MARINE POLLUTION BULLETIN
·
2015
·Vol. 102
·期 1
·142-147
·
IF 2.991
Xiuping He,Xiaoqi Mei,Jiangtao Wang,Ziru Lian,Liju Tan,Wei Wu
An effective and highly selective molecularly imprinted material was prepared by suspension polymerization for the isolation and pre-concentration of synthetic estrogen diethylstilbestrol (DES) in seawater . The obtained MIPMs were proved to have more uniform size and porous structure, with maximum adsorption capacity of 8.43 mg g − 1 almost two times more than NIPMs (4.43 mg g − 1 ). The MIPMs showed no significant deterioration of the adsorption capacity after five rounds of regeneration. An off-line molecularly imprinted solid phase extraction (MISPE) method followed by HPLC–DAD was proposed for the detection of DES in seawater , and recoveries were satisfactorily higher than 77%. Four seawater samples in aquaculture area were analyzed and 0.61 ng mL − 1 DES was detected in one sample. The result demonstrated that this method can be used for the rapid separation and clean up of trace residual of DES in seawater.
研究领域:
环境分析化学
·
海洋环境污染
·
分子印迹技术
·
药物残留检测
·
水体污染物
✓ 已验证
DOI
高影响因子
FOOD CHEMISTRY
·
2023
·
IF 8.8
Jiameng Liu,Mengfei Wang,Chuanpan Guo,Zheng Tao,Minghua Wang,Linghao He,Baozhong Liu,Zhihong Zhang
An electrochemical aptasensor was prepared for the efficient, sensitive, and selective detection of 17β-estradiol. The sensor was based on a defective two-dimensional porphyrin-based metal–organic framework derived from V 2 CT x MXene. The resulting metal–organic framework nanosheets benefited from the advantages of V 2 CT x MXene nanosheets and porphyrin-based metal–organic framework, two-dimensional porphyrin-based metal–organic framework nanosheets demonstrated amplified electrochemical response and enhanced aptamer-immobilization ability compared with V 2 CT x MXene nanosheets. The sensor’s detection limit was ultralow at 0.81 fg mL −1 (2.97 fM), and the 17β-estradiol concentration range was wide, thereby outperforming most reported aptasensors. The high selectivity, superior stability and reproducibility, and excellent regeneration performance of the constructed aptasensor indicated its remarkable potential application for 17β-estradiol determination in diverse real samples. This aptasensing strategy can be used to analyze other targets by replacing the corresponding aptamer.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
·
2023
·
IF 8.8
Lixia Lu,Xinyu Shao,Jianwen Gao,Bingchan Song,Linhe Ding,Jianhua Zhou
The endocrine system's interference caused by environmental estrogens (EEs) residue in food is a topic of public concern. Here, we construct an aptasensor for the sensitive detection of EEs based on luminescence resonance energy transfer (LRET). With MoS 2 nanosheets acting as the energy acceptor and upconversion luminescence [email protected] nanoparticles ( [email protected] ) as the luminescence donor, autofluorescence from food is prevented from interfering. The in-situ deposition of AuNPs not only induces local field enhancement to significantly increase the luminescence intensity of UCNPs, but also conduces to the modification of aptamer through Au-S bond. This aptasensor can respond to multiple estrogens thanks to the choice of a universal aptamer that recognizes phenolic hydroxyl group, and it offers the probability to screen unidentified phenolic estrogens. This method has a high sensitivity and a low limit of detection (LOD), and the satisfactory recovery rates acquired from water and milk samples confirmed its considerable application value.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHIMICA ACTA
·
2022
·Vol. 189
·期 12
·1-10
·
IF 6.408
Sun Min,Wang Xiuqin,Ding Yali,Feng Juanjuan
