A Microfluidic Contact Lens to Address Contact Lens-Induced Dry Eye

The contact lens (CL) industry has made great strides in improving CL-wearing experiences. However, a large amount of CL wearers continue to experience ocular dryness, known as contact lens-induced dry eye (CLIDE), stemming from the reduction in tear volume, tear film instability, increased tear osmolarity followed by inflammation and resulting in ocular discomfort and visual disturbances. In this article, to address tear film thinning between the CL and the ocular surface, the concept of using a CL with microchannels to deliver the tears from the pre-lens tear film (PrLTF) to the post-lens ocular surface using in vitro eye-blink motion is investigated. This study reports an eye-blink mimicking system with microfluidic poly(2-hydroxyethyl methacrylate) (poly(HEMA)) hydrogel with integrated microchannels to demonstrate eye-blink assisted flow through microchannels. This in vitro experimental study provides a proof-of-concept result that tear transport from PrLTF to post-lens tear film can be enhanced by an artificial eyelid motion in a pressure range of 0.1–5 kPa (similar to human eyelid pressure) through poly(HEMA) microchannels. Simulation is conducted to support the hypothesis. This work demonstrates the feasibility of developing microfluidic CLs with the potential to help prevent or minimize CLIDE and discomfort by the enhanced transport of pre-lens tears to the post-lens ocular surface.     

Low-Cost Customized Color-Blind Contact Lenses using 3D Printed Molds

Prominence of color perception in our day-to-day routine is unequivocally pronounced, yet visual ramifications due to color vision deficiency (CVD) or color blindness impede carriers of this disorder from functioning normally. To circumvent this deficiency, patients opt for tinted glasses/contact lenses to complement their color distinction capabilities. Red-green color blindness, the most prevalent form of CVD, can be alleviated using such glasses/lenses that filter out problematic wavelengths (540–580 nm). Nonetheless, nearly all contact lenses established by companies and developed by researchers are tinted throughout their entire surface, causing patients discomfort and needless attention as people can easily note their deficiency. Ideally, the tint within the lens should only cover the eye's pupil as it is responsible for perceiving light. Hence herein, CVD contact lenses are fabricated by solely tinting the midportion of commercial lenses utilizing two additively manufactured molds with 4 and 8 mm-diameter holes to emulate the humans’ average pupil size. The tinted lenses filter light effectively at 530–590 nm with their transmission dip being at 558 nm. The contact lenses show excellent wettability and water retention capabilities along with demonstrating superior wavelength-filtering properties to most of the commercial and research-based CVD wearables.     

角膜接触镜专用顶焦度标准器的研制

论述了建立角膜接触镜专用顶焦度标准器的必要性和研制方案所用的原理,并给出接触镜专用项焦度标准器的测试结果和误差分析,最后讨论了对检测角膜接触镜的焦度计如何校准的问题。     

N-异丙基丙烯酰胺对软接触镜材料性能的影响

以0.2%的2-羟基-甲基苯基丙烷-1-酮(1173)为引发剂,0.5%的二乙二醇甲基丙烯酸酯(EGDM A)为交联剂,常温下用紫外灯合成了N-异丙基丙烯酰胺(N IPAm)/甲基丙烯酸2-羟基乙酯(HEM A)/N-乙烯吡咯烷酮(NVP)三元共聚物;与相同条件下合成的HEM A/NVP共聚物进行了试验对比。凝胶在水中的溶胀实验证明,含N IPAm的三元共聚物溶胀率对温度的敏感性强于HEM A-NVP共聚物;傅立叶红外光谱与热重测试显示了两种材料的结构差异。     

Light‐Governed Capillary Flow in Microfluidic Systems

Light‐based flow systems for point‐of‐care devices are of interest because, in principle, sunlight could be used to operate them, potentially allowing for high functionality with minimal device complexity and expense. A light‐operated method to drive flow using poly(N‐isopropylacrylamide), a ‘smart’ polymer that changes wettability as a function of temperature, is introduced. It is grafted onto a carbon black‐polydimethylsiloxane surface, which converts light into a thermal pattern that valves flow at user‐defined locations. Flow rates are demonstrated ranging from 4 μL min^?1 at 25 °C to 0.1 μL min^?1 at 40 °C. The valving dynamics are also characterised, and a response time of less than 4 s is shown. Light‐operated flow could provide the simple architecture and advanced functionality needed in low‐resource point‐of‐care devices.     

