Edison Gerena; Stéphane Régnier; Sinan Haliyo
Optical robots are microscale structures actuated using laser trapping techniques. However, the lack of robust and real-time three-dimensional (3-D) actuation techniques reduces most applications to planar space. We present here a new approach to generate and control several optical traps synchronously in 3-D with low latency and high bandwidth (up to 200 Hz). This time-shared technique uses only mirrors, hence, is aberration free. Simultaneous traps are used to actuate optical robots and provide 6-DoF telemanipulation. Experiments demonstrate the flexibility and dexterity of the implemented user control, paving the way to novel applications in microrobotics and biology.
DOI
Concisely bringing the latest news and relevant information regarding optical trapping and micromanipulation research.
.
Showing posts with label IEEE Robotics & Automation Magazine. Show all posts
Showing posts with label IEEE Robotics & Automation Magazine. Show all posts
Tuesday, January 29, 2019
Monday, October 27, 2014
Optical Tweezers: Autonomous Robots for the Manipulation of Biological Cells
Banerjee, A. ; Chowdhury, S. ; Gupta, S.K.
Optical tweezers (OTs) are a popular tool for manipulating biological objects, especially cells [1], [2]. Using a tightly focused laser beam, they exert sufficient forces to tweeze, i.e., hold (trap) and move, freely diffusing cells in the vicinity of the beam focus. The beam can be focused at any point in the workspace, which is typically a liquid-filled glass slide. The trapped cell can, thus, be translated and rotated (transported) in three dimensions by changing the beam focus position. OTs provide certain advantages over other cell-manipulation techniques. They are able to manipulate cells with a greater degree of precision as compared with microfluidic flow. Significant contact forces are not exerted on the cells, unlike in mechanical manipulation, thereby avoiding damages due to contact friction or surface chemistry. The cells are also easily released at the end of the manipulation by simply switching off the laser beam. Hence, OTs have been extensively used for mechanical characterization of cells by measuring their viscoelastic properties to distinguish between normal and diseased cells [3]. They have also been used for separating cells of different types [4] and investigating the response of cells to external stimuli [5]. However, manual or teleoperated control of the laser beam has limited their applicability for multicellular studies.
DOI
Optical tweezers (OTs) are a popular tool for manipulating biological objects, especially cells [1], [2]. Using a tightly focused laser beam, they exert sufficient forces to tweeze, i.e., hold (trap) and move, freely diffusing cells in the vicinity of the beam focus. The beam can be focused at any point in the workspace, which is typically a liquid-filled glass slide. The trapped cell can, thus, be translated and rotated (transported) in three dimensions by changing the beam focus position. OTs provide certain advantages over other cell-manipulation techniques. They are able to manipulate cells with a greater degree of precision as compared with microfluidic flow. Significant contact forces are not exerted on the cells, unlike in mechanical manipulation, thereby avoiding damages due to contact friction or surface chemistry. The cells are also easily released at the end of the manipulation by simply switching off the laser beam. Hence, OTs have been extensively used for mechanical characterization of cells by measuring their viscoelastic properties to distinguish between normal and diseased cells [3]. They have also been used for separating cells of different types [4] and investigating the response of cells to external stimuli [5]. However, manual or teleoperated control of the laser beam has limited their applicability for multicellular studies.
DOI
Subscribe to:
Comments (Atom)