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Materials Science and Engineering B-Advanced Functional Solid-State Materials · 2023 · IF 3.6

Textile-based dual-mode organic electrochemical transistors for lactate biosensing

Yang Tao,Rufeng Zhu,Panpan Hao,Wei Jiang,Mufang Li,Qiongzhen Liu,Liyan Yang,Yuedan Wang,Dong Wang

The dual-mode organic electrochemical transistors (OECT) were successfully assembled on fabric. The property of different devices has been compared. In the depletion mode, the PEDOT: PSS/textile-based OECT exhibit high transconductance of 75 mS, and the switching ratio of 8 × 10 2 . In accumulation mode, the PEDOT: PSS/DETA/textile-based OECT exhibit transconductance of 0.55 mS, switching ratio can reach 31.7. Both modes have good cycle stability. A lactate (LA) sensor was prepared by modifying the gate electrode with lactate oxidase. The sensitivity of the sensor is 69.97 mV/decade and 47.8 mV/decade in the depletion and accumulation mode, respectively. The LA sensor in both modes has good linear response in a wide concentration range of 100 pM-10 mM. The sensor has been successfully applied to the detection of LA in sweat sample. It has the advantages of simple preparation, good performance, and convenient integration into clothes, which provides a feasible platform for intelligent wearable and portable medical detection.

CAS / MDL: 50-21-5 69-93-2 50-70-4
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Materials · 2023 ·Vol. 16 ·期 3 ·1261 · IF 3.4

Electrophoretic Deposition of Co3O4 Particles/Reduced Graphene Oxide Composites for Efficient Non-Enzymatic H2O2 Sensing

Qian Wang,Yuzhe Wang,Guiyong Xiao,Xinde Zhu

In this work, the facile fabrication of Co3O4particles/reduced graphene oxide (Co3O4/rGO) composites on Indium tin oxide (ITO) slide was achieved by an electrophoretic deposition and annealing process. The deposition time and ratio of the precursors were optimized. Structural characterization and chemical composition investigation indicated successful loading of Co3O4particles on graphene sheets. When applied as a non-enzymatic H2O2sensor, Co3O4/rGO showed significant electrocatalytic activity, with a wide linear range (0.1–19.5 mM) and high sensitivity (0.2247 mA mM−1cm−2). The good anti-interference ability, reproducibility, and long-term stability of the constructed sensor were also presented. The application of Co3O4/rGO in real sample analysis was evaluated in human urine sample with satisfactory results, indicating the feasibility of the sensor in physiological and medical applications.

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ANALYTICAL CHEMISTRY · 2023 · IF 7.4

Flexible Point-of-Care Electrodes for Ultrasensitive Detection of Bladder Tumor-Relevant miRNA in Urine

Duo Chen,Na Chen,Fangning Liu,Yiming Wang,Huageng Liang,Yanbing Yang,Quan Yuan

Portable point-of-care testing (POCT) is currently drawing enormous attention owing to its great potential for disease diagnosis and personal health management. Electrochemical biosensors, with the intrinsic advantages of cost-effectiveness, fast response, ease of miniaturization, and integration, are considered as one of the most promising candidates for POCT application. However, the clinical application of electrochemical biosensors-based POCT is hindered by the decreased detection sensitivity due to the low abundance of disease-relevant biomolecules in extremely complex biological samples. Herein, we construct a flexible electrochemical biosensor based on single-stranded DNA functionalized single-walled carbon nanotubes (ssDNA-SWNTs) for high sensitivity and stability detection of miRNA-21 in human urine to achieve bladder cancer (BCa) diagnosis and classification. The ssDNA-SWNT electrodes with a 2D interconnected network structure exhibit a high electrical conductivity, thus enabling the ultrasensitive detection of miRNA-21 with a detection limit of 3.0 fM. Additionally, the intrinsic flexibility of ssDNA-SWNT electrodes endows the biosensors with the capability to achieve high stability detection of miRNA-21 even under large bending deformations. In a cohort of 40 BCa patients at stages I–III and 44 negative control samples, the constructed ssDNA-SWNT biosensors could detect BCa with a 92.5% sensitivity, an 88.6% specificity, and classify the cancer stages with an overall accuracy of 81.0%. Additionally, the flexible ssDNA-SWNT biosensors could also be utilized for treatment efficiency assessment and cancer recurrence monitoring. Owing to their excellent sensitivity and stability, the designed flexible ssDNA-SWNT biosensors in this work propose a strategy to realize point-of-care detection of complex clinical samples to achieve personalized healthcare.

