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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Real-time blood gas analysis using pH, PO2 and PCO2 multifunctional fluorescent capillary sensing system

Jinhua Liu,Lan Guan,Zhe Li,Li Huang,Dan Li,Zhe Li,Xiaohui Wang,Yingqun Zhu,Yuanan Liu

Real-time blood gas analysis is of great significance in disease diagnosis and treatment. Here we have developed a pH, PO 2 and PCO 2 multifunctional fluorescent capillary sensing system. The pH, O 2 and CO 2 fluorescent indicators with same excitation wavelength are fixed into a single capillary tube. The sensing system possesses sensitive fluorescence response to pH, O 2 and CO 2 , and the changes of pH, O 2 and CO 2 in buffer, in vitro, and in vivo can be detected simultaneously by measuring the fluorescence signals of sensor probe. The PO 2 , PCO 2 and pH of rabbits in four disease models were assessed efficiently by the sensing system, exhibiting similar variation trend with the results by blood gas analyzer. Studies in living rabbit display the reasonable and favorable feasibility of capillary sensing system in real-time arterial blood gas analysis. Overall, the multifunctional fluorescent capillary sensing system exhibits significant potential in real-time arterial blood gas analysis and clinical application of disease diagnosis.

研究领域: 医学诊断 · 生物传感技术
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2021 · IF 4.098

Two-phase activated colorimetric and ratiometric fluorescent sensor for visual detection of phosgene via AIE coupled TICT processes

Qinghua Hu,Tao Gong,Yu Mao,Qiang Yin,Yuyuan Wang,Hongqing Wang

In this paper, we specifically designed and synthesized an excellent colorimetric and ratiometric fluorescent sensor DPA-CI for rapid and convenient detection of the highly toxic phosgene. DPA-CI was developed by incorporated a diphenylamine (DPA) and a 2-imine-3-benzo[d]imidazole as the enhanced push–pull electronic structure into the coumarin fluorophore matrix. The sensor DPA-CI towards phosgene sensing exhibited both visible colorimetric and ratiometric fluorescent color change in solution and in gaseous conditions with TICT and AIE mechanism respectively, which can be easily distinguished by using the naked eye. Also, the sensor DPA-CI showed splendid sensing performance such as excellent selectivity, rapid response (less than 8 s in THF and 2 min in gaseous condition), and fair sensitivity (limit of detection less than 0.11 ppm in gaseous condition and 0.27 μM in solution). The design strategy based on enhanced push–pull electronic structure with AIE and TICT properties will be helpful to construct a solid optical sensor with excellent potential application prospects for portable and visual sensing of gaseous phosgene through distinct color and ratiometric fluorescence change by the naked eyes.

研究领域: 化学 · 材料科学
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Materials Science & Engineering C-Materials for Biological Applications · 2021 · IF 7.328

Carbon dots for specific “off-on” sensing of Co2+ and EDTA for in vivo bioimaging

Xiangping Wen,Guangming Wen,Wenyan Li,Zhonghua Zhao,Xine Duan,Wenjun Yan,John F. Trant,Yingqi Li

Fluorescent carbon dots (CDs) were hydrothermally synthesized from a mixture of frozen tofu, ethylenediamine and phosphoric acid in an efficient 64% yield. The resulting CDs exhibit good water solubility, low cytotoxicity, high stability, and excellent biocompatibility. The CDs selectively and sensitively detect Co 2+ through fluorescent quenching with a detection limit of 58 nM. Fluorescence can be restored through the introduction of EDTA, and this phenomenon can be used to quantify EDTA in solution with a detection limit of 98 nM. As both analytes are detected by the same CD platform, this is an “off-on” fluorescence sensor for Co 2+ and EDTA. The technique's robustness for real-world samples was illustrated by quantifying cobalt in tap water and EDTA in contact lens solution. The CDs were also evaluated for in vivo imaging as they show low cytotoxicity and excellent cellular uptake. In a zebrafish model, the CDs are rapidly adsorbed from the intestine into the liver, and are essentially cleared from the body in 24 h with no appreciable bioaccumulation. Their simple and efficient synthesis, combined with excellent physical and chemical performance, renders these CDs attractive candidates for theranostic applications in targeted “smart” drug delivery and bioimaging.

