journal article·2013-05-29

Directed self-assembly of microscale hydrogels by electrostatic interaction

Yu Long Han, Yanshen Yang, Shaobao Liu, Jinhui Wu, Yongmei Chen, Tian Jian Lu, Feng Xu

Biofabrication· Volume 5· Issue 3
Publisher page

Abstract

The unique benefit of electrostatic self-assembly of microscale components in solution is demonstrated for the first time. In particular, positive and negative treatment of poly(ethylene glycol) (PEG) facilitates a novel bottom-up assembly approach using electrostatic interaction from microgels with opposite charges. Fundamental investigations of electrostatic interaction of microgels reveal that the contact area of microgels determines the total energy of construct and thus the final patterns. The electrostatic self-assembly approach enables the fabrication of large and complex biological related structures (e.g., multi-layer spheroid) with accurate control. By the design of the microgels, the thickness and number of microgels in each layer can be controlled. Biological investigations of positive and negative treatments of PEG further prove the possibility of using this approach in tissue engineering, regenerative medicine and drug delivery.
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Research context

OpenAlex topics: 3D Printing in Biomedical Research · Hydrogels: synthesis, properties, applications · Microfluidic and Bio-sensing Technologies

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

References (45)

Show source-provided references
1. 10.1038/nature0220910.1038/nature02209 ↗
2. 10.1038/nphoton.2007.25210.1038/nphoton.2007.252 ↗
3. 10.1126/science.289.5482.117010.1126/science.289.5482.1170 ↗
4. Costanzo L · Physiology · 2006
5. 10.1038/nri241410.1038/nri2414 ↗
6. 10.1038/nri166910.1038/nri1669 ↗
7. 10.1126/science.106921010.1126/science.1069210 ↗
8. 10.1039/b814285h10.1039/b814285h ↗
9. 10.1002/adhm.20120001110.1002/adhm.201200011 ↗
10. 10.1073/pnas.080186610510.1073/pnas.0801866105 ↗
11. 10.1002/adma.20110196210.1002/adma.201101962 ↗
12. 10.1016/j.biomaterials.2011.07.01010.1016/j.biomaterials.2011.07.010 ↗
13. 10.1002/adfm.20120170810.1002/adfm.201201708 ↗
14. 10.1021/nl015684310.1021/nl0156843 ↗
15. 10.1126/science.112512410.1126/science.1125124 ↗
16. 10.1039/c1sm05881a10.1039/c1sm05881a ↗
17. 10.1039/c2sm26192h10.1039/c2sm26192h ↗
18. 10.1021/ma970897t10.1021/ma970897t ↗
19. 10.1080/0021846090329148610.1080/00218460903291486 ↗
20. 10.1016/j.biomaterials.2006.12.00510.1016/j.biomaterials.2006.12.005 ↗
21. 10.1063/1.167215710.1063/1.1672157 ↗
22. 10.1021/j100570a01310.1021/j100570a013 ↗
23. Bhattacharjee S · Croat. Chem. Acta · 1998 · 71 · 883
24. 10.1021/nn100869j10.1021/nn100869j ↗
25. 10.1038/416811a10.1038/416811a ↗
26. Sleisenger M H · Sleisenger & Fordtran's Gastrointestinal and Liver Disease: Pathophysiology, Diagnosis, Management · 2009
27. 10.1369/jhc.5C6684.200510.1369/jhc.5C6684.2005 ↗
28. 10.1002/bit.2255210.1002/bit.22552 ↗
29. 10.1002/adma.20090389310.1002/adma.200903893 ↗
30. 10.1021/bm025610110.1021/bm0256101 ↗
31. 10.1021/la981574910.1021/la9815749 ↗
32. 10.1038/3500661010.1038/35006610 ↗
33. 10.1063/1.471422110.1063/1.4714221 ↗
34. 10.1063/1.275715610.1063/1.2757156 ↗
35. 10.1126/science.115458610.1126/science.1154586 ↗
36. 10.1016/j.copbio.2011.02.00610.1016/j.copbio.2011.02.006 ↗
37. 10.1002/biot.20100034010.1002/biot.201000340 ↗
38. 10.1063/1.358075210.1063/1.3580752 ↗
39. 10.1096/fj.06-7117com10.1096/fj.06-7117com ↗
40. 10.1016/j.addr.2004.05.00110.1016/j.addr.2004.05.001 ↗
41. 10.1016/j.biomaterials.2004.04.02410.1016/j.biomaterials.2004.04.024 ↗
42. 10.1039/c2sm26126j10.1039/c2sm26126j ↗
43. 10.1016/j.biomaterials.2008.06.01710.1016/j.biomaterials.2008.06.017 ↗
44. 10.1038/nprot.2010.13910.1038/nprot.2010.139 ↗
45. 10.1126/science.116949410.1126/science.1169494 ↗