Dynamic optical manipulation of colloidal systems using a spatial light modulator

Abstract

A method and mathematical foundation are presented for generating multiple-beam optical tweezers capable of introducing complex trapping beam configurations that enable optical manipulation for a variety of colloidal structures. The method is based on the generalized phase contrast technique for generating high intensity beam patterns from an input phase modulation encoded on a spatial light modulator. The mathematical foundation describes issues concerning how the method provides high photon efficiency adequate for generating large array traps while maintaining dynamic features. Experimental results show multiple trapping of up to 25 particles using a 200 mW laser diode operating at 830 nm. Arbitrary array beam configurations are also shown where the shape, position and size can easily be reconfigured and applied for dynamic manipulation of colloidal particles.     

Optical selection, manipulation, trapping, and activation of a microgear structure for applications in micro-optical-electromechanical systems

The optical processes involved in laser trapping and optical manipulation are explored theoretically and experimentally as a means of activating a micrometer-size gear structure. We modeled the structure by using an enhanced ray-optics technique, and results indicate that the torque present on the gear can induce the gear to rotate about the gear-arm plane center with light as the driving energy source. We confirmed these findings experimentally by using gears manufactured with conventional semiconductor techniques and from a layer of polyimide. It is expected that such a simple gear design activated by use of light could lead to an entire new class of micro-optical-electromechanical systems.     

Confocal Raman microscopy for monitoring chemical reactions on single optically trapped,solid-phase support particles

Optical trapping of small structures is a powerful tool for the manipulation and investigation of colloidal and particulate materials. The tight focus excitation requirements of optical trapping are well suited to confocal Raman microscopy. In this work, an inverted confocal Raman microscope is developed for studies of chemical reactions on single, optically trapped particles and applied to reactions used in solid-phase peptide synthesis. Optical trapping and levitation allow a particle to be moved away from the coverslip and into solution, avoiding fluorescence interference from the coverslip. More importantly, diffusion of reagents into the particle is not inhibited by a surface, so that reaction conditions mimic those of particles dispersed in solution. Optical trapping and levitation also maintain optical alignment, since the particle is centered laterally along the optical axis and within the focal plane of the objective, where both optical forces and light collection are maximized. Hour-long observations of chemical reactions on individual, trapped silica particles are reported. Using two-dimensional least-squares analysis methods, the Raman spectra collected during the course of a reaction can be resolved into component contributions. The resolved spectra of the time-varying species can be observed, as they bind to or cleave from the particle surface.     

Optical manipulation in combination with multiphoton microscopy for single-cell studies

We demonstrate how optical tweezers can be incorporated into a multiphoton microscope to achieve three-dimensional imaging of trapped cells. The optical tweezers, formed by a cw 1064 nm Nd:YVO4 laser, were used to trap live yeast cells in suspension while the 4',6-diamidino-2-phenylindole-stained nucleus was imaged in three dimensions by use of a pulsed femtosecond laser. The trapped cell was moved in the axial direction by changing the position of an external lens, which was used to control the divergence of the trapping laser beam. This gives us a simple method to use optical tweezers in the laser scanning of confocal and multiphoton microscopes. It is further shown that the same femtosecond laser as used for the multiphoton imaging could also be used as laser scissors, allowing us to drill holes in the membrane of trapped spermatozoa.     

Trapping and manipulating gas bubbles in water with ultrashort laser pulses at a high repetition rate

We have experimentally observed the trapping of a gas bubble in water by focused laser radiation. The optical trap was provided by 200-fs pulses of a Ti-sapphire laser operating at a repetition rate of 100 kHz. The laser radiation was focused in water by an objective with a numerical aperture of 0.5. The trapping force in water is estimated as ∼200 pN at an average laser power of 20 mW, which is by two orders of magnitude greater than the efficiency of a traditional laser tweezers. The trapping force arises upon local heating of gas inside a bubble due to nonlinear absorption in the focal region.     

