A Highly Selective and Sensitive Fluorescent Probe Based on Quinolone Derivative for Hg2+ in Aqueous Solution

2012 ◽  
Vol 549 ◽  
pp. 229-233
Author(s):  
Juan Juan Tian ◽  
Xin Zhou ◽  
Hui Juan Hao ◽  
Xue Wu
Keyword(s):  
Aqueous Solution ◽  
Fluorescent Probe ◽  
Limit Of Detection ◽  
Transition Metal Ions ◽  
Quinoline Derivative ◽  
Ligand Complex ◽  
Quinolone Derivative ◽  
Ph Range ◽  
Metal Ligand ◽  
Tof Ms

A new fluorescent probe, quinoline derivative DPQ bearing a methyl pyrrolidine-1-carbodithioate group, was synthesized and characterized by IR, Tof-MS and NMR. Its fluorescent behaviors toward transition metal ions were investigated. The results indicate that DPQ shows unique selective and high sensitive for Hg2+ in aqueous solution with a broad pH range 4-10. DPQ forms a 1:2 metal-ligand complex with Hg2+ ions with a limit of detection as low as 1.7×10-6 mol/L.

scholarly journals Selective and Sensitive Detection of Cyanide Based on the Displacement Strategy Using a Water-Soluble Fluorescent Probe

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Ming La ◽  
Yuanqiang Hao ◽  
Zhaoyang Wang ◽  
Guo-Cheng Han ◽  
Lingbo Qu
Keyword(s):  
Aqueous Solution ◽  
Fluorescent Probe ◽  
Limit Of Detection ◽  
Aqueous Media ◽  
Water Soluble ◽  
World Health ◽  
Selective Detection ◽  
Highly Sensitive ◽  
Health Organization

A water-soluble fluorescent probe (C-GGH) was used for the highly sensitive and selective detection of cyanide (CN−) in aqueous media based on the displacement strategy. Due to the presence of the recognition unit GGH (Gly-Gly-His), the probeC-GGH can coordinate with Cu2+and consequently display ON-OFF type fluorescence response. Furthermore, thein situformed nonfluorescentC-GGH-Cu2+complex can act as an effective OFF-ON type fluorescent probe for sensing CN−anion. Due to the strong binding affinity of CN−to Cu2+, CN−can extract Cu2+fromC-GGH-Cu2+complex, leading to the release ofC-GGH and the recovery of fluorescent emission of the system. The probeC-GGH-Cu2+allowed detection of CN−in aqueous solution with a LOD (limit of detection) of 0.017 μmol/L which is much lower than the maximum contaminant level (1.9 μmol/L) for CN−in drinking water set by the WHO (World Health Organization). The probe also displayed excellent specificity for CN−towards other anions, including F−, Cl−, Br−, I−, SCN−,PO43-,N3-,NO3-, AcO−,SO42-, andCO32-.

A rhodamine-based Hg2+-selective fluorescent probe in aqueous solution

2009 ◽  
Vol 63 (3) ◽  
Author(s):  
Minglei Zhao ◽  
Xiao-Feng Yang ◽  
Shenfeng He ◽  
Liping Wang
Keyword(s):  
Aqueous Solution ◽  
Detection Limit ◽  
Transition Metal ◽  
Fluorescent Probe ◽  
Fluorescence Emission ◽  
Transition Metal Ions ◽  
Fluorescent Product ◽  
Compound I ◽  
Strong Fluorescence ◽  
Fluorogenic Probe

AbstractA new rhodamine-based Hg2+-selective fluorescent probe (I) was designed and synthesized. Compound I displays excellent selective and sensitive response to Hg2+ over other transition metal ions in neutral aqueous solutions. I itself is a colorless, nonfluorescent compound. Upon addition of Hg2+ to its solution, the thiosemicarbazide moiety of I undergoes an irreversible desulfurization reaction to form the corresponding 1,3,4-oxadiazole (II), a colorful and fluorescent product, causing instantaneous development of visible color and strong fluorescence emission. Based on this mechanism, a fluorogenic probe for Hg2+ was developed. The fluorescence increases linearly with the Hg2+ concentration up to 0.8 μmol L−1 with the detection limit of 9.4 nmol L− (3σ).

