ANALYTICAL CHEMISTRY
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2025
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IF 6.7
Xue-Hui Shi,Wei Zhao,Zhimou Yang,Lei Wang,Wenjie Ren
The development of sophisticated nanomaterials with synergistically enhanced functionalities and applications has been greatly promoted via the construction of Janus nanoparticles with controlled compositions. In this work, we described and demonstrated the formation of Janus Au-PbS nanoparticles (NPs) by Au NPs-mediated spontaneous epitaxial nucleation and growth. The mechanism of formation of Janus Au-PbS NPs was investigated in detail. Then, we also found that there was a strong electronic interaction between the Au NPs and PbS quantum dots (QDs) in Janus Au-PbS NPs, where electrons were transferred from the Au NPs domain to the PbS QDs domain. Moreover, the Janus Au-PbS NPs integrated the high-brightness tunable second near-infrared (NIR-II) photoluminescence emission and surface-enhanced Raman scattering (SERS), which achieved good intraoperative tumor resection. This complementary dual-functional imaging had the potential to enable more accurate tumor imaging and resection.
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ACS Sensors
·
2024
·
IF 8.2
Yahui He,Jian Zhou,Jinbo Zhang,Yihao Guo,Zhangbin Ji,Hui Chen,Yongqing Fu
Love-mode surface acoustic wave (SAW) sensors show great promise for biodetection applications owing to their low cost, digital output, and wireless passive capability, but their performance is often restricted by the availability of suitable sensitive membrane layers. Herein, a composite layer of electrospun fibers made from cellulose acetate and polyethylenimine, coated with gold nanoparticles, is proposed as a porous and sensitive membrane coated onto a love-mode SAW biosensor for monitoring gene sequences of Staphylococcus aureus. The results showed that the developed sensor exhibited an impressive sensitivity of 122.56 Hz/(nmol/L) for detecting gene sequences of S. aureus, surpassing the sensitivity of conventional SAW sensors employing a bare Au film as the sensitive layer by 5-fold. The analysis revealed a remarkably linear detection (R2 of 0.97827) of S. aureus gene sequences within the range of 0 to 100 nmol/L. The limit of detection was impressively low at 0.9116 nmol/L. The good stability and specificity of the biosensor in liquid environments were demonstrated for clinical diagnostics.
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Small
·
2025
·
IF 12.1
Wenli Lei,Shuang Zhang,Jiaxi Shu,Fudong Li,Zixuan Deng,Juejing Liu,Xiaofeng Guo,Yuanmeng Zhao,Changsheng Shan
Self-powered biosensors (SPBs) based on biofuel cells (BFCs) use electrical output as a sensing signal without the need of external power supplies, providing a feasible approach to constructing miniaturized implantable or portable devices. In this work, a novel nanozyme of gold nanoclusters/palladium nanocubes (AuNCs/PdNCs) heterostructure is successfully fabricated to develop an innovatively self-powered and non-enzymatic glucose sensing system. The AuNCs/PdNCs with glucose oxidase (GOD)-like activity exhibits superior electrocatalytic and non-enzymatic sensing performance toward glucose. The non-enzymatic BFCs-based SPBs system, established on the AuNCs/PdNCs (anodic catalyst) and single atomic Fe sites coupled with carbon-encapsulated Fe 3 C crystals (Fe 3 C@C-Fe SACs as a cathodic catalyst) platform, exhibits an exceptional sensitivity to glucose with 0.151 µW cm −2 m m −1 (3.4 times higher than the PdNCs), outstanding selectivity and robust stability. The outstanding performance of the BFCs-based SPBs system can be attributed to the synergistic cooperation between the PdNCs and AuNCs.
