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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

Atractylodin targeted visual fluorescence sensor based on N-acetyl-L-cysteine capped CdTe QDs for the rapid identification of the geographical origin of Atractylodis Rhizome

Xintian Wang,Hengye Chen,Yao Fan,Wei Lan,Juan He,Haiyan Fu,Xiaolong Yang

The economic and medicinal value of Atractylodis Rhizoma (AR) is intricately tied to its geographical origin and mainly depends on the atractylodin (IUPAC Name: 2-[(1E,7E)-nona-1,7-dien-3,5-diynyl]furan) content in it. In this study, a green fluorescent sensor using N-acetyl-L-cysteine (NAC, IUPAC Name: (2R)-2-acetamido-3-sulfanylpropanoic acid)-capped CdTe quantum dots (QDs) was developed for the detection of AR origin discrimination. Both electron transfer and internal filtration effects was introduced into sensor to improve the sensitivity and selectivity. The sensors can achieve visual quantitative analysis of atractylodin using the partial least squares regression (PLSR) model. This model with a detection limit of 0.321 µg /mL and the quantification range of 0.002–0.030 mg /mL. Furthermore, the visual sensor also could be applied to the quantification of atractylodin in the actual AR samples with recoveries as high as 95.36 % to 105 %. Their sensor was also able to identify different origin of AR with an accuracy of 100 % for the training set and 95.29 % for the prediction set using the Partial Least Squares Discriminant Analysis (PLSDA) model. The method offers direction for verifying the authenticity of traditional Chinese medicine and precise analysis of intended constituents in complex systems.

研究领域: 分析化学 · 药学 · 中药学 · 光谱学 · 材料科学
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MICROCHIMICA ACTA · 2019 ·Vol. 186 ·期 8 ·1-10 · IF 5.479

Molecularly imprinted mesoporous silica incorporating C3N4 dots and CdTe quantum dots as ratiometric fluorescent probe for determination of Malachite Green

Shi Han,Zhang Liang,Yu Guoliang,Liu Yuting,Chen Ligang

A new dual-emission ratiometric fluorescent probe was synthesized and successfully used for the determination of Malachite Green (MG) in fish farming water. The ratiometric fluorescent probe was successfully composited by sol-gel method using C 3 N 4 and CdTe quantum dots as fluorescent materials combined with mesoporous molecularly imprinted polymers. MG quenches the red fluorescence of the CdTe QDs (with excitation/emission wavelengths at 350/680 nm) while the blue fluorescence of C 3 N 4 (with excitation/emission wavelengths at 350/458 nm) remains unchanged. The change of fluorescence color and fluorescence intensity ratio can be successfully used for quantification of malachite green. In addition, the mesoporous structure has a large surface and good adsorption capacity for malachite green. The normalized intensity of fluorescence increases linearly in the 50–1000 ng·mL −1 MG concentration range, and the detection limit is 10 ng·mL −1 . The imprinting factor is 3.2. The nanoprobe was applied to the determination of MG in fish farming water samples. Recoveries and relative standard deviations were 92.5–97.8% and 2.5–6.2%, respectively. Schematic representation of synthesis of molecularly imprinted mesoporous silica ratiometric fluorescent probes incorporating C 3 N 4 dots and CdTe quantum dots for determination of malachite green.

研究领域: 分析化学 · 环境科学 · 材料科学 · 纳米技术
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TALANTA · 2019 · IF 4.916

Electrochemiluminescent aptasensor based on resonance energy transfer system between CdTe quantum dots and cyanine dyes for the sensitive detection of Ochratoxin A

Jingwen Gao,Ziyi Chen,Lebao Mao,Wei Zhang,Wei Wen,Xiuhua Zhang,Shengfu Wang

In this work, an innovative aptasensor based on electrochemiluminescence resonance energy transfer (ECL-RET) from CdTe quantum dots (QDs) to a cyanine dye (Cy5) fluorophore for the determination of Ochratoxin A (OTA) was fabricated. A strong cathodic ECL emission was obtained by the CdTe QDs modified glassy carbon electrode (GCE). After the immobilization with the capture DNA (cDNA) and the sequential hybridization with the probe DNA-modified Cy5 (pDNA, the aptamer of OTA), the ECL signal enhanced obviously through the ECL-RET. Meanwhile, the spectrum- and distance-related ECL enhancement effect was investigated. When the target OTA was in the presence, the pDNA-Cy5 molecules were released from the electrode surface owing to the specific interaction between OTA and aptamer, resulting in an evident decrease of ECL signal. Under optimal conditions, the developed aptasensor displayed the linear response toward OTA in the wide range of 0.0005–50 ng/mL with a low detection limit of 0.17 pg/mL. With the excellent selectivity , stability and repeatability, the strategy provided an efficient and universal method for the sensitive detection of target in practical application.

