ANALYST
·
2026
·
IF 3.6
Jiannan Jia,Hongjian Chen,Songle Wang,Yunpeng Wang,Qike Wang,Dong Chen,Shisheng Ling,Zhenzhen Ge,Wenkun Dong,Mi Yan,Zhiyu Wang,Xianping Fan,Xu Liang,Qiang Xu,Xvsheng Qiao
Eu-complex-swollen polystyrene (PS) fluorescent microspheres have attracted considerable attention in the field of lateral flow immunoassay (LFIA) bio-detection. However, the excessive swelling and induced concentration quenching effect of Eu complexes often deteriorate their fluorescence intensity and fluorescence efficiency. To address this issue, herein, we synthesized Eu(TTA)3(TPPO)2 and introduced divinylbenzene (DVB) to fabricate three-dimensionally cross-linked PS-DVB-Eu microspheres in order to obtain a moderate swelling capacity of the Eu complexes without obvious fluorescence concentration quench. This cross-linked structure effectively promotes the homogeneous distribution of swollen Eu(TTA)3(TPPO)2 in PS-DVB-Eu microspheres. This thus resulted in improved fluorescence properties with a high internal quantum efficiency (IQE) of 52.36% and a lifetime of 539 μs. The fluorescence of the cross-linked PS-DVB-Eu microspheres was 3.85 times stronger than that of the non-crosslinked PS-Eu microspheres. The cross-linked structures also helped the PS-DVB-Eu microspheres maintain a relatively high zeta potential and a large surface carboxyl concentration. These merits support PS-DVB-Eu microspheres in obtaining an enhanced lateral flow immunoassay (LFIA) performance, including an LOD of 0.08 ng mL−1 and a CV value of less than 7.34% on detecting C-reactive protein (CRP). This demonstrates that cross-linked PS-DVB-Eu microspheres are promising materials for high performance LFIA point-of-care testing techniques.
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CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Yihan Wu,Biyun Li,Xiangxue Wang,Shujun Yu,Hongwei Pang,Yue Liu,Xiaoyan Liu,Xiangke Wang
The water stable core-shell microspheres (Fe 3 O 4 @ZIF-8) with strong magnetism were successfully fabricated through a facile modification strategy. Concrete procedures included firstly pretreatment of Fe 3 O 4 core with anionic polyelectrolyte to acquire negatively charged Fe 3 O 4 particle surface, followed by nucleation through attracting Zn 2+ cation, and then growth of a thin layer of ZIF-8 (~25 nm). Various characterization techniques (SEM, TEM, FT-IR, XRD, VSM, BET and XPS) indicated that the Fe 3 O 4 @ZIF-8 microspheres were highly stable and magnetic with a large specific surface area (606.91 m 2 /g) and fairly sufficient functional groups ( NH , OH, COOH, Zn O, N O and C N ). Multi-factors affecting the radionuclides removal performance on Fe 3 O 4 @ZIF-8 was adequately explored, comprising contact time, temperature, pH, ionic strength, co-existing ions and extreme conditions. And the results showed that Fe 3 O 4 @ZIF-8 exhibited fast reaction kinetics (~30 min to achieve equilibrium), excellent uptake capabilities (539.7 mg U/g and 255.6 mg Eu/g), remarkable selectivity and favorable physicochemical stability. These researches suggested that Fe 3 O 4 @ZIF-8 could not only simultaneously achieve favorable stability and functionality, but also easily to be separated by external magnetic field after used in radioactive sewage treatment, which was of considerable practical utility in extracting radioactive wastes though in harsh circumstance.
