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Transparent Cross-Flow Platform as Chemiluminescence Detection Cell in Cross Injection Analysis
(2023-02-01)
Somboonsuk, Thachkorn
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Saetear, Phoonthawee
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Mantim, Thitirat
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Ratanawimarnwong, Nuanlaor
;
Wilairat, Prapin
This work presents the use of a transparent ‘Cross Injection Analysis’ (CIA) platform as a flow system for chemiluminescence (CL) measurements. The CL-CIA flow device incorporates introduction channels for samples and reagents, and the reaction and detection channels are in one acrylic unit. A photomultiplier tube placed above the reaction channel detects the emitted luminescence. The system was applied to the analysis of (i) Co(II) via the Co(II)-catalyzed H<inf>2</inf>O<inf>2</inf>-luminol reaction and (ii) paracetamol via its inhibitory effect on the catalytic activity of Fe(CN)<inf>6</inf>3− on the H<inf>2</inf>O<inf>2</inf>-luminol reaction. A linear calibration was obtained for Co(II) in the range of 0.002 to 0.025 mg L−1 Co(II) (r2 = 0.9977) for the determination of Co(II) in water samples. The linear calibration obtained for the paracetamol was 10 to 200 mg L−1 (r2 = 0.9906) for the determination of pharmaceutical products. The sample throughput was 60 samples h−1. The precision was ≤4.2% RSD. The consumption of the samples and reagents was ca. 170 µL per analysis cycle.
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Simple flow system with in-line gas-diffusion unit for determination of ethanol employing hypsochromic shift of visible absorbance band of methyl orange
(2020-01-01)
Ratanawimarnwong, Nuanlaor
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Sinpun, Montatip
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Chankaw, Panuwat
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Choengchan, Nathawut
;
Nacapricha, Duangjai
The effect of solvent composition on the uv–visible spectrum of methyl orange was investigated for application to the quantitative determination of ethanol. At fixed pH, there was a hypsochromic shift of the absorbance band of methyl orange with increasing ethanol concentration. Using acetate buffer at pH 3.40 the change of absorbance at 530 nm of a solution of methyl orange containing known concentrations of standard ethanol was measured to provide a calibration curve. In order to apply this method to the analysis of alcoholic samples, such as distilled spirits, blended spirits and liquid herbal medicines, a simple gas-diffusion unit coupled with flow system was employed to separate the ethanol from sample matrices. Using the gas diffusion-flow system and employing an evaporation time of 2 min, a linear calibration range of 5–45% (v/v) ethanol was achieved ((ΔA = (0.0078 ± 0.0002)x(ethanol, %(v/v)) + (0.040 ± 0.005)), r2 = 0.998). The limit of detection (3σ blank/slope) was 2.23% (v/v). The developed gas diffusion-flow system was applied to the analysis of colorless distilled spirits, yellow blended spirits and dark brown herbal medicines that are available in the local markets of Bangkok, Thailand. Validation of the method was carried out by comparing the results with analysis using gas chromatography. There was no statistically significant difference at the 95% confidence level for all alcoholic samples analyzed.
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Microfluidic paper-based analytical device for convenient use in measurement of iodate in table salt and irrigation water
(2020-01-01)
Duangdeewong, Chomphunud
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Sitanurak, Jirayu
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Wilairat, Prapin
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Nacapricha, Duangjai
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Teerasong, Saowapak
We report a convenient microfluidic paper-based analytical device (µPAD) for the determination of iodate. The µPAD was fabricated using an ink-stamp with a simple circle design. Colorimetric detection of iodate employs the oxidation of hydroxylamine by the iodate to generate nitrite which reacts with the Griess reagent producing an intense magenta color. The images were recorded by a digital camera, and converted to a green scale color intensity by ImageJ. Calibration of iodate was linear in the range of 50–400 mg L−1 with a detection limit of 38.1 mg L−1. With such a wide linear range, the method can be applied to various kinds of samples with the entire process completed in 50 s. Good precision of measurement was obtained (<2 %RSD). Iodate levels were determined using the µPADs in table salt and irrigation water samples. The measured concentrations of the samples correlated well with the values as found by the standard iodometric titration (no statistical difference at a 95% confidence level). The developed device is simple with easy fabrication and rapid operation. It is portable and cost-effective and therefore suitable for quality control of iodate levels in the manufacturing and agricultural industries.
