Switching the Biointerface of Displaceable Poly-p-xylylene Coatings
Source abstract
Abstract
A new class of functionalized poly-p-xylyene coating has been synthesized to provide switchable and displaceable surface properties for biomaterials. The switchability is achieved through a mechanism for detaching/attaching biomolecules and/or a mechanism through which the programmed restoration of functions or their replacement by other functions can be carried out. This advanced version of poly-p-xylylene comprises an integrated disulfide moiety within the functional side group, and the switching phenomenon between the immobilized functional molecules is triggered by the redox thiol-disulfide interchange reaction. These dynamically well-defined molecules on the surfaces respond simultaneously to altered biological properties and controlled biointerfacial functions, for example, switching wettability or reversibly altered cell adhesion activity. Poly-p-xylylenes are a key player in controlling surface properties for many important applications, such as medical implants, biosensors, bioMEMS devices, and microfluidics. The introduction of this new facet of poly-p-xylylenes enables the dynamic mimicry of biological functions relevant to the design of new biomaterials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer Surface Interaction Studies · Molecular Junctions and Nanostructures · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan
Funding
Ministry of Science and Technology, Taiwan
References (42)
Show source-provided references
1. Murphy W. L. · Nat. Mater. · 2014 · 13 · 54710.1038/nmat3937 ↗
2. Klee D. · 1999 · 1
3. Fisher O. Z. · Acc. Chem. Res. · 2010 · 43 · 41910.1021/ar900226q ↗
4. Stevens M. M. · Science · 2005 · 310 · 113510.1126/science.1106587 ↗
5. Sun T. · Chem. Soc. Rev. · 2011 · 40 · 290910.1039/c0cs00124d ↗
6. Cole M. A. · Biomaterials · 2009 · 30 · 182710.1016/j.biomaterials.2008.12.026 ↗
7. Yang Y.-W. · Acc. Chem. Res. · 2014 · 47 · 195010.1021/ar500022f ↗
8. Stuart M. A. C. · Nat. Mater. · 2010 · 9 · 10110.1038/nmat2614 ↗
9. Dolbier W. R. · J. Fluorine Chem. · 2003 · 122 · 9710.1016/S0022-1139(03)00100-3 ↗
10. Senkevich J. J. · J. Vac. Sci. Technol., A · 2002 · 20 · 144510.1116/1.1487870 ↗
11. Vaeth K. M. · Adv. Mater. · 1999 · 11 · 81410.1002/(SICI)1521-4095(199907)11:10<814::AID-ADMA814>3.0.CO;2-Z ↗
12. Chen H.-Y. · Adv. Mater. · 2008 · 20 · 347410.1002/adma.200800455 ↗
13. Zhang C. · Acta Biomater. · 2011 · 7 · 374610.1016/j.actbio.2011.06.003 ↗
14. Jeon B.-J. · Sens. Actuators, B · 2011 · 154 · 8910.1016/j.snb.2010.01.035 ↗
15. Ko H. · Biosens. Bioelectron. · 2011 · 30 · 5610.1016/j.bios.2011.08.026 ↗
16. Chen H.-Y. · Proc. Natl. Acad. Sci. U. S. A. · 2007 · 104 · 1117310.1073/pnas.0702749104 ↗
17. Nandivada H. · Angew. Chem., Int. Ed. · 2006 · 45 · 336010.1002/anie.200600357 ↗
18. Elkasabi Y. · Adv. Mater. · 2006 · 18 · 152110.1002/adma.200502454 ↗
19. Chen H.-Y. · Chem. Commun. (Cambridge, U. K.) · 2013 · 49 · 453110.1039/c3cc41491d ↗
20. Sun H.-Y. · Adv. Mater. Interfaces · 2014 · 1 · 140009310.1002/admi.201400093 ↗
21. Wu J.-T. · Macromol. Rapid Commun. · 2012 · 33 · 92210.1002/marc.201200011 ↗
22. Chen H.-Y. · J. Am. Chem. Soc. · 2010 · 132 · 1802310.1021/ja108679m ↗
23. Chang C.-H. · J. Mater. Chem. B · 2014 · 2 · 849610.1039/C4TB00992D ↗
24. Li C. · Angew. Chem., Int. Ed. · 2006 · 45 · 351010.1002/anie.200600324 ↗
25. Roy D. · Prog. Polym. Sci. · 2010 · 35 · 27810.1016/j.progpolymsci.2009.10.008 ↗
26. Szajewski R. P. · J. Am. Chem. Soc. · 1980 · 102 · 201110.1021/ja00526a042 ↗
27. Keire D. A. · J. Org. Chem. · 1992 · 57 · 12310.1021/jo00027a023 ↗
28. Cuozzo J. W. · Nat. Cell Biol. · 1999 · 1 · 13010.1038/11047 ↗
29. Tian F. · Proc. Natl. Acad. Sci. U. S. A. · 2014 · 111 · 176610.1073/pnas.1321237111 ↗
30. Williams K. · 2011 · 7710.1007/978-1-61737-960-4_7 ↗
31. Lahann J. · Macromolecules · 2002 · 35 · 438010.1021/ma011769e ↗
32. Castner D. G. · Langmuir · 1996 · 12 · 508310.1021/la960465w ↗
33. Xia Y. · Annu. Rev. Mater. Sci. · 1998 · 28 · 15310.1146/annurev.matsci.28.1.153 ↗
34. Perl A. · Adv. Mater. · 2009 · 21 · 225710.1002/adma.200801864 ↗
35. Caswell K. K. · J. Am. Chem. Soc. · 2003 · 125 · 1391410.1021/ja037969i ↗
36. Sletten E. M. · Angew. Chem., Int. Ed. · 2009 · 48 · 697410.1002/anie.200900942 ↗
37. Forsberg P. · Soft Matter · 2011 · 7 · 10410.1039/C0SM00595A ↗
38. Sun T. · Angew. Chem., Int. Ed. · 2004 · 43 · 35710.1002/anie.200352565 ↗
39. Zhang M. · Biomaterials · 1998 · 19 · 95310.1016/S0142-9612(98)00026-X ↗
40. Hersel U. · Biomaterials · 2003 · 24 · 438510.1016/S0142-9612(03)00343-0 ↗
41. Chen Y.-C. · ACS Appl. Mater. Interfaces · 2014 · 6 · 2190610.1021/am5071865 ↗
42. Chen H.-Y. · Langmuir · 2010 · 27 · 3410.1021/la101623n ↗