Plasmonic Optical Tweezers for Particle Manipulation: Principles, Methods, and Applications.
Ya-Tao RenQin ChenMingjian HeXiangzhi ZhangHong QiYuying YanPublished in: ACS nano (2021)
Inspired by the idea of combining conventional optical tweezers with plasmonic nanostructures, a technique named plasmonic optical tweezers (POT) has been widely explored from fundamental principles to applications. With the ability to break the diffraction barrier and enhance the localized electromagnetic field, POT techniques are especially effective for high spatial-resolution manipulation of nanoscale or even subnanoscale objects, from small bioparticles to atoms. In addition, POT can be easily integrated with other techniques such as lab-on-chip devices, which results in a very promising alternative technique for high-throughput single-bioparticle sensing or imaging. Despite its label-free, high-precision, and high-spatial-resolution nature, it also suffers from some limitations. One of the main obstacles is that the plasmonic nanostructures are located over the surfaces of a substrate, which makes the manipulation of bioparticles turn from a three-dimensional problem to a nearly two-dimensional problem. Meanwhile, the operation zone is limited to a predefined area. Therefore, the target objects must be delivered to the operation zone near the plasmonic structures. This review summarizes the state-of-the-art target delivery methods for the POT-based particle manipulating technique, along with its applications in single-bioparticle analysis/imaging, high-throughput bioparticle purifying, and single-atom manipulation. Future developmental perspectives of POT techniques are also discussed.
Keyphrases
- label free
- high throughput
- high resolution
- single molecule
- high speed
- energy transfer
- atomic force microscopy
- living cells
- single cell
- mass spectrometry
- molecular dynamics
- fluorescent probe
- sensitive detection
- staphylococcus aureus
- visible light
- high frequency
- pseudomonas aeruginosa
- cystic fibrosis
- circulating tumor cells