Fiber Optic Spectrometer Research Articles

A Portable Fiber Optic Real-time Smartphone-based Visible Spectrometer

A Portable Fiber Optic Real-time Smartphone-based Visible Spectrometer

Opalescence and Fluorescence of 46 Resin-Based Composites Exposed to Ultraviolet Light

Identifying the boundary between the tooth and the resin-based composite (RBC) is difficult when replacing restorations. Ultraviolet (UV) light has been reported to assist the viewer by causing the RBC to fluoresce. Using a laboratory-grade fiberoptic spectrometer, 46 RBCs were exposed to UV light from the Woodpecker O-Star curing light. The opalescence and fluorescence were measured relative to a human tooth that contained just dentin and a tooth that contained both enamel and dentin. After these quantitative measurements, 10 RBCs with large differences in light emittance were compared qualitatively to assess their brightness when exposed to UV light compared to the dentin specimen and the specimen containing both enamel and dentin. It was found that, when exposed to UV light, some of the RBCs were less bright compared to the two samples of teeth used for comparison, but most were brighter; some were up to six times brighter. The filler appears to affect the opalescence peaks, while the resin appears to affect the fluorescence peaks. It was concluded that because RBCs emit very different levels of opalescence and fluorescence, UV light from the Woodpecker O-Star cannot be relied upon to detect all brands of RBC on the tooth. The opalescence and fluorescence can also be used to detect changes in the formulation of the RBC.

Enhanced luminescence efficiency in GaN-based blue laser diodes by H plasma technology

To the best of our knowledge, this paper is the first to report the application of H plasma treatment technology to the treatment of laser diode ridge. Through the H plasma passivation on the ridge of the laser diode, a neutral complexes layer (i.e., Mg-H) is formed on the ridge, which effectively reduces ridge leakage current, thus reducing the threshold current of the laser diode and significantly improving the slope efficiency. The ridge were treated with H plasma using the Oxford Plasmalab System 100 ICP 180. The lasers' leakage current, optical power, emission wavelength, and other parameters were measured using a Cascade150 + B1505A probe station system, along with matched optical power meters and fiber optic spectrometers. Specifically, this study successfully fabricates a GaN-based blue laser diode characterized by a threshold current as low as 0.42 A and a slope efficiency as high as 1.96 W/A. Compared with the traditional silicon oxide-mediated ridge treated laser, the threshold current of the laser passivated by H plasma is reduced by 0.13 A, and the slope efficiency is increased by 0.56 W/A. This research not only enhances the performance of laser diodes but also has the potential to expand their application in multiple fields.

A custom-made integrated system for thermoluminescence and radioluminescence spectroscopy

Thermoluminescence (TL) and Radioluminescence (RL) are widely used in dosimetry applications. We present a custom-built integrated system, designated LUMI22, for measuring TL, TL spectroscopy, RL, and RL as a function of temperature. LUMI22 includes a heating system based on Kanthal® A1 alloy (FeCrAl), a microcontroller to regulate the temperature ramps (e.g. 1–5 °C/s). To irradiate samples an X-ray tube (Moxtek 50 kV, 50 μA) is powered, controlled, and monitored by an FTC-200 standard controller. The dose rate at the sample position is 0.43 Gy/min. Light collection includes a Photomultiplier Tube (PMT, Hamamatsu H10493-012:HA, 185–850 nm). Additionally, a miniature fiber optic spectrometer (Ocean Optics, QE65000, range 200–1100 nm) coupled with a 1000 μm diameter fiber optic (QP1000- 2-UV-VIS) was employed for TL and RL spectroscopy measurements. To assess the functionality of the system, it was used to measure TL and RL from Al2O3:C,Mg, Al2O3:C and TLD-100 phosphors which have been previously well investigated. The measured TL and RL data were well compared to the published ones, confirming the functionality of the system.