Optical trapping of a spherically symmetric sphere in the ray-optics regime: a model for optical tweezers upon cells

Since their invention in 1986, optical tweezers have become a popular manipulation and force measurement tool in cellular and molecular biology. However, until recently there has not been a sophisticated model for optical tweezers on trapping cells in the ray-optics regime. We present a model for optical tweezers to calculate the optical force upon a spherically symmetric multilayer sphere representing a common biological cell. A numerical simulation of this model shows that not only is the magnitude of the optical force upon a Chinese hamster ovary cell significantly three times smaller than that upon a polystyrene bead of the same size, but the distribution of the optical force upon a cell is also much different from that upon a uniform particle, and there is a 30% difference in the optical trapping stiffness of these two cases. Furthermore, under a small variant condition for the refractive indices of any adjacent layers of the sphere, this model provides a simple approximation to calculate the optical force and the stiffness of an optical tweezers system.     

Confocal light absorption and scattering spectroscopic microscopy

We have developed a novel optical method for observing submicrometer intracellular structures in living cells, which is called confocal light absorption and scattering spectroscopic (CLASS) microscopy. It combines confocal microscopy, a well-established high-resolution microscopic technique, with light-scattering spectroscopy. CLASS microscopy requires no exogenous labels and is capable of imaging and continuously monitoring individual viable cells, enabling the observation of cell and organelle functioning at scales of the order of 100 nm.     

Measurement of particle size distribution in mammalian cells in vitro by use of polarized light spectroscopy

We demonstrate the feasibility of measuring the particle size distribution (PSD) of internal cell structures in vitro. We use polarized light spectroscopy to probe the internal morphology of mammalian breast cancer (MCF7) and cervical cancer (Siha) cells. We find that graphing the least-squared error versus the scatterer size provides insight into cell scattering. A nonlinear optimization scheme is used to determine the PSD iteratively. The results suggest that 2-microm particles (possibly the mitochondria) contribute most to the scattering. Other subcellular structures, such as the nucleoli and the nucleus, may also contribute significantly. We reconstruct the PSD of the mitochondria, as verified by optical microscopy. We also demonstrate the angle dependence of the PSD.     

Digital in-line soft x-ray holography with element contrast

Digital in-line soft x-ray holography (DIXH) was used to image immobilized polystyrene and iron oxide particles and to distinguish them based on their different x-ray absorption cross sections in the vicinity of the carbon K-absorption edge. The element-specific information from the resonant DIXH images was correlated with high-resolution scanning electron microscopy (SEM) pictures. We also present DIXH images of a cell nucleus and compare the contrast obtained for nuclear components with the appearance in optical microscopy.     

飞秒激光空间选择性诱导玻璃微结构及应用

利用飞秒激光与玻璃的非线性相互作用，可以对玻璃进行空间选择性微观改性与修饰，赋予新的光功能．本文介绍飞秒激光的持点及其对玻璃微结构的改性，以及近年来利用飞秒激光进行玻璃的缺陷控制、光活性离子(稀土、过渡和重金属离子)价态操作、微晶析出与折射率调控及其在光开关、波分复用、波导型有源器件、光子晶体等微光学器件的制备及光学集成领域应用的进展．     

Optical tweezers: 20 years on

In 1986, Arthur Ashkin and colleagues published a seminal paper in Optics Letters, 'Observation of a single-beam gradient force optical trap for dielectric particles' which outlined a technique for trapping micrometre-sized dielectric particles using a focused laser beam, a technology which is now termed optical tweezers. This paper will provide a background in optical manipulation technologies and an overview of the applications of optical tweezers. It contains some recent work on the optical manipulation of aerosols and concludes with a critical discussion of where the future might lead this maturing technology.     