CAS / MDL: 128446-36-6 6119-70-6
研究领域: 分析化学 · 生物医学工程 · 材料科学
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MOLECULES · 2022 ·Vol. 27 ·期 19 ·6749 · IF 4.927

Sensitive, Selective and Reliable Detection of Fe3+ in Lake Water via Carbon Dots-Based Fluorescence Assay

Zhuang Xiang,Yuxiang Jiang,Chen Cui,Yuanping Luo,Zhili Peng

In this study, C-dots were facilely synthesized via microwave irradiation using citric acid and ethylenediamine as carbon precursors. The fluorescence emissions of the C-dots could be selectively quenched by Fe3+, and the degree of quenching was linearly related to the concentrations of Fe3+presented. This phenomenon was utilized to develop a sensitive fluorescence assay for Fe3+detection with broad linear range (0–250, 250–1200 μmol/L) and low detection limit (1.68 μmol/L). Most importantly, the assay demonstrated high reliability towards samples in deionized water, tap water and lake water, which should find potential applications for Fe3+monitoring in complicated environments.Keywords:Fe3+;fluorescence sensing;carbon dots;lake water;limit of detection

CAS / MDL: 107-15-3
研究领域: 环境科学 · 分析化学
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2024 · IF 4.3

Recognition and detection of histamine in foods using aptamer modified fluorescence polymer dots sensors

Gan Wu,Zhaoyang Ding,Xilin Dou,Ze Chen,Jing Xie

Histamine has been known as a momentous cause of biogenic amine poisoning. Therefore, the content of histamine in foods is strictly required to be controlled within a certain range. Here, an aptamer fluorescent sensor was developed for detection of histamine. Poly [(9, 9-di-n-octylfluorenyl-2, 7-diyl)-alt-(benzo [2,1,3] thiadia-zol-4, 8-diyl)] (PF8BT) and the styrene maleic anhydride copolymer (PSMA) were used for the preparation of PF8BT-Polymer dots (PF8BT-Pdots). PF8BT-Pdots and the cyanine3-phosphoramidite (Cy3) were linked through aptamer to achieve the ratiometric detection for histamine. PF8BT-Pdots were partly quenched by Cy3 due to the fluorescence resonance energy transfer (FRET), when the histamine molecule was recognized by aptamer on the surface of PF8BT-Pdots. A linear range (3–21 μmol/L) was obtained for histamine detection with a low limit of detection (LOD = 0.38 μmol/L). PF8BT aptamer Pdots (PF8BT-A) were used to detect histamine in simply treated aquaculture water and tuna. The cell imaging of HeLa cells presented a good biosecurity and outstanding fluorescent imaging capability of PF8BT-A. The aptamer fluorescent sensors provided a new platform for rapid and accurate detection of histamine in aquatic products and had great potential for the application in food safety and quality control.

研究领域: 食品安全 · 生物化学 · 分析化学
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Journal of Inorganic and Organometallic Polymers and Materials · 2019 ·Vol. 29 ·期 6 ·2124-2132 · IF 1.637

Eu3+/TFA Functionalized MOF as Luminescent Enhancement Platform: A Ratiometric Luminescent Sensor for Hydrogen Sulfide in Aqueous Solution

Wang Zirui,Wang Xinyu,Li Jingfang,Li Weizuo,Li Guangming

In this work, a facile and fast luminescence sensing platform for the ratiometric detection of hydrogen sulfide (H 2 S/HS − ) has been constructed by encapsulating the Eu 3+ /β-diketone chromophore into the host framework of MIL-140 (Eu 3+ /TFA@MIL-140C, TFA = 1,1,1-Trifluoro-2,4-pentanedione). It is well known that the energy transfer from the host framework or/and TFA to the Eu 3+ ions can be disturbed easily by some metal ions, such as Cu 2+ ions. Therefore, the ratiometric sensor was constituted with the Eu 3+ /β-diketone moiety as the response signal and the host framework moiety as the reference signal. Furthermore, on the basis of the hard–soft acid–base theory, the Cu 2+ ions could be rapidly caught by HS − , profiting from the low solubility of CuS, realizing the real-time detection by luminescence color change. This sensor shows remarkable property on the detection of H 2 S (HS − in water solution) with low limit of detection (LOD = 7.43 μM) and short response time (< 0.5 min). The good linearity between luminescent intensity and concentration makes the luminescent ratio meter feasible.

