).
1
These authors contributed equally to this work.
is a crucial requirement for the successful construction of a highly
sensitive biosensor system.
We previously developed an effective method for fabricating
high-aspect-ratio pillar-like nanostructures on a quartz surface
(Lee et al., 2010). Our method finely controls the spacing and height
of the resulting nanopattern in nanometer-scale resolution over
several centimeters by simple two-step reactive ion etching (RIE)
with O
2
and CF
4
plasma without any expensive mask, additional
equipment or complicated technology. The spacing was controlled
by the O
2
RIE time, and the height and shape of features in the
nanopattern were mainly controlled by CF
4
RIE time.
DNA chips, also called as DNA microarrays, have been devel-
oped to analyze the concentration of specific DNA of which the
sequences are related to genetic disease, pathogenic microorgan-
ism, or gene expression (Bittel et al., 2005; Cho et al., 2006; Ito
et al., 2007; Wen et al., 2004). This technology using immobilized
DNA oligonucleotides allows highly parallel analysis by hybridiza-
tion process, after which the DNA chip is analyzed by various
methods such as surface plasmon resonance, electrochemical sig-
naling or fluorescence level (Ahmed et al., 2007; Bin Lim et al.,
2008; Lao et al., 2009; Wakai et al., 2004). Although DNA chips
have great potential as a high-throughput detection method, their
sensitivity on planar substrates is not particularly high due to the
limitation of mixing efficiency and probe immobilization capacity
(Oillic et al., 2007a). Therefore, pillar-like nanostructures have been
synthesized on solid substrate for the detection of biomolecules
(Kuwabara et al., 2008; Murthy et al., 2008; Park et al., 2009).
In this study, we controlled the height and spacing of pillar-like
nanostructures and examined their impact on DNA detection sen-
0956-5663/$ – see front matter © 2010 Elsevier B.V. All rights reserved.
doi:10.1016/j.bios.2010.09.010