Selective encapsulation of single cells and subcellular organelles into picoliter- and femtoliter-volume droplets

This paper describes a method, which combines optical trapping and microfluidic-based droplet generation, for selectively and controllably encapsulating a single target cell or subcellular structure, such as a mitochondrion, into a picoliter- or femtoliter-volume aqueous droplet that is surrounded by an immiscible phase. Once the selected cell or organelle is encased within the droplet, it is stably confined in the droplet and cannot be removed. We demonstrate in droplet the rapid laser photolysis of the single cell, which essentially "freezes" the state that the cell was in at the moment of photolysis and confines the lysate within the small volume of the droplet. Using fluorescein di-beta-d-galactopyranoside, which is a fluorogenic substrate for the intracellular enzyme beta-galactosidase, we also assayed the activity of this enzyme from a single cell following the laser-induced lysis of the cell. This ability to entrap individual selected cells or subcellular organelles should open new possibilities for carrying out single-cell studies and single-organelle measurements.     

Laser manipulation in liquid crystals: an approach to microfluidics and micromachines

Laser trapping of particles in three dimensions can occur as a result of the refraction of strongly focused light through micrometre-sized particles. The use of this effect to produce laser tweezers is extremely common in fields such as biology, but it is only relatively recently that the technique has been applied to liquid crystals (LCs). The possibilities are exciting: droplets of LCs can be trapped, moved and rotated in an isotropic fluid medium, or both particles and defects can be trapped and manipulated within a liquid crystalline medium. This paper considers both the possibilities. The mechanism of transfer of optical angular momentum from circularly polarized light to small droplets of nematic LCs is described. Further, it is shown that droplets of chiral LCs can be made to rotate when illuminated with linearly polarized light and possible mechanisms are discussed. The trapping and manipulation of micrometre-sized particles in an aligned LC medium is used to provide a measure of local shear viscosity coefficients and a unique test of theory at low Ericksen number in LCs.     

Optothermal escape of plasmonically coupled silver nanoparticles from a three-dimensional optical trap

We demonstrate that optical trapping of multiple silver nanoparticles is strongly influenced by plasmonic coupling of the nanoparticles. Employing dark-field Rayleigh scattering imaging and spectroscopy on multiple silver nanoparticles optically trapped in three dimensions, we experimentally investigate the time-evolution of the coupled plasmon resonance and its influence on the trapping stability. With time the coupling strengthens, which is observed as a gradual red shift of the coupled plasmon scattering. When the coupled plasmon becomes resonant with the trapping laser wavelength, the trap is destabilized and nanoparticles are released from the trap. Modeling of the trapping potential and its comparison to the plasmonic heating efficiency at various nanoparticle separation distances suggests a thermal mechanism of the trap destabilization. Our findings provide insight into the specificity of three-dimensional optical manipulation of plasmonic nanostructures suitable for field enhancement, for example for surface-enhanced Raman scattering.     

An integrated microfabricated cell sorter

We have developed an integrated microfabricated cell sorter using multilayer soft lithography. This integrated cell sorter is incorporated with various microfluidic functionalities, including peristaltic pumps, dampers, switch valves, and input and output wells, to perform cell sorting in a coordinated and automated fashion. The active volume of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of optical interrogation is approximately 100 fL. Different algorithms of cell manipulation, including cell trapping, were implemented in these devices. We have also demonstrated sorting and recovery of Escherichia coli cells on the chip.     

Manipulation and light-induced agglomeration of carbon nanotubes through optical trapping of attached silver nanoparticles

A simple experimental method has been demonstrated for manipulating multi-walled carbon nanotube (MWCNT) bundles through the optical trapping of attached silver nanoparticles (SNPs). In our experiments, without the SNPs, the MWCNTs cannot be trapped due to their irregular shapes and large aspect ratio. However, when mixed with SNPs, the MWCNTs can be successfully trapped along with the SNPs using a TEM(00) mode laser at 532?nm. This is attributed to the optical trapping of the SNPs and attractive interaction or binding between the SNPs and MWCNTs due to electrostatic and van der Waals forces. Therefore, optical manipulation of MWCNT bundles is achieved through the manipulation of the attached silver nanoparticles/aggregates. In addition, we have observed the phenomenon of light-induced further agglomeration of SNPs/MWCNTs which could potentially be exploited for fabricating patterned MWCNT films for future nanoscale devices and other applications.     