研究领域: 材料科学 · 分析化学 · 环境科学
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DALTON TRANSACTIONS · 2018 ·Vol. 47 ·期 46 ·16696-16703 · IF 4.099

Eu3+/Tb3+ functionalized Bi-based metal–organic frameworks toward tunable white-light emission and fluorescence sensing applications

Lifei Xu,Yan Xu,Xianliang Li,Zhuopeng Wang,Ting Sun,Xia Zhang

The rational design strategy to construct lanthanide ion functionalized metal organic frameworks (MOFs) has attracted tremendous attention as they are promising candidates for developing novel luminescence materials and optical sensors owing to their intense, long-lived and tunable luminescence performances. In this work, a series of Eu3+/Tb3+ singly doped or codoped bismuth-based MOFs were prepared under in situ facile solvothermal conditions using BiOBr nanoplates as bismuth resources. A red-green-blue-based trichromatic white-light emission can be finely achieved by modulating the doping ratio of Eu3+/Tb3+ in the blue-emitting Bi-MOF host material and such photoluminescence tuning can also be realized by controlling the excitation wavelength. In addition, the Eu3+/Tb3+ singly incorporated Bi-MOF can serve as a multifunctional fluorescent probe for sensing Fe3+ and Cr2O72− ions in aqueous solution, as well as small organic pollutants of acetone molecules, and their sensing mechanisms have also been analyzed. These lanthanide ion functionalized Bi-MOF materials exhibit great potential in exploring white-light emitting devices and construction of supersensitive multifunctional sensors.

研究领域: 材料科学 · 光学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Three-step post-synthetic modification metal-organic framework as a ratiometric fluorescent probe for the detection of creatinine

Ning Wu,Hao Guo,Liping Peng,Yuan Chen,Lei Sun,Yinsheng Liu,Xiaoqing Wei,Wu Yang

Creatinine (Cre) measurement in biological fluids is an increasingly important clinical measure for evaluating renal insufficiency, thyroid dysfunction, and muscle injury. Therefore, a simple, fast, and reliable Cre analysis method is of great significance to human health. Herein, a novel ratiometric fluorescence sensor, Ag-Eu-MOF-808-EDTA, was synthesized by introducing ethylenediaminetetraacetic acid (EDTA), Ag + , and Eu 3+ into the framework of MOF-808 through three steps of post-synthesis modification, and was used to detect Cre in PBS buffer of pH 7.2 at 35 °C with a “turn-on” ratio response in the presence of various interfering ions and several biomolecules. In this strategy, the characteristic emission of Eu 3+ at 551 nm can be turned on due to coordination between Cre and Ag + , while emission at 613 nm is independent of Cre, which produces a significant ratio response change throughout the cycle. Experimental results showed that the ratio fluorescence sensor displayed a wide linear range for Cre from 0.5 to 350 μM with a low detection limit of 0.42 μM. Finally, a good recovery rate (96.7–102.9%) and appropriate relative standard deviation (RSD <2.39%, n = 3) were obtained during the determination of creatinine in real urine and serum. This work provides additional insights into the detection of creatinine in clinical blood samples.

研究领域: 分析化学 · 生物医学
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2017 · IF 2.536

Highly sensitive “turn-on” fluorescent chemical sensor for trace analysis of Cr3 + using electro-synthesized poly(N-(9-fluorenylmethoxycarbonyl)-l-histidine)

Hui Zhang,Ge Zhang,Jingkun Xu,Yangping Wen,Shouli Ming,Jie Zhang,Wanchuan Ding

Trivalent chromium (Cr 3   + ) can cause severely environment pollution, declining quality of edible agro-products in plants and animals, and human diseases. Poly( N -(9-fluorenylmethoxycarbonyl)- l -histidine) (PFLH) synthesized by the direct electro-polymerization of its corresponding commercially available monomer in both boron trifluoride diethyl etherate and dichloromethane mixed system. The “turn-on” type fluorescent sensor based on PFLH displayed high sensitivity and selectivity for Cr 3   + detecting. The structure of PFLH was rationally proved by 1 H NMR spectra, FT-IR spectra, quantum chemical calculations , and its optical properties were characterized. The electro-synthesized PFLH exhibited a “turn-on” fluorescent response towards Cr 3   + , which was employed as a sensing platform for the “turn-on” fluorescent analysis of Cr 3   + in a wide linear range from 5.1   nM to 25   μM with a low limit of detection as low as 1.7   nM. The possible mechanism of fluorescent “turn-on” sensor based on PFLH for Cr 3   + was proposed. The sensor displayed high sensitivity, good selectivity, satisfactory practicability, suggesting that PFLH has potential fluorescent application for “turn-on” sensing Cr 3   + in agricultural environments and edible agro-products of plants and animals.

