scholarly journals Development of paper-based microfluidic strips for quantification of ammonia

2019 ◽  
Author(s):  
◽  
Nonhlazeko Loveday Nxumalo
Keyword(s):  
Spectrophotometric Method ◽  
Limit Of Detection ◽  
Low Cost ◽  
Yellow Colour ◽  
Chromatographic Paper ◽  
Hydrophobic Paper ◽  
Nessler Reagent ◽  
Ammonia Sensors ◽  
Wastewater Samples ◽  
Sizing Agents

Water is one of the most valuable and crucial of life and therefore accurate monitoring and assessment of water resources for sustainability is imperative. Conventional water investigation includes manual gathering of tests, their transportation and resulting examination in the research center. This is time and labour-intensive, costly and requires exceptionally qualified personnel. Sovereign of this procedure empowers more continuous examination, sparing time and cash for analysts, ventures and administering bodies. Consequently, there is requirement for advancement of minimal effort ecological microfluidic paper-based expository gadget that is fundamental for compelling administration of our profitable water assets. This will address the huge and growing demand for low-cost ammonia sensors as legislation becomes more stringent and as more frequent monitoring becomes essential for legislative compliance. Subsequently, this thesis reports on the development of a low-cost, colorimetric, wax- printed microfluidic paper-based analytical device (µPAD) to detect ammonia in industrial wastewaters. Microfluidic innovation was utilized to facilitate the examination of analytes on the colorimetric explanatory techniques onto a convenient detecting gadget. This therefore empowers the blending of little volumes of analytes with synthetic reagents to form a coloured/hued product in the sight of the analyte of interest. The µPAD fabricated was an oval shaped pattern which was designed on Corel draw software. The hydrophilic segments were made by printing a chromatographic paper with hydrophobic paper sizing agents utilizing a standard Xerox wax printer (Xerox colorqube 8570). The quantification of ammonia in wastewater was performed on the µPADs using two typical colorimetric methods namely, Nessler reagent and Salicylate. The reaction of ammonia with the Nessler reagent resulted in a brown or intense yellow colour whereas with the salicylate method, the final colour was green. For both methods, the colour intensity increased proportionally with the analyte concentration, and all images of the μPADs were captured and colorimetrically analyzed with ImageJ software for quantification. The analytical performances of the µPAD were linear from 0 to 5 mg L-1 with a limit of detection of 3.37 mg L-1 and 3.20 mg L-1 for the Nessler vii reagent and salicylate methods respectively. The validity and accuracy of aforementioned methods was supported by the standard UV Visible spectrophotometric method and applied to the measurement of wastewater effluent samples. Wastewater samples were analyzed and the results obtained were similar to those obtained with a spectrophotometric method, demonstrating that the µPAD is suitable to determine ammonia in wastewater.

scholarly journals Development of a paper-based microfluidic device for the quantification of ammonia in industrial wastewater

Water SA ◽  
2020 ◽  
Vol 46 (3 July) ◽  
Author(s):  
Nonhlazeko Loveday Nxumalo ◽  
Lawrence Mzukisi Madikizela ◽  
Hendrik Gert Kruger ◽  
Stanley Chibuzor Onwubu ◽  
Phumlane Selby Mdluli
Keyword(s):  
Surface Water ◽  
Industrial Wastewater ◽  
Wastewater Treatment Plants ◽  
Limit Of Detection ◽  
Low Cost ◽  
Colorimetric Method ◽  
Chromatographic Paper ◽  
Run Off ◽  
Toxic Pollutant ◽  
Nessler Reagent

Ammonia is a toxic pollutant increasingly found in urban and industrial wastewater and unprotected surface water. Industry discharges and fertilizer run-off release ammonia into sewers and streams, overloading wastewater treatment plants and causing fish deaths in surface water such as rivers, sea and lakes. The purpose of this study was to develop and evaluate the effectiveness of the microfluidic paper-based device (µPAD) for the quantification of ammonia in wastewater. The µPAD fabricated had an oval-shaped pattern which was designed using CorelDraw software. The hydrophilic zones were created by printing a chromatographic paper with a Xerox wax printer (Xerox colorqube 8570). The modified version of the colorimetric method using Nessler reagent was combined with microfluidic technologies to create a low-cost monitoring system for detection of ammonia in wastewater. The method allows for ammonia determination in the range of 0–5 ppm (mg/L) with a limit of detection of 3.34 ppm. This study indicated that a µPAD was successfully used to quantify the concentration of ammonia in wastewater.

