journal article·2020-10-14

Metachronal Actuation of Microscale Magnetic Artificial Cilia

Srinivas Hanasoge, Peter J. Hesketh, Alexander Alexeev

ACS Applied Materials & Interfaces· Volume 12· Issue 41
Publisher page

Abstract

Biological cells often interact with the environment through carpets of microscopic hair-like cilia. These elastic structures are known to beat in a synchronized wavy fashion called metachronal motion to produce fluid transport. Metachronal motion emerges due to a phase difference between beating cycles of neighboring cilia and appears as traveling waves propagating along the ciliary carpet. We demonstrate submerged in water microscale magnetic cilia that are externally actuated to beat in a metachronal fashion. Two approaches are used to induce coordinated phase differences among the beating cilia. In the first case, we fabricate cilia with an imposed gradient of geometrical properties that are subject to a rotating uniform magnetic field. In the second scenario, a ciliary array is composed of identical cilia that experience a magnetic field that varies spatiotemporally. We demonstrate that magnetic cilia can achieve symplectic, antiplectic, and leoplectic metachrony.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Micro and Nano Robotics · Microfluidic and Bio-sensing Technologies · Characterization and Applications of Magnetic Nanoparticles

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

Affiliations

George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States

Funding

National Institute of Food and Agriculture · Division of Chemical, Bioengineering, Environmental, and Transport Systems

References (42)

Show source-provided references
1. 10.1146/annurev.physiol.69.040705.14123610.1146/annurev.physiol.69.040705.141236 ↗
2. 10.1093/humupd/dml01210.1093/humupd/dml012 ↗
3. 10.1089/jam.2006.19.11010.1089/jam.2006.19.110 ↗
4. 10.1016/j.tibtech.2012.11.00510.1016/j.tibtech.2012.11.005 ↗
5. 10.1073/pnas.100512710710.1073/pnas.1005127107 ↗
6. 10.1021/nl070190c10.1021/nl070190c ↗
7. 10.1002/smll.20190387210.1002/smll.201903872 ↗
8. 10.1039/c0sm00185f10.1039/c0sm00185f ↗
9. 10.1164/ajrccm/137.3.72610.1164/ajrccm/137.3.726 ↗
10. 10.1152/ajpgi.00064.200610.1152/ajpgi.00064.2006 ↗
11. 10.1146/annurev.en.11.010166.00053510.1146/annurev.en.11.010166.000535 ↗
12. 10.1073/pnas.110788910810.1073/pnas.1107889108 ↗
13. 10.1063/1.367606810.1063/1.3676068 ↗
14. 10.1103/PhysRevE.100.04240510.1103/PhysRevE.100.042405 ↗
15. 10.1073/pnas.121886911010.1073/pnas.1218869110 ↗
16. 10.1529/biophysj.106.08489710.1529/biophysj.106.084897 ↗
17. 10.1017/jfm.2011.35510.1017/jfm.2011.355 ↗
18. 10.1063/1.493855810.1063/1.4938558 ↗
19. 10.1038/s41567-018-0174-010.1038/s41567-018-0174-0 ↗
20. 10.7567/JJAP.55.06GP1910.7567/JJAP.55.06GP19 ↗
21. 10.1039/C1JM13787E10.1039/C1JM13787E ↗
22. 10.1021/la902926w10.1021/la902926w ↗
23. 10.1039/c1sm05423f10.1039/c1sm05423f ↗
24. 10.1088/1402-4896/ab207a10.1088/1402-4896/ab207a ↗
25. 10.1038/s41467-020-16458-410.1038/s41467-020-16458-4 ↗
26. 10.1073/pnas.94.12.600110.1073/pnas.94.12.6001 ↗
27. 10.1073/pnas.96.22.1224010.1073/pnas.96.22.12240 ↗
28. 10.1083/jcb.54.3.49310.1083/jcb.54.3.493 ↗
29. 10.1126/science.120396310.1126/science.1203963 ↗
30. 10.1016/S0960-9822(01)00581-410.1016/S0960-9822(01)00581-4 ↗
31. Machemer H. · J. Exp. Biol. · 1972 · 57 · 23910.1242/jeb.57.1.239 ↗
32. 10.1017/jfm.2012.30610.1017/jfm.2012.306 ↗
33. 10.1038/s41378-018-0010-910.1038/s41378-018-0010-9 ↗
34. 10.1039/C7LC00556C10.1039/C7LC00556C ↗
35. 10.1039/c0lc00411a10.1039/c0lc00411a ↗
36. 10.1103/PhysRevE.82.02730210.1103/PhysRevE.82.027302 ↗
37. 10.1039/C8SM00549D10.1039/C8SM00549D ↗
38. 10.1103/PhysRevE.79.04630410.1103/PhysRevE.79.046304 ↗
39. 10.1002/adfm.20150269610.1002/adfm.201502696 ↗
40. 10.1038/nature0409010.1038/nature04090 ↗
41. 10.1038/nbt.298910.1038/nbt.2989 ↗
42. 10.1007/s10404-019-2306-y10.1007/s10404-019-2306-y ↗