Controllable Cellular Micromotors Based on Optical Tweezers
Source abstract
Abstract
Abstract Micromotors hold exciting prospects in biomedical applications but still face a great challenge. To date, there have been few reports of micromotors with high safety, flexible controllability, and full biocompatibility. Here, a multifunctional method based on an optical tweezer system is presented to realize controllable cellular micromotors. The method not only satisfies all of the above criteria but is also independent of the cell types and materials. Optical tweezers are used to generate a dynamic scanning optical trap along a given circular trajectory, which can trap and drive a microparticle or a single cell to move along the trajectory and thus generate a microvortex. Cells within the microvortex will be controllably rotated under an action of shear stress or torque and their rotation rate and direction can be controlled by changing the scanning frequency and direction of the dynamic optical trap. The proposed method is effective for both immotile target cells and swimming target cells. Additionally, it is further applied to realize synchronous translation and rotation of cellular micromotors and to assemble controllable and fully biocompatible cellular micromotor assays. The proposed method is believed to have potential applications in targeted drug delivery, biological microenvironment monitoring and sensing, and biomedical treatment.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Orbital Angular Momentum in Optics · Micro and Nano Robotics · Microfluidic and Bio-sensing Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering State Key Laboratory of Optoelectronic Materials and Technologies Sun Yat‐Sen University Guangzhou Guangdong 510275 China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province
References (40)
Show source-provided references
1. 10.1039/C7CS00516D10.1039/C7CS00516D ↗
2. 10.1021/ja406090s10.1021/ja406090s ↗
3. 10.1038/nphoton.2011.28710.1038/nphoton.2011.287 ↗
4. 10.1021/acsami.7b1659510.1021/acsami.7b16595 ↗
5. 10.1364/OL.11.00028810.1364/OL.11.000288 ↗
6. 10.1073/pnas.172078511610.1073/pnas.1720785116 ↗
7. 10.3390/cryst910051510.3390/cryst9100515 ↗
8. 10.1039/c2lc40538e10.1039/c2lc40538e ↗
9. 10.1038/2856610.1038/28566 ↗
10. 10.1021/acsnano.5b0631110.1021/acsnano.5b06311 ↗
11. 10.1021/nl401081710.1021/nl4010817 ↗
12. 10.1103/PhysRevLett.104.10360110.1103/PhysRevLett.104.103601 ↗
13. 10.1103/PhysRevLett.75.82610.1103/PhysRevLett.75.826 ↗
14. 10.1038/s41467-018-06947-y10.1038/s41467-018-06947-y ↗
15. 10.1088/1367-2630/15/6/06301610.1088/1367-2630/15/6/063016 ↗
16. 10.3390/act202001910.3390/act2020019 ↗
17. 10.1021/acsnano.5b0356510.1021/acsnano.5b03565 ↗
18. 10.1039/C5NR08768F10.1039/C5NR08768F ↗
19. 10.1038/s41467-019-08968-710.1038/s41467-019-08968-7 ↗
20. Yang W. · Small · 2017 · 13
21. 10.1109/TBME.2011.214678110.1109/TBME.2011.2146781 ↗
22. 10.1364/OL.36.00004010.1364/OL.36.000040 ↗
23. 10.1364/OL.40.00188110.1364/OL.40.001881 ↗
24. 10.1515/nanoph-2019-005510.1515/nanoph-2019-0055 ↗
25. 10.1016/j.jphotobiol.2013.02.00610.1016/j.jphotobiol.2013.02.006 ↗
26. 10.3390/s1711264010.3390/s17112640 ↗
27. 10.3390/mi1008050710.3390/mi10080507 ↗
28. 10.1021/ac203002z10.1021/ac203002z ↗
29. 10.1039/C3LC50689D10.1039/C3LC50689D ↗
30. 10.1038/micronano.2017.8510.1038/micronano.2017.85 ↗
31. 10.1002/smll.20180442110.1002/smll.201804421 ↗
32. 10.1039/B913587A10.1039/B913587A ↗
33. 10.1002/cpcb.7010.1002/cpcb.70 ↗
34. 10.1146/annurev-control-053018-02380310.1146/annurev-control-053018-023803 ↗
35. 10.1002/adma.20180413010.1002/adma.201804130 ↗
36. 10.1039/C7LC00017K10.1039/C7LC00017K ↗
37. 10.1016/j.bbrc.2009.01.04910.1016/j.bbrc.2009.01.049 ↗
38. 10.1038/lsa.2016.15810.1038/lsa.2016.158 ↗
39. 10.1021/acs.accounts.8b0025410.1021/acs.accounts.8b00254 ↗
40. 10.1038/ncomms280610.1038/ncomms2806 ↗