First spectroscopic study of HFRC plasma

An advanced spectral diagnostic system was developed to measure the electron temperature (T e), electron density (N e), and ion temperature (T i) of the Huazhong University of Science and Technology field-reversed configuration plasma. The system consists of an optic fiber spectrometer with a wide spectral band and a 670 mm focal length high throughout Czerny–Turner monochromator equipped with both a 3600 g mm−1 grating and a 2400 g mm−1 grating to measure the line spectrum. Accompanying these components is an electron-multiplying charge-coupled device camera to capture spectral data. The relative intensity of the optical fiber spectrometer was calibrated using a standard luminance source, and the wavelength calibration of the spectrometer was accomplished using a Hg/Ar lamp. This diagnostic setup was configured to measure electron density based on the Stark effect of Hγ (n = 5 → n = 2; 434.04 nm). Doppler broadening of an O III (2s22p(2P0)3p → 2s22p(2P0)3s; 375.988 nm) emission line was measured and analyzed to obtain the ion temperature, and electron temperatures were estimated from the relative strength of Hβ (n = 4 → n = 2; 486.14 nm) (Dβ) and Hγ (Dγ) spectral lines when the electron density was obtained from Stark effect measurements. The initial experimental results indicate that the highest electron temperature of the formation region was approximately 8 eV, the electron density of the colliding-and-merging region was approaching 1020 m−3, and the ion temperature reached about 40 eV.

Relationship among intramuscular fat, crude protein, and moisture in porcine longissimus thoracis muscle and their prediction by a handheld fiber-optic near-infrared spectrometer

The handheld fiber-optic near-infrared (NIR) spectrometer with special probe, which is widely used for Wagyu beef carcass in all Japan, was determined to predict the chemical composition in pork. Since intramuscular fat (IMF) is related to eating quality and the relationships among chemical compositions were examined. The intact longissimus dorsi muscles collected from meat markets in Japan (N = 914) were scanned at three sites in the same cut, and analyzed chemically. The data were used for calibration (N = 553 out of 605), prediction (N = 300) and repeatability (N = 9). One-point increase in IMF resulted in linear decreases in moisture and crude protein at approximate rate of 0.7- and 0.3- points, respectively (N = 905). The spectrometer had high repeatability, and the optical values had interaction between the individual pork and the measurement site. The coefficients of determination in the prediction were 0.81, 0.91 and 0.66 for moisture, IMF and crude protein, respectively. The agreements between chemical and optical methods was strong for IMF (intraclass correlation coefficients 0.92) and moisture (0.81), and moderate for crude protein (0.64). These results showed that the handheld fiber-optic NIR spectrometer can quickly evaluate chemical composition for intact pork.

Superparamagnetic photonic crystals with DNA probes for rapid visual detection of mercury

A novel superparamagnetic photonic crystal DNA probe (Fe3O4@SiO2@amino@DNA SPC) was developed to enable rapid visual detection of Hg2+. This unique photonic crystal (PC) was synthesized by combining superparamagnetic nanospheres with DNA probes. The DNA probe, rich in thymine (T), detects mercury ions through base mismatch, resulting in the formation of T–Hg2+–T loop hairpin structures. With the binding of Hg2+ to the probe attached to superparamagnetic nanospheres, the PC structure assembled by these nanospheres, formed by the magnetic field, was changed. This change enhanced the reflection intensity; it could be quantified using a fiber optic spectrometer and was visible to the naked eye. The Fe3O4@SiO2@amino@DNA SPC, specific to Hg2+, exhibited a reflection peak at 679 nm, which intensified with increasing Hg2+ concentration. The reflection intensity increased by 132.58 a.u., and the PC color shifted from red to yellow as the Hg2+ concentration increased from 0.1 μg/L to 1 mg/L.

Compact Numerical Aperture 0.5 Fiber Optic Spectrometer Design Using Active Image Plane Tilt.

