journal article·2013-01-09

Hydrodynamic Shaping, Polymerization, and Subsequent Modification of Thiol Click Fibers

Darryl A. Boyd, Adam R. Shields, Jawad Naciri, Frances S. Ligler

Publisher page

Abstract

Hydrodynamic focusing in microfluidic channels is used to produce highly uniform, shaped polymer fibers at room temperature and under "green" conditions. Core streams of thiol-ene and thiol-yne prepolymer solutions were guided using a phase-matched sheath stream through microfluidic channels with grooved walls to determine shape. Size was dictated by the ratio of the flow rates of the core and sheath streams. Thiol click reactions were initiated using UV illumination to lock in predesigned cross-sectional shapes and sizes. This approach proved to be much more flexible than electrospinning in that highly uniform fibers can be produced from prepolymer solutions with varying compositions and viscosities with made-to-order sizes and shapes. Furthermore, a very simple manipulation of the composition provided reactive groups on the fiber surface for attachment of active ligands and biological components. A proof-of-principle experiment demonstrated that biotin attached to thiol groups on the fiber surface could specifically bind a fluorescent protein.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polymer Surface Interaction Studies · Surface Modification and Superhydrophobicity · Advanced Sensor and Energy Harvesting Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, 4555 Overlook Avenue SW, Washington, D.C. 20375, United States

References (29)

Show source-provided references
1. Posner T. · Ber. Dtsch. Chem. Ges. · 1905 · 38 · 64610.1002/cber.190503801106 ↗
2. Kharasch M. S. · Chem. Ind. (London) · 1938 · 57 · 75210.1002/jctb.5000573206 ↗
3. Kohler E. P. · J. Am. Chem. Soc. · 1935 · 57 · 131610.1021/ja01310a045 ↗
4. Hoyle C. E. · Angew. Chem., Int. Ed. · 2010 · 49 · 154010.1002/anie.200903924 ↗
5. Hoyle C. E. · Chem. Soc. Rev. · 2010 · 39 · 135510.1039/b901979k ↗
6. Lowe A. B. · J. Mater. Chem. · 2010 · 20 · 474510.1039/b917102a ↗
7. Aimetti A. A. · Biomaterials · 2009 · 30 · 604810.1016/j.biomaterials.2009.07.043 ↗
8. Lin C.-C. · Biomaterials · 2011 · 32 · 968510.1016/j.biomaterials.2011.08.083 ↗
9. Nimmo C. M. · Bioconjugate Chem. · 2011 · 22 · 219910.1021/bc200281k ↗
10. 10.1002/adfm.20120225810.1002/adfm.201202258 ↗
11. Killops K. L. · J. Am. Chem. Soc. · 2008 · 130 · 506210.1021/ja8006325 ↗
12. Montanez M. I. · Macromolecules · 2010 · 43 · 600410.1021/ma1009935 ↗
13. Service R. F. · Science · 2008 · 320 · 86810.1126/science.320.5878.868 ↗
14. Lu H. · Dent. Mater. · 2005 · 21 · 112910.1016/j.dental.2005.04.001 ↗
15. Carioscia J. A. · Dent. Mater. · 2005 · 21 · 113710.1016/j.dental.2005.04.002 ↗
16. Davis A. R. · J. Am. Chem. Soc. · 2011 · 133 · 2054610.1021/ja2088579 ↗
17. Kwisnek L. · Macromolecules · 2010 · 43 · 385910.1021/ma1001113 ↗
18. Shanmuganathan K. · Chem. Mater. · 2011 · 23 · 472610.1021/cm2015093 ↗
19. Chan J. W. · Macromolecules · 2010 · 43 · 638110.1021/ma101069c ↗
20. Lee T. Y. · J. Polym. Sci. Polym. Chem. · 2009 · 47 · 250910.1002/pola.23327 ↗
21. Cramer N. B. · Macromolecules · 2002 · 35 · 536110.1021/ma0200672 ↗
22. Hensarling R. M. · J. Am. Chem. Soc. · 2009 · 131 · 1467310.1021/ja9071157 ↗
23. Fairbanks B. D. · Macromolecules · 2009 · 42 · 21110.1021/ma801903w ↗
24. Fairbanks B. D. · Macromolecules · 2010 · 43 · 411310.1021/ma1002968 ↗
25. Howell, P. B.; Ligler, F. S.; Shields, A. R.Sheath Flow Device and Method. U.S. Patent Application 20110193259, August 11, 2011.
26. Mott D. R. · Lab Chip · 2006 · 6 · 54010.1039/b516459a ↗
27. Shields A. R. · Soft Matter · 2012 · 8 · 265610.1039/c2sm07429j ↗
28. Thangawng A. L. · Lab Chip · 2009 · 9 · 312610.1039/b910581f ↗
29. Thangawng A. L. · Lab Chip · 2011 · 11 · 115710.1039/c0lc00392a ↗