A colorimetric and ratiometric fluorescence sensor for sensitive detection of fluoride ions in water and toothpaste

RSC Advances ◽  
2016 ◽  
Vol 6 (54) ◽  
pp. 49158-49163 ◽  
Author(s):  
Bo Qiu ◽  
Yi Zeng ◽  
Lixia Cao ◽  
Rui Hu ◽  
Xiaohui Zhang ◽  
...  

The colorimetric and ratiometric sensor shows significant spectral response towards fluoride ions in water with a detection limit as low as 2.7 ppb, enabling direct observation with the bare eye as well as quantitative determination of F− in toothpaste.

1987 ◽  
Vol 70 (6) ◽  
pp. 1031-1032
Author(s):  
Yuuko S Endoh ◽  
Ryozo Yamaoka ◽  
Nobuo Sasaki

Abstract A liquid chromatographic (LC) method is described for the quantitative determination of sulfamoyldapsone (2-sulfamoyl-4,4'-diaminodiphenyl sulfone) in swine muscle, liver, kidney, and fat. Sulfamoyldapsone was extracted from tissues with acetonitrile saturated with n-hexane. The extract was washed with n-hexane saturated with acetonitrile, concentrated, and cleaned up by alumina column chromatography. Sulfamoyldapsone was separated on an ODS column by using acetonitrile-methanol-water (6 + 18 + 76) and was detected at 292 nm. Overall average recovery of sulfamoyldapsone added to tissues at levels of 0.1 and 0.5 /μg/g was 93.3% ± 6.0. Detection limit was 0.02 μg/g in these tissues.


2019 ◽  
Vol 43 (46) ◽  
pp. 18259-18267 ◽  
Author(s):  
Hang Lei ◽  
Cui-Xing Qi ◽  
Xuan-Bo Chen ◽  
Tian Zhang ◽  
Ling Xu ◽  
...  

Tb3+0.6/Eu3+0.4@Ni-BTC is a quantitative ratiometric fluorescence sensor for DPA detection with high sensitivity, anti-interference, rapid response and durability.


2020 ◽  
Vol 1 (1) ◽  
pp. 72-77
Author(s):  
Naresh Pant ◽  
Anup Subedee ◽  
Ram Bahadur Gharti ◽  
Santu Shrestha

Quantitative determination of heavy metals; Fe, Zn, Co, Pb and Ni in Mango fruit of Nepali origin, locally sourced was carried out. Fifteen Mango samples were collected by random sampling method, converted into analyte sample by standard method and analyzed by using Atomic absorption spectrometric method. The amount of heavy metals Fe, Zn, Co and Ni present in sample was, 0.570±0.48, 0.510±0.031, 0.431±0.021, 0.106±0.003 mg/kg respectively. The results indicated the concentration of Zn & Co were higher (WHO 0.320 & 0.05), and the concentration of Nickel (Ni) was below the maximum permissible limit issued by WHO. The concentration of the Lead (Pb) was found below the detection limit of the instrument used.


1981 ◽  
Author(s):  
L L M Thomas ◽  
A Sturk ◽  
M C Schaap ◽  
H ten Cate ◽  
J W ten Cate

A method, its optimalization and a solution to specific problems is described for the quantitative determination of endotoxins in blood. The method is based upon the endotoxin-dependent activation of a proenzyme, present in limulus ame- bocyte lysate. This activated enzyme is measured with the chromogenic substrate S2222. Possible inhibitors and activated coagulationfactors interfering in the assay are removed by dilution and boiling. The method is shown to be fast (2½ hr), sensitive and reproducible with a detection limit of 10 pg/ml.The endotoxin assay was found to have a good correlation with results of blood cultures.The detection threshold of the endotoxin assay compared with the number of circulating gramnegative organisms and CRD-measurements will also be shown.


2002 ◽  
Vol 48 (3) ◽  
pp. 526-532 ◽  
Author(s):  
Marius Ulleland ◽  
Ingar Eilertsen ◽  
Edward V Quadros ◽  
Sheldon P Rothenberg ◽  
Sergey N Fedosov ◽  
...  

