I. Introduction
Increasing demand for both efficiency and productivity in the manipulation of biological cells highlights the need for advancement in micromanipulation with techniques such as atomic force microscope (AFM) [1], dielectrophoretic (DEP) traps [3], micro pipe injection tool [3]–[5], and optical tweezers [6], etc. The intrinsic advantages and disadvantages of these methods were discussed in [7]. Optical tweezers exhibits high accuracy in flexible and noninvasive manipulation of microparticles [10], and has been extensively utilized as a unique tool for manipulating biological cells in recent years. With strongly focusing beams of light, an optical tweezers can trap and move a biological cell with a size ranging from several nanometers up to tens of micrometers. Micromanipulation of cells with optical tweezers has been utilized in many cell-based biomedical applications such as cell sorting or isolation [8], [9], cell microinjection [3], cell property characterization [10]–[12], actin cytoskeleton study [13], and cell-cell interaction [14], to name a few.