The numerical aperture of the spectrometer is crucial for weak signal detection. The transmission lens-based configuration has more optimization variations, and the grating can work approximately in the Littrow condition; thus, it is easier to acquire high numerical aperture (NA). However, designing a large aperture focusing lens remains challenging, and thus, ultra-high NA spectrometers are still difficult to acquire. In this paper, we propose a method of setting image plane tilt ahead directly when designing the large aperture focusing lens to simplify the high NA spectrometer design. By analyzing the accurate demands of the focusing lens, it can be concluded that a focusing lens with image plane tilt has much weaker demand for achromatism, and other monochromatic aberration can also be reduced, which is helpful to increase the NA. An NA0.5 fiber optic spectrometer design is given to demonstrate the proposed method. The design results show that the NA can achieve 0.5 using four lenses of two materials, and the MTF is higher than 0.5 when the spectral dispersion length is 12.5 mm and the pixel size is 25 μm, and thus, the spectral resolution can achieve 6.5 nm when the spectral sampling ratio is 2:1. The proposed method can provide reference for applications when appropriate materials are limited and high sensitivity is necessary.

Feasibility study of one-dimensional imaging with an optical fiber for radiation dose-rate monitoring system in the decommissioning process

Real-time dose-rate monitoring system under the high dose-rate situation is required for the decommissioning of Fukushima Daiichi Nuclear Plants to remove the debris remaining inside the plants. We have proposed a dose-rate monitor consisting of a scintillator, over 100-m long optical fiber and CCD spectrometer. Some noises with a dominant emission wavelength of below 550 nm originating from the optical fiber itself must be separated from the signal from the scintillator, and the signal region has been defined as 650–1000 nm to use significant data, up to now. In this paper, we investigated if the noise region defined as below 550 nm can be supporting data for the monitoring system, because such noises are expected to include position information through the fiber. In the emission spectrum, the intensities of the noise emission or absorption band are expected to depend on the position of the fiber, and we demonstrated such dependence, “one-dimensional dose-rate distribution”, with 20 m-long optical fiber and CCD spectrometer. Optical fiber was placed around a 60Co source with an activity of approximately 60 TBq, and emission spectra of the fiber were acquired with different dose-rate conditions from 10 to 700 Gy/h. The noise intensities were well fitted with the power function as a function of the product of fiber length and dose rate, and we found that fiber noise has rate information in one-dimensional imaging.

Research on ionization characteristics of atmospheric pressure pulse-modulated microwave He/air plasma jet

The atmospheric pressure pulsed microwave He plasma jet has the advantages of high electron density and abundant active particles, but its shrinking on the discharge electrode morphology limits its application range. In order to modulate a He plasma jet with a longer plume and study its ionization development characteristics, we constructed a dual-channel pulsed microwave coaxial discharge device. He and air were, respectively, injected into the inner and outer gas channels of the resonator to generate a double-layer atmospheric pressure microwave plasma jet with a longer plume. It is observed that the bifurcation of the stratified plasma jet will occur by changing the gas flow. The ionization development of plasma jet was observed by using enhanced charge-coupled device and microwave Rayleigh scattering apparatus measured the space-time evolution of plasma and observed the three times ionization enhancement process of plasma jet development. The spectral lines of the active products associated with Penning ionization were observed by using a fiber optic spectrometer. A fluid model was constructed to simulate and analyze that under the condition of sufficient He flow rate (He flow rate is above 0.6 slm), there will be sufficient and stable He mole fraction (64%) at the stratification of the plasma jet. The experimental and simulation results show that the jet profile of the microwave He plasma is related to the inlet structure of the discharger and He flow rate. Stratified intake structure can produce stratified He plasma jet, and the unique appearance of bifurcation of jet can be produced by changing the flow rate of He. In the bifurcation process of the plasma jet, the product of Penning ionization inhibits the development of the main branch of the plasma jet, and the secondary electron avalanche of the local electric field promotes the formation of the branch of the plasma jet and is accompanied by the enhancement of the second ionization. The ionization mechanism of microwave He plasma is the resonance excitation of local enhanced electric field, the advance of ionizing waves, and the interaction between the spatially distributed active particles.

