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The present work exhibits a novel design of surface plasmon resonance (SPR) biosensor, which comprises CaF2 prism, TiO2, metal (Ag/Au), PtSe2, 2D materials (graphene/ transition metal dichalcogenides (MoS2/WS2)) and sensing medium, for point-of-care detection of various stages of malaria diseases. The transfer matrix method (TMM) is employed to examine the angular reflectivity of the proposed structure after judiciously optimizing the layer thicknesses and layer numbers. Phase interrogation technique is utilised to validate the position of occurrence of resonance angles. Additionally, the proposed SPR structure is designed using COMSOL Multiphysics, to assay the electric field intensity and electric field enhancement factor near the edge of 2D material-sensing layer interface. Simulation upshots revealed that the use of new class of 2D materials catapult the sensor performance to a new height compared to the traditional SPR configuration. A maximum sensitivity of 240.10°/RIU, quality factor of 78.46 RIU-1 and detection accuracy of 1.99 is attained for Ag-based SPR configuration with bilayer of WS2. Sensing parameters are compared with previously reported works to prove the superiority of the present research. Moreover, the real-time and label-free detection of malaria diseases makes the suggested sensor worth to fabricate as a SPR chip with the recent nanofabrication technologies.

We report on an extrinsic surface plasmon-enhancedrefractometer based on cladding mode resonance excitation in a photonic crystal fiber (PCF) equipped with a straight fiber Bragggrating (FBG). First, we show that the lattice pitch and the air hole diameter of the PCF microstructure define the spectral locationof the excited cladding mode resonances. Second, we demonstrate that if the PCF parameters are properly selected, those resonancesare sensitive to increases in steps of 1×10−4 refractive index units(RIU) of the refractive index value close to that of water. To thebest of our knowledge, this is the first time that the sensitivity of PCF cladding mode resonances to refractive index changesin water-based solutions is reported. We achieved experimental values of 40.3 nm/RIU in terms of wavelength sensitivity and −801dB/RIU in terms of amplitude sensitivity. The performance of our sensor is therefore comparable to that of tilted FBGs in step-indexfibers used for water refractometry, which indicates the potential ofour PCF sensor for biosensing. In addition, the sensor fabricationdoes not require any post-processing such as etching or polishing,which allows preserving the integrity of the fiber probe. Finally, thenarrowspectrum within which the PCF operates, allows envisagingmulti-target detection with a single fiber probe by using cascadedwavelength-multiplexed gratings.

Highly sensitive, simple and multiplex detection capabilities are key criteria of point-of-care (POC) diagnosis in clinical samples. Here, a simple and highly sensitive multi-analyte detection technique is proposed by using photonic crystal fiber (PCF) based surface plasmon resonance (SPR) sensor that employs both internal and external sensing approaches. The proposed sensor can detect two different analytes simultaneously by the internal and external plasmonic micro-channels. The light propagation through the sensor is controlled by the scaled-down air-holes to excite the free electrons of the plasmonic metal layers. The light-guiding and sensing properties of the sensor is numerically analyzed by using the Finite Element Method (FEM). The proposed sensor shows the maximum wavelength sensitivities (WS) of 12,000 nm/refractive index unit (RIU), and 10,000 nm/RIU, for the internal and external sensing approaches, respectively, and corresponding resolution of 8.33×10-6 RIU and 1.0×10-5 RIU. Moreover, the hybrid sensor is applicable to detect unknown analyte refractive index (RI) in the range of 1.33 to 1.40 which covers extensively investigating analytes such as viruses, different cancer cells, glucose, proteins and DNA/RNA. Due to high sensing performance with multi-analyte detection capability, the proposed sensor can play a significant role to detect bio targets at the POC platform.

We present a microfluidic device compatible with high resolution light sheet and super-resolution microscopy. The device is a 150 μm thick chamber with a transparent fluorinated ethylene propylene (FEP) cover that has a similar refractive index (1.34) to water (1.33), making it compatible with top-down imaging used in light sheet microscopy. We provide a detailed fabrication protocol and characterize the optical performance of the device. We demonstrate that the device supports long-term imaging of cell growth and differentiation as well as the rapid addition and removal of reagents while simultaneously maintaining sterile culture conditions by physically isolating the sample from the dipping lenses used for imaging. Finally, we demonstrate that the device can be used for super-resolution imaging using lattice light sheet structured illumination microscopy (LLS-SIM) and DNA PAINT. We anticipate that FEP-based microfluidics, as shown here, will be broadly useful to researchers using light sheet microscopy due to the ability to switch reagents, image weakly adherent cells, maintain sterility, and physically isolate the specimen from the optics of the instruments.

Tomographic coherent imaging requires the reconstruction of a series of two-dimensional projections of the object. We show that using the solution for the image of one projection as the starting point for the reconstruction of the next projection offers a reliable and rapid approach to the image reconstruction. The method is demonstrated on simulated and experimental data. This technique also simplifies reconstructions using data with curved incident wavefronts.

Imaging platforms that enable long-term, high-resolution imaging of biofilms are required to study cellular level dynamics within bacterial biofilms. By combining high spatial and temporal resolution and low phototoxicity, lattice light sheet microscopy (LLSM) has made critical contributions to the study of cellular dynamics. However, the power of LLSM has not yet been leveraged for biofilm research because the open-on-top imaging geometry using water-immersion objective lenses is not compatible with living bacterial specimens; bacterial growth on the microscope's objective lenses makes long-term time-lapse imaging impossible and raises considerable safety concerns for microscope users. To make LLSM compatible with pathogenic bacterial specimens, we developed hermetically sealed, but optically accessible, microfluidic flow channels that can sustain bacterial biofilm growth for multiple days under precisely controllable physical and chemical conditions. To generate a liquid- and gas-tight seal, we glued a thin polymer film across a 3D-printed channel, where the top wall had been omitted. We achieved negligible optical aberrations by using polymer films that precisely match the refractive index of water. Bacteria do not adhere to the polymer film itself, so that the polymer window provides unobstructed optical access to the channel interior. Inside the flow channels, biofilms can be grown on arbitrary, even nontransparent, surfaces. By integrating this flow channel with LLSM, we were able to record the growth of S. oneidensis MR-1 biofilms over several days at cellular resolution without any observable phototoxicity or photodamage.

International audience; Evanescent-wave scattering is a topic in classical electrodynamics and in the study of colloidal particles near a boundary. However, how such near-surface scattering at subcellular refractive-index heterogeneities degrades the excitation confinement in biological total internal reflection fluorescence microscopy has not been well studied. An elegant theoretical work by Axelrod and Axelrod now addresses this very relevant question and reveals that-even when scattered-evanescent light preserves some of its surprising optical properties.

