ANALYTICAL CHEMISTRY
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2022
·
IF 8.008
Jian Song,Kaiyu He,Bingcong Xing,Yong Pei,Dingnan Wang,Yang Wang,Shiyan Li,Jie Li,Weiwei Huan,Yiming Zhang,Bruce. D. Hammock
The development of highly specific biomimetic recognition material is a challenge for rapid detection of harmful residues in foodstuff. In this study, a paper-based boronate affinity metal–organic framework/molecularly imprinted polymer microfluidic chip (FZS-BA@MIP) was constructed based on the in situ construction strategy, which was also designed as a highly specific biomimetic recognition module. Here, the homogeneous zeolitic imidazole framework-8 (ZIF-8) membrane served as a great scaffold and enrichment layer. Besides, the recognition layer of MIP was prepared based on a highly oriented boronate affinity surface imprinting strategy. With the aid of the liquid flow channel, the highly specific enrichment and visual detection for antibiotic residues like kanamycin in actual products were achieved on the paper chip module of an integrated lateral flow platform. The whole analysis process could be accomplished within 30 min. In brief, this study offered a new integrated biomimetic recognition platform for visually detecting harmful veterinary residues containing cis-diols, which demonstrated promising commercial value in point-of-care testing of foodborne hazardous compounds.
研究领域:
食品安全
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分析化学
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材料科学
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DOI
PubMed
高影响因子
FOOD CHEMISTRY
·
2024
·
IF 8.5
Shiqi Huang,Xiao Song,Shiyu Wang,Hao Liu,Chengyi Xiong,Shengfu Wang,Xiuhua Zhang,Miao-Miao Chen
Paper chip as a representative microfluidic device has been mushroomed for rapid identification of contaminants in agro-food. However, the sensitivity and accuracy have still been challenged by inevitable background noise or interference in food matrix. Herein, we designed and fabricated a dual-mode paper chip (DPC) by assembling a patterned paper electrode with a platinum nanoparticles-treated colorimetric region through a flow channel. Dual-mode outputs were guided by an aptamer-gated UiO-66-NH 2 metal-organic frameworks (MOFs). UiO-66-NH 2 loaded with 3, 3′, 5, 5′-tetramethylbenzidine (TMB) was controlled by a switch comprised of CdS quantum dots-aptamer. Aflatoxin B1 (AFB1, a kind of carcinogenic mycotoxin) target came and induced TMB release, triggering colorimetric and ECL signals on DPC, ultra-high sensitivity with a detection limit of 7.8 fg/mL was realized. The practicability of the DPC was also confirmed by spiking AFB1 in real corn samples. This portable paper-based device provides an ideal rapid detection platform tailored for diverse food contaminants analysis.
研究领域:
食品安全检测
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分析化学
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生物传感技术
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产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Lu Shi,Wei Liu,Baoxin Li,Chaoyong James Yang,Yan Jin
Simultaneous detection of multi-biomarkers not only enhances the accuracy of disease diagnosis but also improves detection efficiency and reduces cost. It is vital to achieve portable, simple, low-cost, and simultaneous detection of biomarkers for point-of-care (POC) diagnostics in a low-resource setting. Herein, a multichannel paper chip-based gas pressure bioassay was developed for the simultaneous detection of multiple biomarkers by combining multichannel paper chips with a portable gas pressure meter. Four DNA tetrahedral probes (DTPs) were used as capture probes and were immobilized in different detection zones of the paper chips to improve hybridization efficiency and reduce nonspecific adsorption. The formation of a sandwich structure between target microRNAs (miRNAs), the capture probe, and platinum nanoparticles (PtNPs)-modified complementary DNA (PtNPs-cDNA) transformed biomolecular recognition into quantitative detection of gas pressure. Four lung cancer-related miRNAs were detected simultaneously by a portable gas pressure meter. There is a good linear relationship between gas pressure and the logarithm of miRNA concentration in the range of 10 pM to 100 nM. Compared with single-stranded DNA capture probe, the signal-to-noise (S/N) of DNA tetrahedral probes improved more than 3 times. Using ring-oven washing, the unbound reagents in all channels of the paper chip were simultaneously and continuously washed away, leading to a more cheap, simple, and fast separation than magnetic separation. Therefore, it offers a promising multichannel paper chip-based gas pressure bioassay for portable and simultaneous detection of multiple biomarkers.