Microfluidic chips for point-of-care immunodiagnostics

We might be at the turning point where research in microfluidics undertaken in academia and industrial research laboratories, and substantially sponsored by public grants, may provide a range of portable and networked diagnostic devices. In this Progress Report, an overview on microfluidic devices that may become the next generation of point-of-care (POC) diagnostics is provided. First, we describe gaps and opportunities in medical diagnostics and how microfluidics can address these gaps using the example of immunodiagnostics. Next, we conceptualize how different technologies are converging into working microfluidic POC diagnostics devices. Technologies are explained from the perspective of sample interaction with components of a device. Specifically, we detail materials, surface treatment, sample processing, microfluidic elements (such as valves, pumps, and mixers), receptors, and analytes in the light of various biosensing concepts. Finally, we discuss the integration of components into accurate and reliable devices.     

Methods of Checking the Optical Characteristics of Soft Contact Lenses

A new classification is proposed for contact lenses based on standard specimens (tolerance monitoring). The best wavelengths have been determined for measuring the spectral transmission coefficients of the standard specimens, and realistic bounds have been defined for the tolerance fields for the most common colors of these lenses.     

Microfluidic Synthesis of Nanohybrids

Nanohybrids composed of two or more components exhibit many distinct physicochemical properties and hold great promise for applications in optics, electronics, magnetics, new energy, environment protection, and biomedical engineering. Microfluidic systems exhibit many advantages due to their unique characteristics of narrow channels, variable length, controllable number of channels and multiple integrations. Particularly their spatial‐temporarily splitting of the formation stages during nanomaterials formation along the microfluidic channels favors the online control of the reaction kinetic parameters and in situ tuning of the product properties. This Review is focused on the features of the current types of microfluidic devices in the synthesis of different types of nanohybrids based on the classification of the four main kinds of materials: metal, nonmetal inorganic, polymer and composites. Their morphologies, compositions and properties can be adjusted conveniently in these synthesis systems. Synthesis advantages of varieties of microfluidic devices for specific nanohybrids of defined surfaces and interfaces are presented according to their process and microstructure features of devices as compared with conventional methods. A summary is presented, and challenges are put forward for the future development of the microfluidic synthesis of nanohybrids for advanced applications.     

CRISPR/Cas13a‐Powered Electrochemical Microfluidic Biosensor for Nucleic Acid Amplification‐Free miRNA Diagnostics

Noncoding small RNAs, such as microRNAs, are becoming the biomarkers of choice for multiple diseases in clinical diagnostics. A dysregulation of these microRNAs can be associated with many different diseases, such as cancer, dementia, and cardiovascular conditions. The key for effective treatment is an accurate initial diagnosis at an early stage, improving the patient's survival chances. In this work, the first clustered regularly interspaced short palindromic repeats (CRISPR)/Cas13a‐powered microfluidic, integrated electrochemical biosensor for the on‐site detection of microRNAs is introduced. Through this unique combination, the quantification of the potential tumor markers microRNA miR‐19b and miR‐20a is realized without any nucleic acid amplification. With a readout time of 9 min and an overall process time of less than 4 h, a limit of detection of 10 pm is achieved, using a measuring volume of less than 0.6 µL. Furthermore, the feasibility of the biosensor platform to detect miR‐19b in serum samples of children, suffering from brain cancer, is demonstrated. The validation of the obtained results with a standard quantitative real‐time polymerase chain reaction method shows the ability of the electrochemical CRISPR‐powered system to be a low‐cost, easily scalable, and target amplification‐free tool for nucleic acid based diagnostics.     

衍射透镜的色散分析

基于标量衍射理论，本文分析了衍射透镜的色差，首次得出了计算其色散的数学表达式。结果表明，衍射透镜的色散包两个部分：材料色散和波长色散，二者所占的比例随孔径值的不同而变化。     

Microfluidic synthesis of nanomaterials

An overview of the current information and analyses on the microfluidic synthesis of different types of nanomaterial, including metallic and silica nanoparticles and quantum dots, is presented. Control of particle size, size distribution, and crystal structure of nanomaterials are examined in terms of the special features of microfluidic reactors.     