研究领域: 分析化学 · 生物传感器 · 毒理学 · 食品安全
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BIOSENSORS & BIOELECTRONICS · 2017 · IF 7.78

Fluorescent “on-off-on” switching sensor based on CdTe quantum dots coupled with multiwalled carbon nanotubes@graphene oxide nanoribbons for simultaneous monitoring of dual foreign DNAs in transgenic soybean

Yaqi Li,Li Sun,Jing Qian,Lingliang Long,Henan Li,Qian Liu,Jianrong Cai,Kun Wang

With the increasing concern of potential health and environmental risk, it is essential to develop reliable methods for transgenic soybean detection. Herein, a simple, sensitive and selective assay was constructed based on homogeneous fluorescence resonance energy transfer (FRET) between CdTe quantum dots (QDs) and multiwalled carbon [email protected] oxide nanoribbons ( [email protected] ) to form the fluorescent “on-off-on” switching for simultaneous monitoring dual target DNAs of promoter cauliflower mosaic virus 35   s (P35s) and terminator nopaline synthase (TNOS) from transgenic soybean. The capture DNAs were immobilized with corresponding QDs to obtain strong fluorescent signals (turning on). The strong π–π stacking interaction between single-stranded DNA (ssDNA) probes and [email protected] led to minimal background fluorescence due to the FRET process (turning off). The targets of P35s and TNOS were recognized by dual fluorescent probes to form double-stranded DNA (dsDNA) through the specific hybridization between target DNAs and ssDNA probes. And the dsDNA were released from the surface of [email protected] , which leaded the dual fluorescent probes to generate the strong fluorescent emissions (turning on). Therefore, this proposed homogeneous assay can be achieved to detect P35s and TNOS simultaneously by monitoring the relevant fluorescent emissions. Moreover, this assay can distinguish complementary and mismatched nucleic acid sequences with high sensitivity. The constructed approach has the potential to be a tool for daily detection of genetically modified organism with the merits of feasibility and reliability.

研究领域: 生物化学 · 分子生物学 · 食品科学
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SENSORS AND ACTUATORS B-CHEMICAL · 2025 · IF 7.7

Colorimetric and fluorescence dual-mode sandwich biosensor for visual detection of multiple foodborne pathogens with concanavalin A modified magnetic nanoparticles and CdTe quantum dots

Wen-Bo Zhao,Xiao Liang,Zi-Tao Zhong,Ji-Tao Li,Dan Mei,Juan Yang,Qin-Qin Han,Ya-Ling Yang

Salmonella ( Sal ) and Escherichia coli ( Esc ) are two common foodborne pathogens that cause significant harm to humans. Therefore, strict control of Esc and Sal in food and the environment is essential. Herein, we developed a colorimetric/fluorescence dual-mode strategy for the detection of two pathogenic bacteria. Taking advantage of the characteristic that concanavalin A (ConA) can capture bacteria via the recognition of the sugar residues, it was coupled with magnetic nanoparticles (MNPs) to form MNPs@ConA as the capture probe. In addition, the antibody (Ab) can specifically recognize the bacteria, and after coupling with CdTe quantum dots (QDs), QDs@Ab was employed as the signal probe. This study shows that MNPs can catalyze 3,3′,5,5′-tetramethylbenzidine (TMB) to generate blue oxTMB to be recognized by the naked eye, while QDs exhibited strong fluorescence, which can also be observed by the naked eye, allowing for a clear differentiation in Sal and Esc detection. The signal was linearly correlated with the target bacteria with a satisfied visualized results. The practicability of the method was verified using milk tea, milk, and juice samples, with recovery rates ranging from 93.5 % to 106 %. The feasibility of this method for the detection of Sal and Esc was validated, and it poses a significant potential for food safety monitoring.

