One‐step Preparation of Monodisperse Multifunctional Macroporous Particles through a Spontaneous Physical Process
Source abstract
Abstract
Abstract Macroporous particles that combine the property features of spherical structures and porous materials are expected to find use over micro‐ and macroscopic length scales from miniaturized systems such as cell imaging, drug and gene delivery to industrial applications. However, the capacity for de novo design of such materials is still limited. Here, a spontaneous process to fabricate monodisperse multifunctional macroporous particles (MMMPs) by high internal phase emulsion templating is reported. An interesting physical phenomenon involving self‐emulsification and synergistic effects between nanoparticles and amphiphilic diblock copolymers is observed in this process. These MMMPs, featured with tailor‐made pore structures, pH responsiveness, and magnetic response, could be used as stimuli‐responsive carriers for multiple functional molecules with a high loading and releasing efficiency. This new understanding regarding the underlying phenomena that control self‐emulsification behavior and synergistic action in emulsion systems provides a unique outlook and a novel approach to the design of potentially multifunctional porous materials for controllable release and delivery processes.
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Research context
OpenAlex topics: Pickering emulsions and particle stabilization · Surfactants and Colloidal Systems · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Laboratory of Biomedical Materials Beijing University of Chemical Technology Beijing 100029 China
Beijing National Laboratory for Molecular Science Institute of Chemistry Chinese Academy of Sciences North First Street 2 Zhongguancun Beijing 100190 China
University of Chinese Academy of Sciences Beijing 100049 China
References (39)
Show source-provided references
1. 10.1021/cr200440z10.1021/cr200440z ↗
2. 10.1039/C6CS00060F10.1039/C6CS00060F ↗
3. 10.1021/ja035874a10.1021/ja035874a ↗
4. 10.1039/C5CS00533G10.1039/C5CS00533G ↗
5. 10.1016/j.progpolymsci.2013.07.00310.1016/j.progpolymsci.2013.07.003 ↗
6. 10.1016/j.polymer.2004.11.09710.1016/j.polymer.2004.11.097 ↗
7. 10.1002/adfm.20100133010.1002/adfm.201001330 ↗
8. 10.1002/adma.20100072910.1002/adma.201000729 ↗
9. 10.1002/adma.20130055210.1002/adma.201300552 ↗
10. 10.1021/ma901867910.1021/ma9018679 ↗
11. 10.1126/science.291.5503.45310.1126/science.291.5503.453 ↗
12. 10.1002/anie.20130500310.1002/anie.201305003 ↗
13. 10.1021/ma301026310.1021/ma3010263 ↗
14. 10.1002/adma.20080198610.1002/adma.200801986 ↗
15. 10.1002/adma.20150635810.1002/adma.201506358 ↗
16. 10.1021/jacs.5b1214910.1021/jacs.5b12149 ↗
17. 10.1038/nature0719710.1038/nature07197 ↗
18. 10.1002/smll.20150139610.1002/smll.201501396 ↗
19. 10.1002/adma.20120491310.1002/adma.201204913 ↗
20. 10.1021/jacs.6b1134610.1021/jacs.6b11346 ↗
21. 10.1002/adma.20160689510.1002/adma.201606895 ↗
22. 10.1002/anie.20161229110.1002/anie.201612291 ↗
23. 10.1002/anie.20080224410.1002/anie.200802244 ↗
24. 10.1002/anie.20090210310.1002/anie.200902103 ↗
25. 10.1002/anie.20090717510.1002/anie.200907175 ↗
26. 10.1021/am503341j10.1021/am503341j ↗
27. 10.1021/ja412172f10.1021/ja412172f ↗
28. 10.1021/ma501253u10.1021/ma501253u ↗
29. 10.1021/la500726v10.1021/la500726v ↗
30. 10.1002/anie.20160215010.1002/anie.201602150 ↗
31. 10.1038/srep2140110.1038/srep21401 ↗
32. 10.1021/acs.langmuir.5b0447710.1021/acs.langmuir.5b04477 ↗
33. 10.1021/acs.langmuir.5b0303710.1021/acs.langmuir.5b03037 ↗
34. 10.1021/acsnano.6b0098510.1021/acsnano.6b00985 ↗
35. 10.1021/ja038142r10.1021/ja038142r ↗
36. 10.1073/pnas.18223399910.1073/pnas.182233999 ↗
37. 10.1002/anie.20160696010.1002/anie.201606960 ↗
38. 10.1021/ja038085210.1021/ja0380852 ↗
39. 10.1002/adma.20120125110.1002/adma.201201251 ↗