Development of an AIE based fluorescent probe for the detection of nitrate anions in aqueous solution over a wide pH range

RSC Advances ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 6997-7001 ◽  
Author(s):  
Shiyan Chen ◽  
Xin-Long Ni
Keyword(s):  
Aqueous Solution ◽  
Fluorescent Probe ◽  
Living Cells ◽  
Selective Detection ◽  
Ionic Interaction ◽  
Turn On ◽  
Wide Ph Range ◽  
New Type ◽  
Ph Range ◽  
Nitrate Anions

A new type of AIE-based turn-on fluorescent probe 1 was reported to highly selective detection of NO3− anion in aqueous solution and living cells by virtue of ionic interaction.

Novel palladium(II) selective membrane electrode based on 4-[(5-mercapto-1,3,4-thiadiazol-2-ylimino)methyl]benzene-1,3-diol

2010 ◽  
Vol 75 (5) ◽  
pp. 563-575 ◽  
Author(s):  
Moslem Mohammadi ◽  
Mehdi Khodadadian ◽  
Mohammad K. Rofouei
Keyword(s):  
Limit Of Detection ◽  
Membrane Electrode ◽  
Aqueous Samples ◽  
Selective Determination ◽  
Poly Vinyl Chloride ◽  
Selective Membrane ◽  
Ph Range ◽  
Palladium Content ◽  
Methyl Benzene

A plasticized poly(vinyl chloride) membrane electrode based on 4-[(5-mercapto-1,3,4-thiadiazol-2-ylimino)methyl]benzene-1,3-diol (L) for highly selective determination of palladium(II) (in PdCl42– form) is developed. The electrode showed a good Nernstian response (29.6 ± 0.4 mV per decade) over a wide concentration range (3.1 × 10–7 to 1.0 × 10–2 mol l–1). The limit of detection was 1.5 × 10–7 mol l–1. The electrode has a response time of about 20 s, and it can be used for at least 2 months without observing any considerable deviation from Nernstian response. The proposed electrode could be used in the pH range of 2.5–5.5. The practical utility of the electrode has been demonstrated by its use for the estimation of palladium content in aqueous samples.

scholarly journals Self-Assembled Nanomaterials Based on Complementary Sn(IV) and Zn(II)-Porphyrins, and Their Photocatalytic Degradation for Rhodamine B Dye

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3598
Author(s):  
Nirmal K. Shee ◽  
Hee-Joon Kim
Keyword(s):  
Aqueous Solution ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Self Assembly ◽  
The Self ◽  
Assembly Process ◽  
Absorption Bands ◽  
Ligand Coordination ◽  
Rhodamine B Dye ◽  
Metal Ligand

A series of porphyrin triads (1–6), based on the reaction of trans-dihydroxo-[5,15-bis(3-pyridyl)-10,20-bis(phenyl)porphyrinato]tin(IV) (SnP) with six different phenoxy Zn(II)-porphyrins (ZnLn), was synthesized. The cooperative metal–ligand coordination of 3-pyridyl nitrogens in the SnP with the phenoxy Zn(II)-porphyrins, followed by the self-assembly process, leads to the formation of nanostructures. The red-shifts and remarkable broadening of the absorption bands in the UV–vis spectra for the triads in CHCl3 indicate that nanoaggregates may be produced in the self-assembly process of these triads. The emission intensities of the triads were also significantly reduced due to the aggregation. Microscopic analyses of the nanostructures of the triads reveal differences due to the different substituents on the axial Zn(II)-porphyrin moieties. All these nanomaterials exhibited efficient photocatalytic performances in the degradation of rhodamine B (RhB) dye under visible light irradiation, and the degradation efficiencies of RhB in aqueous solution were observed to be 72~95% within 4 h. In addition, the efficiency of the catalyst was not impaired, showing excellent recyclability even after being applied for the degradation of RhB in up to five cycles.