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FOOD CHEMISTRY
·
2021
·
IF 7.514
Kuiyu Yi,Lei Zhang
An ingenious nanoscale fluorescent sensor derived from Eu 3+ -postfunctionalized MIL-53 (Al) (Eu 3+ @MIL-53 [Al]) was fabricated though a simple and effective approach. Malachite green (MG) effectively turned off the luminescence of Eu 3+ @MIL-53 (Al) via fluorescence resonance energy transfer (FRET), thus enabling MG sensing. The developed probe exhibited instantaneous reusability after being cleaned with deionized water. The fluorescence intensity, quenching efficiency, and crystal structure of the recoverable sensor after five recycling processes were unchanged compared with those of the original sample. Moreover, the potential mechanism of MG detection was revealed in detail. This work represents the first attempt to determine MG in aquaculture water and products by using metal–organic frameworks (MOFs). The Eu 3+ @MIL-53 (Al) probe proved to be a remarkable fluorescence probe for MG with high selectivity, sensitivity, and excellent regeneration capability. It provides a promising functional platform for the recognition of illegal MG addition to aquaculture water and products.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2019
·
IF 2.931
Hongwei Ren,Xue Wang,Ruiquan Gong,Meiyu Li,Hongyu Zhu,Jinfeng Zhang,Erhong Duan
Heavy metal ions in wastewater have brought serious environmental pollution. To improve the detection efficiency, it is important to find useful fluorescent probes . The emerging green natural deep eutectic solvents (NADESs) offer attractive option for “green” detection for its good biocompatibility, easy preparation, and high sensitivity. In this study, a multi-functionalized fluorescent probe with atomically dispersed EuCl 3 ·6H 2 O in amino acid-based NADESs ( l -Glutamic acid/Glycerol, l -Glu/Gly) was synthesized by metal-ligand coordination interactions with a mass ratio of 15:1. Combined with the NADESs and rare earth metal , the l -Glu/Gly/EuCl 3 ·6H 2 O could form the amino site and Eu 2+ site fluorescent centers. Under the excitation wavelength of 370 nm, it had dual emission peaks at 425 nm and 470 nm with efficient resonance energy transfer . The stable optoelectronic properties of l -Glu/Gly/EuCl 3 ·6H 2 O under external factors, such as mass ratio (13,1 to 18:1), temperature (30–50 °C), pH (1 to 14) and storage time ( >42 days), approved l -Glu/Gly/EuCl 3 ·6H 2 O an excellent fluorescence probe. In the application of water-quality monitoring, Fe 3+ and Cu 2+ could react with l -Glu/Gly/EuCl 3 ·6H 2 O in different reactive patterns. The blue fluorescence was quenched by Fe 3+ and enhanced by Cu 2+ , thus metal ions could be distinguished with high sensitivity. The detective process was determined and the fluorescent mechanism was also proposed. l -Glu/Gly/EuCl 3 ·6H 2 O fluorescent probe was demonstrated to be an efficient fluorescent probe for metal detection avoiding the hydrothermal process, and the cumbersome of ilter, dialysis, freeze drying.
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Frontiers in Chemistry
·
2018
·
IF 4.155
Li Yinong,Tian Chen,Liu Weizhen,Xu Si,Xu Yunyun,Cui Rongxin,Lin Zhang
Nano-Mg(OH)2 is attracting great attention as adsorbent for pre-concentration and recovery of rare earth elements (REEs) from low-concentration solution, due to its superior removal efficiency for REEs and environmental friendliness. However, the nanoparticles also cause some severe problems during application, including aggregation, blockage in fixed-bed column, as well as the difficulties in separation and reuse. Herein, in order to avoid the mentioned problems, a carbon cloth (CC) supported nano-Mg(OH)2 (nano-Mg(OH)2@CC) was synthesized by electrodeposition. The X-ray diffraction and scanning electron microscopy analysis demonstrated that the interlaced nano-sheet of Mg(OH)2 grew firmly and uniformly on the surface of carbon cloth fibers. Batch adsorption experiments of Eu(III) indicated that the nano-Mg(OH)2@CC composite maintained the excellent adsorption performance of nano-Mg(OH)2 toward Eu(III). After adsorption, the Eu containing composite was calcined under nitrogen atmosphere. The content of Eu2O3 in the calcined material was as high as 99.66%. Fixed-bed column experiments indicated that no blockage for Mg(OH)2@CC composite was observed during the treatment, while the complete blockage of occurred to nano-Mg(OH)2 at an effluent volume of 240 mL. Moreover, the removal efficiency of Mg(OH)2@CC was still higher than 90% until 4,200 mL of effluent volume. This work provides a promising method for feasible application of nanoadsorbents in fixed-bed process to recycle low-concentration REEs from wastewater.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
·
IF 4.3
Xuequan Jing,Meina Guo,Jiarong Li,Wei Xu,Haonan Qin,Weidong Xiao,Yinhua Wan,Jieliang Chen,Zhangwei Yao,Weijie Song,Hongdong Yu,Kang Hu,Tinggang Li
The overuse of quinolone antibiotics has led to a series of health and environmental issues. Herein, we combine the distinct luminescence properties of Eu 3+ with the unique structure of covalent organic frameworks (COFs) to develop a precise and sensitive fluorescent probe for detecting Flumequine (Flu) in water. Eu 3+ is thoroughly anchored into the channels of COFs as recognition sites, while the synthesized probe material still maintains its intact framework structure. The unique structure of COFs provides excellent support and protection for Eu 3+ . Therefore, COF-Eu can rapidly bind with Flu which can transfer the absorbed energy to Eu 3+ through an “antenna effect”, resulting in red fluorescence. Moreover, there is a good linear relationship between Flu concentration in the range of 0–30 µM, with a detection limit of 41 nM. Simultaneously, the material maintains remarkable reproducibility, with its performance remaining almost unchanged after five cycles of use. Remarkably, the probe demonstrates excellent Flu recovery rates in real samples. This study provides a viable approach for the recognition of flumequine in the environment through a customized fluorescence detection method.