UV-Visible Spectrophotometric Determination of Lambda-Cyhalothrin Insecticide in Vegetables, Soil and Water Samples

2019 ◽  
Vol 31 (1) ◽  
pp. 1-9
Author(s):  
Deepak Kumar Sahu ◽  
Joyce Rai ◽  
Chhaya Bhatt ◽  
Manish K. Rai ◽  
Jyoti Goswami ◽  
...  
Keyword(s):  
Crop Production ◽  
Limit Of Detection ◽  
Low Cost ◽  
Molar Absorptivity ◽  
Agricultural Field ◽  
Limit Of Quantification ◽  
Yellow Colour ◽  
Modern Age ◽  
Lambda Cyhalothrin

In modern age pesticide is used widely in agriculture. Lambda-cyhalothrin (LCT) is one of the most used pesticides which are used as a insecticide to kill pest, tricks, flies etc in agricultural field and it is also used for crop production. We have developed new method to detect LCT insecticide in agriculture field and reduce its uses. In this method we found the maximum absorbance at 460 nm for yellow colour dye. We also calculated limit of detection and limit of quantification 0.001 mg kg-1 and 0.056 mg kg-1 respectively. Molar absorptivity and Sandell’s sensitivity was also calculated and obtained 1.782 ×107 mol-1 cm-1 and 9.996 ×10-6 µg cm-2 respectively. The obtained yellow colour dye obeyed Beer’s law limit range of 0.5 µg ml -1 to 16 µg ml-1 in 25 ml. This method is less time consuming, selective, simple, sensitive and low cost. Present method is successfully applied in various soil, water and vegetable samples.

Development of Rapid Colorimetric Assay for Detection of Gluconic Acid Using Iron(Ⅱ) and Indigo Carmine

2020 ◽  
Vol 42 (4) ◽  
pp. 525-525
Author(s):  
Yifeng Lan Yifeng Lan ◽  
Lixiang Zuo Lixiang Zuo ◽  
Yangyang Zhou Yangyang Zhou ◽  
Yanli Wei and Chuan Dong Yanli Wei and Chuan Dong
Keyword(s):  
Spectrophotometric Method ◽  
Gluconic Acid ◽  
Limit Of Detection ◽  
Colorimetric Assay ◽  
Low Cost ◽  
Indigo Carmine ◽  
Colorimetric Method ◽  
Food Samples ◽  
Reducing Agent ◽  
Acid Complex

In this work, a simple and rapid spectrophotometric method, which is based on the fact that Iron(Ⅱ) -gluconic acid complex as a kind of reducing agent deterioration of indigo carmine dyes, was developed to detect gluconic acid in food. Under the optimal experimental condition, a linear range of 3.6 M to 900 M was obtained for gluconic acid with a limit of detection of 1.1 μM. The colorimetric method was rapid and robust with a low cost and can be applied to gluconic acid detection in food samples.

scholarly journals Determination of ?iroctone Olamine (Octopirox) in Bulk by UV Spectrophotometric Method

2017 ◽  
Vol 16 (1) ◽  
pp. 37-42
Author(s):  
Lyudmyla M Antypenko ◽  
Vitaliy A Solodovnyk
Keyword(s):  
Spectrophotometric Method ◽  
Limit Of Detection ◽  
Low Cost ◽  
Limit Of Quantification

A simple and low-cost UV-spectrophotometric method has been developed and validated for the quantification of Octopirox in bulk. The linearity was found at 307 ± 1 nm in 10-50 ?g/ml solution of ethanol-water (1:3, v:v) with r2 = 0.99. The limit of detection was found to be 1.18 µg/ml, while the limit of quantification was 3.58 µg/ml. The method was validated for linearity, accuracy, precision, range, ruggedness and robustness.Dhaka Univ. J. Pharm. Sci. 16(1): 37-42, 2017 (June)

scholarly journals A Sensitive UV Spectrophotometric Method for the Determination of Gabapentin

2009 ◽  
Vol 6 (s1) ◽  
pp. S163-S170 ◽  
Author(s):  
R. Singh Gujral ◽  
S. Manirul Haque ◽  
P. Shanker
Keyword(s):  
Spectrophotometric Method ◽  
Good Accuracy ◽  
Limit Of Detection ◽  
Low Cost ◽  
Pharmaceutical Formulations ◽  
Accuracy And Precision ◽  
Ich Guidelines ◽  
Limit Of Quantitation ◽  
Precision Limit

