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    Smartphone-based disposable cotton-swab sensor loaded with creatinine/Cu–chlorophyllin–stabilized AuNPs for ultrasensitive RGB colorimetric detection of mercury (II) ions in aquatic environments
    (2026-05-01)
    Lerdpiriyaskulkij, Natee
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    Detsri, Ekarat
    ;
    Teerasong, Saowapak
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    Chansai, Sarayute
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    Mathaweesansurn, Arjnarong
    A simple, rapid, selective, and sensitive colorimetric sensor based on a disposable cotton swab loaded with Au nanoparticle–modified Cu-chlorophyllin (Au<sup>0</sup>–NPs<inf>CHL</inf>) and creatinine was developed for mercury (II) detection in aquatic environments using smartphone–based RGB analysis. Au<sup>0</sup>–NPs<inf>CHL</inf> were synthesized by ultrasonic-assisted chemical reduction, employing Cu-chlorophyllin as a stabilizing and NaBH<inf>4</inf> as a reducing agent. A vivid red Au<sup>0</sup>–NPs<inf>CHL</inf> colloidal (7.96 ± 0.29 nm) with a sharp SPR peak at 515 nm was successfully obtained. An aliquot of 75 µL of Au<sup>0</sup>-NPs<inf>CHL</inf> (0.103 ± 0.03 nmol L<sup>−1</sup>) and 25 µL of creatinine solution (40 mg L<sup>−1</sup>) were sequentially loaded into an 8.0 × 0.5 cm cotton swab, separated by a 0.5 cm air gap. Detection began by immersing the swab into Hg<sup>2+</sup>–contaminated samples for 3 min, allowing Hg<sup>2+</sup> adsorption. Breaking the swab generated pressure differential, which, along with gravity, drove the Au<sup>0</sup>–NPs<inf>CHL</inf> to mix with creatinine. The resulting mixture migrated toward the swab tip by capillary action and reacted with adsorbed Hg<sup>2+</sup> through metallophilic 5d<sup>10</sup>–5d<sup>10</sup> interactions. Creatinine acted as a bridging ligand, inducing Au<sup>0</sup>–NPs<inf>CHL</inf> aggregation and shifting the SPR to 620 nm, causing a visible red-to-blue transition. This sensor enables rapid and visual detection and quantitative evaluation via smartphone RGB analysis. The system demonstrated excellent linearity from 1 to 100 µg L<sup>−1</sup> with a low LOD of 0.82 µg L<sup>−1</sup>. Recoveries of 97.6–101.8 % confirmed high accuracy and minimal matrix interference. The disposable cotton swab RGB sensor provides a rapid, portable, and practical tool for on-site primary assessment of Hg<sup>2+</sup> contamination in environmental samples.
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    Ultrasonic-driven chemical reduction synthesis of alizarin complexone-modified gold nanoparticles for dual-signal colorimetric and fluorometric sensing of histamine in seafood products
    (2024-12-01)
    Phoungsiri, Ampika
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    Lerdpiriyaskulkij, Natee
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    Mathaweesansurn, Arjnarong
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    Detsri, Ekarat
    Alizarin complexone-modified gold nanoparticles (Au<sup>0</sup>-NPs<inf>ALz</inf>) were synthesized using a proposed ultrasonic irradiation-assisted chemical reduction method. Ultrasonic irradiation powers, reaction time and alizarin complexone concentration had been proven to be the main parameters for controlling the nucleation and growth of Au<sup>0</sup>-NPs<inf>ALz</inf>. In the synthesized ultrasonic irradiation-assisted chemical reduction conditions, Au<sup>0</sup>-NPs<inf>ALz</inf> had a spherical oriented morphology with a uniform size of 17.84 ± 1.37 nm and are shiny red with a surface plasmon resonance (SPR) of 535 nm. A rapid colorimetric and fluorometric dual-mode detection strategy for selective detection of histamine in seafood was developed based on the self-assembly of Au<sup>0</sup>-NPs<inf>ALz</inf>-Ni (II) complexes. Ni (II) can capture the histamine molecules close to Au<sup>0</sup>-NPs<inf>ALz</inf> surfaces, making changes in the colorimetric and fluorometric responses of the solution. The quantitative analysis of histamine was realized through the variation of dual-signal colorimetric and fluorometric responses. Such Au<sup>0</sup>-NPs<inf>ALz</inf> sensor offered good detection sensitivity for histamine with a detection limit (LOD) of 59.32 μmol L<sup>−1</sup> and 116.20 μmol L<sup>−1</sup> and wide linear response within the range of 10–10000 μmol L<sup>−1</sup> (R<sup>2</sup> = 0.9952) and 100–5000 μmol L<sup>−1</sup> (R<sup>2</sup> = 0.9947) for colorimetric and fluorometric measurement, respectively. Recoveries ranging from 94.99 to 103.29 % and 97.67–106.88 % for colorimetric and fluorometric assay were obtained, showing low levels of matrix effects. Particularly, the results of the dual-mode sensor were also validated by comparing with the HPLC method for improving the assay accuracy and dependability. Ultimately, the developed Au<sup>0</sup>-NPs<inf>ALz</inf> colorimetric and fluorometric probe performs excellently in practical applications, with promising results for detecting histamine in seafood products.
