Microfluidic Routing via Dynamic Optical Lattices Ryan L. Smith*, G. C. Spalding*, M. P. MacDonald, S. L. Neale, K. Dholakia *Department of Physics, Illinois Wesleyan University, P.O. Box 2900, Bloomington, IL USA 61702-2900. SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St. Andrews, Fife, KY16 9SS ABSTRACT All optical manipulation has been shown to provide unprecedented non-invasive control over a variety of different substances in the micro regime. It is especially useful for passive sorting of colloid in a microfluidic flow. When sorting a flow it is not only how well the particles intended to be routed are routed but also the throughput of the system. Any commercial system needs the time it takes the colloid to be sorted to be practical in order for mainstream acceptance. We investigate injection widths as well as various methods of lattice control to maximize efficiency throughput for microfluidic sorting. 1. INTRODUCTION Non-invasive control at the micro-scale has become a subject of great interest and enormous promise. Methods utilizing optical forces alone offer a number of clear advantages, including ease of integration and reconfigurability. In particular, several geometries have recently been demonstrated for sorting materials entrained in microfluidic flows. All-optical chromotagraphy has now been used to sort designed proxies for anthrax spores and other bioterrorism agents from a background of pollen and other species1. Elsewhere, the response to optical forces has been used to separate metastatic cancer cells from less aggressive cancer cells and from normal cells2 and, separately, to sort stem cells out from a background of differentiated cells. These new approaches have been incorporated into lab-on-a-chip technology for clinical trials that are currently underway. 2. SORTING IN STATIC OPTICAL LATTICES Our own approach3, which holds potential for higher throughput screening, has centered upon the use of passive optical lattices. Optical lattices of this type can be generated in a number of ways. One method is through use of a spatial light modulator (SLM) to modify the phase of your light. Real-time 3D control over multiple trapping sites has been shown (cite Miles, Jean-Marc’s Talbot effect). In addition, the use of a 3D lattice with multiple trappable particles has been used to create assisted self-assembly of 3D lattices (cite alfons). Jesper Gluckstad has demonstrated the fine level of control by using an SLM to modify the phase of the light and thus change the position, size, shape and intensity of each individual trap (cite OE paper by Jesper). Although SLMs provide precision control over multiple optical traps, for some applications multibeam interference has its advantages. We interfere between two and five beams to create a symmetric lattice of varying geometries5. The beams are created by passing a single beam through a static diffractive optical element (DOE). This is ideal in many cases due to the fact that they are relatively cheap to produce and allow the setup to be fairly compact compared to the table space required for a setup using an SLM. In addition using multibeam interference grants control that is not attainable using an SLM. We require a polarization change on a single one of the incident beams. SLMs cannot grant you this level of control and thus are not ideal for our setup. In addition, for many applications the refresh rates attainable by liquid crystal phase modulating SLMs are not fast enough. We have used studies of “wide-band” injection of monodisperse colloid into optical lattices to determine the optimal injection and collection geometries for microfluidic devices. Fig. 1. Collection into optical channels vs. flow speed. Fig. 2. We observe a one-third micron shift in the deflected output for each microliter/hour increase in flow speed It is evident from Figure 2 that increasing the flow speed will reduce the uptake stream centriod in a linear manner. This is important when trying to maximize efficiency throughput for a given stream due to the fact that as we increase throughput, we reduce efficiency. Fig. 3. Measure of efficient throughput for different injector centers and an injection width of 6 microns In addition we analyzed the efficient throughput based on where the injector center is located. We also did analysis on lateral velocity based on position in the lattice. That is shown in Figure 4 below. Fig. 4. Y velocity vs Y position. It is evident that the lateral velocity is at a maximum when the colloid is in the center of the Gaussian lattice profile. One of the main problems with filling a close-packed lattice of traps is that the periphery traps fill with colloid and then block the interior traps from being filled (cite Ming Wu). A similar problem occurs in our setup at lower flow rates. As colloid is being passed through the lattice, if the gradient force from the light is stronger than the force exerted by stokes drag, the particles will not exit the lattice and “jamming” will occur. This problem is countered by using the Angular Doppler (AD) effect to translate the lattice. This effectively eliminates the jamming that was evident in the static lattice. 3. SORTING IN DYNAMIC LATTICES From this we can introduce a frequency shift by using a rotating waveplate and the AD effect (cite Arlt, kishan, mike, etc). To produce this effect we used circularly polarized incident light. We then select one of the five incident beams and pass it though a half-waveplate. Under normal circumstances this would simply switch the “handedness” of the circularly polarized light from to . In our setup we have the half-waveplate rotating. This rotation grants a constant phase shift that is equivalent to a frequency change in the beam that is passing through the half-waveplate. When this beam interferes with the other beams that are not observing the frequency shift, it creates a dynamic three-dimensional lattice that translates in a certain direction. We investigate how this effects three-dimensional routing of colloid passing through the lattice in a microfluidic flow. We first examined a lattice with a 10-degree orientation with respect to the input flow. From this data we were able to gather that the static lattice provided a lower failure rate when the injection stream was set at 30 pixels. With this said, it was evident that the particles that were being routed in the AD stream were being routed further up in the y direction than necessary. Based on this observation, we looked at the routing efficiency for larger input stream values. As we suspected, increasing the size of the input stream made the efficiency of the Angular Doppler data greater than that of the static lattice. Fig 5. Routing efficiency for the static lattice (left) and the AD lattice (right) at a lattice angle of 10 degrees. The yellow portion is the injection width, the red tracks are unrouted tracks and the green tracks are routed tracks. We also examined the tracks at a lattice angle of 35 degrees. From this data we found that for narrower input streams the AD lattice offered a higher routing efficiency but for wider input streams the static lattice offered greater routing efficiency. This is displayed in Figure 6. Fig 6. Routing efficiency vs. Injection width for a static and AD lattice. 4. CONCLUSION In two dimensions, we have successfully demonstrated an approach that allows optical forces alone to assemble and/or guide large ensembles of microparticles over macroscopic areas4. The formation of static three-dimensional structures pose greater challenges, as the scattering of light by particles in one layer perturbs the optical landscape that is applied to particles in subsequent layers. At powers low enough to avoid unacceptable heating/convection, optical forces are typically weak, and scattering greatly complicates efforts to build 3D static structures via optical trapping alone. Early efforts at filling a 3D lattice of optical traps led to an appreciation for the dynamics of injected microparticle streams, which yield a surprisingly successful method of sorting or rerouting within microfludic environments3. We have investigated the optimal injection widths to maximize efficiency throughput of sorted colloid in a microfluidic flow. In addition we have introduced a novel method for translating the lattice in an effort to prevent jamming in the flow. Although results from this method are not currently conclusive, the method overall provides a promising landscape for future studies. 5. ACKNOWLEDGEMENTS R.L.S. and G.C.S. were supported by a grant from the Petroleum Research Fund. 6. REFERENCES 1 2 S. J. Hart, A. Terray, K. L. Kuhn et al., "Optical chromatography of biological particles," Am. Lab. 36 (24), 13-+ (2004). J. Guck, S. Schinkinger, B. Lincoln et al., "Optical deformability as an inherent cell marker for testing malignant transformation and metastatic competence," Biophys. J. 88 (5), 3689-3698 (2005). 3 4 5 M. P. MacDonald, G. C. Spalding, and K. Dholakia, "Microfluidic sorting in an optical lattice," Nature 426 (6965), 421-424 (2003). V. Garces-Chavez, K. Dholakia, and G. C. Spalding, "Extended-area optically induced organization of microparticies on a surface," Appl. Phys. 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