An accurate and validated spectrophotometric method was developed for the determination of gabapentin. This is simple, sensitive and low cost UV spectrophotometric method. The method is based on the direct measurement of the native absorbance of the drug. The detection was done at 210 nm. The method was linear in the range of 0.25 - 3.5 µ g/mL with correlation coefficient of 0.9999. It is validated according to the ICH guidelines with respect to linearity, selectivity, accuracy and precision, limit of quantitation and limit of detection. The method has been applied to assess gabapentin in pharmaceutical formulations with good accuracy and precision and relatively free of interference from coexisting substances.

scholarly journals Total polyphenols from Syzygium cumini (L.) Skeels fruit extract

2009 ◽  
Vol 45 (1) ◽  
pp. 121-126 ◽  
Author(s):  
Ketylin Fernanda Migliato ◽  
Elisângela Simões de Carvalho ◽  
Luis Vitor Silva do Sacramento ◽  
João Carlos Palazzo de Mello ◽  
André Rolim Baby ◽  
...  
Keyword(s):  
Statistical Analysis ◽  
Spectrophotometric Method ◽  
Limit Of Detection ◽  
Low Cost ◽  
Syzygium Cumini ◽  
Fruit Extract ◽  
Total Polyphenols ◽  
Limit Of Quantification ◽  
Pyrogallic Acid

A precise, accurate and low cost spectrophotometric method was developed and validated for routine determination of total polyphenols, as pyrogallic acid equivalents, from the percolated and lyophilized extract of Syzygium cumini (L.) Skeels fruits. Validation was assessed experimentally and data were rigorously treated by statistical analysis. Analytical parameters were: linearity, interval (range), precision and recovery/accuracy, limit of detection (LOD, μg mL-1) and limit of quantification (LOQ, μg mL-1). The visible spectrophotometric method presented linearity (r² = 0.9979 ± 0.0010) over the concentration range 0.25-7.5 μg mL-1 of standard pyrogallic acid, precision < 2.918171%, recovery/accuracy ranging from 96.228693 to 107.17701%, LOD = 0.21 μg mL-1 and LOQ = 0.64 μg mL-1.

scholarly journals A rapid, accurate, scalable, and portable testing system for COVID-19 diagnosis

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Guanhua Xun ◽  
Stephan Thomas Lane ◽  
Vassily Andrew Petrov ◽  
Brandon Elliott Pepa ◽  
Huimin Zhao
Keyword(s):  
Limit Of Detection ◽  
Low Cost ◽  
High Volume ◽  
N Gene ◽  
Testing System ◽  
Target Sequence ◽  
One Pot ◽  
Sequence Detection ◽  
Highly Sensitive ◽  
Speed Accuracy

AbstractThe need for rapid, accurate, and scalable testing systems for COVID-19 diagnosis is clear and urgent. Here, we report a rapid Scalable and Portable Testing (SPOT) system consisting of a rapid, highly sensitive, and accurate assay and a battery-powered portable device for COVID-19 diagnosis. The SPOT assay comprises a one-pot reverse transcriptase-loop-mediated isothermal amplification (RT-LAMP) followed by PfAgo-based target sequence detection. It is capable of detecting the N gene and E gene in a multiplexed reaction with the limit of detection (LoD) of 0.44 copies/μL and 1.09 copies/μL, respectively, in SARS-CoV-2 virus-spiked saliva samples within 30 min. Moreover, the SPOT system is used to analyze 104 clinical saliva samples and identified 28/30 (93.3% sensitivity) SARS-CoV-2 positive samples (100% sensitivity if LoD is considered) and 73/74 (98.6% specificity) SARS-CoV-2 negative samples. This combination of speed, accuracy, sensitivity, and portability will enable high-volume, low-cost access to areas in need of urgent COVID-19 testing capabilities.

scholarly journals Rapid and Sensitive Detection of miRNA Based on AC Electrokinetic Capacitive Sensing for Point-of-Care Applications

Sensors ◽  
2021 ◽  
Vol 21 (12) ◽  
pp. 3985
Author(s):  
Nan Wan ◽  
Yu Jiang ◽  
Jiamei Huang ◽  
Rania Oueslati ◽  
Shigetoshi Eda ◽  
...  
Keyword(s):  
Limit Of Detection ◽  
Point Of Care ◽  
Low Cost ◽  
Clinical Diagnostics ◽  
Detection Methods ◽  
Capacitive Sensing ◽  
Application Potential ◽  
Mirna Detection ◽  
Mirna 25 ◽  
Low Sensitivity