Microfluidic Approaches for Microactuators: From Fabrication,Actuation, to Functionalization

Microactuators can autonomously convert external energy into specific mechanical motions. With the feature sizes varying from the micrometer to millimeter scale, microactuators offer many operation and control possibilities for miniaturized devices. In recent years, advanced microfluidic techniques have revolutionized the fabrication, actuation, and functionalization of microactuators. Microfluidics can not only facilitate fabrication with continuously changing materials but also deliver various signals to stimulate the microactuators as desired, and consequently improve microfluidic chips with multiple functions. Herein, this cross-field that systematically correlates microactuator properties and microfluidic functions is comprehensively reviewed. The fabrication strategies are classified into two types according to the flow state of the microfluids: stop-flow and continuous-flow prototyping. The working mechanism of microactuators in microfluidic chips is discussed in detail. Finally, the applications of microactuator-enriched functional chips, which include tunable imaging devices, micromanipulation tools, micromotors, and microsensors, are summarized. The existing challenges and future perspectives are also discussed. It is believed that with the rapid progress of this cutting-edge field, intelligent microsystems may realize high-throughput manipulation, characterization, and analysis of tiny objects and find broad applications in various fields, such as tissue engineering, micro/nanorobotics, and analytical devices.     

Microfluidic Single‐Cell Omics Analysis

The commonly existing cellular heterogeneity plays a critical role in biological processes such as embryonic development, cell differentiation, and disease progress. Single‐cell omics‐based heterogeneous studies have great significance for identifying different cell populations, discovering new cell types, revealing informative cell features, and uncovering significant interrelationships between cells. Recently, microfluidics has evolved to be a powerful technology for single‐cell omics analysis due to its merits of throughput, sensitivity, and accuracy. Herein, the recent advances of microfluidic single‐cell omics analysis, including different microfluidic platform designs, lysis strategies, and omics analysis techniques, are reviewed. Representative applications of microfluidic single‐cell omics analysis in complex biological studies are then summarized. Finally, a few perspectives on the future challenges and development trends of microfluidic‐assisted single‐cell omics analysis are discussed.     

Pulsatile Flow in Microfluidic Systems

This review describes the current knowledge and applications of pulsatile flow in microfluidic systems. Elements of fluid dynamics at low Reynolds number are first described in the context of pulsatile flow. Then the practical applications in microfluidic processes are presented: the methods to generate a pulsatile flow, the generation of emulsion droplets through harmonic flow rate perturbation, the applications in mixing and particle separation, and the benefits of pulsatile flow for clog mitigation. The second part of the review is devoted to pulsatile flow in biological applications. Pulsatile flows can be used for mimicking physiological systems, to alter or enhance cell cultures, and for bioassay automation. Pulsatile flows offer unique advantages over a steady flow, especially in microfluidic systems, but also require some new physical insights and more rigorous investigation to fully benefit future applications.     

Microfluidic one-step synthesis of alginate microspheres immobilized with antibodies

Micrometre- and submicrometre-size functionalized beads are frequently used to capture targets of interest from a biological sample for biological characterizations and disease diagnosis. The main challenge of the microbead-based assay is in the immobilization of probe molecules onto the microbead surfaces. In this paper, we report a versatile droplet microfluidics method to fabricate alginate microspheres while simultaneously immobilizing anti-Mycobacterium tuberculosis complex IgY and anti-Escherichia coli IgG antibodies primarily on the porous alginate carriers for specific binding and binding affinity tests. The binding affinity of antibodies is directly measured by fluorescence intensity of stained target bacteria on the microspheres. We demonstrate that the functionalized alginate microspheres yield specificity comparable with an enzyme-linked immunosorbent assay. The high surface area-to-volume ratio of the functionalized porous alginate microspheres improves the detection limit. By using the droplet microfluidics, we can easily modify the size and shape of alginate microspheres, and increase the concentration of functionalized alginate microspheres to further enhance binding kinetics and enable multiplexing.