A technique is implemented for altering the multimodal resonance generated in an ultrathin silicon ring resonator-based terahertz (THz) absorber. The absorber provides the dual-band resonance with the excitation of magnetic and electric dipole in the lower and upper band, respectively. The field of magnetic and electric dipoles is altered using a non-resonant graphene ring placed in the center of the generated dipolar arrangement and the tunability and perfect absorption is achieved. A circuit model is prepared using transmission line method and absorber operation is verified. The proposed absorber can be utilized as a biosensor for the detection of malaria virus and glucose percentage in water. The sensor offers highest sensitivity as 0.29 and 0.27 THz per thickness unit change and quality factor as 117.53 and 245 in the lower and upper band, respectively during the sensing of analyte thickness. Also, it offers the sensitivity as 0.20 and 0.10 THz per refractive index unit change and quality factor as 105.28 and 211.84 in the lower and upper band, respectively during refractive index sensing. Moreover, the structure remains insensitive to polarization angle of the incident electromagnetic wave.

Both the nonclose-packed structure and the large refractive index contrast of guanine nanocrystals and cytosols in iridophores play a vital role in the dynamic camouflage of chameleons, including the bright skin color and color tuning sensitivity to external stimulus. Here, the nonclose-packed photonic crystals consisting of ZnS nanospheres and polymers, which have similar refractive indices with guanine nanocrystals and cytosols, respectively, are constructed by a two-step filling strategy. ZnS@SiO2 nanospheres are self-assembled to build intermediate close-packed photonic crystals followed by filling polymers in their interstices. The nonclose-packed photonic crystal is successfully achieved when the silica portion is etched by HF solution and refilled by polymers. Excitingly, the stimulus response of the designed photonic crystal is as sensitive as the skin of chameleons due to the similar contrast of refractive indices and nonclose-packed structure. The reflection peak of the structure can blue-shift more than 200 nm as the temperature increases from 30 to 55 °C or under 20% compressional strain. This work not only builds the nonclose-packed photonic crystals by introducing a two-step filling strategy but also proves that high refractive contrast in photonic crystals is an effective strategy to achieve ultrasensitivity, which is highly desirable for various applications.

Purpose: To examine the refractive lens power (RLP) and lens thickness and their associated factors in children from North-Western China.Methods: Children from two schools (primary school and junior high school) in the North-Western Chinese province of Qinghai underwent a comprehensive ophthalmic examination including biometry and cycloplegic refractometry. The RLP was calculated using Bennett’s equation. Results: The study included 596 (77.9%) individuals (mean age: 11.0±2.8 years; range: 6-16 years) with a mean axial length of 23.65±1.24mm (range: 20.02-27.96mm). Mean lens thickness was 3.30±0.16mm (range: 2.85-3.99mm) and mean RLP was 24.85±1.98D (range: 19.40-32.97). In univariate analysis, girls as compared to boys had a significantly thicker lens and greater RLP, shorter axial length, smaller corneal curvature radius and shorter corneal curvature radius (all PP=0.11) and corneal thickness (P=0.16). RLP was positively associated with refractive error (correlation coefficient r=0.33; PPPPβ=−0.07), female sex (Pβ=−0.08), shorter axial length (Pβ=−0.48) and higher lens thickness (Pβ=0.42). Conclusions: In Chinese children, RLP with a mean of 24.85±1.98D decreases with older age, male sex, longer axial length, and thinner lens thickness. Changes in RLP and axial length elongation are important players in the emmetropization and myopization.

Herein, a novel liquid crystal microarray (LCM) film with optical regulation ability is first constructed by combining liquid crystals (LC) and the highly ordered microporous structure of inverse opal photonic crystals (IOPhCs). The LCM films are fabricated by infiltrating LC molecules into the LC polymer with the structure of IOPhCs, and their properties are very different from those without the LC. Interestingly, the optical property of LCM films can be controlled by changing the orientation of LC molecules, which varies with the interfacial force. In combination with polarization images, spectral reflection peak, circular dichroism spectra, potential difference, and fluorescence images of LCM films, the mechanism of this change is investigated. It is found that the exposed basic group of single-stranded DNA is the key to the change of the optical property of LC microarrays. Meanwhile, the optical signals of LC microarrays based on the PhCs provide a novel LC signal mode for an LC sensing system (microspectral signal mode), and it can be recorded by a fiber-optic spectrometer, which is a great improvement on LC sensing signals. Therefore, the LC microarray sensing signal can be used for accurate analysis of targets by the change of the reflection peak intensity of PhCs. When the LC molecules are induced by different aptamers, the LC microarray sensing interface can be further used for the determination of different targets, such as cocaine and Hg2+. The research on LCM films is of significant value for the development of LC sensing technology and also shows great application prospects in biochemical sensing fields.

Critical angle refractometry is an established technique for determining the refractive index of liquids and solids. For transparent samples, the critical angle refractometry precision is limited by incidence angle resolution. For lossy samples, the precision is also affected by reflectance measurement error. In the present study, it is demonstarted that reflectance error can be practically eliminated, provided that the sample’s extinction coefficient is a priori known with sufficient accuracy (typically, better than 5%) through an independent measurement. Then, critical angle refractometry can be as precise with lossy media as with transparent ones.

Phycobiliproteins are a class of light-harvesting fluorescent proteins existing in cyanobacteria and microalgae, which harvest light and convert it into electricity. Owing to recent demands on environmental-friendly and renewable apparatuses, phycobiliproteins have attracted substantial interest in bioenergy and sustainable devices. However, converting energy from biological materials remains challenging to date. Herein, we report a novel scheme to enhance biological light-harvesting through light-matter interactions at the biointerface of whispering-gallery modes (WGMs), where phycobiliproteins were employed as the active gain material. By exploiting microdroplets as a carrier for light-harvesting biomaterials, strong local electric field enhancement and photon confinement at the cavity interface resulted in significantly enhanced bio-photoelectricity. A threshold-like behavior was discovered in photocurrent enhancement and the WGM modulated fluorescence. Systematic studies of biologically produced photoelectricity and optical mode resonance were carried out to illustrate the impact of the cavity quality factor, structural geometry, and refractive indices. Finally, a biomimetic system was investigated by exploiting cascade energy transfer in phycobiliprotein assembly composed of three light-harvesting proteins. The key findings not only highlight the critical role of optical cavity in light-harvesting but also offer deep insights into light energy coupling in biomaterials. Ministry of Education (MOE) Nanyang Technological University This research is supported by the Ministry of Education Singapore (Tier 1-RG 158/19(S)). We would like to thank Internal Grant NAP SUG -M4082308.040 from NTU.