Super‐Resolution Nonlinear Photothermal Microscopy

Super‐resolution fluorescence microscopy enables imaging of fluorescent structures beyond the diffraction limit. However, this technique cannot be applied to weakly fluorescent cellular components or labels. As an alternative, photothermal microscopy based on nonradiative transformation of absorbed energy into heat has demonstrated imaging of nonfluorescent structures including single molecules and ~1‐nm gold nanoparticles. However, previously photothermal imaging has been performed with a diffraction‐limited resolution only. Herein, super‐resolution, far‐field photothermal microscopy based on nonlinear signal dependence on the laser energy is introduced. Among various nonlinear phenomena, including absorption saturation, multiphoton absorption, and signal temperature dependence, signal amplification by laser‐induced nanobubbles around overheated nano‐objects is explored. A Gaussian laser beam profile is used to demonstrate the image spatial sharpening for calibrated 260‐nm metal strips, resolving of a plasmonic nanoassembly, visualization of 10‐nm gold nanoparticles in graphene, and hemoglobin nanoclusters in live erythrocytes with resolution down to 50 nm. These nonlinear phenomena can be used for 3D imaging with improved lateral and axial resolution in most photothermal methods, including photoacoustic microscopy.     

Direct observation of nanomechanical properties of chromatin in living cells

Precise manipulation of nanometer-sized magnetic particles using magnetic tweezers has yielded insights into the rheology of the cell cytoplasm. We present first results using this approach to study the nanomechanics of the cell nucleus. Using a custom-designed micro-magnetic-tweezers instrument, we can achieve sufficiently high magnetic forces enabling the application and measurement of controlled distortion of the internal nuclear structure on the nanometer scale. We precisely measure the elasticity and viscosity inside the nucleus of living HeLa cells. The high value of the Young's modulus (Y = 2.5 x 10(2) Pa) measured relative to the cytoplasm is explained by a large-scale model for in vivo chromatin structure using a polymer network model.     

Optical manipulation of microscopic objects by means of vertical-cavity surface-emitting laser array sources

We report on experimental verification of optical trapping using multiple beams generated by a vertical-cavity surface-emitting laser (VCSEL) array. Control of the spatial and temporal emission of a VCSEL array provides flexibility for manipulation of microscopic objects with compact hardware. Simultaneous capture of multiple objects and translation of an object without mechanical movement are demonstrated by an experimental system equipped with 8 x 8 VCSEL array sources. Features and applicability of the method are also discussed.     

Application of plasmonic bowtie nanoantenna arrays for optical trapping, stacking, and sorting

We present the use of Au bowtie nanoantenna arrays (BNAs) for highly efficient, multipurpose particle manipulation with unprecedented low input power and low-numerical aperture (NA) focusing. Optical trapping efficiencies measured are up to 20× the efficiencies of conventional high-NA optical traps and are among the highest reported to date. Empirically obtained plasmonic optical trapping "phase diagrams" are introduced to detail the trapping response of the BNAs as a function of input power, wavelength, polarization, particle diameter, and BNA array spacing (number density). Using these diagrams, parameters are chosen, employing strictly the degrees-of-freedom of the input light, to engineer specific trapping tasks including (1) dexterous, single-particle trapping and manipulation, (2) trapping and manipulation of two- and three-dimensional particle clusters, and (3) particle sorting. The use of low input power densities (power and NA) suggests that this bowtie nanoantenna trapping system will be particularly attractive for lab-on-a-chip technology or biological applications aimed at reducing specimen photodamage.