研究领域:
生物医学工程
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分子诊断学
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纳米技术
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产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Ying Zhou,Donghui Wang,Dingnan Wang,Yang Wang,Yang Li,Jie Li,Yiming Zhang
Mimetic recognition materials for rapid and selective analysis of foodborne contamination from complex foodstuff becomes a hot research topic in the field of food safety. In this work, borate-affinity-functionalized MOF/molecularly imprinted polymer paper-based microfluidic chips (FSU-BA@MIP) were prepared by growing functionalized MOFs on paper surface with 3-carboxyphenylboronic acid (3-CPBA) as the ligands, followed by coating of a MIP layer of salbutamol (SAL) through a borate-affinity surface imprinting strategy. Using the obtained paper-based chip as a mimetic recognition and specific enrichment module, the fluorescence sensing platform achieved visual rapid quantitative analysis of SAL with a linear range of 0.1 × 10 −2 –5.0 mg L −1 . The limits of detection and quantification were calculated to be 0.095 and 0.290 μg kg −1 , respectively, and the sample loading via lateral flow aid could be completed within 30 min. The obtained MOFs/MIPs paper chips provide an effective way for the rapid analysis of harmful contaminants from different animal-derived foods.
研究领域:
食品安全
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分析化学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
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IF 15.1
Qian Lin,Jiaqi Huang,Yiling Zhang,Miaomiao Chen,Yuzhi Xu,Xiaoyong Zou,Si-Yang Liu,Zong Dai
Noninvasive glucose detection for diabetes monitoring, in comparison with the conventional finger-prick test that causes inevitable pain, is on demand. Salivary glucose level that possesses a well-established correlation with blood glucose level can be a promising alternative for noninvasive detection, however, the sensitivity and user-friendliness remained to be improved. Herein, an “all-in-one” paper chip was fabricated by one-pot method for sensitive and user-friendly detection of salivary glucose level. Glucose oxidase (GOx) and the chromogenic reagent, luminol, were both in situ encapsulated in a metal–organic framework, ZIF-67, to form the GOx& [email protected] @Paper (G& [email protected] @Paper). Owing to the specificity of GOx and the peroxidase activity of ZIF-67, the paper chips are highly sensitive and specific for glucose with a linear range from 0.2 to 2 mM, and a limit of detection of 0.12 mM (S/N = 3). Moreover, ascribing to the protection and “all-in-one” structure by ZIF-67, the chip is highly stable that maintains the detection performance after storage at room temperature in air for 4 weeks, and this strategy also facilitates the one-pot detection without multiple steps of sampling and incubation. With the assistance of a smartphone application, the glucose level in saliva can be accurately detected with “sample-in-result-out” manner, and the results were highly consistent with those measured by commercial kit. This paper chip is a promising device for daily glucose monitoring, and the highly-integrated strategy provides an innovative resolution for the construction of colorimetric paper chips.
研究领域:
生物医学工程
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分析化学
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糖尿病技术
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产品关联
DOI
高影响因子
Nature Communications
·
2023
·Vol. 14
·期 1
·1-12
·
IF 16.6
Li Bowei,Qi Ji,Liu Feng,Zhao Rongfang,Arabi Maryam,Ostovan Abbas,Song Jinming,Wang Xiaoyan,Zhang Zhiyang,Chen Lingxin
Fluorescence analysis is a fast and sensitive method, and has great potential application in trace detection of environmental toxins. However, many important environmental toxins are non-fluorescent substances, and it is still a challenge to construct a fluorescence detection method for non-fluorescent substances. Here, by means of charge transfer effect and smart molecular imprinting technology, we report a sensitive indirect fluorescent sensing mechanism (IFSM) and microcystin (MC-RR) is selected as a model target. A molecular imprinted thin film is immobilized on the surface of zinc ferrite nanoparticles (ZnFe 2 O 4 NPs) by using arginine, a dummy fragment of MC-RR. By implementation of IFSM on the paper-based microfluidic chip, a versatile platform for the quantitative assay of MC-RR is developed at trace level (the limit of detection of 0.43 μg/L and time of 20 min) in real water samples without any pretreatment. Importantly, the proposed IFSM can be easily modified and extended for the wide variety of species which lack direct interaction with the fluorescent substrate. This work offers the potential possibility to meet the requirements for the on-site analysis and may explore potential applications of molecularly imprinted fluorescent sensors.