Relationship of single crystal growth and luminescence properties of Cr-doped gadolinium gallium garnet crystals for radiation dose-rate monitoring systems

For the decommissioning of Fukushima Daiichi Nuclear Plants, a novel real-time dose-rate monitor consisting of a scintillator, 100-m long optical fiber and CCD spectrometer has been proposed, and this scintillation material is required to have an emission wavelength of longer than approximately 650 nm. In this paper, as a candidate material for the system, we focused on Ce/Cr co-doped Gd3Ga5O12 (Ce/Cr:GGG) single crystals grown by the micro-pulling down method. Since the light output of this material was expected to depend on the Cr3+ concentration, we investigated the relationship between Cr segregation and luminescence properties in Ce/Cr:GGG crystal. Generally, a single photon counting method is not available to evaluate its light output accurately due to the long decay time, we used a novel technique “emission-intensity two-dimensional- mapping method” (2D-image method) to verify the light intensity at each point of the sample. This method realized estimation of the light intensity within the sample, though segregation of Cr3+ is observed. The results showed that Cr was concentrated in the center part along the radial direction in the grown crystals, while all parts had an emission wavelength of approximately 730 nm excited by X-ray. Using the 2D-image method, emission intensity was found to correspond to the Cr concentration, and its correlation coefficients between emission intensity and Cr concentration were over 0.8. We found that our material is available for the monitoring system when the Cr dense part of the crystal is cut and used.

Chemical sensor thin film-based carbon quantum dots (CQDs) for the detection of heavy metal count in various water matrices.

Rising pollution of heavy metals is one of the greatest concerns, especially in water resources globally and has led to significant adverse effects to human health. To uplift the status of human health, detection of heavy metals is of key importance. This study establishes the ability of carbon quantum dot (CQD)-based thin films for the detection of total heavy metal counts based on a fluorescence-based mechanism in various water resources using a fiber optic spectrometer (FOS) device. CQDs and CQD thin films were characterized using various techniques, such as X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), X-ray diffraction (XRD), and confocal laser scanning microscopy (CLSM), and the sensing capability was evaluated for the detection of heavy metals using an optical fiber system. The analytical parameters of the CQD-based thin film were compared with the estimation carried out using a micro plasma-atomic emission spectroscopy (MP-AES) method. The sensing performances of CQD thin films indicate that they are able to detect five heavy metals individually (lead, nickel, manganese, cobalt and chromium) in combination with a response time of 1 minute. The CQD thin films were able to detect heavy metals with a detection limit of 0.006-0.019 ppm for the analyzed heavy metals with a linear range of estimation analyzed as 0-100 μM. The accuracy of the estimation of all five heavy metals when spiked in various real water samples lies in the range of 100-103%. The result of the study clearly indicates that CQD thin films associated with a fiber optic device have the potential to play a role in point-of-care devices for total heavy metal count detection in complex matrices of water.

Autofluorescence spectroscopy in photodynamic therapy for skin rejuvenation: A theranostic approach in aesthetic medicine