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MOLECULES · 2022 ·Vol. 27 ·期 23 ·8200 · IF 4.927

Disposable Electrochemical Sensors for Highly Sensitive Detection of Chlorpromazine in Human Whole Blood Based on the Silica Nanochannel Array Modified Screen-Printed Carbon Electrode

Qianqian Han,Tongtong Zhang,Meifang Wang,Fei Yan,Jiyang Liu

Rapid and highly sensitive quantitative analysis of chlorpromazine (CPZ) in human whole blood is of great importance for human health. Herein, we utilize the screen-printed carbon electrodes (SPCE) as the electrode substrates for growth of highly electroactive and antifouling nanocomposite materials consisting of vertically ordered mesoporous silica films (VMSF) and electrochemically reduced graphene oxide (ErGO) nanosheets. The preparation of such VMSF/ErGO/SPCE could be performed by using an electrochemical method in a few seconds and the operation is controllable. Inner ErGO layer converted from graphene oxide (GO) in the growth process of VMSF provides oxygen-containing groups and two-dimensional π-conjugated planar structure for stable fabrication of outer VMSF layer. Owing to the π-π enrichment and excellent electrocatalytic abilities of ErGO, electrostatic preconcentration and antifouling capacities of VMSF, and inherent disposable and miniaturized properties of SPCE, the proposed VMSF/ErGO/SPCE sensor could be applied for quantitative determination of CPZ in human whole blood with high accuracy and sensitivity, good stability, and low sample consumption.Keywords:vertically ordered mesoporous silica films;screen-printed carbon electrodes;electrochemically reduced graphene oxide;chlorpromazine;electrochemical sensors;human whole blood

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MICROCHEMICAL JOURNAL · 2022 · IF 5.304

Ag-Ti3C2Tx MXenes nanoribbons coupled with carbon nanotubes: Preparation, characterization and application for highly sensitive ratiometric voltammetric sensing of paracetamol

Yong Zhao,Yixuan Xia,Juerui Zhang,Hongde Liu,Yinhui Yi,Gangbing Zhu

In this work, based on the unique self-adsorption and reduction capacities of Ti 3 C 2 T x MXenes toward silver ion, silver nanoparticles (Ag NPs) as reference probe are synthesized and immobilized on the surface of Ti 3 C 2 T x nanoribbons (Ti 3 C 2 T x R) to form Ag-Ti 3 C 2 T x R nanohybrid with a simple stirring-method, and carbon nanotubes (CNTs) are introduced to conjugate Ag-Ti 3 C 2 T x R for inhibiting their aggregation and improving further the sensing performance. Via selecting paracetamol (PA) as a model analyte, a ratiometric voltammetric sensing strategy is proposed by using Ag-Ti 3 C 2 T x R/CNTs as electrode materials on the basic of the collaborative advantages of Ag NPs, Ti 3 C 2 T x R and CNTs: in the absence of PA, Ag-Ti 3 C 2 T x R/CNTs modified electrode displays only an electrochemical signal from the oxidation of Ag 0 ; while in the presence of PA, a varied signal of PA along with its concentration can be observed coupled with a quite stable oxidation signal of Ag 0 . Based on this principle, a highly sensitive and reliable ratiometric sensing platform is designed for PA detection by recording the ratio of signals between PA and Ag 0 . It’s expected that this work exploits a new research field in electrochemical sensors by combining the synthetic advantages of MXenes and metal elements.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2023 · IF 4.4

Blue-emitting tryptophan-protected gold nanoclusters acted as a sensitive nanosensor for fluorescence sensing and visual imaging detection of furaltadone

Zhifeng Cai,Huinan Li,Xin Yang,Ming Zhang,Jinhao Guo,Yani Su,Taotao Liu

Herein, blue-emitting gold nanoclusters (Au NCs) were carried out through tryptophan as the protecting and reducing agents. In aqueous solution of Au NCs@tryptophan, the addition of furaltadone guaranteed the interaction of furaltadone with tryptophan around Au NCs. The propinquity of furaltadone to Au NCs caused that the fluorescence of Au NCs was weakened by furaltadone based on the inner filter effect (IFE). Under the optimal measurement conditions, the logarithm of relative fluorescence intensity of Au NCs@tryptophan was linearly carried out with the furaltadone amount increasing from 0.5 to 100 μM, the corresponding detection limit was 0.087 μM. The fluorescence change of Au NCs@tryptophan displayed excellent selectivity and sensitivity for furaltadone than other possible substance in the human body. In view of Au NCs@tryptophan, the as-performed fluorescence nanosensor suggested outstanding ability for furaltadone sensing in real samples. Obviously, this nanoprobe of furaltadone could implement the naked-eye visual fluorescence determination of furaltadone.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2023 · IF 4.4

Physicochemically modulated fluorescence-scattering ratiometric sensor for selective and visual detection of levodopa