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JOURNAL OF HAZARDOUS MATERIALS
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2025
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IF 11.3
Yudie Sun,Aobo Feng,Ruilai Zhang,Kehong Quan,Zefeng Hua,Kui Zhang
Bacterial contamination is a very serious health and environmental problem, with the main source of toxicity being lipopolysaccharides in the cell walls of Gram-negative bacteria. Therefore, the development of effective analytical methods is crucial for the detection of lipopolysaccharide content. This work facilitates the efficient generation of precisely adjustable dual-mode signals for LPS detection in surface-enhanced Raman spectroscopy (SERS) and electrochemiluminescence (ECL) by inducing anisotropic morphological evolution of Au@Ag nanocubes (Au@AgNCs) through poly-cytosine (poly-C) DNA. In the presence of LPS, the released probe triggers rolling circle amplification (RCA) and generates cyclic poly-C DNA, which subsequently induces the etching of Ag composites on Au@AgNCs. This etching process leads to changes in both the morphology and composition of Au@AgNCs composite materials, resulting in a decrease in SERS signals. The poly-C DNA was subsequently adsorbed with Ag + and then reduced to silver nanoclusters (AgNC) by NaBH 4 , serving as an ECL signal source. Under optimal experimental conditions, both SERS and ECL demonstrated linear ranges spanning from 1 fg/mL to 1 ng/mL, with detection limits of 0.29 fg/mL and 0.14 fg/mL, respectively. Moreover, the SERS-ECL dual-mode sensor facilitates the accurate discrimination of Gram-negative bacteria in diverse real samples. It demonstrates promising applications in the areas of food safety, water quality monitoring, and clinical bacterial detection.
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MICROCHIMICA ACTA
·
2024
·Vol. 191
·期 10
·1-13
·
IF 5.3
Guo Liang,Zhou Shijin,Xue Jinyan,Liu Zenghui,Xu Shuqing,He Zhangxu,Yang Huaixia
A sandwich electrochemical sensor was fabricated based on multi-walled carbon nanotubes/ordered mesoporous carbon/AuNP (MWCNTs/CMK-3/AuNP) nanocomposites and porous core–shell nanoparticles Au@PdNPs to achieve rapid and sensitive detection of AFB 1 in complex matrices. MWCNTs/CMK-3/AuNP nanocomposite, which was prepared by self-assembly method, served as a substrate material to increase the aptamer loading and improve the conductivity and electrocatalytic activity of the electrode for the first signal amplification. Then, Au@PdNPs, which were synthesized by one-pot aqueous phase method, were applied as nanocarriers loaded with plenty of capture probe antibody (Ab) and signal molecule toluidine blue (Tb) to form the Au@PdNPs-Ab-Tb bioconjugates for secondary signal amplification. The sensing system could still significantly improve the signal output intensity even in the presence of ultra-low concentration target compound due to the dual signal amplification of MWCNTs/CMK-3/AuNP nanocomposites and Au@PdNPs-Ab-Tb. The method exhibited high selectivity, low detection limit (9.13 fg/mL), and strong stability to differentiate AFB 1 from other mycotoxins. Furthermore, the sensor has been successfully applied to the quantitative determination of AFB 1 in corn, malt, and six herbs, which has potential applications in food safety, quality control, and environmental monitoring. Graphical Abstract
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2024
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IF 4.9
Jin Wang,Xu Guo,Qixiang Zhou,Yan Cai,Bing Lu,Yang Wang,Yong Yao