研究领域: 生物传感器 · 食品安全 · 纳米技术 · 微生物学 · 分析化学
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2013 ·Vol. 14 ·期 5 ·10397-10411 · IF 2.464

An Ultrasensitive Electrochemiluminescence Immunoassay for Carbohydrate Antigen 19-9 in Serum Based on Antibody Labeled Fe3O4 Nanoparticles as Capture Probes and Graphene/CdTe Quantum Dot Bionanoconjugates as Signal Amplifiers

Ning Gan,Jing Zhou,Ping Xiong,Tianhua Li,Shan Jiang,Yuting Cao,Qianli Jiang

The CdTe quantum dots (QDs), graphene nanocomposite (CdTe-G) and dextran–Fe3O4magnetic nanoparticles have been synthesized for developing an ultrasensitive electrochemiluminescence (ECL) immunoassay for Carcinoembryonic antigen 19-9 (CA 19-9) in serums. Firstly, the capture probes (CA 19-9 Ab1/Fe3O4) for enriching CA 19-9 were synthesized by immobilizing the CA 19-9’s first antibody (CA 19-9 Ab1) on magnetic nanoparticles (dextran-Fe3O4). Secondly, the signal probes (CA 19-9 Ab2/CdTe-G), which can emit an ECL signal, were formed by attaching the secondary CA 19-9 antibody (CA 19-9 Ab2) to the surface of the CdTe-G. Thirdly, the above two probes were used for conjugating with a serial of CA 19-9 concentrations. Graphene can immobilize dozens of CdTe QDs on their surface, which can emit stronger ECL intensity than CdTe QDs. Based on the amplified signal, ultrasensitive antigen detection can be realized. Under the optimal conditions, the ECL signal depended linearly on the logarithm of CA 19-9 concentration from 0.005 to 100 pg/mL, and the detection limit was 0.002 pg/mL. Finally, five samples of human serum were tested, and the results were compared with a time-resolved fluorescence assay (TRFA). The novel immunoassay provides a stable, specific and highly sensitive immunoassay protocol for tumor marker detection at very low levels, which can be applied in early diagnosis of tumor.Keywords:dextran-Fe3O4magnetic nanoparticles;sandwich immunoassay;graphene CdTe QD nanocomposite;carcinoembryonic antigen 19-9;electrochemiluminescence

CAS / MDL: 7782-42-5
研究领域: 生物医学工程 · 肿瘤学 · 纳米技术
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MICROCHIMICA ACTA · 2019 ·Vol. 186 ·期 11 ·1-9 · IF 5.479

Ratiometric fluorometric determination of silver(I) by using blue-emitting silicon- and nitrogen-doped carbon quantum dots and red-emitting N-acetyl-L-cysteine-capped CdTe quantum dots

Wu Huifang,Tong Changlun

A ratiometric fluorometric assay for silver(I) is described. The method makes use of a dually emitting quantum dot hybrid, which is composed of (a) blue-fluorescent silicon- and nitrogen-doped carbon quantum dots (CQDs), and (b) of red-emitting CdTe quantum dots (QDs) capped with N-acetyl-L-cysteine. The red-emitting CdTe QDs undergo strong and specific quenching by Ag(I), whereas the blue-emitting N,Si-CQDs are not quenched. The two kinds of QDs are mixed and used as a ratiometric fluorescent probe. A linear relationship is found between the log of intensities  [(I 608 /I 441 ) 0 /(I 608 /I 441 )] and the concentration of Ag(I) in the range from 5.0–1000 nM, and the limit of detection (at S/ N  = 3) is 1.7 nM. Possible interferents (including 17 general metal ions, 12 anions and fulvic acid) do not interfere with the determination. The assay was successfully used for the determination of Ag(I) in surface water and wastewater samples. The fluorescence quenching mechanism of the ratiometric assay system was also discussed in detailed. Schematic representation of a ratiometric probe composed of silicon- and nitrogen-doped carbon quantum dots (N,Si-CQDs) and CdTe quantum dots capped by N-acetyl-L-cysteine (CdTe QDs). This dual-emission QDs hybrid was fabricated for ultrasensitive and highly selective detection of silver(I) in water samples.