In order to improve the selectivity and stability of melamine–formaldehyde (MF) aerogel, it was composited with TiO 2 aerogel. A TiO 2 -MF hybrid aerogel was in situ prepared on the surface of carbon fibers for in-tube solid-phase microextraction (SPME). The extraction performance of TiO 2 -MF aerogel was regulated by changing the ratio of TiO 2 sol and MF sol during the material preparation. Coupled with high-performance liquid chromatography-diode array detection (HPLC–DAD), the extraction tube filled by TiO 2 -MF aerogel-coated carbon fibers was evaluated with several types of environmental pollutants including polycyclic aromatic hydrocarbons (PAHs), estrogens, and ultraviolet filters. Because of favourable extraction performance of PAHs they were selected as model analytes, and some important influence factors were optimized for satisfactory sensitivity. The detection limits were in the range 0.05–0.10 μg L −1 , owing to high enrichment factors (653–1007). The online in-tube SPME-HPLC–DAD method was verified for the determination of trace PAHs in environmental water samples, and acceptable recovery (70–118%) was achieved. The analytical methods also displayed some advantages in comparison with other reports. Moreover, the extraction tube exhibited satisfactory chemical stability. Graphical abstract
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF SEPARATION SCIENCE
·
2022
·Vol. 45
·期 23
·4224-4235
·
IF 3.614
Ruozhu Xu,Yuan Tao,Wang Yao,Honglin Qin,Lizhen Qiao
In this study, three-dimensional flower-like tin disulfide materials were prepared, and a highly efficient dispersive solid-phase extraction method was developed using the obtained three-dimensional tin disulfide adsorbents for the preconcentration and determination of six endocrine-disrupting phenols in combination with high-performance liquid chromatography-ultraviolet detection. Several important experimental parameters influencing extraction efficiency were investigated, including the amount of adsorbent, ultrasound time, sample solution pH, sample volume, type of elution solvent, desorption time, and the number of desorption times. Under the optimized experimental conditions, the developed method showed good linearity with the determination coefficients of 0.993–0.998 in the linear range of 0.5–400 ng/ml and low limits of detection in the range of 0.15–1.0 ng/ml, as well as satisfactory intra-day and inter-day precisions with relative standard deviations of 0.1–9.8%. Finally, the proposed method was successfully applied for the enrichment and determination of trace endocrine-disrupting phenols in milk, tea beverage, and plastic bottled water samples, and acceptable recoveries were obtained from 70.1% to 119.1% under four different spiked concentration levels. The results showed that the three-dimensional tin disulfide materials had great potential for the extraction of endocrine-disrupting phenols contaminants in environmental and food samples.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Yan Wu,Panpan Cao,Yanhao Jiang,Yanjuan Liu,Yuefei Zhang,Wei Chen,Zhengwu Bai,Sheng Tang
Nowadays, the efficient detection of environmental organic pollutants has been a research focus in the field of chromatographic analysis . In this work, aminopropylimidazole was designedly introduced to adjust the hydrophobicity of the long-chain alkyl group , and a novel chromatographic stationary phase for the separation and analysis of environmental organic pollutants was specially prepared. Specifically, the waste aminopropyl silica gel (5 μm) was first recycled as the raw material, which was calcined at high temperature and then acidified with hydrochloric acid solution to obtain the activated silica gel. Afterwards, a new type of aminopropylimidazole/dodecyl dual-functionalized silica stationary phase (Sil-API-DD) was synthesized via one-pot reaction of the activated silica gel with 3-chloropropyltrimethoxysilane, dodecyltrimethoxysilane and 1-(3-aminopropyl)imidazole. The separation performance of Sil-API-DD was evaluated using environmental organic pollutants as the model analytes, and the results showed that an effective separation of seven alkylphenols, five bisphenols , six phthalates , seven steroid hormones and six benzophenones in reversed-phase chromatography was achieved. Moreover, the developed Sil-API-DD was found to exhibit more flexible selectivity and superior separation efficiency compared with the commercial C18 column under the tested conditions, suggesting a good application prospect.