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MICROCHIMICA ACTA
·
2020
·Vol. 187
·期 8
·1-13
·
IF 6.232
Min Jie,Qu Xiang-Long,Yan Bing
A novel fluorescent and electron-deficient hybrid, N -methylated [Eu (pddb)phen(ox) 0.5 ] n (Eu-MOF-Me) has been prepared via post-synthetic modification. Considering its special luminescent properties and cationic framework, Eu-MOF-Me is developed as a visualized fluorescent probe. Notably, water-stable Eu-MOF-Me exhibits advantages like good structural and fluorescent stability in a wide range of pH value (3.39–10.86), excellent identification ability for F − , I − , and S 2− (it can easily distinguish F − and I − from other halogen ions and can realize naked eye identification of F − , I − , and S 2− ), relatively low detection limits (6.61 μM for S 2− , 7.57 μM for F − ), and reusability. More importantly, it has been utilized for the construction of a Boolean logic gate system. In this system, Eu-MOF-Me serves as the gate, by taking F − , I − , and S 2− as the inputs and fluorescence emission bands (UV380, B437, and R612) as the outputs; some primary logic gates (NOR, IMP, YES, NOT) and the combination of them have been realized. Moreover, we achieved a cascaded logic gate (NOR+OR). For further application, a molecular computing keypad-lock security system has been obtained.
A novel fluorescent and electron-deficient hybrid named Eu-MOF-Me has been prepared via post-synthetic methylation. Considering its special luminescent properties and cationic framework, Eu-MOF-Me was developed as a fluorescent probe for the visual monitoring of important anions. In addition, it was used for the construction of Boolean logic library and a keypad-lock system was achieved
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2024
·Vol. 333
·期 4
·2195-2206
·
IF 1.5
Li Junze,Zhao Chuang,Guo Wenbin,Gao Yang,Liu Tingting,Zhou Yu,Hou Hongguo,Jiao Caishan,Zhang Meng
Using DMDODGA as the carrier, the transportation and separation behavior of Eu(III) and La(III) were studied using a plate-type supported liquid membrane. La(III) and Eu(III) reach their maximum transport rates at feed phase nitric acid concentrations of 2 and 4 mol/L, which are 72.41 (± 2.12)% and 77.80 (± 2.45)%; Increasing the concentration of NO 3 − in feed phase will promote the transport of both ions. The change of HNO 3 concentration in feed phase had major effect on the separation of Eu(III)/La(III), and the co-transport of Eu(III)/La(III) was observed when the concentration of NO 3 − was 3 mol/L.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2026
·
IF 5.4
Raj Kumar Parajuli,Govinda Gurung,Shree Krishna Tamang,Dinesh Acharya,Xinzhi Wang,Jun Li,Du Zhonglin,Yao Wang,Yanxin Wang,Xinze Yu,Soo Wohn Lee,Laurence A. Belfiore,Jianguo Tang
Polymeric drug nanocarriers still face critical challenges, including poor water solubility, limited biocompatibility, insufficient drug loading capacity, uncontrolled drug release, and the lack of in situ sensing capabilities. This work aims to develop new polymeric drug nanocarriers with multifunctionalization of drug loading, releasing, and in situ sensing (D-LRS). Firstly, water-dispersible Eu 3+ -induced polymeric nanoaggregates (EIPAs) composed of EuCl 3 , 1,10-phenanthroline, and 2-thenoyltrifluoroacetone are synthesized as drug nanocarriers in a polystyrene- block -poly(acrylic acid) aqueous system. The as-synthesized EIPAs have an average diameter of 200 nm and intrinsic luminescence in an aqueous environment, as well as good biocompatibility. Secondly, both doxorubicin ( dox ) and paclitaxel ( pac ) are encapsulated with EIPAs for co-delivery, either separately or together, and the encapsulated drugs are found to be able to achieve pH-responsive controlled release. More importantly, the loading and releasing of the dox and pac drugs could be efficiently in situ monitored by tuning the emission intensity of EIPAs. Thanks to desired water solubility and biocompatibility, as well as intense aqua-luminescence and pH-responsive drug-releasing ability, the smart Eu 3+ -fluorescence-sensible drug carriers could have potential for D-LRS in the combinatory therapy of cancer.