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A Screen Printed Graphene Based Electrochemical Sensor for Single Drop Analysis of Hydroquinone in Cosmetic Products
(2019-08-01)
Duekhuntod, Wannida
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Karuwan, Chanpen
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Tuantranont, Adisorn
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Nacapricha, Duangjai
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Teerasong, Saowapak
A graphene modified carbon paste sensor (or so-called graphene based sensor) was developed for electrochemical detection of hydroquinone. The sensor was fast fabricated using screen-printing technique. By integrating three fundamental electrodes on a single device, the sensor is small and portable. A determination is based on a one drop analysis. A 60 μ.L-drop of sample was placed onto the sensor prior to cyclic voltammetric measurement. The method relies on green analysis since it lowers the consumption of sample and waste generation. Under the optimal conditions, a linear calibration was achieved in range of 1.0 x 10-4 to 5.0 x 10-3 M hydroquinone. The detection limit was 7 x 10-5 M, a sensitive adequate for measuring hydroquinone in cosmetic products. The sensor provided good precision (%RSD = 2.78) and accuracy (recoveries = 87-114%), with analysis times of less than a minute. The sensor was applied to determine the presence of hydroquinone in whitening creams. The results obtained from the developed sensor satisfactorily agreed with the HPLC method, indicating the reliability of the method. Due to its advantages in terms of rapidity, low-cost and portability, the device is a viable choice for on-site screening for hydroquinone contamination in whitening products.
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Simple and green method for direct quantification of hypochlorite in household bleach with membraneless gas-separation microfluidic paper-based analytical device
(2018-09-01)
Sitanurak, Jirayu
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Wangdi, Nidup
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Sonsa-ard, Thitaporn
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Teerasong, Saowapak
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Amornsakchai, Taweechai
This work presents development of a microfluidic paper-based analytical device (µPAD) for direct determination of hypochlorite in household bleach. The recent design of a membraneless gas-separation microfluidic paper-based analytical device (MBL-GS µPAD) was employed to fabricate the hypochlorite-µPAD. Chlorine gas is generated in the µPAD via acidification of an aliquot of sample loaded on to the donor reservoir located at the bottom layer of the μPAD. The liberated chlorine gas diffuses through the air space to oxidize iodide ion previously impregnated in the acceptor reservoir at the top layer of the μPAD, leading to formation of the brown color of the tri-iodide ions. Digital image of the brown zone was captured at exactly 5 min after loading the acid. Image J program is used for analysis of the image for quantification of the hypochlorite in unit of g Cl<inf>2</inf> L−1. It was found that employing a relatively large volume of the air space (ca. 270 µL) direct analysis of the high concentration of hypochlorite in the bleach was achieved without prior dilution. The method thus provides a linear working range of 25–100 g Cl<inf>2</inf> L−1, which is suitable for most commercial household products. The calibration line has a coefficient of determination of 0.999. The precision of measurements is 0.96% RSD and 0.30% RSD at 30 g Cl<inf>2</inf> L−1 and 80 g Cl<inf>2</inf> L−1 (n = 10), respectively. Using the paired t-test (P = 0.05, n = 8), the method agreed well with the iodometric titration method. Our μPAD for hypochlorite is portable and cost-effective. The method is also “green” since there is a significant reduction in use of reagents compared to other conventional methods.