Refereed/Peer-reviewed A multifunction, high-sensitivity, and temperature-compensated optical fiber DNA hybridization sensor combining surface plasmon resonance (SPR) and Mach–Zehnder interference (MZI) has been designed and implemented. We demonstrate, for the first time to our knowledge, the dual-parameter measurement of temperature and refractive index (RI) by simultaneously using SPR and MZI in a simple single-mode fiber (SMF)–no-core fiber (NCF)–SMF structure. The experimental results show RI sensitivities of 930 and 1899 nm/RIU and temperature sensitivities of 0.4 and −1.4 nm/°C for the MZI and SPR, respectively. We demonstrate a sensitivity matrix used to simultaneously detect both parameters, solving the problem of temperature interference of RI variation-based biosensors. In addition, the sensor can also distinguish biological binding events by detecting the localized RI changes at the fiber’s surface. We realize label-free sensing of DNA hybridization detection by immobilizing probe DNA (pDNA) onto the fiber as the probe to capture complementary DNA (cDNA). The experimental results show that the sensor can qualitatively detect cDNA after temperature compensation, and the limit of detection (LOD) of the sensor reaches 80 nM. The proposed sensor has advantages of high sensitivity, real time, low cost, temperature compensation, and low detection limit and is suitable for in situ monitoring, high-precision sensing of DNA molecules, and other related fields, such as gene diagnosis, kinship judgment, environmental monitoring, and so on.

A method to enable surface plasmon resonance (SPR) sensors to discriminate between bulk and surface-localized refractive index changes is demonstrated with modified gold-coated tilted fiber Bragg grating SPR sensors (TFBG-SPR). Without this capability, all high-resolution SPR sensors should be using reference channels and strict temperature control to prevent the contamination of the desired detection of surface-localized chemical or binding events by drift of the refractive index of the medium, in which the experiment is carried out. The very fine comb of high-quality-factor resonances of a TFBG-SPR device coupled to the large differential sensitivity of some of the resonances to various perturbations is used to measure unambiguously the refractive index changes within a surface layer thinner than 25 nm from those of the bulk surrounding. The enabling modification of the conventional TFBG-SPR is a reduction of the gold coating from its optimum value near 50-30 nm: at this lower thickness, a surface plasmon wave can still be excited by a limited number of cladding mode resonances, but at the same time, the metal is thin enough to allow modes away from the SPR to tunnel across the metal and probe the bulk RI value. Measurements and simulations of the deposition of a self-assembled monolayer of 1-dodecanethiol in ethanol show that the bulk refractive index changes as small as 0.0004 can be distinguished from the formation of a 1 nm thick coating on the surface of the fiber.

Quantification of molecular interactions on a surface is typically achieved via label-free techniques such as surface plasmon resonance (SPR). The sensitivity of SPR originates from the characteristic that the SPR angle is sensitive to the surface refractive index change. Analogously, in another interfacial optical phenomenon, total internal reflection, the critical angle is also refractive index dependent. Therefore, surface refractive index change can also be quantified by measuring the reflectivity near the critical angle. Based on this concept, we develop a method called critical angle reflection (CAR) imaging to quantify molecular interactions on glass surface. CAR imaging can be performed on SPR imaging setups. Through a side-by-side comparison, we show that CAR is capable of most molecular interaction measurements that SPR performs, including proteins, nucleic acids and cell-based detections. In addition, we show that CAR can detect small molecule bindings and intracellular signals beyond SPR sensing range. CAR exhibits several distinct characteristics, including tunable sensitivity and dynamic range, deeper vertical sensing range, fluorescence compatibility, broader wavelength and polarization of light selection, and glass surface chemistry. We anticipate CAR can expand SPR′s capability in small molecule detection, whole cell-based detection, simultaneous fluorescence imaging, and broader conjugation chemistry., Here, the authors present a method for quantifying molecular interactions on a glass surface, based on measuring surface refractive index changes via the reflectivity near the critical angle. They demonstrate tunable sensitivity and dynamic range, deep vertical sensing range, also for intracellular signals.

When developing oil fields, there is an urgent task to quickly determine the type of pumped formation fluid, which includes formation gas, formation oil and formation water. In this paper, we propose a new type of a sensor element designed for flow refractometry of formation fluid based on the effect of total internal reflection. The sensor element is a taper tip of a conical shape made of sapphire and is 20 mm in length and 20 mm in diameter. The original shape of the sensor element is determined by a modified ray tracing method, taking into account analytical relations that determine the conditions for providing a larger dynamic range of measurements under specified physical, technological and design constraints. The conversion dependence of the tip is obtained for the wavelengths of 405 nm, 1064 nm and 3300 nm and allows determining the type of formation fluid (gas/water/oil). The proposed method enables the development of conical sensor elements based on the total internal reflection for downhole monitoring systems and optical threshold sensors of the refractive index.

For biomedical photoacoustic applications, an ongoing challenge in simultaneous volumetric imaging and spectroscopic analysis arises from ultrasonic detectors lacking high sensitivity to pressure transients over a broad spectral bandwidth. Photoacoustic impulses can be measured on the basis of the ultrafast temporal dynamics and highly sensitive response of surface plasmon polaritons to the refractive index changes. Taking advantage of the ultra-sensitive phase shift of surface plasmons caused by ultrasonic perturbations instead of the reflectivity change [as is the case for traditional surface plasmon resonance (SPR) sensors], a novel SPR sensor based on phase-shifted interrogation was developed for the broadband measurement of photoacoustically induced pressure transients with improved detection sensitivity. Specifically, by encoding the acoustically modulated phase change into time-varying interference intensity, our sensor achieved an almost five-fold sensitivity enhancement (∼98 Pa noise-equivalent pressure) compared with the reflectivity-mode SPR sensing technologies (∼470 Pa) while retaining a broadband acoustic response of ∼174 MHz. Incorporating our sensor into an optical-resolution photoacoustic microscope, we performed label-free imaging of a zebrafish eye in vivo, enabling simultaneous volumetric visualization and spectrally resolved discrimination of anatomical features. This novel sensing technology has potential for advancing biomedical ultrasonic and/or photoacoustic investigations.