Jin Yuan Zhang,Ying Zhang,Yu Zou,Ze Li Bo Xu,Bo Zhang,Wang Ren

In this study, a facile fluorescence-scattering ratiometric sensor was designed for visual and selective detection of levodopa (LD) via a clever physicochemical modulation scheme. The alkalized products of LD can rapidly react with polyethyleneimine (PEI) to exhibit an intense blue fluorescence and decrease the second-order scattering (SOS) signal of PEI. As the concentration of LD increased, the fluorescence intensity at 420 nm increased and the SOS intensity at 675 nm decreased synchronously. Thus the fluorescence-scattering ratiometric sensor was constructed by virtue of the two simultaneously changed signals. Furthermore, red light-emitting Au nanoclusters (AuNCs) were added into the above mixture solution to enlarge the SOS signal and provide a stable red background fluorescence. The intensity ratio of fluorescence to SOS ( F /( S / S blank )) is linear dependent on C LD in the wide range of 50.0–––30000.0 nM, and LD as low as 50.0 nM can be identified with the naked eye via change of fluorescence color. The developed ratiometric sensor is smart, simple and efficient, and has been applied to the convenient assay of LD in real samples. The proposed physicochemical modulation strategy provides a new and facile path for selectively and visually identifying the target from its analogues.

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Journal of Physical Chemistry C · 2023 · IF 3.7

Pyrene as a Triplet Acceptor Enhancing Triplet Energy Transfer of g-C3N4 in Heterogeneous Photooxidation

Longjian Li,Qinhua Zhang,Congcong Han,Xiaohui Sun,Tao Xing,Mingqing Wang,Mingbo Wu,Nopphon Weeranoppanant,Wenting Wu

Triplet photosensitizers have great potential in selective photooxidation by generating 1O2 through triplet energy transfer. However, the heterogeneous bulk photosensitizers easily trap triplet excitons and inhibit photocatalysis efficiency. Previous work focused on controlling ultra-small size to reduce the transfer distance, but we propose a new strategy using triplet acceptor molecules (e.g., pyrenecarboxylic acid, PCA) with proper energy levels to modify the surface of heterogeneous photosensitizers (e.g., g-C3N4), facilitate the transfer of triplet excitons from the interior to the surface of the catalyst, and enhance catalytic reactions on its surface. In the photooxidation reaction of uric acid (UA), the conversion of UA catalyzed by pg-C3N4/PCA can reach 91.3% at 60 min, higher than that without modification (24.0%). DFT calculations and spectroscopic characterization show that the triplet acceptor in pg-C3N4/PCA could reduce the ΔEST value and grab triplet excitons in g-C3N4, thereby enhancing the 1O2 generation. This work provides another approach for high-efficiency utilization of heterogeneous triplet photosensitizers in wide applications.

CAS / MDL: 461-58-5 69-93-2
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BIOSENSORS & BIOELECTRONICS · 2023 · IF 12.6

Triple-enhanced Raman scattering sensors from flexible MXene/Au nanocubes platform via attenuating the coffee ring effect

Xin Liu,Alei Dang,Tiehu Li,Tung-Chun Lee,Yiting Sun,Yuhui Liu,Fei Ye,Shuze Ma,Yong Yang,Weibin Deng

Developing substrates that combine sensitivity and signal stability is a major challenge in surface enhanced Raman scattering (SERS) research. Herein, we present a flexible triple-enhanced Raman Scattering MXene/Au nanocubes (AuNCs) sensor fabricated by selective filtration of Ti 3 C 2 T x MXene/AuNCs hybrid on the Ti 3 C 2 T x MXene membrane and subsequent treatment with 1H,1H,2H,2H-perfluoro-octyltriethoxysilane (FOTS). The resultant superhydrophobic MXene/AuNCs-FOTS membrane not only provides the SERS substrate with environmental stability, but also imparts analyte enrichment to enhance the sensitivity (LOD = 1 × 10 −14  M) and reliability (RSD = 6.41%) for Rhodamine 6G (R6G) molecules owing to the attenuation of the coffee ring effect. Moreover, the triple enhancement mechanism of combining plasmonic coupling enhancement from plasmonic coupling (EM) of nearby AuNCs at lateral and longitudinal direction of MXene/AuNCs-FOTS membrane, charge transfer (CT) from Ti 3 C 2 T x MXene and target molecules and analyte enrichment function provides the substrate with excellent SERS performance (EF = 3.19 × 10 9 ), and allows efficient quantification of biomarkers in urine. This work could provide new insights into MXenes as building blocks for high-performance substrates and fill existing gaps in SERS techniques.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2023 · IF 4.4

Ag triangle nanoplates assembled on PVC/SEBS membrane as flexible SERS substrates for skin cortisol sensing

