Melanie Jimenez

Cascading and Parallelising Curvilinear Inertial Focusing Systems for High Volume, Wide Size Distribution, Separation and Concentration of Particles

Inertial focusing is a microfluidic based separation and concentration technology that has expanded rapidly in the last few years. Throughput is high compared to other microfluidic approaches although sample volumes have typically remained in the millilitre range. Here we present a strategy for achieving rapid high volume processing with stacked and cascaded inertial focusing systems, allowing for separation and concentration of particles with a large size range, demonstrated here from 30 μm–300 μm. The system is based on curved channels, in a novel toroidal configuration and a stack of 20 devices has been shown to operate at 1 L/min. Recirculation allows for efficient removal of large particles whereas a cascading strategy enables sequential removal of particles down to a final stage where the target particle size can be concentrated. The demonstration of curved stacked channels operating in a cascaded manner allows for high throughput applications, potentially replacing filtration in applications such as environmental monitoring, industrial cleaning processes, biomedical and bioprocessing and many more.

Microfluidics for effective concentration and sorting of waterborne protozoan pathogens

We report on an inertial focussing based microfluidics technology for concentrating waterborne protozoa, achieving a 96% recovery rate of Cryptosporidium parvum and 86% for Giardia lamblia at a throughput (mL/min) capable of replacing centrifugation. The approach can easily be extended to other parasites and also bacteria.

A NEW METHOD FOR MEASURING DIFFUSION COEFFICIENT OF GASES IN LIQUIDS BY PLIF

Gas–liquid mass transfer is a major issue in engineering processes such as wastewater treatment or biogas production since this phenomenon is directly linked to their design and efficiency. In recent years, much research has been done in this area but some gaps still remain in our knowledge of gas–liquid transfer, in particular concerning molecular diffusivity. The determination of molecular diffusivity is commonly based on empirical correlations, such as the widely used Wilke and Chang13 expression, valid under specific conditions and with relatively high uncertainties. In the present work, an innovative and promising technique is proposed to determine diffusion coefficients of gases in liquids. This technique is based on visualizing and quantifying oxygen diffusion across a flat gas–liquid interface, in a Newtonian medium, using planar laser induced fluorescence (PLIF) with inhibition. Particle image velocimetry (PIV) experiments were conducted to confirm the hydrodynamic flow field in the liquid phase. Results included the visualization of oxygen diffusion over time, and the quantification of this visualization. The oxygen diffusivity thus determined is in agreement with values found in the literature.

Angry pathogens, how to get rid of them: introducing microfluidics for waterborne pathogen separation to children

The purpose of this paper is to present a new approach for introducing to a non-scientific audience a major public health issue: access to safe drinking water. Access to safe drinking water is a privilege in developed countries and an urgent need in the third world, which implies always more efficient and reliable engineering tools to be developed. As a major global challenge it is important to make children aware of this problem for understanding (i) what safe drinking water is, (ii) how ingenious techniques are developed for this purpose and (iii) the role of microfluidics in this area. This paper focuses on different microfluidic-based techniques to separate and detect pathogens in drinking water that have been adapted to be performed by a young audience in a simplified, recreational and interactive way.

Multi-objective optimization of solar assisted absorption cooling system

This work presents a multi-period and multi-objective optimization based on mathematical programming of solar assisted absorption cooling systems. Seven solar collector models combined with a gas fired heater and an absorption cooling cycle are considered. The optimization task is formulated as a multi-objective multi-period mixed-integer nonlinear programming (MINLP) problem that accounts for the minimization of the total cost of the cooling system and the associated environmental impact. The environmental performance is measured following the Life Cycle Assessment (LCA) principles. The capabilities of the proposed method are illustrated in a case study that addresses the design of a solar assisted ammonia-water absorption cooling system using the weather conditions of Tarragona (Spain).