研究领域: 分析化学 · 环境科学 · 材料科学
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JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE · 2020 ·Vol. 101 ·期 6 ·2552-2560 · IF 2.614

Determination of l-theanine in tea water using fluorescence-visualized paper-based sensors based on CdTe quantum dots/corn carbon dots and nano-porphyrin with chemometrics

Hengye Chen,Liuna Wei,Xiaoming Guo,Chengying Hai,Lu Xu,Lei Zhang,Wei Lan,Chunsong Zhou,Yuanbin She,Haiyan Fu

BACKGROUND The quality of tea is influenced by numerous factors, especially l- theanine, which is one of the important markers used to evaluate the sweetness and freshness of tea. Sensitive, rapid, and accurate detection of l -theanine is therefore useful to identify the grade and quality of tea. RESULTS A high-sensitivity, paper-based fluorescent sensor combined with chemometrics was established to detect l- theanine in tea water based on CdTe quantum dots / corn carbon dots and nano tetra pyridel-porphine zinc (ZnTPyP). To verify the reliability of this method, fluorescence spectra and fluorescence-visualized paper-based sensors were compared. The fluorescence spectrum method demonstrated a linear range of 1 to 10 000 nmol L −1 and a limit of detection (LOD) of 0.19 nmol L −1 . In the fluorescence-visualized paper-based sensors there was a linear range of 10–1000 nmol L −1 , and the LOD was 10 nmol L −1 . Partial least squares discriminant analysis (PLSDA) and partial least squares regression analysis (PLSR) were used successfully to determine l -theanine accurately in tea water with this approach. The accuracy of the PLSDA model was 100% both in the training set and the predicting set, and the correlation coefficient between the actual concentration and the predicted concentration was greater than 0.9997 in the PLSR model. CONCLUSION This fluorescence-visualized paper-based sensor, combined with chemometrics, could be applied efficiently to the practical analysis of tea water samples, which provides a new idea to ensure the flavor and quality of tea. © 2020 Society of Chemical Industry

研究领域: 分析化学 · 食品科学 · 化学传感器 · 化学计量学
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FOOD CHEMISTRY · 2023 · IF 8.8

A sensitized ratiometric fluorescence probe based on N/S doped carbon dots and mercaptoacetic acid capped CdTe quantum dots for the highly selective detection of multiple tetracycline antibiotics in food

Yao Fan,Lu Shen,Yaqi Liu,Ying Hu,Wanjun Long,Haiyan Fu,Yuanbin She

A ratiometric fluorescent probe based on N/S doped carbon dots (N/S-CQDs) and mercaptoacetic acid capped CdTe quantum dots (TGA-CdTe QDs) with sensitized and self-calibration functions was constructed to sensitively detect multiple tetracycline antibiotics (TCs). N/S-CQDs could attach stably to TGA-CdTe QDs and form a new composite ratiometric fluorescent probe that had a more than tenfold increase in sensitivity to TCs compared with each single QD. The probe could detect four common TCs as the color of the probe changed from bright red to dark red, and the limit of detection (LOD) was 1.47 × 10 −2 –1.78 × 10 −2 mg/L. Practical applications of the probe in food and urine were also verified with recovery rates of 95.21%-104.97%. Due to the abundant spectral fingerprints provided by both QDs, this novel probe could accurately recognize not only different single TCs but also mixed TC samples even in actual samples combined with chemometrics.

CAS / MDL: 10108-64-2
研究领域: 分析化学 · 食品科学 · 纳米技术 · 环境科学
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ANALYST · 2019 ·Vol. 145 ·期 2 ·619-625 · IF 4.019

A photoelectrochemical immunosensor based on CdS/CdTe-cosensitized SnO2 as a platform for the ultrasensitive detection of amyloid β-protein

Nuo Zhang,Yaoguang Wang,Guanhui Zhao,Chao Wang,Yueyuan Li,Yong Zhang,Huan Wang,Qin Wei

An ultrasensitive label-free photoelectrochemical (PEC) immunosensor was developed to detect amyloid β-protein (Aβ) based on CdS/CdTe-cosensitized SnO2 nanoflowers. Specifically, SnO2 with a flower-like porous nanostructure was utilized as a perfect substrate for the construction of PEC immunosensors, and the SnO2-modified electrode was first coated with CdTe quantum dots (QDs) and then further deposited with CdS by successive ionic layer adsorption and reaction techniques. The formed SnO2/CdS/CdTe-cosensitized structure exhibited excellent photocurrent intensity and was employed as an excellent photoactive matrix to immobilize Aβ antibody to further construct the immunosensor. Under optimal conditions, the as-constructed PEC immunosensor was used to detect Aβ and exhibited a wide linear concentration range from 0.5 pg mL−1 to 10 ng mL−1, with a low limit of detection (LOD, 0.18 pg mL−1, S/N = 3). Meanwhile, it also presented good reproducibility, specificity, and stability and may open a new promising platform for the clinical detection of Aβ or other biomarkers.