BackgroundThe method of photodynamic therapy for skin rejuvenation (PDT-SR) provides an improvement in appearance with a safe and painless effect. The quality of treatment is most often assessed subjectively. The most informative morphological control methods are rarely used due to the invasiveness of the sampling procedure. AimThis study aimed to find out the possibility of using skin autofluorescence spectroscopy (SAF) for an objective assessment of changes occurring in the skin during PDT-SR. MethodsThis study included 12 volunteers (10 women, 2 men) aged 32 to 79 years. Two (n = 6) or three (n = 6) PDT sessions were performed at intervals of 13–30 days. Photosensitizer chlorin e6, exposure 20 min, energy density 18–24 J/cm2 were used. SAF spectra were recorded using a two-wavelength fiber optic spectrometer under excitation at wavelengths (λex) of 365 nm and 440 nm. Measurements were made both before and after each PDT session and up to 25–238 days from the start of treatment. For the evaluation, we used the spectra AF365(λ) and AF440(λ) averaged over 40 points corrected for diffuse reflection at λex=440 nm in the range λem= 460–700 nm, as well as the spectra of the ratios AFN365(λ) and AFN440(λ), which were obtained by dividing the intensities of the current spectra by the intensities collected before PDT-SR. ResultsPDT-SR led to changes in both the intensity and shape of the spectra. Analysis of the spectra using numerical fitting of the spectra showed that the main changes can be explained by changes in the content of advanced glycation end products (AGEs), as well as lipofuscin-like lipopigments (LPs) and porphyrins (PPs). The spectra of AGEs upon excitation at wavelengths of 365 and 440 nm differ, which may be due to the formation of two types of bonds, with collagen and elastin. By the end of the study, the vast majority of the examined volunteers showed a significant decrease of the parameters characterizing both of these types of AGEs, AGE365 (0.56–1.2) and AGE440 (0.58–1.01), relative to the beginning of the study. In most cases, a decrease was also noted for LPs and PPs. AGE365 and AGE440 were positively correlated with the age of the volunteers (r2 = 0.26–0.46 %). A steady decrease in the content of AGEs occurred approximately on the 40th day. ConclusionSAF spectroscopy makes it possible to assess changes in the content of AGEs, LPs, and PPs in the skin during PDT-SR. The method has great potential for non-invasive monitoring of the treatment process, as well as its improvement, including through its personalization. In addition, the method can be used to study the mechanisms of age-related skin changes at the molecular level and to study the processes of rejuvenation.

Recombinant Organophosphorus acid anhydrolase (OPAA) enzyme-carbon quantum dot (CQDs)-immobilized thin film biosensors for the specific detection of Ethyl Paraoxon and Methyl Parathion in water resources

Organophosphates pesticide (OP) toxicity through water resources is a large concern globally among all the emerging pollutants. Detection of OPs is a challenge which needs to be addressed considering the hazardous effects on the health of human beings. In the current research thin film biosensors of recombinant, Organophosphorus acid anhydrolase (OPAA) enzyme along with carbon quantum dots (CQDs) immobilized in thin films were developed. OPAA-CQDs thin film biosensors were used for the specific detection of two OPs Ethyl Paraoxon (EP) and Methyl Parathion (MP) in river water and household water supply. Recombinant OPAA enzyme was expressed in E. Coli, purified and immobilized on the CQD containing chitosan thin films. The CQDs used for this purpose were developed by a one-pot hydrothermal method from phthalic acid and Tri ethylene diamine. The properties of CQDs, OPAA and thin films were characterized using techniques like XPS, TEM, XRD, enzyme activity and CLSM measurements. Biosensing studies of EP and MP were performed by taking fluorescence measurements using a fiber optic spectrometer. The analytical parameters of biosensing were compared against an estimation carried out using the HPLC method. The biosensing performance indicates that the OPAA-CQDs thin film-based biosensors were able to detect both EP and MP in a range of 0–100 μM having a detection limit of 0.18 ppm/0.69 ppm for EP/MP, respectively with a response time of 5 min. The accuracy of estimation of EP/MP when spiked in water resources lie in the range of ∼100–102% which clearly indicates the OPAA-CQD based thin film biosensors can function as a point-of-use method for the detection of OP pesticides in complex water resources.