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    A new colorimetric method for determination of formaldehyde in sea food based on anti-aggregation of gold nanoparticles
    (2022-12-01)
    Mathaweesansurn, Arjnarong
    ;
    Detsri, Ekarat
    A new colorimetric method based on anti-aggregation of gold nanoparticles (AuNPs) in the presence of melamine for sensitive and selective determination of formaldehyde was developed. The citrate capped AuNPs was synthesized by Turkevich method. A certain concentration of melamine is responsible for color change of AuNPs from red to purple. The surface plasmon resonance peak was shifted from 520 to 640 nm. In the presence of formaldehyde, the reaction between melamine and formaldehyde to form methylol melamine was occurred, which resulted in the decreasing of aggregation of AuNPs. Based on the anti-aggregation mechanism, formaldehyde can be detected by observing the color change of AuNPs solution containing melamine, which was monitored by UV–visible spectrophotometer. Calibration curve plotted between absorbance ratio (A640/A520) and formaldehyde concentration was made with linearity of 0 – 2000 µg L<sup>−1</sup>. The limit of detection and the limit of quantitation were found at 26.0 µg L<sup>−1</sup> and 88.0 µg L<sup>−1</sup>, respectively. The method also provided high accuracy (%recovery in range 97.3 – 104%) and high precision (%RSD < 5.6).
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    Low-cost synthesis of gold nanoparticles from reused traditional gold leaf and its application for sensitive and selective colorimetric sensing of creatinine in urine
    (2020-01-01)
    Mathaweesansurn, Arjnarong
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    Choengchan, Nathawut
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    Khongkaew, Putthiporn
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    Phechkrajang, Chutima M.
    Background: Gold nanoparticles (Au NPs) are normally prepared using standard gold (III) trichloride which is much expensive and irritant. This work is aimed at demonstrating simple and low-cost synthesis of Au NPs from the reused traditional gold leaf which is cost-free and less toxic. Methods: The reused gold leaf was donated by the local temple. It was digested and used as the precursor for the preparation of the Au NPs by Turkevich method. Poly (vinyl alcohol) (PVA) was em-ployed as a stabilizer. The as-prepared Au NPs were applied for the colorimetric determination of creatinine in urine without any sample pretreatment. Results: Long-term stability of the gold colloids was achieved for at least 3 months. Morphology and purity of the as-prepared Au NPs were the same as the ones prepared from standard gold (III) salt and standard gold foil. Colorimetric response of the Au NPs was linear to the standard creatinine up to 200 mg L<sup>-1</sup>. The limit of detection (0.16 mg L<sup>-1</sup> or 1.41 µM) was enough sensitive for urinary cre-atinine detection in patients with kidney disease. Good recoveries (97-108%) and fast analysis time (3 min) were achieved. The developed method was successfully validated against the HPLC method. Conclusion: Facile and cost-effective synthesis of the Au NPs from the reused traditional gold leaf, was accomplished. The as-prepared Au NPs were successfully applied for the determination of urinary creatinine with high sensitivity and selectivity.