研究领域:
环境科学
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分析化学
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纳米技术
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毒理学
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产品关联
DOI
PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
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IF 4.3
Lifan Zhang,Ziyue Lang,Bozhi Lu,Tinglan Yang,Xinyi Zhang,Muxue Wang,Xiaomei Zhang,Hongmei Cao,Daixin Ye
Carbofuran (CBF), which exhibit high toxicity, persistent residues, ease of accumulation, and resistance to degradation, pose serious threats to human health and harm the ecological environment. Therefore, there is an urgent need to develop a rapid and accurate method for detecting CBF. In this work, a low-cost, portable, and easy-to-use paper chip biosensor was developed, integrating smartphones for the detection of CBF pesticide residues. This biosensor facilitates rapid on-site testing, meeting the needs for immediate analysis. CBF has the ability to inhibit acetylcholinesterase (AChE) activity. In the presence of AChE, acetylthiocholine (ATCh) is hydrolyzed to produce thiocholine (TCh). TCh, in turn, can inhibit the catalytic activity of Ni-N-C single-atom nanozymes (SAzyme) synthesized using Ni(OH) 2 nanochip as a metal precursor, which possess high peroxidase activity. Consequently, the concentration of CBF can be determined by observing the resultant color changes. The results showed that this sensor had a good linear response in the range of CBF concentration from 10 to 500 ng/mL, and the LOD was as low as 8.79 ng/mL. In testing three actual samples—Chinese cabbage, cabbage, and lettuce—the recoveries ranged from 81.09% to 125.27%. This demonstrated that the proposed smartphone-based colorimetric paper chip sensor, utilizing Ni-N-C SAzyme, offers an immediate, convenient, and rapid new strategy for detecting CBF.
研究领域:
环境科学
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分析化学
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生物传感器
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食品安全
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农药检测
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产品关联
DOI
PubMed
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2023
·
IF 8.4
Zimu Li,Min Zhu,Fang Li,Zhi Li,Anqi Zhao,Mohammad A. Haghighatbin,Hua Cui
The development of chemiluminescence (CL) sensing strategy with multiple-parameters for discrimination of small molecules remains a great challenge. Herein, a multicolor CL sensing strategy for the discrimination of five antioxidants , including dopamine, catechin, cysteine, glutathione , and thioctic acid was presented. Firstly, multilayer paper chips modified with luminol-Co(II), luminol-fluorescein-Co(II), and luminol-rhodamine B-Co(II) that can produce strong blue, green and purple colored light emission, respectively, via CL and CL resonance energy transfer (CRET) reactions were fabricated. The presence of antioxidants exhibits different inhibition or enhancement effect on the CL reactions, creating unique multicolor CL response pattern to each antioxidant. The red (R), green (G), and blue (B) channel split from the purple, green and blue CL image, respectively, generate cross-reactive sensing parameters for the discrimination of the five antioxidants. The distinct R, G, and B values of the CL images to each antioxidant are created as analytical fingerprints to identify five antioxidants by using principal component analysis and hierarchical cluster analysis. Satisfied results were obtained for discrimination antioxidant mixtures and spiked antioxidants in serum samples. Identification of 10 unknown samples resulted in 100% accuracy. This work presents the first example of multicolor CL sensing strategy for the discrimination of small molecules.
研究领域:
分析化学
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材料科学
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生物技术
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产品关联
DOI
高影响因子
MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 12
·1-8
·
IF 5.833
Li Shuhuai,Pang Chaohai,Ma Xionghui,Zhang Yanling,Xu Zhi,Li Jianping,Zhang Meng,Wang Mingyue
The rapid detection of insecticides such as parathion-methyl (PM) requires methods with high sensitivities and selectivities. Herein, a dual catalytic amplification strategy was developed using Fe 3 O 4 nanozyme-supported carbon quantum dots and silver terephthalate metal–organic frameworks (Fe 3 O 4 /C-dots@Ag-MOFs) as current amplification elements. Based on this strategy, a novel electrochemical microfluidic paper-based chip was designed to detect PM. Fe 3 O 4 /C-dots@Ag-MOFs were synthesised by a hydrothermal method, and a molecularly imprinted polymer (MIP) was then synthesised on the surface of Fe 3 O 4 /C-dots@Ag-MOFs using PM as a template molecule. Finally, the reaction zone of a chip was modified with MIP/Fe 3 O 4 /C-dots@Ag-MOFs. PM from a sample introduced into the reaction zone was captured by the MIP, which generated a reduction current response at − 0.53 V in a three-electrode system embedded in the chip. Simultaneous catalysis by Fe 3 O 4 /C-dots and Ag-MOFs significantly enhanced the signal. The chip had a detection limit of 1.16 × 10 −11 mol L −1 and was successfully applied to the determination of PM in agricultural products and environmental samples with recovery rates ranging from 82.7 to 109%, with a relative standard deviation (RSD) of less than 5.0%. This approach of combining a dual catalytic amplification strategy with an MIP significantly increased the sensitivity as well as selectivity of chips and can potentially be used to detect a wide variety of target analytes using microfluidic paper-based chips. Graphical abstract
研究领域:
分析化学
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环境科学
·
材料科学
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DOI
PubMed
高影响因子
MICROCHIMICA ACTA
·
2020
·Vol. 187
·期 10
·1-9
·
IF 6.232
Wei Shengnan,Li Juan,He Jingya,Zhao Wei,Wang Feng,Song Xiuling,Xu Kun,Wang Juan,Zhao Chao
A rapid and sensitive colorimetric assay is described for Salmonella typhimurium ( S. typhimurium ) detection using urea/phenol red impregnated test paper. Aptamer-modified Fe 3 O 4 @Ag multifunctional hybrid nanoprobes (apt-Fe 3 O 4 @Ag NPs) were used to specifically captured S. typhimurium ; the nanoprobes were quickly etched by H 2 O 2 to form Ag + . The generated Ag + can inhibit the urease-catalyzed hydrolysis reaction of urea to produce NH 4 + . Consequently, the as-prepared test paper displayed a yellow color. In the presence of S. typhimurium , the target bacteria can cause aggregation of apt-Fe 3 O 4 @Ag NPs, and the deposited Ag on the nanoprobe’s surface is shielded against H 2 O 2 -induced oxidative decomposition leading to reduced Ag + production. The catalytic activity of urease cannot be inhibited completely by inadequate amount of Ag + . An obvious color change from yellow to pink can be monitored directly using our test paper as a result of increased NH 4 + . The entire assay procedure could be completed within 1 h. A limit of detection of 48 cfu/mL is achieved with a linear range of 1 × 10 2 to 1 × 10 6 cfu/mL. The recoveries of S. typhimurium spiked in pure milk samples were 92.48–94.05%.