The functional photoelectric materials based on bismuth oxyhalides (BiOX, X = Cl, Br and I) have been widely used in the field of photo-electrochemistry (PEC) due to their excellent physical, chemical and optical properties. Herein, a series of BiOX nanoflowers conjugated water-soluble pillar[5]arenes functionalized Au (Au@WP5/BiOX) modified PEC sensor are constructed and investigated for the PEC detection of serotonin. Upon exploring the physical properties, such as size, visible light absorption capacity, band gap and impedance, of the three BiOX materials, it is discovered that BiOBr is more effective in detecting 5-HT due to its high redox ability, moderate band gap (∼2.03 eV), and low impedance. BiOBr can provide a high and stable starting photocurrent compared to the other two bismuth oxyhalides. When used in acidic or neutral environments, 5-HT with a positive charge can undergo electrostatic adsorption and host-guest complexation behavior with WP5, which has a negative charge. By using WP5, the recognition ability of the material to 5-HT molecules can be enhanced, and the adsorption of 5-HT molecules on Au@WP5/BiOBr can be accelerated. The local surface plasmon resonance effect (LSPR) of gold nanoparticles (Au NPs) can accelerate the electrochemical reaction rate and charge transfer rate, which ultimately leads to the amplification of the photocurrent signal. As a result, the 5-HT detection sensor based on Au@WP5/BiOBr has a wide detection range from 0.01 to 100 μM and a low detection limit of 3 nM (S/N = 3) compared to other sensors, including Au@WP5/BiOCl and Au@WP5/BiOI. The proposed PEC sensor also exhibits good stability and selectivity, making it a promising strategy for detecting biological small molecules using pillar[5]arene functionalized PEC active materials.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Yuejia Yin,Yajie Chen,Xinyan Yu,Qiuyu Zhang,Yaxin Ru,Guohui Tian
During the photocatalytic CO 2 reduction process, fast charge transport, abundant active sites, and high visible light utilization in photocatalysts are key to achieving excellent CO 2 conversion efficiency. In this work, we have designed and prepared hierarchical CuS@SnS 2 p-n heterostructure hollow cubes for photocatalytic CO 2 reduction. First, a monolayer of CuS was in situ generated on the pre-prepared Cu 2 O cubes to construct core–shell Cu 2 O@CuS cubes by sulfidation of Cu 2 O cubes. The following etching process led to the formation of CuS hollow cubes. Finally, the hierarchical CuS@SnS 2 p-n heterostructure hollow cubes were obtained by growing SnS 2 nanosheets on the CuS hollow cubes. The prepared CuS@SnS 2 p-n heterostructure hollow cubes showed an improved photocatalytic CO 2 reduction activity compared with the bare CuS and SnS 2 control samples. The p-n heterojunction formed between SnS 2 and CuS as well as its hollow structure enhanced the charge carrier separation efficiency and the light absorption capacity of the hybrid catalyst. Furthermore, after the decoration of Au nanoparticles, the formed Schottky junction further discouraged the charge carrier recombination. Thus, the cooperative p-n heterojunction and Schottky junction greatly facilitated photocatalytic CO 2 reduction, and exhibiting the maximum CO and CH 4 yields of 140.1 and 77.5 μmol g −1 h −1 , respectively. This work presents an efficient design of high-performance catalysts for photocatalytic CO 2 reduction.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Yulin Xu,Qin Luo,Lichun Yang,Shenghao Zhang,Yuanbo Huang,Yan Sun,Wei Wei,Min Xie,Yongjun Hu
Sensitive, flexible and rapid SERS substrate for the on-site detection of pesticide residues on the fruit peel is of great significance. In this study, the three-dimensional nanofiber network of bacterial nanocellulose (BNC) serves as a matrix template material in the composite system. The highly antioxidative silver@gold nanoparticles (Ag@Au NPs), featuring a ∼ 45 nm diameter Ag core and an ultrathin ∼2 nm Au shell, were first synthesized via a ligand-assisted complexation approach. Subsequently, these nanoparticles were uniformly incorporated into the bacterial nanocellulose (BNC) matrix through a facile vacuum filtration method to fabricate the flexible Ag@Au NPs-BNC SERS substrate. The prepared flexible SERS substrate achieved an exceptional detection sensitivity of 5 × 10 −9 M for the detection of crystal violet (CV), excellent signal uniformity (RSD = 5.4 %), and exhibited a remarkable SERS enhancement factor of 1.19 × 10 6 . The substrate demonstrated excellent performance for detecting thiram in apple and pear peels, exhibiting a linear dynamic range of 0.1–10 ppm with ultralow detection limits (LODs: 0.0498 ppm and 0.0621 ppm, respectively), and these values are two orders of magnitude below the U.S. Environmental Protection Agency's maximum residue limit (MRL: 5 ppm) for thiram in agricultural products. Remarkably, the substrate maintained stable SERS signal intensity after 57 days of ambient storage, confirming its outstanding long-term stability. The flexible Ag@Au NPs-BNC SERS substrate offers high sensitivity, excellent stability, and reliable detection of trace hazardous chemicals in real applications.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE
·
2025
·Vol. 36
·期 1
·1-18
·
IF 4.5
Fang Cuifu,Duan Qing,Tang Ying,Fu Lifeng,Chen Juzheng,Zhou Weimin,Liu Fengen
Venous thromboembolism ranks as the third most prevalent cardiovascular disease. Nanotechnology-based drug carriers show significant potential for thrombolytic therapy. However, existing systems face challenges, including environmental impact and limited accessibility. To address these, we developed a novel delivery system using human black hair-derived nanoparticles (HNPs). These HNPs were loaded with the thrombolytic agent urokinase plasminogen activator (uPA) and a minimal concentration of gold nanoparticles (AuNPs). These components were encapsulated within a polyvinyl alcohol (PVA) membrane to create the nanocapsule drug delivery system, uPA-Au@HNP@PVA. Upon intravenous injection into a rat model with venous thrombosis, the system leveraged targeted blood flow to reach thrombus sites. Under 1064 nm NIR irradiation, the PVA membrane dissolved, exposing and releasing the drugs for intelligent thrombolysis. This system demonstrated excellent thrombolytic efficacy both in vivo and in vitro, coupled with robust biocompatibility in various biological tests, suggesting a wide range of potential applications. Graphical Representation: a. Depiction of the uPA-Au@HNP@PVA synthesis process. b. Diagrammatic explanation of intelligent thrombolytic therapy for specific drug delivery in a rat venous thrombosis model: I. Intravenous administration of uPA-Au@HNP@PVA; II. Targeted delivery to thrombus sites, navigation of uPA-Au@HNP@PVA to the thrombus location through targeted blood circulation, whereupon exposure to 1064 nm NIR irradiation causes a temperature rise, resulting in PVA dissolution, and drug release; III. NIR-triggered drug release and thrombolysis. Intelligent thrombolysis facilitated by 1064 nm NIR irradiation.
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Carbon Energy
·
2024
·
IF 19.5
Hongyu Gong,Guanliang Sun,Wenhua Shi,Dongwei Li,Xiangjun Zheng,Huan Shi,Xiu Liang,Ruizhi Yang,Changzhou Yuan
Enhancing both the number of active sites available and the intrinsic activity of Co-based electrocatalysts simultaneously is a desirable goal. Herein, a ZIF-67-derived hierarchical porous cobalt sulfide decorated by Au nanoparticles (NPs) (denoted as HP-Au@Co x S y @ZIF-67) hybrid is synthesized by low-temperature sulfuration treatment. The well-defined macroporous–mesoporous–microporous structure is obtained based on the combination of polystyrene spheres, as-formed Co x S y nanosheets, and ZIF-67 frameworks. This novel three-dimensional hierarchical structure significantly enlarges the three-phase interfaces, accelerating the mass transfer and exposing the active centers for oxygen evolution reaction. The electronic structure of Co is modulated by Au through charge transfer, and a series of experiments, together with theoretical analysis, is performed to ascertain the electronic modulation of Co by Au. Meanwhile, HP-Au@Co x S y @ZIF-67 catalysts with different amounts of Au were synthesized, wherein Au and NaBH 4 reductant result in an interesting “competition effect” to regulate the relative ratio of Co 2+ /Co 3+ , and moderate Au assists the electrochemical performance to reach the highest value. Consequently, the optimized HP-Au@Co x S y @ZIF-67 exhibits a low overpotential of 340 mV at 10 mA cm –2 and a Tafel slope of 42 mV dec –1 for OER in 0.1 M aqueous KOH, enabling efficient water splitting and Zn–air battery performance. The work here highlights the pivotal roles of both microstructural and electronic modulation in enhancing electrocatalytic activity and presents a feasible strategy for designing and optimizing advanced electrocatalysts.
