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Effects of Ionic Strength in the Medium on Sample Preconcentration Utilizing Nano-interstices between Self-Assembled Monolayers of Gold Nanoparticles

  • Nguyen, Ngoc-Viet (Department of Mechanical Engineering, National Chung Cheng University) ;
  • Wu, Jian-Sheng (Department of Mechanical Engineering, National Chung Cheng University) ;
  • Jen, Chun-Ping (Department of Mechanical Engineering, National Chung Cheng University)
  • Received : 2018.05.31
  • Accepted : 2018.07.10
  • Published : 2018.12.20

Abstract

This paper investigated the effects of ionic strength in the medium on a preconcentrator for a protein sample with low concentration. The preconcentration chip was designed and fabricated using a polydimethylsiloxane replica through standard lithophotography. A glass substrate is silanized prior to functionalizing the nanoparticles for self-assembly at a designed region. Due to the overlap of electrical double layers in a nanofluidic channel, a concentration polarization effect can be achieved using an electric field. A nonlinear electrokinetic flow is induced, resulting in the fast accumulation of proteins in front of the induced ionic depletion zone, so called exclusion-enrichment effect. Thus, the protein sample can be driven by electroosmotic flow and accumulated at a specific location. The chip is used to collect fluorescein isothiocyanate-labeled bovine serum albumin (FITC-BSA) diluted in phosphate-buffered saline (PBS) buffer solution. Different concentrations of the buffer media were studied herein. Fluorescence intensity images show that the buffer concentration of 4 mM is more appropriate than all the other ones. The sample of FITC-BSA with an initial concentration of $10{\mu}M$ in the 4 mM PBS solution increases its concentration at the desired region by up to 50 times within 30 min, demonstrating the results in this investigation.

