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Online proceedings - EDA Publishing Association

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11-13 <br />

May, 2011, Aix-en-Provence, France<br />

<br />

y 0.0062x0.932<br />

ln( R(t)/ R(0))<br />

y 0.0069x1.292<br />

y 0.007x1.973<br />

Figure 5. Diffusion induced i-t curves for various AAO membranes<br />

Figure 6 displays the trajectories of the ratio of conductance<br />

difference ( Rt<br />

( ) / R(0)<br />

) with respect to the i-t curves shown in<br />

Figure 5. The conductance difference data were measured using<br />

the Wheatstone bridge circuit shown in Figure 2.<br />

Figure 6. Trajectories of the ratio of conductance difference ( Rt<br />

( ) / R(0)<br />

)<br />

The ( ln( Rt<br />

( ) / R(0))<br />

, t) curves are plotted in Figure 7.<br />

Since the ion diffusion induced currents as shown in Figure 5<br />

almost reached their steady-state conditions in less than 200 sec,<br />

the ( ln( Rt<br />

( ) / R(0))<br />

, t) curves were linearly approximated for<br />

the period from 0 to 180 sec. The approximation equations are<br />

listed adjacent to each curve. The slope of each<br />

( ln( Rt<br />

( ) / R(0))<br />

, t) curve can thus be calculated as depicted in<br />

Table 1. The diffusivity for each sample is calculated using<br />

Equation (11) and shown in Table 1. It can be observed that the<br />

diffusivities are close.<br />

R()<br />

t<br />

ln( )<br />

R(0)<br />

t<br />

D<br />

(m 2 /sec)<br />

Table 1. Diffusivity for various AAO membrane<br />

#1 #2 #3 mean<br />

-0.0070 -0.0062 -0.0069<br />

-0.0067<br />

0.00036<br />

2.5410 -8 2.2510 -8 2.5010 -8 2.430.13<br />

10 -8<br />

Figure 7. ( ln( Rt<br />

( ) / R(0))<br />

, t) curves for different samples<br />

IV. CONCLUSION<br />

Most of the physiological reactions in a cell are owing to<br />

the small changes of the surrounding environment. The in-vivo<br />

detection of the physiological reaction induced molecular<br />

variations can provide a very useful tool for better<br />

understanding of the physiological reaction. The small<br />

variations of the ambient environment are carried out by way of<br />

the diffusion of ions through the ion channels of the cell<br />

membrane. In this study, a simple principle for the detection of<br />

the diffusivity of nanoparticles in a nanochannel based on the<br />

Fick’s first law is proposed. Anodic aluminum oxide (AAO)<br />

membranes are used to replace membranes with single<br />

nanochannel for the measurement of the diffusivity. An<br />

electrochemical bath that can hold an AAO membrane to<br />

separate vessels with different ion concentrations is built. The<br />

across channel ionic concentration difference can be estimated<br />

in terms of the conductance difference that is measured using a<br />

Wheatstone bridge circuit. The diffusivity in the nanochannel<br />

can be estimated by simply plotting the natural logarithmic<br />

value of the electrolyte conductance difference across the<br />

nanochannel versus time and calculating its slope. The average<br />

diffusivity in an AAO membrane with nanopore diameter being<br />

around 80 nm and the thickness being 60 m was measured to<br />

be 2.430.1310 -8 m 2 /sec.<br />

ACKNOWLEDGEMENTS<br />

The authors would like to address their thanks to the<br />

National Science Council of Taiwan for their financial support<br />

of this work under grant NSC-98-2212-E-005-072- MY3.<br />

REFERENCES<br />

[1] Z. Siwy, and A. Fulinski, Am. J. Phys. 72, 567, 2004.<br />

[2] H. Uno, Z. L. Zhang, M. Suzui, R. Tero, Y. Nonogaki, S. Nakao, S. Seki,<br />

S.Tagawa, S. Oiki, and T. Urisu, Jpn. J. Appl. Phys. 45, L1334, 2004.<br />

[3] S. Howorka, S. Cheley, and H. Bayley, Nature. Biotechnol. 19, 636, 2001.<br />

[4] A. F. Sauer-Budge, J. A. Nyamwanda, D. K. Lubensky, and D. Branton,<br />

Phys. Rev.Lett. 90, 238101, 2003.<br />

[5] S. M. Bezrukov, I. Vodyanoy, and V. A. Parsegian, Nature 390, 279-291,<br />

385

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