研究领域: 环境科学 · 分析化学
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Sensors & Diagnostics · 2023 ·Vol. 3 ·期 1 ·79-86 · IF 0

Highly selective fluorescent sensor for ammonium ions

Min Shen,Tingting Pan,Yonghao Chen,Juewei Ning,Fengyu Su,Yanqing Tian

Ammonium ions (NH4+) are one of the important metabolic products and are closely related to human health. Currently, many NH4+ detection methods are inevitably disturbed by amino acids, K+, or other substituted amines (such as trimethylamine). To alleviate this problem, a new sensor was designed in this study, which consisted of the fluorescent indicator KS, hydrogel medium D4, and a hydrophobic membrane. In this sensing system, NH4+ and NH3 coexisted in equilibrium; NH3 could pass through a suitable hydrophobic film and transform into NH4+, which complexed with KS, resulting in a change of the probe's fluorescence intensity. By adjusting the internal composition of the sensing matrix, an excellent NH4+ sensor NS-1 was obtained; it demonstrated effective detection of NH4+ in the range 0.3–15.6 mM with a limit of detection (LOD) of 258 μM, and it was not disturbed by K+ or other substituting amines.

研究领域: 生物化学 · 分析化学
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Foods · 2022 ·Vol. 11 ·期 17 ·2650 · IF 5.561

A Rapid Fluorescence Sensor for the Direct Quantification of Rongalite in Foodstuffs

Hongfang Li,Jie Chen,Baowei Huang,Lingwei Kong,Feifei Sun,Lin Li,Chuanyi Peng,Huimei Cai,Ruyan Hou

Rongalite was reported illegally used as a food additive for bleaching purposes and improving the tenderness of foodstuffs, which may endanger public health. At present, rongalite was mostly detected by indirect methods via derivatization or determining its decomposition products. In this study, we developed a new fluorescence sensor for the direct quantification of rongalite based on the principles: (1) dopamine reacts with resorcinol and generates strong fluorophore (azamonardine); (2) rongalite could inhibit the production of fluorophores and then result in lower fluorescence intensity. Hence, the rongalite concentration was inversely proportional to fluorescence intensity of fluorophore. Several crucial reaction conditions of fluorescence sensor were further optimized, such as dopamine and resorcinol concentration, pH values, and reaction time. Under the optimal conditions, the limit of detection of fluorescence sensor was 0.28–0.38 μg/g in vermicelli, wheat and rice powder samples, exhibiting almost 3.5-fold improvement compared to that of lateral flow immunoassay. Moreover, the detection time was substantially decreased to 20 min. The recoveries in spiked samples were 80.7–102.1% with a coefficient of variation of less than 12.6%. In summary, we developed a direct, high throughput, selective and accurate fluorescence sensor that poses a promising application for the rapid detection of rongalite in foodstuffs.Keywords:rongalite;fluorescence sensor;rapid detection;foodstuffs

研究领域: 食品科学 · 分析化学
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2024 · IF 4.1

A “turn-on” fluorescent sensor for folic acid based on thiourea-decorated bis-cyanostilbene

Bowen Zha,Xinhui Huang,Liangbin Lin,Hongyu Guo,Fafu Yang

Although some detection methods for folic acid have been developed based on the conventional instruments, the rapid, simple and in-situ detection for folic acid was rarely reported. In this work, a “turn-on” and “color-changing” fluorescence sensor ( TBCS ) on detecting folic acid was designed and synthesized. TBCS emits the green fluorescence, which transferred to the strong blue fluorescence after binding folic acid. The high sensing selectivity was observed among various ions and biomolecules. The detection limitation of TBCS for folic acid was 4.32 × 10 −7  M. The sensing mechanism was proposed as that the ICT effectiveness of TBCS was interrupted by sensing folic acid. The application experiments on test paper, folic acid tablets and simulated sample displayed the good in-situ detecting ability of TBCS for folic acid, suggesting the good application prospect on rapid, simple and in-situ detecting folic acid in real environments.

研究领域: 分析化学 · 生物医学
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