Accurate color characterization of solar photovoltaic modules for building integration

Accurate and reproducible color characterization is essential for colored building integrated photovoltaic products, both for manufacturing quality control and assessing long-term color stability. However, existing characterization techniques struggle to accurately determine color when a surface is behind a transparent layer like a solar PV laminate. In this study, we compare different colorimetric techniques and propose an innovative colorimeter based on a fiber optic spectrometer and large area illumination to address this issue. Samples with varying transparent glass thicknesses and underlying colors are laminated and characterized using a scanner, an integrated sphere spectrometer, a commercial portable colorimeter, and the proposed large area illumination colorimeter. Results show that common scanners produce darker images and inaccurate color determination due to light losses in the glass. As glass thickness increases, reflectance decreases with the integrated sphere spectrometer and portable colorimeter. However, the large area illumination colorimeter exhibits only minimal signal reduction. High reflective foils experience more reflectance reduction with thicker glass than low reflective ones. All devices yield comparable results without the glass layer. The large area illumination colorimeter, compensating for light losses, proves to be a suitable solution for accurately measuring color under glass laminates using reflected light. For example, it reduces the color change from 57 (commercial portable colorimeter) to only 3 for an ivory colored glass laminate. This innovative tool has the potential to improve color characterization in building integrated photovoltaic products, enabling better manufacturing quality control and assessment of long-term color stability.

A novel sulfhydryl-modified superparamagnetic photonic crystal sensing material for the simultaneous heavy metal ions detection and adsorption treatment

A novel superparamagnetic photonic crystal (Fe3O4@SiO2@Sulfhydryl SPC) was successfully created for simultaneous visual detection and absorption of harmful heavy metal ions. This SPC was made by combining photonic crystal and superparamagnetic nanosphere technologies. During detection, Fe3O4@SiO2@Sulfhydryl nanospheres can move in the liquid sample and fully absorb the target substances. The detection range is from 1 μg/L to 5 mg/L, which corresponds to the critical concentration range for heavy metal ions in drinking water and sewage. The detection limit is 1 μg/L. In the detection process, the signal responded rapidly and remained stable when analyzed with a fiber optic spectrometer. Notably, the signal intensity decreased significantly, with a reduction of 62.22 a.u. for Hg2+ and 124.31 a.u. for Ag+. Simultaneously, the visual results were striking. The SPC changed color from orange (PC structural color) to the original reddish-brown color of the solution with the formation of magnetic aggregates (PC structural color disappeared). This SPC exhibits excellent sensitivity, offers a clear visual display, possesses strong absorption detection capabilities, is easy to use, cost-effective, and, importantly, does not cause secondary pollution. Furthermore, the harmful heavy metal ions absorbed by the SPC can be easily removed from the water sample using an external magnetic field, overcoming challenges related to efficient separation of the adsorbent material from wastewater. As a result, this SPC holds great promise for real-time visual monitoring and practical sewage purification processes.

Label-free Raman microspectroscopic imaging with chemometrics for cellular investigation of apple ring rot and nondestructive early recognition using near-infrared reflection spectroscopy with machine learning

Apple ring rot caused by Botryosphaeria dothidea can cause fruit decay during the growth and storage stages of apple fruit. Understanding the infection process and cellular defense response at the cellular micro-level holds immense importance in the field of prevention and control. Consequently, there is a pressing need to develop suitable chemical imaging analysis methods. Here we proposed a label-free, high-throughput imaging method for cellular investigation of apple fruit ring rot infected by Botryosphaeria dothidea, based on confocal Raman microspectroscopic imaging technology combined with multivariate curve resolution-alternating least squares algorithm (MCR-ALS). We conducted Raman measurements on every apple fruit and obtain an image cube. This cube was then unfolded into an augmented matrix in a column-wise manner. We proceeded with simultaneous MCR-ALS analysis, resolving the single-substance spectrum and concentration profile from the mixed signals. Lastly, the accurate and pure molecular imaging of low methoxyl pectin, high methoxyl pectin, cellulose, lignin, and phenols were realized by refolding the resolved concentration data to construct the composition image. Thereafter, we realized the study of the spatial-temporal changes distribution of the above substances in the cuticle and cell wall of green and red apples at different stages of infection. The imaging method proposed in this paper is expected to provide a chemical imaging strategy for studying pathogen infection process and fruit defense response at the cellular level. In addition, by utilizing a fiber-optic probe near-infrared reflection spectrometer in conjunction with machine learning, we developed a rapid and non-destructive classification method. This method allows for the timely identification of apples exhibiting early infection by Botryosphaeria dothidea. Notably, both principal component analysis-quadratic discriminant analysis and support vector machine achieved a classification accuracy of 100%.