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Microfluidic analysis with front-face fluorometric detection for the determination of total inorganic iodine in drinking water
(2018-01-01)
Inpota, Prawpan
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Strzelak, Kamil
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Koncki, Robert
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Sripumkhai, Wisaroot
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Jeamsaksiri, Wutthinan
A microfluidic method with front-face fluorometric detection was developed for the determination of total inorganic iodine in drinking water. A polydimethylsiloxane (PDMS) microfluidic device was employed in conjunction with the Sandell-Kolthoff reaction, in which iodide catalyzed the redox reaction between Ce(IV) and As(III). Direct alignment of an optical fiber attached to a spectrofluorometer was used as a convenient detector for remote front-face fluorometric detection. Trace inorganic iodine (IO <inf>3</inf> - and I - ) present naturally in drinking water was measured by on-line conversion of iodate to iodide for determination of total inorganic iodine. On-line conversion efficiency of iodate to iodide using the microfluidic device was investigated. Excellent conversion efficiency of 93 - 103% (%RSD = 1.6 - 11%) was obtained. Inorganic iodine concentrations in drinking water samples were measured, and the results obtained were in good agreement with those obtained by an ICP-MS method. Spiked sample recoveries were in the range of 86%(±5) - 128%(±8) (n = 12). Interference of various anions and cations were investigated with tolerance limit concentrations ranging from 10-6 to 2.5 M depending on the type of ions. The developed method is simple and convenient, and it is a green method for iodine analysis, as it greatly reduces the amount of toxic reagent consumed with reagent volumes in the microfluidic scale.
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A "dual-acceptor channel" membraneless gas-diffusion unit for simultaneous determination of ethanol and acetaldehyde in liquors using reverse flow injection
(2018-01-01)
Choengchan, Nathawut
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Poontong, Bangerdsuk
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Mathaweesansurn, Arjnarong
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Maneerat, Noppadol
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Motomizu, Shoji
A new design of membraneless gas-diffusion unit with dual acceptor channels for separation, collection and simultaneous determination of two volatile analytes in liquid sample is presented. The unit is comprised of three parallel channels in a closed module. A sample is aspirated into the central channel and two kinds of reagents are introduced into the other two channels. Two analytes are isolated from the sample matrix by diffusion into head-space and absorbed into the specific reagents. Non-absorbed vapor is released by opening the programmable controlled lid. The unit was applied to liquors for measurement of ethanol and acetaldehyde using reverse flow injection. Dichromate and nitroprusside were exploited as reagents for colorimetric detection of ethanol and acetaldehyde, respectively. Good linearity ranges (r2 > 0.99) with high precision (RSD < 2%) and high accuracy (recovery: 90 - 105%) were achieved. The results were compared to the results by GC-FID and no significant difference was observed by paired t-test (95% confidence).
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Poly(vinyl alcohol) capped silver nanoparticles for antioxidant assay based on seed-mediated nanoparticle growth
(2017-08-01)
Teerasong, Saowapak
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Jinnarak, Amornrassamee
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Chaneam, Sumonmarn
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Wilairat, Prapin
;
Nacapricha, Duangjai
A simple and rapid method for measurement of total antioxidant capacity (TAC) was developed. In this work, gallic acid was used as the antioxidant standard. Poly(vinyl alcohol) embedded silver nanoparticles (PVA-AgNPs) were employed as a colorimetric sensor. The detection principle was based on the seed-mediated nanoparticle growth technique. The PVA-AgNPs act as a catalyst in the reduction of Ag+ by gallic acid by providing nucleation seeds. Ag+ was reduced to Ag° and accumulated on the PVA-AgNP surface, leading to an increase in the size of particles. The absorbance of the colloidal solution was drastically enhanced with a small red shift. Under optimal conditions, a linear response was established between the change in absorbance and the TAC value expressed in terms of gallic acid equivalents. The linear range was from 25 to 200 μM with a detection limit of 22.1 μM. Satisfactory precision was obtained with % relative standard deviation (RSD) of 2.17. The developed sensor was successfully applied for TAC assessment of commercial ginger products. The PVA-AgNP sensor offers rapid analysis (within 5 min) compared to other nanoparticle-based antioxidant assays. Synthesis of the particles and assay involved less-toxic chemicals, and is therefore a “greener” method.