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TALANTA
·
2024
·
IF 5.6
Feifan Qi,Mengdie Wu,Simin Liu,Wendi Mu,Chunyan Wu,Xinshui Ren,Chuang Rui,Fangfang Wu,Dong Chang,Hongzhi Pan
Carbohydrate antigen 199 (CA199) is the most sensitive marker reported for pancreatic cancer, and it is a difficult task to develop a highly sensitive assay for CA199. During the experiment, a ratiometric electrochemical immunosensor for quantitative analysis of CA199 was prepared for NiCo@Fc-MWCNTs-LDH as the electrode sensing surface and 3D-rGOF@Ag/Au as the label of Ab 2 . NiCo@Fc-MWCNTs-LDH not only provide the required signal for the immunosensor, but also have a layered structure to obtain a large specific surface area, which can provide more sites for the placement of biological molecules. rGOF has the advantages of large specific surface area and high porosity, which can adsorb Ag electrochemical probe through redox reaction. The modification of gold nanoparticles can not only enhance the electrical conductivity of nano-composites, but also immobilize more biomolecules to improve the sensitivity of electrochemical sensors. With the beefing up of CA199 concentration, the oxidation peak current of Ag increases and the oxidation peak current of Fc-COOH decreases. The ratio (y = I Ag /I Fc-COOH ) of two different signals was linear with the logarithm of CA199 concentration in a certain value range. Under optimal conditions, the immunosensor showed excellent performance in the concentration range of 0.0001 U/mL to 10 U/mL, and the detection limit was 5.55 × 10 −4 U/mL. The strategy could clearly discriminate between matched and mismatched targets, demonstrating high specifificity. This approach further detects CA199 in human plasma to differentiate pancreatic cancer patients from healthy individuals with high accuracy. This method also provided a new idea for the ultrasensitive quantitative detection of other biomarkers.
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Nanoscale Advances
·
2025
·
IF 4.6
Mengting Tong,Guangpeng Chen,Yong Dong,Yubin Pan,Yanan Xue,Da Li
Despite the progress made in novel immunotherapy for hepatocellular carcinoma (HCC), drug resistance remains a challenging problem. In this study, we developed a stepwise nanodrug delivery system, known as Au-SS-PEG/Sor/ATP aptamer /LHRH-MPG ΔNLS , to adapt to the high concentrations of glutathione (GSH) and adenine nucleoside triphosphate/adenosines (ATP/ADO) found in cancer cells and the tumor microenvironment (TME). This system utilizes novel Au nanoclusters conjugated with disulfide-linked PEG as vectors to transport sorafenib (Sor) and an ATP-binding nucleic acid aptamer (ATP apt ). It can enter HCC cells through luteinizing hormone-releasing hormone (LHRH)-MPG ΔNLS (LM). Within the cells, the disulfide bonds of the nanoclusters are cleaved by the high levels of GSH, leading to the release of Sor/ATPapt. This release can be further triggered by ATP/ADO, resulting in a stepwise drug release mechanism. Furthermore, this nanodrug system has exhibited the ability to overcome αPD-1 resistance in HCC tumors. In summary, our novel drug delivery system demonstrates a dramatic anti-HCC effect and holds great potential for treating HCC patients. Synthesis and mechanistic illustration of Au-SS-PEG/Sor/ATP apt /LM nanoclusters for the treatment of hepatocellular carcinoma (HCC).
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