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2020
·
IF 4.551
Jun Yao,Ming Xie,Yang Li
In order to protect human health from the threat of excessive acrylamide in heat-processed foods, swift, uncomplicated, highly selective and sensitive online monitoring methods for acrylamide are urgently needed. In this study, a rare earth metal/transition metal-organic frameworks Eu/Zr-MOFs fluorescence sensor with dual-band luminescence was prepared by the solvothermal method for detection of acrylamide in fried potatoes and cookie crumbs. This sensor exhibited two different fluorescence emission peaks at 430 and 615 nm under excitation of 365 nm, and the ratio of fluorescence intensity was linear with the experimental concentration of acrylamide in the range of 1 × 10 −4 to 1 × 10 −3 M. Under the optimal conditions, the proposed fluorescence analysis method showed that the detection limit of acrylamide was as low as 2.4 × 10 −8 M, and the satisfactory recoveries of 94.05–104.04% were obtained for various spiked samples. More importantly, the sensor has ultra-high selectivity for the detection of acrylamide while other small organic molecules hardly interfere with it in the measurement environment. These studies confirmed that the ratiometric fluorescence sensing method was expected to achieve on-line rapid detection of acrylamide in real foods. In addition, the mechanism of Eu/Zr-MOFs sensing of acrylamide was analyzed and discussed in depth, and the analog computation was carried out by Materials Studio software, and the entire sensing system was studied at the micro level in combination with density functional theory.
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MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 10
·1-8
·
IF 5.705
Pang Jiawei,Lu Yuexiang,Gao Xinyu,Song Panshu,Yang Fengyi,Liu Yueying
A selective phosphorescent on-off-on probe with long decay lifetime has been designed for the detection of pyrophosphate ions (PPi). The detection scheme is based on the use of europium(III)-modulated Mn(II)-doped ZnS quantum dots capped with N-acetyl-L-cysteine. Both the aggregation of quantum dots and electron transfer induced by Eu(III) ions cause phosphorescence to be quenched (“off” state). Phosphorescence is, however, restored on addition of PPi to the system (“on” state). The effect is attributed to the removal of Eu(III) from the carboxy groups on the surface of the quantum dots owing to the stronger interaction between PPi and Eu(III). A linear relationship exists between phosphorescence intensity (best measured at excitation/emission wavelengths of 316/594 nm) and PPi concentration in the 400 nM to 6000 nM with a detection limit of 145 nM. An additional attractive feature is provided by the long-lived phosphorescence (1920 μs) of the quantum dots. It can be used to eliminate interference by short-lived fluorescence in biological samples by performing time resolved measurements. The probe was applied to the determination of PPi in spiked in urine samples and gave recoveries in the range from 98 to 105% with RSDs of <2.0%.
Schematic of a long-lived phosphorescent on-off-on probe for the sensitive and selective detection of pyrophosphate ions (PPi). It is based on the use of Eu(III)-modulated Mn(II)-doped ZnS quantum dots (QDs). Phosphorescence is quenched of QDs after the addition of Eu 3+ but restored after the addition of PPi.
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INORGANIC CHEMISTRY
·
2023
·
IF 4.6
Dongsheng Zhao,Wenqian Li,Rongmei Wen,Nana Lei,Wencui Li,Xin Liu,Xiutang Zhang,Liming Fan
With the introduction of Eu3+ ions as the secondary fluorescent signal reporter and sensing active sites, a dual-emission ratiometric sensor of Eu3+@NiMOF (Eu3+ functional NiMOF) for hippuric acid (HA) detection in urine and serum was fabricated via the postsynthetic encapsulating strategy. Based on the two emission signals at 441 nm (turn-on) and 628 nm (turn-off), the produced Eu3+@NiMOF ratiometric sensor provided enhanced sensitivity, higher selectivity, and 9.7 times lower limits of detection (LOD) for the detection of HA (2.38 μM, 0.42 μg·mL–1) than that of the pristine NiMOF. Considering the high sensitivity and visualization results, further exploration of intelligent applications in the HA sensing process was carried out by constructing a tandem combinational logic gate to improve the practicability and convenience with the help of a smartphone. This work provides a promising approach for developing MOF-based ratiometric sensors to detect biomarkers.
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