Optical microfiber-based refractometer, which relies on modal interference operating near the dispersion turning point (DTP), has attracted a high level of research interest. The ultrahigh sensitivity can be achieved by mitigating the group effective refractive index difference between the modes in the coupling. Through modifying the microfiber diameter, the group effective refractive index difference can be modified to zero which is defined as DTP. However, all the DTP-based sensors report low fabrication tolerance and narrow operation bandwidth of probing wavelength for the high-sensitivity region where the refractive index (RI) sensitivities higher than 104 nm/RIU can be achieved, which extremely limits the practical applications. To address the challenge, we manipulate and optimize the mode dispersion by using a tapered specially-designed single stress-applying fiber (SSAF). By introducing the stress-applying part (SAP) into the cladding, the wavelength sensitivity of the group effective RI difference can be significantly reduced through the flexibly engineerable control over the material index. In this way, the operation bandwidth is dramatically broadened for 500 nm in comparison with that of conventional microfiber with the same diameter based on DTP, indicating a broad range of optional probing wavelength and high fabrication tolerance. We experimentally verify the ultrahigh sensitivity and broadband operation around the DTP using an SSAF-based microfiber with a waist diameter of about 2.3 μm. The maximum RI sensitivity of 30563 nm/RIU is obtained.

In modern large-sized tokamaks and those under construction, for example, in ITER, when measuring the average plasma electron density using the refractometry technique, it becomes necessary to study different effects that affect the measurement accuracy. This paper presents the results from studies of the high-temperature effects that can affect the interpretation of delay time measurements of the probing microwave signal in the ITER refractometry diagnostics. The criteria for applicability of different plasma models (“cold” plasma, modified “cold” plasma, and “hot plasma”) are obtained for calculating the plasma refractive index and interpreting the delay times that will be measured using the refractometry diagnostics of the ITER plasma. In the second article, based on the results obtained in this article, we will consider the influence of the high-temperature effects on the accuracy of determining the mean density using the refractometry diagnostics.

Chip-scale SARS-CoV-2 testing was demonstrated using silicon nitride (Si3N4) nanoslot fluidic waveguides to detect a tagged oligonucleotide with a coronavirus DNA sequence. The slot waveguides were fabricated using complementary metal-oxide-semiconductor (CMOS) fabrication processes, including multiscale lithography and selective reactive ion etching (RIE), forming femtoliter fluidic channels. Finite difference method (FDM) simulation was used to calculate the optical field distribution of the waveguide mode when the waveguide sensor was excited by transverse electric (TE) and transverse magnetic (TM) polarized light. For the TE polarization, a strong optical field was created in the slot region and its field intensity was 14× stronger than the evanescent sensing field from the TM polarization. The nanoscale confinement of the optical sensing field significantly enhanced the light-analyte interaction and improved the optical sensitivity. The sensitivity enhancement was experimentally demonstrated by measuring the polarization-dependent fluorescence emission from the tagged oligonucleotide. The photonic chips consisting of femtoliter Si3N4 waveguides provide a low-cost and high throughput platform for real-time virus identification, which is critical for point-of-care (PoC) diagnostic applications.

In this work, the splitting of resonance lines in a Fabry-Perot resonator formed by a section of a standard curved single-mode fiber with metal-coated ends is investigated numerically and experimentally. It is shown that this splitting is similar to the Autler-Townes splitting and results from a strong coupling between the fundamental mode of the core and the whispering gallery mode of the cladding of the curved fiber. The influence of all basic parameters of the curved resonator on the splitting of its resonance lines in the reflection and transmission spectra is considered. Prospects for the practical application of the effects studied for high-resolution optical refractometry, as well as the direction of further research are outlined.

Okadaic acid (OA) is one of the marine toxins that are widely distributed and harmful to humans. However, the current detection methods for OA involve complex procedures, need long detection time, and rely on large-scale laboratory equipment. In this work, a multi-channel handheld automatic spectrometer (MHAS) based on a spectral sensor was developed with the advantages of small size, simple operation and low cost. It could achieve rapid detection within 30 s and a wide spectral detection range of 470–780 nm with a broadband LED as the light source and a microplate containing 8 wells as a sample cell. Moreover, through the combination of gold nanoparticles (AuNPs) and aptamer-OA34, a highly sensitive and rapid system for OA detection was established with a LOD of 1.80 μg L−1 and a wide detection range of 20–10 000 μg L−1, which is comparable to a microplate reader. Compared with other studies, the proposed MHAS realized rapid on-site detection of OA with a wider detection range, shorter detection time and higher portability. Therefore, the MHAS promises to be a stable and efficient optical detection instrument for on-site detection in the fields of food safety, disease diagnosis and environmental monitoring.

Resumen Introducción. Los sustitutos de calostro han aumentado su popularidad en Costa Rica como una alternativa al calostro de mala calidad, reservas limitadas, o para romper el ciclo de transmisión de ciertas enfermedades infecciosas. Sin embargo, es importante asegurarse de que estos productos sean efectivos y capaces de proporcionar concentraciones séricas de IgG adecuadas. Objetivo. Evaluar la eficacia de un sustituto del calostro versus el calostro materno en terneras de lechería. Materiales y métodos. El experimento se llevó a cabo durante el primer semestre del 2019 en sesenta terneras Jersey (veinte terneras por tratamiento) que fueron asignadas aleatoriamente a uno de tres tratamientos que consistieron en suplementar a las terneras con: 3 l de calostro materno (tratamiento 1), 335 g de sustituto de calostro que contenía 150 g de IgG (tratamiento 2) y 2 l de calostro materno + 110 g de suplemento de calostro que contenía 55 g de IgG (tratamiento 3). Se recogieron muestras de sangre de todas las terneras 48 h después de la administración del calostro y se analizaron las concentraciones de proteína sérica total e IgG. Resultados. Las terneras alimentadas con calostro materno y con calostro materno + suplemento de calostro tuvieron concentraciones más altas de proteína sérica total (p10 g de IgG) y tuvieron una mayor eficiencia aparente de absorción. No hubo diferencias significativas (p>0,05) con respecto a los parámetros de crecimiento y el estado de salud de las terneras. Conclusiones. El reemplazador de calostro evaluado proporcionó una adecuada concentración de IgG en las terneras evaluadas y se podría utilizar como una alternativa cuando no se cuenta con calostro materno. Abstract Introduction. Colostrum substitutes have increased in popularity in Costa Rica as an alternative to poor quality colostrum, limited colostrum reserves, or to break the cycle of transmission of certain infectious diseases. However, it is important to make sure that these products are effective and capable of providing adequate serum IgG concentration. Objective. To evaluate the efficacy of a colostrum substitute versus maternal colostrum in dairy heifer calves. Materials and methods. The experiment was carried out during the first semester of 2019 in sixty Jersey calves (twenty calves per treatment) that were randomly assigned to 1 of 3 treatment groups that consisted of supplementing the calves with: 3 l of maternal colostrum (group 1), 335 g of a colostrum replacer product containing 150 g of IgG (group 2), and 2 l of maternal colostrum + 110 g of colostrum supplement containing 55 g of IgG (group 3). Blood samples from all calves were collected 48 h after colostrum administration and analyzed for total serum protein and IgG concentration. Results. Calves fed maternal colostrum and maternal colostrum + colostrum supplement had significantly higher (p 10 g of IgG) and had a higher apparent efficiency of absorption. There were no significant differences (p>0.05) on calf growth parameters and health status of the calves. Conclusions. The evaluated colostrum replacer product provided an adequate IgG concentration in the assessed Jersey heifer calves and could be used as an alternative when there is no maternal colostrum.

