journal article·2015-03-10

Stimuli-Responsive and Hemocompatible Pseudozwitterionic Interfaces

Antoine Venault, Yong-Sheng Zheng, Arunachalam Chinnathambi, Sulaiman Ali Alharbi, Hsin-Tsung Ho, Yu Chang, Yung Chang

Langmuir· Volume 31· Issue 9
Publisher page

Abstract

We report a novel biomacromolecular formula for the design of hemocompatible gel interfaces of N-isopropylacrylamide (NIPAAm) and mixed-charge pairs of [2-(methacryloyloxy)ethyl]trimethylammonium (TMA) and 3-sulfopropyl methacrylate (SA) with overall electrical neutrality. The study stresses on how well-defined compositions of nonionic NIPAAm and pseudozwitterionic TMA/SA in the poly(NIPAAm-co-TMA/SA) hydrogels along with environmental conditions (temperature, ionic strength, and solution pH) affect swelling and adhesion of biofoulants on their surfaces. When challenged with plasma proteins, bacteria, recalcified platelets, or whole blood, stimuli-responsive hydrogels better resisted their adhesion as the content of mixed charges in the copolymer increased, to reach nonbiofouling for the gels made of 100% TMA/SA. The low hemolytic activity (0.5%) associated with a long plasma clotting time (10 min) suggests excellent hemocompatibility excellent hemocompatibility. Finally, hydrogels containing both NIPAAm and TMA/SA tend to exhibit preferential adhesion of leukocytes.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polymer Surface Interaction Studies · Hydrogels: synthesis, properties, applications · Advanced Sensor and Energy Harvesting Materials

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

Affiliations

R&D Center for Membrane Technology and Department of Chemical Engineering, Chung Yuan Christian University, Jhong-Li, Taoyuan 320, Taiwan

Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Kingdom of Saudi Arabia

Laboratory Medicine, Mackay Memorial Hospital, Taipei 104, Taiwan

Department of Obstetrics and Gynecology, Kaohsiung Medical University Hospital, Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

Department of Obstetrics and Gynecology, E-Da Hospital, I-Shou University, No. 1, Yida Road, Jiaosu Village, Yanchao District, Kaohsiung City, Taiwan

Funding

Chung Yuan Christian University · Ministry of Science and Technology, Taiwan

References (43)

Show source-provided references
1. Gilron J. · Desalination · 2001 · 140 · 16710.1016/S0011-9164(01)00366-6 ↗
2. Glinel K. · Bioconjugate Chem. · 2009 · 20 · 7110.1021/bc800280u ↗
3. Chen W. · Environ. Sci. Technol. · 2011 · 45 · 654510.1021/es200994n ↗
4. Li M. · Langmuir · 2012 · 28 · 1640810.1021/la303438t ↗
5. Bellotti N. · Ind. Eng. Chem. Res. · 2012 · 51 · 1662610.1021/ie301524r ↗
6. Gudipati C. S. · Langmuir · 2005 · 21 · 304410.1021/la048015o ↗
7. Misra A. · Macromolecules · 2009 · 42 · 729910.1021/ma9002193 ↗
8. Peng J. · Ind. Eng. Chem. Res. · 2010 · 49 · 485810.1021/ie9018963 ↗
9. Zhao J. · J. Membr. Sci. · 2011 · 369 · 510.1016/j.memsci.2010.10.046 ↗
10. Yang R. · Chem. Mater. · 2011 · 23 · 126310.1021/cm1031392 ↗
11. Li Y. · Langmuir · 2012 · 28 · 1250910.1021/la3022563 ↗
12. Chapman R. G. · J. Am. Chem. Soc. · 2000 · 122 · 830310.1021/ja000774f ↗
13. Holmlin R. E. · Langmuir · 2001 · 17 · 284110.1021/la0015258 ↗
14. Reich L. · J. Appl. Polym. Sci. · 1969 · 13 · 97710.1002/app.1969.070130513 ↗
15. Kuo W. H. · Biomacromolecules · 2011 · 12 · 434810.1021/bm2013185 ↗
16. Chang Y. · ACS Appl. Mater. Interfaces · 2011 · 3 · 122810.1021/am200055k ↗
17. Beltrán-Osuna A. A. · Langmuir · 2012 · 28 · 970010.1021/la301561j ↗
18. Nagumo R. · Ind. Eng. Chem. Res. · 2012 · 51 · 445810.1021/ie2029305 ↗
19. Kuang J. · Langmuir · 2012 · 28 · 725810.1021/la300738e ↗
20. Hu R. · Langmuir · 2013 · 29 · 377310.1021/la304708b ↗
21. Schroeder M. E. · Biomacromolecules · 2013 · 14 · 311210.1021/bm4007369 ↗
22. Chen S. · Langmuir · 2006 · 22 · 818610.1021/la061012m ↗
23. Chang Y. · Langmuir · 2010 · 26 · 352210.1021/la903172j ↗
24. Dai H. · Macromolecules · 2006 · 39 · 658410.1021/ma060486p ↗
25. Chan A. W. · Biomacromolecules · 2009 · 10 · 60910.1021/bm801316z ↗
26. Zarzar L. D. · Acc. Chem. Res. · 2014 · 47 · 53010.1021/ar4001923 ↗
27. Gil E. S. · Prog. Polym. Sci. · 2004 · 29 · 117310.1016/j.progpolymsci.2004.08.003 ↗
28. Li Y. Y. · Biomacromolecules · 2006 · 7 · 295610.1021/bm060080k ↗
29. Cheng H. · Bioconjugate Chem. · 2008 · 19 · 136810.1021/bc700478s ↗
30. Cheng C. · Bioconjugate Chem. · 2008 · 19 · 119410.1021/bc8000062 ↗
31. Chang Y. · Biomacromolecules · 2010 · 11 · 110110.1021/bm100093g ↗
32. Chang Y. · Langmuir · 2012 · 28 · 430910.1021/la203504h ↗
33. Venault A. · ACS Appl. Mater. Interfaces · 2014 · 6 · 320110.1021/am404780w ↗
34. Katime I. · Adv. Mater. Lett. · 2013 · 4 · 11510.5185/amlett.2012.6377 ↗
35. Shang J. · Biomacromolecules · 2008 · 9 · 120810.1021/bm701204j ↗
36. Liu Q. · Biomacromolecules · 2013 · 14 · 22610.1021/bm301646y ↗
37. Corum L. E. · Langmuir · 2011 · 27 · 831610.1021/la201064d ↗
38. Riedel T. · Langmuir · 2013 · 29 · 338810.1021/la304886r ↗
39. Birdsall H. H. · AIDS · 2002 · 16 · 510.1097/00002030-200201040-00002 ↗
40. Gawaz P. M. · Kidney Int. · 1994 · 46 · 48910.1038/ki.1994.299 ↗
41. Furman M. I. · Am. Heart J. · 2001 · 142 · 79010.1067/mhj.2001.119128 ↗
42. Zeller J. A. · J. Neurol. Psychiatry · 2004 · 75 · 98410.1136/jnnp.2003.019638 ↗
43. Xiang T. · Langmuir · 2014 · 30 · 511510.1021/la5001705 ↗