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The extracellular matrix (ECM) is a complex, dynamic network present within all tissues and organs that not only acts as a mechanical support and anchorage point but can also direct fundamental cell behavior, function, and characteristics. Although the importance of the ECM is well established, the integration of well-controlled ECMs into Organ-on-Chip (OoC) platforms remains challenging and the methods to modulate and assess ECM properties on OoCs remain underdeveloped. In this review, current state-of-the-art design and assessment of in vitro ECM environments is discussed with a focus on their integration into OoCs. Among other things, synthetic and natural hydrogels, as well as polydimethylsiloxane (PDMS) used as substrates, coatings, or cell culture membranes are reviewed in terms of their ability to mimic the native ECM and their accessibility for characterization. The intricate interplay among materials, OoC architecture, and ECM characterization is critically discussed as it significantly complicates the design of ECM-related studies, comparability between works, and reproducibility that can be achieved across research laboratories. Improving the biomimetic nature of OoCs by integrating properly considered ECMs would contribute to their further adoption as replacements for animal models, and precisely tailored ECM properties would promote the use of OoCs in mechanobiology.
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Técnicas de Cultura de Células , Matriz Extracelular , Animais , Reprodutibilidade dos Testes , Matriz Extracelular/química , Técnicas de Cultura de Células/métodos , Sistemas MicrofisiológicosRESUMO
Basic human functions such as breathing and digestion require mechanical stretching of cells and tissues. However, when it comes to laboratory experiments, the mechanical stretching that cells experience in the body is not often replicated, limiting the biomimetic nature of the studies and the relevance of results. Herein, we establish the importance of mechanical stretching during in vitro investigations by reviewing seminal works performed using cell-stretching platforms, highlighting important outcomes of these works as well as the engineering characteristics of the platforms used. Emphasis is placed on the compatibility of cell-stretching devices (CSDs) with live-cell imaging as well as their limitations and on the research advancements that could arise from live-cell imaging performed during cell stretching.
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Pesquisa Biomédica , Diagnóstico por Imagem , HumanosRESUMO
Microfabricated systems are increasingly being utilized in biotechnological, biomedical, and pharmaceutical research and development as replacements for traditional in vitro cell cultures, bioreactors, and animal experiments (Figure 1) [...].
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Reatores Biológicos , Biotecnologia , Animais , Técnicas de Cultura de CélulasRESUMO
In recent years, perovskite solar cells (PSCs) have experienced rapid development and have presented an excellent commercial prospect as the PSCs are made from raw materials that are readily and cheaply available depending on simple manufacturing techniques. However, the commercial production and utilization of PSCs remain immature, leading to substantial efforts needed to boost the development of scalable fabrication of PSCs, pilot scale tests, and the establishment of industrial production lines. In this way, the PSCs are expected to be successfully popularized from the laboratory to the photovoltaic market. In this review, the history of power conversion efficiency (PCE) for laboratory-scale PSCs is firstly introduced, and then some methods for maintaining high PCE in the upscaling process is displayed. The achievements in the stability and environmental friendliness of PSCs are also summarized because they are also of significance for commercialization. Finally, this review evaluates the commercialization prospects of PSCs from the economic view and provides a short outlook.
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This Perspective discusses the literature related to two-phase biocatalysis in microfluidic droplets. Enzymes used as catalysts in biocatalysis are generally less stable in organic media than in their native aqueous environments; however, chemical and pharmaceutical compounds are often insoluble in water. The use of aqueous/organic two-phase media provides a solution to this problem and has therefore become standard practice for multiple biotransformations. In batch, two-phase biocatalysis is limited by mass transport, a limitation that can be overcome with the use of microfluidic systems. Although, two-phase biocatalysis in laminar flow systems has been extensively studied, microfluidic droplets have been primarily used for enzyme screening. In this Perspective, we summarize the limited published work on two-phase biocatalysis in microfluidic droplets and discuss the limitations, challenges, and future perspectives of this technology.
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Microfluídica , Água , BiocatáliseRESUMO
Monitoring process parameters in the manufacture of composite structures is key to ensuring product quality and safety. Ideally, this can be done by sensors that are embedded during production and can remain as devices to monitor structural health. Extremely thin foil-based sensors weaken the finished workpiece very little. Under ideal conditions, the foil substrate bonds with the resin in the autoclaving process, as is the case when polyetherimide is used. Here, we present a temperature sensor as part of an 8 µm thick multi-sensor node foil for monitoring processing conditions during the production and structural health during the lifetime of a construction. A metallic thin film conductor was shaped in the form of a space-filling curve to suppress the influences of resistance changes due to strain, which could otherwise interfere with the measurement of the temperature. FEM simulations as well as experiments confirm that this type of sensor is completely insensitive to the direction of strain and sufficiently insensitive to the amount of strain, so that mechanical strains that can occur in the composite curing process practically do not interfere with the temperature measurement. The temperature sensor is combined with a capacitive sensor for curing monitoring based on impedance measurement and a half-bridge strain gauge sensor element. All three types are made of the same materials and are manufactured together in one process flow. This is the key to cost-effective distributed sensor arrays that can be embedded during production and remain in the workpiece, thus ensuring not only the quality of the initial product but also the operational reliability during the service life of light-weight composite constructions.