Schematic diagram of the proposed colorimetric assay for S. typhimurium detection based on etching of bifunctional apt-Fe 3 O 4 @Ag NPs and inhibiting catalytic activity of urease by Ag + . A color change from yellow to pink can be observed and correlated to the concentration of S. typhimurium.
研究领域:
分析化学
·
微生物学
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纳米技术
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食品安全
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产品关联
DOI
PubMed
高影响因子
LAB ON A CHIP
·
2016
·Vol. 17
·期 1
·120-127
·
IF 5.586
Jin-Wen Shangguan,Yu Liu,Jian-Bin Pan,Bi-Yi Xu,Jing-Juan Xu,Hong-Yuan Chen
In this paper, we propose a generalized concept of microfluidic polydimethylsiloxane (PDMS) on paper (POP) devices, which combines well the merits of paper chips and PDMS chips. First, we optimized the conditions for accurate PDMS spatial patterning on paper, based on screen printing and a high temperature enabled superfast curing technique, which enables PDMS patterning to an accuracy of tens of microns in less than ten seconds. This, in turn, makes it available for seamless, reversible and reliable integration of the resulting paper layer with other PDMS channel structures. The integrated POP devices allow for both porous paper and smooth channels to be spatially defined on the devices, greatly extending the flexibility for designers to be able to construct powerful functional structures. To demonstrate the versatility of this design, a prototype POP device for the colorimetric analysis of liver function markers, serum protein, alkaline phosphatase (ALP) and aspartate aminotransferase (AST), was constructed. On this POP device, quantitative sample loading, mixing and multiplex analysis have all been realized.
研究领域:
微流控技术
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生物医学工程
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分析化学
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产品关联
DOI
PubMed
高影响因子
ANALYTICAL CHEMISTRY
·
2022
·
IF 8.008
Lang Zhang,Wen Yin,Yanli Tong,Yanfei Zhang,Yuzhi Xu,Si-Yang Liu,Zong Dai,Xiaoyong Zou
Small extracellular vesicles (sEVs) play important roles in mediating intercellular communication and regulating biological processes. Facile sEV isolation is the essential and preliminary issue for their function investigation and downstream biomedical applications, while the traditional methods are challenged by tedious procedures, low purity, low yield, and potential damage. In this work, we developed an sEV isolation paper-based device (sEV-IsoPD) based on a three-dimensional (3D) paper chip, which is composed of a porous membrane for size exclusion and a metal–organic framework (MOF)/antibody-modified paper for immunoaffinity capture. In combination with a peristaltic pump-driven flow system, the sEV-IsoPD can efficiently isolate EV from cell culture medium and serum. Compared with the ultracentrifugation method, sEV-IsoPD exhibited a 5.1 times higher yield (1.7 × 109 mL–1), 1.6 times higher purity (1.6 × 1011 mg–1), and 7.5 times higher recovery (77.3%) with only 8.3% of the time (30 min) and 1.0% of the instrument cost ($710). Moreover, sEV concentration can be visually detected in a quantitative manner with this paper-based device with a linear range from 3.0 × 106 to 3.0 × 1010 mL–1 and a detection limit of 2.2 × 106 mL–1. The sEV-IsoPD provides an efficient and practical approach for the rapid isolation and visible detection of sEVs, which are promising for the preparation of sEVs and diagnosis of disease.
研究领域:
生物技术
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医学诊断
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纳米技术
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生物工程
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产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）