Adaptive iterative optimization method for spectral calibration based on deep learning

The miniature fiber optic spectrometer is smaller, cheaper and has a wide range of applications. However, the measurement error is larger. In order to solve this problem, the adaptive iterative optimization method for spectral calibration is proposed. In this study, a trinity neural network model is built based on spectral wavelength segmentation to improve the calibration degree. Based on the ‘pseudo-label’, a self-optimization method for spectral calibration is proposed to reduce the amount of data required. This study optimizes the measurement accuracy without changing the structure of the spectrometer. And the self-optimization of calibration model in practical application is realized. After experiment, the calibration degree of the calibration model can reach 75.72%. After a self-optimization, it can be increased to 87.45%. The calibration time of 401 spectral values (380 nm–780 nm) is less than 0.01 s. The results show that the operator can use this method to calibrate spectral data without having optical knowledge. This method has low cost, high calibration speed, good reliability and application value.

High-resolution compact spectrometer based on periodic tapered coreless fiber.

This Letter proposes a method that balances miniaturization and high performance of fiber optic speckle spectrometers. The periodically tapered coreless fiber is used as the scattering element to excite more higher-order modes in the coreless fiber. As a result, a remarkable spectral resolution of 0.03 nm in the near-infrared spectrum can be achieved with a 5-cm-long fiber. Narrow linewidth and broadband spectra in the wavelength of 1540-1560 nm are reconstructed separately, demonstrating the excellent performance of the designed all-fiber spectrometer. The spectral resolution of our proposed spectrometer is comparable to that of a 2-m multimode fiber spectrometer and has a significant improvement in miniaturization.

Passive Solid Chemosensor as Saliva Point of Need Analysis for Ammonium Determination by Using a Smartphone

Point-of-need analysis is of great interest nowadays. It refers to the timely analysis or detection of a specific parameter or substance at the location or moment it is needed, often with the aim of providing rapid and on-site results for informed decision-making or immediate interventions. This approach has gained interest in various fields but has not been extensively explored in bioanalytical chemistry. In order to contribute in this way, the analysis of ammonium in saliva as a biological fluid is proposed here. For that purpose, a passive solid sensor of 1,2-naphthoquinone-4-sulfonic acid sodium salt (NQS) embedded in polydimethylsiloxane (PDMS) doped with silica nanoparticles and an ionic liquid was proposed. The assay was developed by delivering ammonia from saliva in a confined atmosphere containing the sensor for 20 to 45 min. Measurements were carried out by absorbance from a benchtop diffuse reflectance spectrophotometer and a fiber optic miniaturized portable spectrometer coupled to a smartphone for point-of-need analysis. Another option for this kind of analysis was the use of the color intensity from digitalized images obtained by a smartphone by isolating the intensity in the color planes R (red), G (green), and B (blue). Good figures of merit were obtained for all three types of instruments, bearing in mind the ammonium content in saliva. Results for 30 samples of male and female volunteers (n = 30) demonstrated the usefulness of the assay, values of mg NH4+/mL saliva between 0.02 and 0.27 were found, and no matrix effect was present. Recoveries for spiked samples were around 100% for all methodologies. Selectivity was demonstrated from spectra obtained from benchtop instruments and the fiber optic mini spectrometer. Two applications were applied for directly determining the ammonium concentration in saliva.