Surface plasmon resonance (SPR) is an important technique for real-time and label-free detection of specific binding biomolecules. However, conventional SPR signals come from both the surface binding biomolecules and the variation in the bulk refractive index. This work demonstrates that Fano resonance in an aluminum capped nanoslit array has the ability to remove the signal of bulk refractive index changes from the SPR signal. As compared to gold nanostructures, the aluminum nanostructure provides an asymmetrical Fano resonance with clear peak and dip wavelengths. The peak wavelength is close to the grating resonance condition. The evanescent depth at the peak wavelength is up to several microns. The dip wavelength comes from the SPR effect. The evanescent depth at the dip wavelength is about 300 nm. By simultaneously measuring the shifts of peaks and the dip wavelengths, the variation in the bulk refractive index can be removed and only the biolayer thickness is measured. The finite-difference time-domain calculation shows that the 470 nm-period nanoslit array with 90 and 70 nm slit depths has the optimal thickness sensitivity. In this experiment, a simple multispectral imaging system is developed for multiple bio-interaction measurements. The measured results verify that the bulk refractive index changes can be removed and the surface biomolecular interactions can be directly obtained without the need of a reference channel.

In this study, a continuous cell-imaging system with subcellular resolution was developed by integrating a microfluidic platform with lattice lightsheet microscopy (LLSM). To reduce aberrations of the lightsheet propagating into the device, a microfluidic channel sealed with a water refractive index-matched thin film was fabricated. When the lightsheet emerged from the water-immersed objectives and penetrated through the water refractive-matched thin film into the microfluidic channel at an incident angle, less light scattering and fewer aberrations were found. Suspended cells flowed across the lattice lightsheet, and an imaging system with the image plane perpendicular to the lightsheet was used to sequentially acquire cell images. By applying a thinner lattice lightsheet, higher-resolution, higher-contrast images were obtained. Furthermore, three-dimensional cell images could be achieved by reconstructing sequential two-dimensional cell images.

We present a numerical and experimental study of resonance splitting in the transmission and reflection spectra of the Fabry–Perot resonator made of a bent section of a conventional single-mode optical fiber with metallized end faces. We show the splitting to be similar in nature to the well-known Autler–Townes effect and to arise from the strong coupling between the core mode and cladding whispering gallery mode of the bent fiber. The effect of all major parameters of the bent resonator on the splitting of its resonances is demonstrated. Potential applications of the observed effects in the field of precision optical refractometry as well as further research directions are discussed.

Background Refractometry is used to assess transfer of passive immunity (TPI), but studies evaluating different refractometers and appropriate thresholds for recommended target immunoglobulin G (IgG) concentrations for beef calves are limited. Objectives To evaluate test performance of digital (DSTP) and optical (OSTP) serum total protein (STP) refractometers and a digital Brix (DBRIX) refractometer for assessment of passive immunity in beef calves. Animals A total of 398 beef calves from 6 herds, 1 to 7 days of age. Methods Serum IgG concentration was estimated by DSTP, OSTP, and DBRIX, and measured by radial immunodiffusion (RID). Correlation coefficients (r) among results were calculated. Optimal STP and Brix thresholds for identification of IgG

Herein, we demonstrate a cavity-enhanced hyperspectral refractometric imaging using an all-dielectric photonic crystal slab (PhCS). Our approach takes advantage of the synergy between two mechanisms, surface-enhanced fluorescence (SEF) and refractometric sensing, both based on high-Q resonances in proximity of bound states in the continuum (BICs). The enhanced local optical field of the first resonance amplifies of 2 orders of magnitude the SEF emission of a probe dye. Simultaneously, hyperspectral refractometric sensing, based on Fano interference between second mode and fluorescence emission, is used for mapping the spatially variant refractive index produced by the specimen on the PhCS. The spectral matching between first resonance and input laser is modulated by the specimen local refractive index, and thanks to the calibrated dependence with the spectral shift of the Fano resonance, the cavity tuning is used to achieve an enhanced correlative refractometric map with a resolution of 10-5 RIU within femtoliter-scale sampling volumes. This is experimentally applied also on live prostate cancer cells grown on the PhCS, reconstructing enhanced surface refractive index images at the single-cell level. This dual mechanism of quasi-BIC spatially variant gain tracked by quasi-BIC refractometric sensing provides a correlative imaging platform that can find application in many fields for monitoring physical and biochemical processes, such as molecular interactions, chemical reactions, or surface cell analysis.

Monitoring the dynamic humidity requires sensors with fast response and anti-electromagnetic interference, especially for human respiration. Here, an ultrafast fiber-optic breath sensor based on the humidity-sensitive characteristics of gelatin film is proposed and experimentally demonstrated. The sensor consists of a microknot resonator superimposed on a Mach-Zehnder (MZ) interferometer produced by a tapered single-mode fiber, which has an ultrafast response (84 ms) and recovery time (29 ms) and a large dynamic transmission range. The humidity in dynamic ambient causes changes in the refractive index of gelatin coating, which could trigger spectral intensity transients that can be explicitly distinguished between the two states. The sensing principle is analyzed using the traditional transfer-matrix analysis method. The influence of coating thickness on the sensor's trigger threshold is further investigated. Experiments on monitoring breath patterns indicate that the proposed breath sensor has high repeatability, reliability, and validity, which enable many other potential applications such as food processing, health monitoring, and other biomedical applications.

The aim of this study is to determine the customized refractive index of ectatic corneas and also propose a method for determining the corneal and IOL power in these eyes. Seven eyes with moderate and severe corneal ectatic disorders, which had been under cataract surgery, were included. At least three months after cataract surgery, axial length, cornea, IOL thickness and the distance between IOL from cornea, and aberrometry were measured. All the measured points of the posterior and anterior parts of the cornea converted to points cloud and surface by using the MATLAB and Solidworks software. The implanted IOLs were designed by Zemax software. The ray tracing analysis was performed on the customized eye models, and the corneal refractive index was determined by minimizing the difference between the measured aberrations from the device and resulted aberrations from the simulation. Then, by the use of preoperative corneal images, corneal power was calculated by considering the anterior and posterior parts of the cornea and refractive index of 1.376 and the customized corneal refractive index in different regions and finally it was entered into the IOL power calculation formulas. The corneal power in the 4 mm region and the Barrett formula resulted the prediction error of six eyes within ± 1 diopter. It seems that using the total corneal power along with the Barrett formula can prevent postoperative hyperopic shift, especially in eyes with advanced ectatic disorders.

