Xiaoshuai Liu

Escherichia coli-based biophotonic waveguides.

The rapid progresses in biological and biomedical applications with optical interfaces have motivated an ever-increasing demand for biocompatible and disposable photonic components. Generally, these biophotonic components are first integrated with biocompatible materials and then interfaced with biological samples, such as living cells, for biological use. Therefore, direct formation of biophotonic components using living cells is greatly desired because the cells would serve simultaneously as samples and optical elements for signal sensing and detection. Here, we report an optical strategy for direct formation of biophotonic waveguides (bio-WGs) with Escherichia coli. The experiments demonstrate that this facile optical strategy enables forming bio-WGs with different lengths and good light propagation performances while the propagating signal can be detected in real-time. This strategy offers a seamless interface between optical and biological worlds with natural materials and provides a new opportunity for direct sensing and detection of biological signal and information in biocompatible microenvironments.

Trapping and Detection of Nanoparticles and Cells Using a Parallel Photonic Nanojet Array

In advanced nanoscience, there is a strong desire to trap and detect nanoscale objects with high-throughput, single-nanoparticle resolution and high selectivity. Although emerging optical methods have enabled the selective trapping and detection of multiple micrometer-sized objects, it remains a great challenge to extend this functionality to the nanoscale. Here, we report an approach to trap and detect nanoparticles and subwavelength cells at low optical power using a parallel photonic nanojet array produced by assembling microlenses on an optical fiber probe. Benefiting from the subwavelength confinement of the photonic nanojets, tens to hundreds of nanotraps were formed in three dimensions. Backscattering signals were detected in real time with single-nanoparticle resolution and enhancement factors of 10(3)-10(4). Selective trapping of nanoparticles and cells from a particle mixture or human blood solution was demonstrated using the nanojet array. The developed nanojet array is potentially a powerful tool for nanoparticle assembly, biosensing, single-cell analysis, and optical sorting.

Optical regulation of cell chain

Formation of cell chains is a straightforward and efficient method to study the cell interaction. By regulating the contact sequence and interaction distance, the influence of different extracellular cues on the cell interaction can be investigated. However, it faces great challenges in stable retaining and precise regulation of cell chain, especially in cell culture with relatively low cell concentration. Here we demonstrated an optical method to realize the precise regulation of cell chain, including removing or adding a single cell, adjusting interaction distance, and changing cell contact sequence. After injecting a 980-nm wavelength laser beam into a tapered optical fiber probe (FP), a cell chain of Escherichia colis (E. colis) is formed under the optical gradient force. By manipulating another FP close to the cell chain, a targeted E. coli cell can be trapped by the FP and removed from the chain. Further, the targeted cell can be added back to the chain at different positions to change the cell contact sequence. The experiments were interpreted by numerical simulations and the impact of cell sizes and shapes on this method was analyzed.

Rotation and deformation of human red blood cells with light from tapered fiber probes

Abstract Dynamic rotation and deformation of human red blood cells (RBCs) are extremely important to investigate the survival and mechanical features of cells, which will be of great physiological and pathological significance. Here, we report an optical approach that is capable of both rotating and deforming RBCs with light from two tapered fiber probes (TFPs). With laser beams at the wavelength of 980 nm injected into the TFPs, a single RBC was rotated around different axes while single or multiple RBCs were stretched by adjusting the points of action and magnitude of the optical forces from the TFPs. The biological safety of the approach was also discussed by taking the laser power required into account.

Non-contact intracellular binding of chloroplasts in vivo

Non-contact intracellular binding and controllable manipulation of chloroplasts in vivo was demonstrated using an optical fiber probe. Launching a 980-nm laser beam into a fiber, which was placed about 3 μm above the surface of a living plant (Hydrilla verticillata) leaf, enabled stable binding of different numbers of chloroplasts, as well as their arrangement into one-dimensional chains and two-dimensional arrays inside the leaf without damaging the chloroplasts. Additionally, the formed chloroplast chains were controllably transported inside the living cells. The optical force exerted on the chloroplasts was calculated to explain the experimental results. This method provides a flexible method for studying intracellular organelle interaction with highly organized organelle-organelle contact in vivo in a non-contact manner.

Enhancing Upconversion Fluorescence with a Natural Bio-microlens

Upconversion fluorescence has triggered extensive efforts in the past decade because of its superior physicochemical features and great potential in biomedical and biophotonic studies. However, practical applications of upconversion fluorescence are often hindered by its relatively low luminescence efficiency (<1%). Here, we employ a living yeast or human cell as a natural bio-microlens to enhance the upconversion fluorescence. The natural bio-microlens, which was stably trapped on a fiber probe, could concentrate the excitation light into a subwavelength region so that the upconversion fluorescence of core-shell NaYF4:Yb3+/Tm3+ nanoparticles was enhanced by 2 orders of magnitude. As a benefit of the fluorescence enhancement, single-cell imaging and real-time detection of the labeled pathogenic bacteria, such as Escherichia coli and Staphylococcus aureus, were successfully achieved in the dark fields. This biocompatible, sensitive, and miniature approach could provide a promising powerful tool for biological imaging, biophotonic sensing, and single-cell analysis.

Optofluidic organization and transport of cell chain

Controllable organization and transport of cell chain in a fluid, which is of great importance in biological and medical fields, have attracted increasing attentions in recent years. Here we demonstrate an optofluidic strategy, by implanting the microfluidic technique with a large-tapered-angle fiber probe (LTAP), to organize and transport a cell chain in a noncontact and noninvasive manner. After a laser beam at 980-nm wavelength launched into LTAP, the E. coli cells were continuously trapped and then arranged into a cell chain one after another. The chain can be transported by adjusting the magnitudes of optical force and flow drag force. The proposed technique can also be applied for the eukaryotic cells (e. g., yeast cell) and human red blood cells (RBCs). Experiment results were interpreted by the numerical simulation, and the stiffness of cell chain was also discussed.

Optically controlled circling of particles with a particle-decorated fiber probe

With the assistance of a particle-decorated fiber probe, optically controlled circling of particles was demonstrated using 3.14 μm diameter silica particles. The method is based on the temperature gradient and thermal convection when a laser beam of 980 nm (power: 108 mW) is injected into the fibre. Specific currents were created by decorating the tip of the drawn fibre probe with specific geometries of silica particles (diameter: 3.14 μm). Thus, the water was being circulated (convective flow driven by heating), and the particles were drowned into the flow. They were circled anticlockwise along a relatively steady trajectory with a period varying from 3 to 7 s. Once the laser switched off, the particles were immediately stopped. Further experiments show that the circular trajectory can be shifted by moving the fiber probe.