Guojun Weng,Jianming Yang,Jianjun Li,Jian Zhu,Junwu Zhao

Surface-enhanced Raman scattering (SERS) based on rigid substrates has been widely used in biomedical detection due to its high sensitivity and specificity. However, the tedious operation steps for preparing SERS rigid substrates limited their applications in real-world detection. Compared with general rigid substrate, the flexible substrate has the advantages of simple preparation and easy portability, which are suitable for rapid, wearable and personalized detection in the field of point-of-care test. Herein, the flexible SERS substrates employing copolymer were fabricated and used for detection of skin cortisol, a biomarker for evaluating psychological stress in sweat. Silver triangle nanoplates with sharp corner were used as enhanced particles, and transferred to polyvinyl chloride/styrene-ethylene-butene-styrene copolymer (PVC/SEBS) film through three-phase interface self-assembly. By adjusting the size of silver nanoparticles, the ratio of PVC to SEBS in the polymer film, and the number of transfers of self-assembled silver films, the enhancement effect of the flexible SERS substrate was maximized. In addition, functionalization of the flexible SERS substrate with cortisol antibodies is used to achieve specific detection of cortisol on the skin surface. Under the optimal conditions, the Raman peak intensities at 1268 and 1500 cm −1 of the cortisol had a good linear relationship with the logarithm of its concentration in the range of 10 −7 to 10 −3 M, and the detection limits were 5.47 × 10 −8 M and 5.51 × 10 −8 M, respectively. The flexible silver triangle nanoplates SERS substrate constructed by self-assembly in the three-phase interface has the characteristics of good specificity and high sensitivity, which has potential for transdermal cortisol wearable detection, providing a feasible method for the rapid evaluating psychological stress level.

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International Journal of Electrochemical Science · 2023 · IF 1.5

Ultrasensitive Determination of Dopamine and Uric Acid Based on Gold Nanoparticles@Carbon Dots/Electrochemical Reduced Graphene Oxide modified glassy carbon electrode

Muyi Li,Xiang Yang,Wenjun Liu,Huixian Wang,Hongmei Jiang,Xiaoying Liu

An ultrasensitive electrochemical sensing platform based on a glassy carbon electrode (GCE) modified with electrochemically reduced graphene oxide (erGO) and gold nanoparticles@carbon dots (GNPs@CDs) was developed. The hydroxyl-rich CDs were electrochemically synthesized, and the GNPs@CDs were obtained by reducing chloroauric acid with hydroxyl-rich CDs. The electrochemical behavior of the fabricated electrode, GNPs@CDs/erGO/GCE, was explored by cyclic voltammetry and electrochemical impedance spectroscopy. The electrochemical performance of the electrode demonstrated a remarkable enhancement in the peak current toward oxidation of dopamine (DA) and uric acid (UA) with a peak potential separation of 0.15 V in the presence of ascorbic acid (AA). Under optimized conditions, the simultaneous determination of DA and UA was investigated using differential pulse voltammetry (DPV) resulting in a linear response in the concentration ranges of 0.01−5.0 μM and 5.0−20.0 μM for DA and of 0.1−20.0 μM and 20.0−50.0 μM for UA and in a sensitivity of 11.96 and 6.48 μA μM -1 , respectively. The prepared electrode also demonstrated long-term stability and good reproducibility and was successfully used for the determination of DA and UA in human serum samples with favorable recoveries.

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IONICS · 2023 ·Vol. 29 ·期 9 ·3795-3803 · IF 2.8

An ultra-sensitive electrochemical dopamine sensor based on Ni@N-doped carbon derived from COF LZU-1 microspheres

Xiong Qinghao,Wan Haifei,Peng Xia,Zhu Yongmei

N-rich carbon (C) microspheres loaded with Ni nanoparticle (NiNP) microspheres (Ni@N-doped C) were obtained by calcination of covalent organic framework (COF) LZU-1 with abundant N atoms/Ni 2+ . Lots of NiNPs with the size of 4 nm are arrayed uniformly and firmly into N-doped C microspheres derived from COF LZU-1 based on the strong coordination between N atoms on the wall of well-ordered pores and Ni atoms, which is more beneficial to rapid electron and mass transfer. The synergistic effect from N-doped C microspheres and small-sized NiNPs in Ni@N-doped C enhances catalytic activity of Ni@N-doped C microspheres greatly, which provides feasibility for the construction of non-enzymatic electrochemical sensor. The non-enzymatic electrochemical sensor based on Ni@N-doped C microspheres is applied to the detection of dopamine (DA) and shows good detection results with a low detection limit of 0.009 μM and a wide detection range of 0.027–70 μM. What is more, this DA sensor has good anti-interference, reproducibility, and stability, which provides new idea for the construction of non-enzymatic electrochemical sensor.

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