A sensitive and efficient method for microRNAs (miRNAs) detection is strongly desired by clinicians and, in recent years, the search for such a method has drawn much attention. There has been significant interest in using miRNA as biomarkers for multiple diseases and conditions in clinical diagnostics. Presently, most miRNA detection methods suffer from drawbacks, e.g., low sensitivity, long assay time, expensive equipment, trained personnel, or unsuitability for point-of-care. New methodologies are needed to overcome these limitations to allow rapid, sensitive, low-cost, easy-to-use, and portable methods for miRNA detection at the point of care. In this work, to overcome these shortcomings, we integrated capacitive sensing and alternating current electrokinetic effects to detect specific miRNA-16b molecules, as a model, with the limit of detection reaching 1.0 femto molar (fM) levels. The specificity of the sensor was verified by testing miRNA-25, which has the same length as miRNA-16b. The sensor we developed demonstrated significant improvements in sensitivity, response time and cost over other miRNA detection methods, and has application potential at point-of-care.

scholarly journals Demonstration of a Label-Free and Low-Cost Optical Cavity-Based Biosensor Using Streptavidin and C-Reactive Protein

Biosensors ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 4
Author(s):  
Donggee Rho ◽  
Seunghyun Kim
Keyword(s):  
Limit Of Detection ◽  
Point Of Care ◽  
Low Cost ◽  
Optical Cavity ◽  
Sample Volume ◽  
Small Sample ◽  
Label Free ◽  
C Reactive Protein ◽  
Reactive Protein ◽  
Cavity Structure

An optical cavity-based biosensor (OCB) has been developed for point-of-care (POC) applications. This label-free biosensor employs low-cost components and simple fabrication processes to lower the overall cost while achieving high sensitivity using a differential detection method. To experimentally demonstrate its limit of detection (LOD), we conducted biosensing experiments with streptavidin and C-reactive protein (CRP). The optical cavity structure was optimized further for better sensitivity and easier fluid control. We utilized the polymer swelling property to fine-tune the optical cavity width, which significantly improved the success rate to produce measurable samples. Four different concentrations of streptavidin were tested in triplicate, and the LOD of the OCB was determined to be 1.35 nM. The OCB also successfully detected three different concentrations of human CRP using biotinylated CRP antibody. The LOD for CRP detection was 377 pM. All measurements were done using a small sample volume of 15 µL within 30 min. By reducing the sensing area, improving the functionalization and passivation processes, and increasing the sample volume, the LOD of the OCB are estimated to be reduced further to the femto-molar range. Overall, the demonstrated capability of the OCB in the present work shows great potential to be used as a promising POC biosensor.

scholarly journals A Real-Time Method for Improving Stability of Monolithic Quartz Crystal Microbalance Operating under Harsh Environmental Conditions

Sensors ◽  
2021 ◽  
Vol 21 (12) ◽  
pp. 4166
Author(s):  
Román Fernández ◽  
María Calero ◽  
Yolanda Jiménez ◽  
Antonio Arnau
Keyword(s):  
Real Time ◽  
Quartz Crystal Microbalance ◽  
Quartz Crystal ◽  
Limit Of Detection ◽  
Quartz Substrate ◽  
Low Cost ◽  
Discrete Wavelet ◽  
Reagent Consumption ◽  
Measurement Cell ◽  
The Stability

Monolithic quartz crystal microbalance (MQCM) has recently emerged as a very promising technology suitable for biosensing applications. These devices consist of an array of miniaturized QCM sensors integrated within the same quartz substrate capable of detecting multiple target analytes simultaneously. Their relevant benefits include high throughput, low cost per sensor unit, low sample/reagent consumption and fast sensing response. Despite the great potential of MQCM, unwanted environmental factors (e.g., temperature, humidity, vibrations, or pressure) and perturbations intrinsic to the sensor setup (e.g., mechanical stress exerted by the measurement cell or electronic noise of the characterization system) can affect sensor stability, masking the signal of interest and degrading the limit of detection (LoD). Here, we present a method based on the discrete wavelet transform (DWT) to improve the stability of the resonance frequency and dissipation signals in real time. The method takes advantage of the similarity among the noise patterns of the resonators integrated in an MQCM device to mitigate disturbing factors that impact on sensor response. Performance of the method is validated by studying the adsorption of proteins (neutravidin and biotinylated albumin) under external controlled factors (temperature and pressure/flow rate) that simulate unwanted disturbances.

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