Abstract Background: Only cobalamin carried by transcobalamin (holo-transcobalamin) is available for cellular uptake and hence is physiologically relevant. However, no reliable or accurate methods for quantifying holo-transcobalamin are available. We report a novel holo-transcobalamin assay based on solid-phase capture of transcobalamin. Methods: A monoclonal antibody specific for human transcobalamin with an affinity constant >1010 L/mol was immobilized on magnetic microspheres to capture and concentrate transcobalamin. The cobalamin bound to transcobalamin was then released and assayed by a competitive binding radioassay. The quantification of holo-transcobalamin was accomplished using calibrators composed of recombinant, human holo-transcobalamin. Results: The assay was specific for holo-transcobalamin and had a detection limit of 5 pmol/L. Within-run and total imprecision (CV) was 5% and 8–9%, respectively. The working range (CV <20%) was 5–370 pmol/L. Dilutions of serum were linear in the assay range. The recovery of recombinant, human holo-transcobalamin added to serum was 93–108%. A 95% reference interval of 24–157 pmol/L was established for holo-transcobalamin in 105 healthy volunteers 20–80 years of age. For 72 of these sera, holo-haptocorrin and total cobalamin were also determined. Whereas holo-haptocorrin correlated well (r2 = 0.87) with total cobalamin, holo-transcobalamin correlated poorly (r2 = 0.23) with total cobalamin or holo-haptocorrin. Conclusions: The solid-phase capture assay provides a simple, reliable method for quantitative determination of holo-transcobalamin in serum.


RSC Advances ◽  
2019 ◽  
Vol 9 (24) ◽  
pp. 13567-13575 ◽  
Author(s):  
Xiafan Hao ◽  
Shuhua Han ◽  
Jingtao Zhu ◽  
Yongfeng Hu ◽  
Lo Yueh Chang ◽  
...  

A novel bis-benzimidazole organic siloxane precursor (BBM-Si) was prepared, and was combined with tetraethylorthosilicate (TEOS) as a mixed Si source.


2020 ◽  
Vol 16 (4) ◽  
pp. 475-484
Author(s):  
Tingting Huang ◽  
Guohong Liu ◽  
Jingxiang Yu ◽  
Meng Liu ◽  
Zhiping Huang ◽  
...  

Background: Sarin is a nerve agent which is lethal to people due to its high toxicity. According to its extreme toxicity, sarin, relatively lack of color, highly toxic, miscible in water, poses viable threats to potable water sources. Therefore, there is an urgent need for portable, rapid and yet reliable methods to monitor for adulteration of potable water sources by sarin on spot. Methods: A stock solution of 30 mg/L sarin was prepared daily by dissolving 300 μg of sarin in 10 mL isopropanol. A certain amount of sarin was added to the glass tube, and then o-dianisidine and hydrogen peroxide were added. The pH value of the solution was adjusted to 9.8. The solution was transferred to the test tube after 10 minutes. A test tube of 2 mL was placed between the light source and the RGB color sensor. The LED light source illuminates directly over the test tube while the RGB sensor obtained the generated spectral response. This RGB voltage output is connected to the ADC and microcontroller to convert these analog voltages to three digital data. This RGB digital data is linked to the microcomputer through the serial port that is interfaced with the user interface. The data thus obtained in the sensor can be processed to display the sarin concentration. Results: Under the optimum conditions as described above, the calibration curve of chromaticity value versus sarin concentration was linear in the range of 0.15 mg/L to 7.8 mg/L. According to the IUPAC definition, theoretical detection limits of this method were 0.147 mg/L and 0.140 mg/L for R and B values, respectively. The practical detection limit was 0.15 mg/L. The sensor was successfully applied to the determination of sarin in artificial water samples and the recoveries were between 86.0% to 95.9%. Conclusion: The results in the present work have demonstrated the feasibility to design a new portable colorimetric sensor based on the RGB chromaticity method for quantitative determination of sarin in water. The influences of chromogenic reagent, oxidant, reaction time, o-dianisidine concentration, hydrogen peroxide concentration, reaction temperature, pH on the chromaticity values were investigated. The results showed that the sensor possessed high selectivity, sensitivity and good repeatability. The method would be potentially applied to the analysis of other toxic compounds in environment, such as other chemical warfare agents.


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