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Polímeros , Sensação Térmica , Reprodutibilidade dos Testes , TemperaturaRESUMO
Electrical impedance is an established technique used for cell and particle characterization. The temporal and spectral resolution of electrical impedance have been used to resolve basic cell characteristics like size and type, as well as to determine cell viability and activity. Such electrical impedance measurements are typically performed across the entire sample volume and can only provide an overall indication concerning the properties and state of that sample. For the study of heterogeneous structures such as cell layers, biological tissue, or polydisperse particle mixtures, an overall measured impedance value can only provide limited information and can lead to data misinterpretation. For the investigation of localized sample properties in complex heterogeneous structures/mixtures, the addition of spatial resolution to impedance measurements is necessary. Several spatially resolved impedance measurement techniques have been developed and applied to cell and particle research, including electrical impedance tomography, scanning electrochemical microscopy, and microelectrode arrays. This review provides an overview of spatially resolved impedance measurement methods and assesses their applicability for cell and particle characterization.
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Técnicas Citológicas , Espectroscopia Dielétrica , Impedância Elétrica , Microscopia Eletroquímica de Varredura , Animais , Membrana Celular/fisiologia , Células Cultivadas , Desenho de Equipamento , Humanos , Camundongos , Microeletrodos , TomografiaRESUMO
Single-cell analysis commonly requires the confinement of cell suspensions in an analysis chamber or the precise positioning of single cells in small channels. Hydrodynamic flow focusing has been broadly utilized to achieve stream confinement in microchannels for such applications. As imaging flow cytometry gains popularity, the need for imaging-compatible microfluidic devices that allow for precise confinement of single cells in small volumes becomes increasingly important. At the same time, high-throughput single-cell imaging of cell populations produces vast amounts of complex data, which gives rise to the need for versatile algorithms for image analysis. In this work, we present a microfluidics-based platform for single-cell imaging in-flow and subsequent image analysis using variational autoencoders for unsupervised characterization of cellular mixtures. We use simple and robust Y-shaped microfluidic devices and demonstrate precise 3D particle confinement towards the microscope slide for high-resolution imaging. To demonstrate applicability, we use these devices to confine heterogeneous mixtures of yeast species, brightfield-image them in-flow and demonstrate fully unsupervised, as well as few-shot classification of single-cell images with 88% accuracy.
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Interfaces between donor and acceptor in a polymer solar cell play a crucial role in exciton dissociation and charge photogeneration. While the importance of charge transfer (CT) excitons for free carrier generation is intensively studied, the effect of blending on the nature of the polymer excitons in relation to the blend nanomorphology remains largely unexplored. In this work, electroabsorption (EA) spectroscopy is used to study the excited-state polarizability of polymer excitons in several polymer:fullerene blend systems, and it is found that excited-state polarizability of polymer excitons in the blends is a strong function of blend nanomorphology. The increase in excited-state polarizability with decreased domain size indicates that intermixing of states at the interface between the donor polymers and fullerene increases the exciton delocalization, resulting in an increase in exciton dissociation efficiency. This conclusion is further supported by transient absorption spectroscopy and time-resolved photoluminescence measurements, along with the results from time-dependent density functional theory calculations. These findings indicate that polymer excited-state polarizability is a key parameter for efficient free carrier generation and should be considered in the design and development of high-performance polymer solar cells.
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Thin-film optoelectronic devices based on polycrystalline organolead-halide perovskites have recently become a topic of intense research. Single crystals of these materials have been grown from solution with electrical properties superior to those of polycrystalline films. In order to enable the development of more complex device architectures based on organolead-halide perovskite single crystals, we developed a process to form epitaxial layers of methylammonium lead iodide (MAPbI3) on methylammonium lead bromide (MAPbBr3) single crystals. The formation of the MAPbI3 layer is found to be dominated by the diffusion of halide ions, leading to a shift in the photoluminescence and absorption spectra. X-ray diffraction measurements confirm the single-crystal nature of the MAPbI3 layer, while carrier transport measurements show that the converted layer retains the high carrier mobility typical of single-crystal perovskite materials. Such heterostructures on perovskite single crystals open possibilities for new types of devices.
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The effect of polymer side chains on device performance was investigated for PBDT(EtHex)-TPD(Oct):PC70BM and PBDT(EtHex)-TPD(EtHex):PC70BM BHJ solar cells. Going from a linear side chain on the polymer's acceptor moiety to a branched side chain was determined to have a negative impact on the overall device efficiency, because of significantly reduced short-circuit current (J(sc)) and fill factor (FF) values. Sub-bandgap external quantum efficiency (EQE) and transient photoluminescence (PL) measurements showed more-efficient carrier generation for the polymer with linear side chains, because of a higher degree of charge-transfer (CT) state delocalization, leading to more-efficient exciton dissociation. Furthermore, the increase in π-π stacking distance and disorder for the bulkier ethylhexyl side chain were shown to result in a lower hole mobility, a higher bimolecular recombination, and a higher energetic disorder. The use of linear side chains on the polymer's acceptor moiety was shown to promote photogeneration, because of more-effective CT states and favorable carrier transport resulting in improved solar cell performance.
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The effect of air processing, with air exposure varying from minutes to hours prior to encapsulation, on photovoltaic device performance has been studied through a series of electrical characterizations and optical simulations for a donor/acceptor polymer-based organic solar cell based on poly(dithienogermole-alt-thienopyrrolodione) p(DTG-TPD)/PC71BM blends. A â¼10% degradation in power conversion efficiency was observed due to air processing with 10 min exposure time, with AM1.5 power conversion efficiencies (PCEs) decreasing from 8.5 ± 0.25% for devices processed in inert nitrogen atmosphere to 7.7 ± 0.18% for devices processed in ambient air. After 3 h air exposure, the PCE leveled off at 7.04 ± 0.1%. This decrease is attributed partially to interface issues caused by exposure of the electrode materials to oxygen and water and partially to a degradation of the hole transport in the active layer.