Background Brix refractometry can be used to assess colostral immunoglobulin G (IgG) concentration, but studies identifying Brix percentages to detect high‐ and low‐IgG colostrum are lacking for beef cows and interlaboratory agreement is unknown. Objectives Evaluate Brix refractometer performance and interlaboratory agreement for assessing beef cow colostrum IgG concentration, including determination of thresholds to identify colostrum containing IgG concentrations

Aluminum has recently attracted considerable interest as plasmonic material due to its unique optical properties, but most work has been limited to nanostructures. We report here novel SPR biosensing with aluminum thin-films using the standard Kretschmann configuration that has previously been dominated by gold films. Electron-beam physical vapor deposition (EBPVD)-prepared Al films oxidize in air to form a nanofilm of Al(2)O(3,) yielding robust stability for sensing applications in buffered solutions. FDTD simulations revealed a sharp plasmonic dip in the visible range that enables measurement of both angular shift and reflection intensity change at a fixed angle. Bulk and surface tests indicated that Al films exhibited superb sensitivity performance in both categories. Compared to Au, the Al/Al(2)O(3) layer showed a marked effect of suppressing non-specific binding from proteins in human serum. Further characterization indicated that Al film demonstrated a higher sensitivity and a wider working range than Au films when used for SPR imaging analysis. Combined with its economic and manufacturing benefits, the Al thin-film has the potential to become a highly advantageous plasmonic substrate to meet a wide range of biosensing needs in SPR configurations.

Plasmonic sensors are promising for ultrasensitive chemical and biological analysis. However, there are increasing experimental findings that cannot be well addressed by theoretical calculations, including the nonlinear dependence of the plasmonic peak wavelength on the refractive index (RI) and the ultrahigh sensitivity beyond the theoretical limit. The gap between experiments and theoretical calculations is that the bulk RI (BRI) used for calculation could be different from the interfacial RI (IRI) determining the electromagnetic response as a result of the interaction of molecules with the surface. But there is still no method to determine the IRI. Herein, we quantitatively determine the IRI by disentangling the surface RI (SRI) from the BRI. The obtained IRI can be directly applied in theoretical calculations to reliably reflect the experimental response and rigorously guide the design of plasmonic sensors. Moreover, it can be a fundamental dimensionless number to describe the light-matter interaction at the interface.

Digital holographic microscopy (DHM) is an important technique that may be used for quantitative phase imaging of unstained biological cell samples. Since the DHM technology is not commonly used in clinics or bioscience research labs, at present there is no well-accepted focusing criterion for unstained samples that users can follow while recording image plane digital holograms of cells. The usual sharpness metrics that are useful for auto-focusing of stained cells do not work well for unstained cells as there is no amplitude contrast. In this work, we report a practical method for estimating the best focus plane for unstained cells in the digital hologram domain. The method is based on an interesting observation that for the best focus plane the fringe pattern associated with individual unstained cells predominantly shows phase modulation effect in the form of bending of fringes and minimal amplitude modulation. This criterion when applied to unstained red blood cells shows that the central dip in the doughnut-like phase profile of cells is maximal in this plane. The proposed methodology is helpful for standardizing the usage of DHM technology across different users and application development efforts. LAY DESCRIPTION: Digital holographic microscopy (DHM) is slowly but steadily becoming an important microscopy modality and gaining acceptability for basic bio-science research as well as clinical usage. One of the important features of DHM is that it allows users to perform quantitative imaging of unstained transparent cells. Instead of using dyes or fluorescent labelling, DHM systems use quantitative phase as a contrast mechanism which depends on the natural refractive index variation within the cell samples. Since minimal wet lab processing is required in order to image cell samples with a DHM, cells can be imaged in their natural state. While DHM is gaining popularity among users, the imaging protocols across the labs or users need to be standardized in order to make sure that the same quantitative phase parameters are used for tasks such as quantitative phased based cell classification. One of the important operational tasks for any microscopy work is to focus the sample under study. While focusing comes naturally to users of brightfield microscopes based on image contrast, the focusing is not straightforward when samples are unstained so that they do not offer any amplitude contrast. When performing quantitative phase imaging, defocus can actually change the phase profile of the cell due to near-zone (Fresnel) diffraction effects. So unless a standardized focusing methodology is used, it will be difficult for multiple DHM users (potentially at different sites) to agree on quantitative results out of their phase images. DHM literature has prior works which perform numerical focusing of recovered complex wave-field in the hologram plane to find the best focus plane. However such methods are not user friendly and do not allow user the same focusing experience as in a brightfield microscope. The numerical focusing is therefore a reasonably good method for an optics researcher but not necessarily so for a microscopy technician looking at cell samples with a DHM system in a clinical setting. The present work provides a simple focusing criterion for unstained samples that works directly in the hologram domain. The technique is based on an interesting observation that the when an unstained cell sample is in the best-focus plane, its corresponding hologram (or fringe pattern) predominantly shows phase modulation manifested by bending of fringes at the location of the cell. This criterion can be converted into a simple numerical method as we have used to find the best-focus plane using a stack of through focus holograms. We believe that the technique can be used manually by visually observing the holograms or can be converted to an auto-focus algorithm for a motorized DHM system.

Background: Proper hydration is vital for both exercise and general health. Although various methods for hydration assessment exist, many are not valid for either use or never tested. Introduction:...