Keywords

Acknowledgement

Supported by : Ministry of Science and Technology of Republic of China

References

  1. Lin, C.C., Hsu, J.L. & Lee, G. Bin. Sample preconcentration in microfluidic devices. Microfluid. Nanofluid. 10, 481-511 (2011). https://doi.org/10.1007/s10404-010-0661-9
  2. Islam, M.R. & Serpe, M.J. Label-free detection of low protein concentration in solution using a novel colorimetric assay. Biosens. Bioelectron. 49, 133-138 (2013). https://doi.org/10.1016/j.bios.2013.05.011
  3. Koh, Y. et al. Nanoslit-concentration-chip integrated microbead-based protein assay system for sensitive and quantitative detection. RSC Adv. 7, 29679-29685 (2017). https://doi.org/10.1039/C7RA02460F
  4. Wang, C., Shi, Y., Wang, J., Pang, J. & Xia, X.H. Ultrasensitive protein concentration detection on a micro/nanofluidic enrichment chip using fluorescence quenching. ACS Appl. Mater. Interfaces 7, 6835-6841 (2015). https://doi.org/10.1021/acsami.5b00383
  5. Duan, C., Wang, W. & Xie, Q. Review article: Fabrication of nanofluidic devices. Biomicrofluidics 7, 026501 (2013). https://doi.org/10.1063/1.4794973
  6. Wang, Y.C., Stevens, A.L. & Han, J. Million-fold preconcentration of proteins and peptides by nanofluidic filter. Anal. Chem. 77, 4293-4299 (2005). https://doi.org/10.1021/ac050321z
  7. Wu, D. & Steckl, A.J. High speed nanofluidic protein accumulator. Lab Chip 9, 1890 (2009). https://doi.org/10.1039/b823409d
  8. Wang, J., Zhang, L., Xue, J. & Hu, G. Ion diffusion coefficient measurements in nanochannels at various concentrations. Biomicrofluidics 8, 1 (2014).
  9. Kim, S.M., Burns, M.A. & Hasselbrink, E.F. Electrokinetic protein preconcentration using a simple glass/poly (dimethylsiloxane) microfluidic chip. Anal. Chem. 78, 4779-4785 (2006). https://doi.org/10.1021/ac060031y
  10. Jeong, H.L., Chung, S., Sung, J.K. & Han, J. Poly(dimethylsiloxane)-based protein preconcentration using a nanogap generated by junction gap breakdown. Anal. Chem. 79, 6868-6873 (2007). https://doi.org/10.1021/ac071162h
  11. Yang, R.-J., Pu, H.-H. & Wang, H.-L. Ion concentration polarization on paper-based microfluidic devices and its application to preconcentrate dilute sample solutions. Biomicrofluidics 9, 014122 (2015). https://doi.org/10.1063/1.4913366
  12. Lee, J.H., Song, Y.-A. & Han, J. Multiplexed proteomic sample preconcentration device using surface-patterned ion-selective membrane. Lab Chip 8, 596 (2008). https://doi.org/10.1039/b717900f
  13. Syed, A., Mangano, L., Mao, P., Han, J. & Song, Y. Creating sub-50 nm nanofluidic junctions in a PDMS microchip via self-assembly process of colloidal silica beads for electrokinetic concentration of biomolecules. Lab Chip 14, 4455-4460 (2014). https://doi.org/10.1039/C4LC00895B
  14. Jen, C.P., Amstislavskaya, T.G., Kuo, C.C. & Chen, Y.H. Protein preconcentration using nanofractures generated by nanoparticle-assisted electric breakdown at junction gaps. PLoS ONE 9, e102050 (2014). https://doi.org/10.1371/journal.pone.0102050
  15. Jen, C.P., Amstislavskaya, T.G., Chen, K.F. & Chen, Y.H. Sample preconcentration utilizing nanofractures generated by junction gap breakdown assisted by self-assembled monolayer of gold nanoparticles. PLoS ONE 10, e0126641 (2015). https://doi.org/10.1371/journal.pone.0126641
  16. Pu, Q., Yun, J., Temkin, H. & Liu, S. Ion-enrichment and ion-depletion effect of nanochannel structures. Nano Lett. 4, 1099-1103 (2004). https://doi.org/10.1021/nl0494811
  17. Quoc, T.V., Wu, M.S., Bui, T.T., Duc, T.C. & Jen, C.P. A compact microfluidic chip with integrated impedance biosensor for protein preconcentration and detection. Biomicrofluidics 11 (2017).
  18. Mani, A., Zangle, T.A. & Santiago, J.G. On the propagation of concentration polarization from microchannel-nanochannel interfaces Part I: Analytical model and characteristic analysis. Langmuir 25, 3898-3908 (2009). https://doi.org/10.1021/la803317p
  19. Rohani, A. et al. Frequency-selective electrokinetic enrichment of biomolecules in physiological media based on electrical double-layer polarization. Nanoscale 9, 12124-12131 (2017). https://doi.org/10.1039/C7NR02376F
  20. Rohani, A., Varhue, W., Liao, K. & Chou, C. Nanoslit design for ion conductivity gradient enhanced dielectrophoresis for ultrafast biomarker enrichment in physiological media. Biomicrofluidics 10, 033109 (2016). https://doi.org/10.1063/1.4954933
  21. Chun, H., Chung, T.D. & Ramsey, J.M. High yield sample preconcentration using a highly ion-conductive charge-selective polymer. Anal. Chem. 82, 6287-6292 (2010). https://doi.org/10.1021/ac101297t
  22. Jung, B., Bharadwaj, R. & Santiago, J.G. On-chip millionfold sample stacking using transient isotachophoresis. Anal. Chem. 78, 2319-2327 (2006). https://doi.org/10.1021/ac051659w
  23. Hofmann, O., Che, D., Cruickshank, K.A. & Muller, U.R. Adaptation of capillary isoelectric focusing to microchannels on a glass chip. Anal. Chem. 71, 678-686 (1999). https://doi.org/10.1021/ac9806660
  24. Schrott, W. et al. Study on surface properties of PDMS microfluidic chips treated with albumin. Biomicrofluidics 3, 1-15 (2009).
  25. Linder, V., Verpoorte, E., Thormann, W., De Rooij, N.F. & Sigrist, H. Surface biopassivation of replicated poly (dimethylsiloxane) microfluidic channels and application to heterogeneous immunoreaction with on-chip fluorescence detection. Anal. Chem. 73, 4181-4189 (2001). https://doi.org/10.1021/ac010421e
  26. Oldham, K.B. A Gouy-Chapman-Stern model of the double layer at a (metal)/(ionic liquid) interface. J. Electroanal. Chem. 613, 131-138 (2008). https://doi.org/10.1016/j.jelechem.2007.10.017
  27. Brown, M.A., Goel, A. & Abbas, Z. Effect of electrolyte concentration on the stern layer thickness at a charged interface. Angew. Chem. Int. Ed. 55, 3790-3794 (2016). https://doi.org/10.1002/anie.201512025

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