High-throughput assessment of mechanical properties of stem cell derived red blood cells, toward cellular downstream processing

Stem cell products, including manufactured red blood cells, require efficient sorting and purification methods to remove components potentially harmful for clinical application. However, standard approaches for cellular downstream processing rely on the use of specific and expensive labels (e.g. FACS or MACS). Techniques relying on inherent mechanical and physical properties of cells offer high-throughput scalable alternatives but knowledge of the mechanical phenotype is required. Here, we characterized for the first time deformability and size changes in CD34+ cells, and expelled nuclei, during their differentiation process into red blood cells at days 11, 14, 18 and 21, using Real-Time Deformability Cytometry (RT-DC) and Atomic Force Microscopy (AFM). We found significant differences (p < 0.0001; standardised mixed model) between the deformability of nucleated and enucleated cells, while they remain within the same size range. Expelled nuclei are smaller thus could be removed by size-based separation. An average Young’s elastic modulus was measured for nucleated cells, enucleated cells and nuclei (day 14) of 1.04 ± 0.47 kPa, 0.53 ± 0.12 kPa and 7.06 ± 4.07 kPa respectively. Our identification and quantification of significant differences (p < 0.0001; ANOVA) in CD34+ cells mechanical properties throughout the differentiation process could enable development of new routes for purification of manufactured red blood cells.

Observing the Dynamics of Waterborne Pathogens for Assessing the Level of Contamination

In environments of scarce hygiene it is of primary importance to detect potentially harmful concentrations of pathogens in drinking water. In many situations, however, accurate analysis of water samples is prohibitively complex and often requires highly specialised apparatuses and technicians. In order to overcome these limitations, a method to employ video processing to assist microfluidics water filtering apparatuses is proposed. Through the automated analysis of videos captured at the output of such devices it is possible to extract useful information that could control an autonomous calibration, hence eliminating the need of an expert and possibly leading to the construction of readily employable water quality assessing devices.

Impact of poloxamer 188 (Pluronic F-68) additive on cell mechanical properties, quantification by real-time deformability cytometry

Advances in cellular therapies have led to the development of new approaches for cell product purification and formulation, e.g., utilizing cell endogenous properties such as size and deformability as a basis for separation from potentially harmful undesirable by-products. However, commonly used additives such as Pluronic F-68 and other poloxamer macromolecules can change the mechanical properties of cells and consequently alter their processing. In this paper, we quantified the short-term effect of Pluronic F-68 on the mechanotype of three different cell types (Jurkat cells, red blood cells, and human embryonic kidney cells) using real-time deformability cytometry. The impact of the additive concentration was assessed in terms of cell size and deformability. We observed that cells respond progressively to the presence of Pluronic F-68 within first 3 h of incubation and become significantly stiffer (p-value < 0.001) in comparison to a serum-free control and a control containing serum. We also observed that the short-term response manifested as cell stiffening is true (p-value < 0.001) for the concentration reaching 1% (w/v) of the poloxamer additive in tested buffers. Additionally, using flow cytometry, we assessed that changes in cell deformability triggered by addition of Pluronic F-68 are not accompanied by size or viability alterations.

Femtosecond laser fabricated integrated chip for manipulation of single cells(Conference Presentation)

Optical micromanipulation techniques and microfluidic techniques can be used in same platform for manipulating biological samples at single cell level. Novel microfluidic devices with integrated channels and waveguides fabricated using ultrafast laser inscription combined with selective chemical etching can be used to enable sorting and isolation of biological cells. In this paper we report the design and fabrication of a three dimensional chip that can be used to manipulate single cells in principle with a higher throughput than is possible using optical tweezers. The capability of ultrafast laser inscription followed by selective chemical etching to fabricate microstructures and waveguides have been utilised to fabricate the device presented in this paper. The complex three dimensional microfluidic structures within the device allow the injected cell population to focus in a hydrodynamic flow. A 1064 nm cw laser source, coupled to the integrated waveguide, is used to exert radiation pressure on the cells to be manipulated. As the cells in the focussed stream flow past the waveguide, optical scattering force induced by the laser beam pushes the cell from out of the focussed stream to the sheath fluid, which can be then collected at the outlet. Thus cells can be controllably deflected from the focussed flow to the side channel for downstream analysis or culture.