PURPOSE To compare refractive error measured by hand-held wavefront aberrometers with postcycloplegic autorefraction (AR) and cycloplegic refraction (CR). METHODS The medical records of patients who received refractive measurements using the wavefront aberrometer, postcycloplegic AR, and CR between January 2014 and January 2016 were retrospectively analyzed. The mean differences, 95% confidence intervals, and limits of agreement (LOA) were calculated for the refractive vector components (M, J₀, and J45 ). RESULTS Fifty-one patients (9.0 ± 5.5 years, male 41.2%) were enrolled in this study, and only the right eye of each was included. Refractive errors ranged from -9.25 to +7.25 diopters (D) for spherical equivalent (median, 0.75 D). The M component was not significantly different among the three methods (p = 0.080). However, the J₀ vector component was significantly different (p < 0.001). After post hoc analysis, the wavefront aberrometer obtained more positive values for J₀ compared to the other methods. The J45 component was not significantly different among the three methods (p = 0.143). The mean difference between the wavefront aberrometer and postcycloplegic AR was -0.115 D (LOA, -1.578 to 1.348 D) for M, 0.239 D (LOA, -0.371 to 0.850 D) for J₀, and -0.015 D (LOA, -0.768 to 0.738 D) for J45 . The mean difference between the wavefront aberrometer and CR was -0.220 D (LOA, -1.790 to 1.350 D) for M, 0.300 D (LOA, -0.526 to 1.127 D) for J₀, and -0.079 D (-0.662 to 0.504 D) for J45 . CONCLUSIONS The wavefront aberrometer showed good agreement with postcycloplegic AR and CR in spherical equivalents, but tended to produce slightly myopic results. The wavefront aberrometer also overestimated with-the-rule astigmatism. Therefore, we recommend that the device be used for estimations of refractive error, which may be useful for patients who have postural difficulties, live in undeveloped countries, or are bedridden.

We propose and experimentally demonstrate a highly flexible and applicable configuration, namely, the “ v ertical-fluid-array i nduced o ptic microfiber l ong per i od grati n g” (VIOLIN), for fully exploring the characteristics of liquids. The presence of flowing liquid in the periodically carved grooves of the designated substrate can activate a long-period grating resonance, as the microfiber is attached. Since the features of the resonance depend strongly on the refractive index of the fluid, the VIOLIN can be utilized as a refractometer with a high sensitivity of 2443 nm/RIU. Modeling and simulation are employed to investigate the mechanism of the sensor, which can be described as follows briefly: “Liquid renders the resonance to light. Light deciphers the secret of liquid.” Moreover, due to the highly elastic control of the fluidic array and the detachable configuration, multiple sensing and easy reconfiguration of the VIOLIN can be realized. The VIOLIN is expected to be highly suitable for microfiber-based chemo/biosensing applications.

A novel refractometer based on multimode fiber (MMF) embedded single mode-no core-single mode (ME-SNS) fiber structure is presented and investigated in detail. The ME-SNS structure has a higher refractive index (RI) sensitivity because of the stronger evanescent field generated by RI modulation. There is an obvious attenuation dip when 3 segment MMFs are embedded in single mode-no core-single mode (SNS) fiber structure. Total length of sensing unit is only 1.8 mm. Experimental results show that the maximal RI and the temperature sensitivity of the ME-SNS fiber structure are 567.158 nm/RIU and 0.009 nm/°C.

This letter reports a novel fused silica microfluidic device with pressure sensing capability that is fabricated by integrated additive and subtractive manufacturing (IASM) method. The sensor consists of a capillary and a 3D printed glass reservoir, where the reservoir volume change under pressure manifests liquid level deviation inside the capillary, thus realizing the conversion between small pressure change into large liquid level variation. Thanks to the design flexibility of this unique IASM method, the proposed microfluidic device is fabricated with liquid-in-glass thermometer configuration, where the reservoir is sealed following a novel 3D printing assisted glass bonding process. And liquid level is interrogated by a fiber-optic sensor based on multimode interference (MMI) effect. This proposed microfluidic device is attractive for chemical and biomedical sensing because it is flexible in design, and maintains good chemical and mechanical stability, and adjustable sensitivity and range.

Direct optical detection has proven to be a highly interesting tool in biomolecular interaction analysis to be used in drug discovery, ligand/receptor interactions, environmental analysis, clinical diagnostics, screening of large data volumes in immunology, cancer therapy, or personalized medicine. In this review, the fundamental optical principles and applications are reviewed. Devices are based on concepts such as refractometry, evanescent field, waveguides modes, reflectometry, resonance and/or interference. They are realized in ring resonators; prism couplers; surface plasmon resonance; resonant mirror; Bragg grating; grating couplers; photonic crystals, Mach-Zehnder, Young, Hartman interferometers; backscattering; ellipsometry; or reflectance interferometry. The physical theories of various optical principles have already been reviewed in detail elsewhere and are therefore only cited. This review provides an overall survey on the application of these methods in direct optical biosensing. The “historical” development of the main principles is given to understand the various, and sometimes only slightly modified variations published as “new” methods or the use of a new acronym and commercialization by different companies. Improvement of optics is only one way to increase the quality of biosensors. Additional essential aspects are the surface modification of transducers, immobilization strategies, selection of recognition elements, the influence of non-specific interaction, selectivity, and sensitivity. Furthermore, papers use for reporting minimal amounts of detectable analyte terms such as value of mass, moles, grams, or mol/L which are difficult to compare. Both these essential aspects (i.e., biochemistry and the presentation of LOD values) can be discussed only in brief (but references are provided) in order to prevent the paper from becoming too long. The review will concentrate on a comparison of the optical methods, their application, and the resulting bioanalytical quality.

Colorimetric sensing, which provides effective detection of bio-molecular signals with one’s naked eye, is an exceptionally promising sensing technique in that it enables convenient detection and simplification of entire sensing system. Though colorimetric sensors based on all-dielectric nanostructures have potential to exhibit distinct color variations enabling manageable detection due to their trivial intrinsic loss, there is crucial limitation that the sensitivity to environmental changes lags behind their plasmonic counterparts because of relatively small region of near field-analyte interaction of the dielectric Mie-type resonator. To overcome this challenge, we proposed all-dielectric metasurface colorimetric sensor which exhibits dual-resonance in the visible region. Thereafter, we confirmed with simulation that, in the elaborately designed dual-Lorentzian-type spectra, highly perceptible variations of structural color were manifested even in minute change of peripheral refractive index. In addition to verifying physical effectiveness of the superior colorimetric sensing performance appearing in the dual-resonance type sensor, by combining advanced optimization technique utilizing deep neural networks, we attempted to maximize sensing performance while obtaining dramatic improvement of design efficiency. Through well-trained deep neural network that accurately simulates the input target spectrum, we numerically verified that designed colorimetric sensor shows a remarkable sensing resolution distinguishable up to change of refractive index of 0.0086.