CAS / MDL: 25952-53-8 6066-82-6
研究领域: 生物传感器 · 纳米技术 · 光电化学 · 分析化学 · 生物医学工程
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ANALYTICAL BIOCHEMISTRY · 2023 · IF 2.9

The fluorescence and colorimetric dual-readout probe for clinical rapid detection of mycophenolic acid by the poly(ethylenimine)/silica-coated CdTe quantum dots

You Quan Shi,Zhao Xu,Le Wang,Kang Wang,Li Xu,Heng Zheng

It is particularly meaningful to therapeutic drug monitoring (TDM) of mycophenolic acid (MPA) for transplant patients to maximize the drug efficacy and minimize the adverse effect. In this study, a novel fluorescence and colorimetric dual-readout probe was put forward to fast and reliable detect MPA. The blue fluorescence of MPA was largely enhanced in the presence of poly (ethylenimine) (PEI), while the red fluorescence of [email protected] 2 (silica-coated CdTe quantum dots) provided a reliable reference signal. Hence, combining PEI 70,000 and [email protected] 2 , a fluorescence and colorimetric dual-readout probe could be constructed. For fluorescence measurement of MPA, the linearity was obtained in the MPA concentration range of 0.5–50 μg/mL, with a limit of detection (LOD) of 33 ng/mL. For the visual detection, the fluorescent colorimetric card was established in the MPA concentration from 0.5 to 50 μg/mL corresponding to the fluorescence color from red to violet and then to blue, which could be used for semi-quantification. Furthermore, in the light of the ColorCollect APP by the smartphone, the ratio of blue and red brightness values was linear with the MPA concentration from 1 to 50 μg/mL; thus, quantification of MPA could be realized by APP with the LOD of 83 ng/mL. The developed method was successfully applied to the analysis of MPA in the plasma samples of three patients after oral administration of mycophenolate mofetil , which was the prodrug of MPA. The result was comparable to those obtained by the clinically widely-used enzyme multiplied immunoassay technique. The developed probe was fast, cost-effective and operational convenience, and possessed high potential for TDM of MPA.

研究领域: 分析化学 · 临床化学 · 药学 · 生物医学工程
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MICROCHIMICA ACTA · 2021 ·Vol. 188 ·期 12 ·1-9 · IF 5.833

Fluorescence and visual immunoassay of HIV-1 p24 antigen in clinical samples via multiple selective recognitions of CdTe QDs

Tang Zhuoyun,Wei Zeliang,Huang Ke,Wei Yinhao,Li Dongdong,Yan Shixin,Huang Jin,Geng Jia,Tao Chuanmin,Chen Piaopiao,Ying Binwu

Human immunodeficiency virus (HIV) infection inflicts significant economic and social burdens on many countries worldwide. Given the substantial morbidity and mortality from HIV infection, there is an urgent need for accurate and early detection of the virus. In this study, immunofluorescence and visual techniques are described that detect the HIV-1 p24 antigen, which relied on selective recognition of Ag + /Ag nanoparticles (Ag NPs) and Cu 2+ /Cu + using cadmium telluride quantum dots (CdTe QDs). After the sandwich immunoreactions were accomplished, the alkaline phosphatase (ALP) hydrolyzed L-ascorbic acid 2-phosphate (AAP) to form ascorbic acid (AA) that further reduces Ag + and Cu 2+ to Ag NPs and Cu + , respectively. This method was highly sensitive and selective and could detect as low as 1 pg/mL of p24 antigen by naked eyes and had a good linearity in the concentration range 1–100 pg/mL. When using Ag + and Cu 2+ as media, the limit of detection (LOD) of the new method was 0.3 pg/mL and 0.2 pg/mL, respectively. Compared with clinical electrochemiluminescence immunoassay (ECLIA) results and clinical data, this method demonstrated good consistency for the quantification of HIV-1 p24 antigen in 34 clinical serum samples. In addition, this method could accurately distinguish HIV from other viruses and infections such as hepatitis B virus , systemic lupus erythematosus , hepatitis C virus , Epstein-Barr virus , cytomegalovirus , lipemia , and hemolysis . Therefore, our dual-mode analysis method may provide additional solutions to identify clinical HIV infection. Graphical abstract An immunofluorescence and visualization dual-mode strategy for the detection of p24 antigen was constructed based on immune recognition reaction and a phenomenon that cadmium telluride quantum dots (CdTe QDs) can selectively recognize Ag + /Ag nanoparticles (Ag NPs) and Cu 2+ /Cu + .

研究领域: 病毒学 · 免疫学 · 医学诊断
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