✓ 已验证
产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Wenjing Wang,Fei Zhai,Fupei Xu,Min Jia
Novel enzyme-free amplified dual-terminal labeled split aptamer (SPA) probes were developed to achieve one-step rapid and sensitive detection of bisphenol A (BPA). By rational split, the original aptamer was divided into two segments named SPA-a and SPA-b to achieve target-driven self-assembly and form BPA/SPA complex. To achieve enzyme-free signal amplification and improved sensitivity, SPA probes were dual-terminal labeled with 6-carboxyfluorescein (FAM) fluorophores and black hole quencher 2 (BHQ 2 ). Two dual-terminal labeled SPA probes were induced to assemble a ternary complex with BPA to produce fluorescence resonance energy transfer effect, generating the decreased fluorescence intensity. The detection limit of dual-terminal labeled SPA probes was 0.89 ng/mL, which was 24-fold lower than that of single-terminal modification. Meanwhile, these SPA probes showed a rapid response to BPA, which could be completed in 5 min for one-step detection without complex cleaning and separation progress. The recovery rates in real samples were 94.17% to 107.28%. In brief, the dual-terminal labeled SPA probes showed substantial potential for onsite detection of BPA.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2022
·
IF 14.224
Xian Liu,Like Chen,Yang Yang,Liping Xu,Junyong Sun,Tian Gan
Rational tailoring of hollow and porous bimetallic structures with excellent electrocatalytic performance is appealing yet challenging. Further, combining independent bimetallic nanoparticles with flexible two-dimensional substrate by forming stable heterocomplex is still highly desired for electrocatalysis. Herein, hierarchical PtCu alloy octahedrons with hollow interiors and nanosheet-assembled nanoshells were synthesized by a facile and efficient chemical transformation strategy using Cu 2 O as sacrificial templates. Such octahedral PtCu nanocages displayed significantly enhanced electrocatalytic activity owing to their unique hollow and porous architectures which provided easy access for analytes to the catalyst surface. Thereafter, introduction of Ti 3 C 2 T x MXene was realized via simple incubation of Ti 3 C 2 T x in solution containing the 3-aminopropyltriethoxysilane-capped PtCu, and their electrostatic interaction guaranteed the firm adsorption of PtCu nanocages on Ti 3 C 2 T x nanosheets. It turned out that the sensitivity of the hybrid sensor was remarkably improved for electrochemical monitoring of endocrine disrupting pollutants in water, exhibiting ultrawide linear ranges and sub-nanomole detection limits. The eminent electrode performance is attributed to the high specific area, fast electrochemical kinetics, decent electrical catalytic ability, and the synergistic effect between Pt, Cu, and MXene.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2022
·
IF 4.598
Qingyuan Song,Xueling Shan,Liyin Bu,Anna Dai,Ding Jiang,Wenchang Wang,Hiroshi Shiigi,Zhidong Chen
A highly efficient electrochemiluminescence resonance energy transfer (ECL-RET) aptasensor was constructed for ultrasensitive detection of diethylstilbestrol (DES). The composite composed of silver orthophosphate and zirconium-based metal–organic frameworks (Ag 3 PO 4 -UiO-66) was prepared as a sensing platform for aptasensor incubation. Ag 3 PO 4 , a novel ECL donor, whose emission could be obviously enhanced through loading on UiO-66. Particularly, the composite of Ag 3 PO 4 -UiO-66 could minimize the aggregation of Ag 3 PO 4 , which provided a novel possibility for the construction of high ECL efficiency sensors. UiO-66 presented ultrahigh surface area to improve the loading capacity of Ag 3 PO 4 and DES-specific aptamer. Notably, Ag 3 PO 4 with superb catalytic properties could immobilize DES aptamer via Ag–NH 2 bond and further ensured the distance between the ECL donor and the energy receptor. To design a novel ECL-RET system, GO nanosheets were synthesized as a suitable ECL acceptor which could be fixed through electrostatic adsorption. Owing to the superior spectral overlap, GO could significantly quench the ECL emission of Ag 3 PO 4 . Under the optimal conditions, the constructed ECL-RET aptasensor showed a satisfactory response to DES in a linear range of 1.0 × 10 −14 ∼ 1.0 × 10 −8 M and the detection limit was 7.2 × 10 −15 M (S/N = 3). This paper not only developed a novel approach for environmental water quality monitoring but also offered more opportunities for building highly sensitive ECL-RET aptasensors.