In this research work, an anisotropic photonic crystal fiber (PCF) biosensor working on a refractive index (RI) variation and based on surface plasmon resonance (SPR) is presented. Liquid analytes (LA) having a RI within the range of 1.340 to 1.380 RIU are investigated from the proposed biosensor. Spectroscopy analysis of LA having RI values of 1.340 RIU, 1.360 RIU, and 1.380 RIU is performed from the developed sensing setup for modeling an ultrasensitive biosensor. The numerical analysis of the sensing parameters for the proposed sensor presents a maximum wavelength sensitivity (WS) of 20000 nm/RIU for x- polarization (x − pol.) and 18000 nm/RIU for y- polarization (y − pol.), respectively, using the wavelength interrogation technique. Maximum amplitude sensitivity (AS) of 2158 RIU−1 and 3167 RIU−1 is obtained for x − pol. and y − pol., respectively, using the amplitude interrogation technique. Maximum sensor resolution (SR) of 5.00 × 10−6 RIU and 5.55 × 10−6 RIU is obtained for x − pol. and y − pol., respectively. The linear relationship of the resonant wavelength (RW) with the RI produces R2 = 0.9972 and R2 = 0.9978, corresponding to a degree (2) for x − pol. and y − pol., respectively. The figure of merit (FOM) for x − pol. and y − pol. are 93.45 RIU−1 and 105.88 RIU−1, respectively. The sensing parameters have obtained the maximum value for the LA having a RI value of 1.375 RIU.

Fourier ptychographic diffraction tomography (FPDT) is a recently developed label-free computational microscopy technique that retrieves high-resolution and large-field 3D tomograms by synthesizing a set of low-resolution intensity images obtained with a low numerical aperture (NA) objective. However, in order to ensure sufficient overlap of Ewald spheres in 3D Fourier space, conventional FPDT requires thousands of intensity measurements and consumes a significant amount of time for stable convergence of the iterative algorithm. Herein, we present accelerated Fourier ptychographic diffraction tomography (aFPDT), which combines sparse annular LED illuminations and multiplexing illumination to significantly decrease data amount and achieve computational acceleration of 3D RI tomography. Compared with existing FPDT technique, the equivalent high-resolution 3D RI results are obtained using aFPDT with reducing data requirement by more than 40 times. The validity of the proposed method is experimentally demonstrated on control samples and various biological cells, including polystyrene beads, unicellular algae, and clustered HeLa cells in a large field of view. With the capability for high-resolution and high-throughput 3D imaging using small amounts of data, aFPDT has the potential to further advance its widespread applications in biomedicine. This article is protected by copyright. All rights reserved.

Rainbow refractometry has been used in the past to measure size and refractive index of spherical particles, typically droplets in a spray. In the present study, conventional optical configurations for point measurements or line measurements have been extended to allow also the particle position in a plane to be determined, and hence, the designation planar rainbow refractometry. However, this extension introduces challenges in accurately calibrating the 2D scattering angles with the image coordinates. This challenge has been met using a novel calibration method, employing a monodispersed droplet stream traversed through the measurement plane. Experiments confirm achievable horizontal and vertical position accuracies of 0.42 mm and 0.36 mm, respectively, and a refractive index uncertainty of 2 × 10 − 4 .

In modern 3D microscopy, holding and orienting arbitrary biological objects with optical forces instead of using coverslips and gel cylinders is still a vision. Although optical trapping forces are strong enough and related photodamage is acceptable, the precise (re-) orientation of large specimen with multiple optical traps is difficult, since they grab blindly at the object and often slip off. Here, we present an approach to localize and track regions with increased refractive index using several holographic optical traps with a single camera in an off-focus position. We estimate the 3D grabbing positions around several trapping foci in parallel through analysis of the beam deformations, which are continuously measured by defocused camera images of cellular structures inside cell clusters. Although non-blind optical trapping is still a vision, this is an important step towards fully computer-controlled orientation and feature-optimized laser scanning of sub-mm sized biological specimen for future 3D light microscopy., Optical manipulation of large objects is challenging as optical trap positions are blindly chosen. Here, the authors present off-focus interferometric tracking, which localises optimal grabbing positions with increased refractive index, by analysing the beam deformations of several holographic optical traps.

The optical properties of biochemical compositions of microalgae are vital for the improvement of biosensor design, photobioreactor design, biofuel, and biophotonics techniques. A combination method using both the double optical pathlength transmission method (DOPTM) and the ellipsometry method (EM) is called DOPTM-EM, and it is used to acquire the optical constants of protein, lipid, and carbohydrate of Haematococcus pluvialis, Nannochloropsis sp., and Spirulina in both a solid state and a solution state within the visible and near-infrared spectral range. For different types of microalgae, the refractive indices of protein and carbohydrate in the solid state are similar to each other, but show an observed difference from lipid in the solid state. The refractive indices of protein and carbohydrate in the solution state presents a visible distinction in the researched spectral range. The absorption indices of protein, lipid, and carbohydrate in the solid state for these three types of microalgae are close to each other in the spectral range of 300–500 nm. However, an observed difference is shown in the spectral range of 500–1700 nm. For ease of application, the refractive index of biochemical composition of microalgae was fitted based on the Sellmeier equation. We believe this work can provide a reference to obtain the optical properties of biomaterial with high accuracy.

The SPR phenomenon results in an abrupt change in the optical phase such that one can measure the phase shift of the reflected light as a sensing parameter. Moreover, many studies have demonstrated that the phase changes more acutely than the intensity, leading to a higher sensitivity to the refractive index change. However, currently, the optical phase cannot be measured directly because of its high frequency; therefore, investigators usually have to use complicated techniques for the extraction of phase information. In this study, we propose a simple and effective strategy for measuring the SPR phase shift based on phase-shift interferometry. In this system, the polarization-dependent interference signals are recorded simultaneously by a pixelated polarization camera in a single snapshot. Subsequently, the phase information can be effortlessly acquired by a phase extraction algorithm. Experimentally, the proposed phase-sensitive SPR sensor was successfully applied for the detection of small molecules of glyphosate, which is the most frequently used herbicide worldwide. Additionally, the sensor exhibited a detection limit of 15 ng/mL (0.015 ppm). Regarding its simplicity and effectiveness, we believe that our phase-sensitive SPR system presents a prospective method for acquiring phase signals.

Developing technologies capable of constantly assessing and optimizing day-to-day activities has been a research priority for several years. A key factor in such technologies is the use of highly sensitive sensors to monitor in real-time numerous parameters, such as temperature and load. Due to their unique features, optical fiber sensors became one of the most interesting and viable solutions for applications dependent on those parameters. In this work, we present an optical fiber load sensor, called load cell, based on Fabry–Pérot hollow cavities embedded in a polymeric material. By using the load cells in a parallel configuration with a non-embedded hollow cavity, the optical Vernier effect was generated, allowing maximum sensitivity values of 0.433 nm N−1 and 0.66 nm °C−1 to be attained for vertical load and temperature, respectively. The proposed sensor’s performance, allied with the proposed configuration, makes it a viable and suitable device for a wide range of applications, namely those requiring high thermal and load sensitivities.