Functional Polymer Zwitterions as Reactive Surfactants for Nanoparticle Capture
Source abstract
Abstract
We describe the synthesis of sulfothetin (ST)-containing polymer zwitterions and their use as polymer surfactants for stabilizing emulsion droplets and for capturing and transporting nanoparticles (NPs) through a flowing aqueous fluid. In contrast to conventional zwitterions, which are chemically inert, the multifunctional ST-containing copolymers we describe both participate in droplet stabilization and embed reactive functionality directly into the zwitterionic framework. Advantageously including these ST zwitterions in phosphorylcholine (PC)-containing copolymers proved particularly useful for producing surfactants that contributed characteristics of droplet stabilization and interfacial reactivity. This was demonstrated by NP pickup, or "capture", experiments that were performed by circulating ST-coated emulsion droplets across a substrate, in a flow cell, containing amine-functionalized silica NPs. The resultant NP adherence to the fluid-fluid interface of the droplets hinged on the available reactivity of both the electrophilic (from ST) and nucleophilic (from the NPs) components as well as the solution pH and extent of amine functionality on the NPs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Surfactants and Colloidal Systems · Pickering emulsions and particle stabilization · Innovative Microfluidic and Catalytic Techniques Innovation
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Polymer Science & Engineering Department Conte Center for Polymer Research, University of Massachusetts, 120 Governors Drive, Amherst 01003, Massachusetts, United States
Funding
Basic Energy Sciences · U.S. Department of Energy
References (42)
Show source-provided references
1. 10.1126/science.270.5244.198010.1126/science.270.5244.1980 ↗
2. 10.1046/j.1365-313x.1998.00219.x10.1046/j.1365-313x.1998.00219.x ↗
3. 10.1371/journal.pcbi.003010110.1371/journal.pcbi.0030101 ↗
4. 10.1073/pnas.070145310410.1073/pnas.0701453104 ↗
5. 10.1038/nri308910.1038/nri3089 ↗
6. 10.1038/nprot.2013.07210.1038/nprot.2013.072 ↗
7. 10.1038/s41467-018-03936-z10.1038/s41467-018-03936-z ↗
8. 10.1295/polymj.22.35510.1295/polymj.22.355 ↗
9. 10.1088/1468-6996/13/6/06410110.1088/1468-6996/13/6/064101 ↗
10. 10.1002/jbm.1021010.1002/jbm.10210 ↗
11. 10.1016/j.memsci.2015.09.03710.1016/j.memsci.2015.09.037 ↗
12. 10.1002/admi.20150052110.1002/admi.201500521 ↗
13. 10.1021/acsami.7b0488410.1021/acsami.7b04884 ↗
14. 10.1038/s41428-018-0026-x10.1038/s41428-018-0026-x ↗
15. 10.1021/acs.langmuir.8b0218410.1021/acs.langmuir.8b02184 ↗
16. 10.1021/bc200667s10.1021/bc200667s ↗
17. 10.7150/thno.1123410.7150/thno.11234 ↗
18. 10.1021/acs.molpharmaceut.8b0076610.1021/acs.molpharmaceut.8b00766 ↗
19. 10.1016/j.csbj.2020.07.01510.1016/j.csbj.2020.07.015 ↗
20. 10.1038/nnano.2011.23510.1038/nnano.2011.235 ↗
21. 10.1002/admi.20140012110.1002/admi.201400121 ↗
22. 10.1002/adfm.20150394710.1002/adfm.201503947 ↗
23. 10.1126/sciadv.160146210.1126/sciadv.1601462 ↗
24. 10.1002/adfm.20180521910.1002/adfm.201805219 ↗
25. 10.1039/c4py01292e10.1039/c4py01292e ↗
26. 10.1021/jacs.5b1315610.1021/jacs.5b13156 ↗
27. 10.1021/acs.langmuir.8b0176410.1021/acs.langmuir.8b01764 ↗
28. 10.1002/app.1969.07013041210.1002/app.1969.070130412 ↗
29. 10.1021/ma971435i10.1021/ma971435i ↗
30. 10.1021/bm501449a10.1021/bm501449a ↗
31. 10.1002/pola.2835910.1002/pola.28359 ↗
32. Bankhead P. · ImageJ · 2014 · 1 · 10
33. 10.1039/d0cc00382d10.1039/d0cc00382d ↗
34. 10.1039/c7ta05171a10.1039/c7ta05171a ↗
35. 10.1021/acs.biomac.9b0062110.1021/acs.biomac.9b00621 ↗
36. 10.1039/c9sm01642b10.1039/c9sm01642b ↗
37. 10.1007/s12274-009-9041-810.1007/s12274-009-9041-8 ↗
38. 10.1021/j150516a00210.1021/j150516a002 ↗
39. 10.1021/j150553a02710.1021/j150553a027 ↗
40. 10.1016/0022-2313(75)90003-410.1016/0022-2313(75)90003-4 ↗
41. 10.1021/ac801134710.1021/ac8011347 ↗
42. 10.1111/j.1475-1313.2009.00703.x10.1111/j.1475-1313.2009.00703.x ↗