TY - JOUR
T1 - Rapid prototyping of nanofluidic systems using size-reduced electrospun nanofibers for biomolecular analysis
AU - Park, Seung Min
AU - Huh, Yun Suk
AU - Szeto, Kylan
AU - Joe, Daniel J.
AU - Kameoka, Jun
AU - Coates, Geoffrey W.
AU - Edel, Joshua B.
AU - Erickson, David
AU - Craighead, Harold G.
PY - 2010/11/5
Y1 - 2010/11/5
N2 - Biomolecular transport in nanofluidic confinement offers various means to investigate the behavior of biomolecules in their native aqueous environments, and to develop tools for diverse single-molecule manipulations. Recently, a number of simple nanofluidic fabrication techniques has been demonstrated that utilize electrospun nanofibers as a backbone structure. These techniques are limited by the arbitrary dimension of the resulting nanochannels due to the random nature of electrospinning. Here, a new method for fabricating nanofluidic systems from size-reduced electrospun nanofibers is reported and demonstrated. As it is demonstrated, this method uses the scanned electrospinning technique for generation of oriented sacrificial nanofibers and exposes these nanofibers to harsh, but isotropic etching/heating environments to reduce their cross-sectional dimension. The creation of various nanofluidic systems as small as 20 nm is demonstrated, and practical examples of single biomolecular handling, such as DNA elongation in nanochannels and fluorescence correlation spectroscopic analysis of biomolecules passing through nanochannels, are provided. A scanned electrospinning technique for the generation of oriented sacrificial nanofibers is presented, and these nanofibers are exposed to harsh but isotropic heating (M1) and etching (M2) environments to reduce their cross-sectional dimension. With new nanofabrication methods, the creation of various nanofluidic systems as small as 20 nm is demonstrated, and practical biomolecular handling applications are provided.
AB - Biomolecular transport in nanofluidic confinement offers various means to investigate the behavior of biomolecules in their native aqueous environments, and to develop tools for diverse single-molecule manipulations. Recently, a number of simple nanofluidic fabrication techniques has been demonstrated that utilize electrospun nanofibers as a backbone structure. These techniques are limited by the arbitrary dimension of the resulting nanochannels due to the random nature of electrospinning. Here, a new method for fabricating nanofluidic systems from size-reduced electrospun nanofibers is reported and demonstrated. As it is demonstrated, this method uses the scanned electrospinning technique for generation of oriented sacrificial nanofibers and exposes these nanofibers to harsh, but isotropic etching/heating environments to reduce their cross-sectional dimension. The creation of various nanofluidic systems as small as 20 nm is demonstrated, and practical examples of single biomolecular handling, such as DNA elongation in nanochannels and fluorescence correlation spectroscopic analysis of biomolecules passing through nanochannels, are provided. A scanned electrospinning technique for the generation of oriented sacrificial nanofibers is presented, and these nanofibers are exposed to harsh but isotropic heating (M1) and etching (M2) environments to reduce their cross-sectional dimension. With new nanofabrication methods, the creation of various nanofluidic systems as small as 20 nm is demonstrated, and practical biomolecular handling applications are provided.
KW - electrospinning
KW - nanofiber control
KW - nanofluidic systems
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U2 - 10.1002/smll.201000884
DO - 10.1002/smll.201000884
M3 - Article
C2 - 20878634
AN - SCOPUS:78349293848
SN - 1613-6810
VL - 6
SP - 2420
EP - 2426
JO - Small
JF - Small
IS - 21
ER -