✓ 已验证
产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Tong Liao,Jia Jia,Kang Tong,Jiuhong Ouyang,Wei Jiang,Xia-ping Zhu
A novel hyper-crosslinked 2, 8, 14, 20-tetraphenyl calix [4] resorcinol arene polymer (HCP-TCRA) was synthesized by using an external crosslinking of 2, 8, 14, 20-Tetraphenyl calix [4] resorcinol arene (TCRA) as monomers and dimethoxymethane as crosslinker. The HCP-TCRA was explored as a SPME fiber coating material. A variety of physicochemical characterization demonstrated that the material has excellent chemical/thermal stability and strong hydrophobicity. The fiber demonstrated fantastic adsorptive property for three synthetic estrogens (diethylstilbestrol, hexestrol, ethinyloestradiol, abbreviated to SESs). In this work, an efficient HCP-TCRA fiber-based SPME method was developed to analyze SESs by coupling with HPLC-MS detection. Under the optimized SPME conditions, this method was shown a wide range of linearity (2.0–100.0 ng mL −1 for diethylstilbestrol, 1.0–100.0 ng mL −1 for hexestrol, and 30.0–480.0 ng mL −1 for ethinyloestradiol), low limits of detection (LODs, 0.5 ng mL −1 for DES 0.3 ng mL −1 for HEX, 10.0 ng mL −1 for EES) and fine reusability (more than 30 times). Finally, the proposed methods had been applied to the determination of SESs in milk samples with a simple pretreatment. At three different levels, relative recoveries presented between 86.7 and 106.4%. The method put up highly sensitive and budget-friendly in detection SESs, and has capacity in quality control of milk products.
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2022
·
IF 6.911
Yanqun Yang,Yipeng Huang,Zhuqiang Wu,Rui Shi,Zhengyi Chen,Guihua Ruan
In this work, a porous capillary monolithic column was simply prepared by in situ thiol-alkyne click polymerization of dipentaerythritol hexakis (3-mercaptopropionate) and dimethyl dipropargylmalonate in fused-silica capillary. The capillary monolithic column shows excellent permeability, high porosity, and thoiether-rich groups, thereby, a high-efficient capacity for trace estrogens from complex samples are obtained via electron-donor-acceptor π-π interaction and hydrophobic interaction. The highest adsorption efficiency for estrogens is achieved at pH = 7.0 with a flow rate of 0.200 mL min −1 . The superior adsorption capacities of the as-prepared capillary column for eight estrogens range from 0.092 mg m −1 to 0.31 mg m −1 . A simple, reliable, and sensitive method for the determination of eight estrogens in biological and environmental samples is developed using the monolithic polymer as in-tube solid-phase microextraction coupled with ultrahigh performance liquid chromatography-tandem mass spectrometry (SPME-UPLC-MS/MS), and the total instrumental analysis time for the SPME-UPLC-MS/MS procedures was about 60 min per sample. The developed method shows a wide linear range (0.0500–5.00 μg L −1 ), and low limits of detection (5.34–9.63 ng L −1 ) for estrogens. The concentrations of estrogens in serum, urine, and pond water samples are found to be no more than 3.69, 0.741, and 1.04 μg L −1 , respectively, and the satisfying recoveries for the eight estrogens range from 80.3% to 113% with relative standard deviations ( n = 5) of 1.5–9.4%. The established method is highly potential for extraction and analysis of ultratrace target estrogens in complex matrices, such as biological and environmental samples.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHROMATOGRAPHIA
·
2022
·Vol. 85
·期 8
·733-741
·
IF 2.213
Zhang Qianchun,Wang Yutong,Yang Bingnian,Bao Linchun,Wu Yun,Wang Xingyi
Estrogen plays a crucial role in various stages of human development and is present in the human body at trace level; therefore, an efficient strategy for the quantitative analysis of trace estrogens is required. However, this analysis is complicated by the presence of extremely complex biological matrices. To address this challenge, a novel method based on monolithic column solid-phase microextraction and ultra-high-performance liquid chromatography-tandem mass spectrometry was developed for the sensitivity analysis of six estrogens: β-estradiol, α-estradiol, 17α-ethynylestradiol, estrone, diethylstilbestrol, and hexestrol, in human urine and serum samples. The method exhibits a low limit of detection (8.6–37 ng L −1 ), with wide linear ranges (0.10–25 μg L −1 ) for each analyte and remarkable correlation coefficients ( R 2 = 0.9953–0.9995). The developed method was successfully used to detect estrogens in urine and serum samples. The six analytes were satisfactorily recovered between 76.2 and 107% with relative standard deviations ranging from 2.5 to 8.3% ( n = 3). The results demonstrated that the developed method, based on a poly(methacrylic acid/3-acrylamidophenylboronic acid-co-ethylene glycol dimethacrylate) monolithic column, is an effective enrichment approach toward the analysis of trace estrogens in human urine and serum samples. Graphical abstract
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）