A novel near-infrared fluorescent probe based on isophorone for the bioassay of endogenous cysteine

2021 ◽  
Author(s):  
Hong-Bo Liu ◽  
Hai Xu ◽  
Xin Guo ◽  
Jian Xiao ◽  
Zheng-Hong Cai ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Fluorescent Probe ◽  
Near Infrared ◽  
Stokes Shift ◽  
Rapid Identification ◽  
Large Stokes Shift

A near-infrared (NIR) fluorescent probe with a large Stokes shift (143 nm) for the rapid identification of Cys over Hcy and GSH in aqueous solution was developed.

scholarly journals A Novel Thiosemicarbazide-Based Fluorescent Chemosensor for Hypochlorite in Near-Perfect Aqueous Solution and Zebrafish

Chemosensors ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 65
Author(s):  
Minji Lee ◽  
Donghwan Choe ◽  
Soyoung Park ◽  
Hyeongjin Kim ◽  
Soomin Jeong ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Reactive Oxygen Species ◽  
Aqueous Solution ◽  
Fluorescence Quenching ◽  
Limit Of Detection ◽  
Fluorescent Sensor ◽  
Ionization Mass ◽  
Oxygen Species ◽  
Marked Selectivity ◽  
Uv Visible

A novel thiosemicarbazide-based fluorescent sensor (AFC) was developed. It was successfully applied to detect hypochlorite (ClO−) with fluorescence quenching in bis-tris buffer. The limit of detection of AFC for ClO− was analyzed to be 58.7 μM. Importantly, AFC could be employed as an efficient and practical fluorescent sensor for ClO− in water sample and zebrafish. Moreover, AFC showed a marked selectivity to ClO− over varied competitive analytes with reactive oxygen species. The detection process of AFC to ClO− was illustrated by UV–visible and fluorescent spectroscopy and electrospray ionization–mass spectrometry (ESI–MS).

Automation and validation of a MALDI-TOF MS (Mass-Fix) replacement of immunofixation electrophoresis in the clinical lab

2021 ◽  
Vol 59 (1) ◽  
pp. 155-163
Author(s):  
Mindy Kohlhagen ◽  
Surendra Dasari ◽  
Maria Willrich ◽  
MeLea Hetrick ◽  
Brian Netzel ◽  
...  
Keyword(s):  
Limit Of Detection ◽  
Turnaround Time ◽  
Automated System ◽  
Serum Samples ◽  
Maldi Tof Ms ◽  
Maldi Tof ◽  
Automated Method ◽  
Positive Specimen ◽  
Specimen Identification ◽  
Tof Ms

AbstractObjectivesA matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) method (Mass-Fix) as a replacement for gel-based immunofixation (IFE) has been recently described. To utilize Mass-Fix clinically, a validated automated method was required. Our aim was to automate the pre-analytical processing, improve positive specimen identification and ergonomics, reduce paper data storage and increase resource utilization without increasing turnaround time.MethodsSerum samples were batched and loaded onto a liquid handler along with reagents and a barcoded sample plate. The pre-analytical steps included: (1) Plating immunopurification beads. (2) Adding 10 μl of serum. (3) Bead washing. (4) Eluting the immunoglobulins (Igs), and reducing to separate the heavy and light Ig chains. The resulting plate was transferred to a second low-volume liquid handler for MALDI plate spotting. MALDI-TOF mass spectra were collected. Integrated in-house developed software was utilized for sample tracking, driving data acquisition, data analysis, history tracking, and result reporting. A total of 1,029 residual serum samples were run using the automated system and results were compared to prior electrophoretic results.ResultsThe automated Mass-Fix method was capable of meeting the validation requirements of concordance with IFE, limit of detection (LOD), sample stability and reproducibility with a low repeat rate. Automation and integrated software allowed a single user to process 320 samples in an 8 h shift. Software display facilitated identification of monoclonal proteins. Additionally, the process maintains positive specimen identification, reduces manual pipetting, allows for paper free tracking, and does not significantly impact turnaround time (TAT).ConclusionsMass-Fix is ready for implementation in a high-throughput clinical laboratory.

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