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Sequential injection for determination of gamma-aminobutyric acid based on its effect on second order light scattering of silver nanoparticles
(2016-08-01)
Jinnarak, Amornrassamee
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Anantavichian, Pattarapon
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Intanin, Apichai
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Fungladda, Suchada
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Choengchan, Nathawut
An automated sequential injection (SI) with second order light scattering (SOS) detection for determination of gamma-aminobutyric acid (GABA) was developed. Quantitation is based on electrostatic interaction between GABA and citrate-capped silver nanoparticles (AgNPs). In acetate buffer at pH 3.8, the positively charged GABA induces the nanoparticles to aggregate. This results in a change of light scattering monitored using a spectrofluorometer. In this work, working standard solutions of GABA were prepared in-line by the SI system pumping appropriate volumes of a stock solution of GABA and acetate buffer into a holding coil. Solution of AgNPs was subsequently drawn into the coil. The reaction zone was then transferred to the spectrofluorometer, set with excitation and detection wavelengths at 300 and 600 nm, respectively. Under optimised condition, the SOS intensity was proportional to the concentration of GABA. As a result, a linear curve was obtained in the range of 100–400 mg L−1 GABA, with a lower limit of detection of 39.6 mg L‐1. Good precision of analysis was achieved, with 0.6 and 3.3% relative standard deviation (RSD) for external calibration (n = 5) and standard addition (n = 3), respectively. The developed method was successfully applied for quantification of GABA in dietary supplements (2 samples) and samples of instant green tea (2 samples).
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Chemometrics-assisted cross injection analysis for simultaneous determination of phosphate and silicate
(2016-07-14)
Uraisin, Kanchana
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Janya, Supavita
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Phechkrajang, Chutima
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Choengchan, Nathawut
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Tiyapongpattana, Warawut
This work presents a novel method for simultaneous spectrophotometric determination of phosphate and silicate by using a cross injection analysis (CIA) coupled with the use of partial least squares (PLS) for data evaluation. The detection principle is based on the well-known ‘molybdenum blue’ method. The molybdate ions in the presence of stannous chloride in acidic medium give phosphomolybdenum blue and silicomolybdenum blue as products. In this work, all the liquids, including sample and reagents were simultaneously introduced into a CIA platform by using two peristaltic pumps for controlling the x-channel and y-channel flow which was automatically manipulated by using in-house control board. Crossflow provides sufficient mixing inside the platform prior detection of the absorption spectra of blue complexes in the wavelength of 400–900 nm. Since spectra of the blue colour product of phosphate and silicate are resemblant, these two analytes therefore reciprocally interfere with one another. This results in difficulty in simultaneous analysis of phosphate and silicate. In this work, PLS was utilised as assistor of CIA system for simultaneous analysis of phosphate and silicate using molybdenum blue reaction without using any modification of reagents and addition of selective masking agent. The calibration ranges are 0.1–6 mgP L−1 and 5–100 mgSi L−1 for phosphate and silicate, respectively. By using CIA coupled with PLS for data evaluation, the analysis of two analytes was achieved within 1.5 min with only single injection. The developed system was applied to natural water samples and the system was validated with the conventional methods. By statistical paired t-test, there was no evidence of significant difference at 95% confidence level (t<inf>stat</inf> = 2.28, t<inf>critical</inf> = 2.31 and t<inf>stat</inf> = 0.62, t<inf>critical</inf> = 2.31 for phosphate and silicate, respectively). This implied that the chemometrics-assisted CIA system was successfully developed for simultaneous spectrophotometric determination of phosphate and silicate.

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