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Pt NPs
MICROCHEMICAL JOURNAL · 2024 · IF 4.9

A novel electrochemical ammonia sensor based on Pt NPs@MIL101(Cr)-NH2 for chemical leaks detection at room temperature

Li Gong,Siwei Jin,Renlong Liu,Zuohua Liu,Yijiao Zhang,Li Zhang,Tengda Zhao,Huanbao Fa,Wei Yin

Achieving the real-time, low-cost, portable and accurate NH 3 detection is of great importance in industry owing to the toxicity of NH 3 . In this paper, Pt NPs@MIL-101-NH 2 composites modified screen-printed electrodes (SPEs) were prepared by solvothermal method and ionic liquids [BMIM][BF 4 ] were used as electrolytes. Finally, the prepared Pt NPs@MIL-101-NH 2 /SPEs were combined with a miniature electrochemical workstation to construct a novel electrochemical NH 3 sensor. The experimental results showed that Pt NPs@MIL-101-NH 2 has excellent adsorption capacity for NH 3 , and the sensor has good linearity in the range of 0.7–600 ppm with low limit of detection (0.58 ppm) and fast response time for 10 ppm NH 3 (8.0 s). Furthermore, this sensor also possesses excellent stability, reproducibility, anti-interference and accuracy. The synthesized Pt NPs@MIL-101-NH 2 nanocomposite was proved to be an excellent candidate for constructing high-performance NH 3 sensor for industry.

CAS / MDL: 174501-65-6
研究领域: 材料科学 · 环境监测 · 工业安全
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BIOSENSORS & BIOELECTRONICS · 2016 · IF 7.476

Pt NPs and DNAzyme functionalized polymer nanospheres as triple signal amplification strategy for highly sensitive electrochemical immunosensor of tumour marker

Honghong Chang,Haochun Zhang,Jia Lv,Bing Zhang,Wenlong Wei,Jingang Guo

Highly sensitive determination of tumour markers is the key for early diagnosis of cancer. Herein, triple signal amplification strategy resulting from polymer nanospheres , Pt NPs, and DNAzyme was proposed in the developed electrochemical immunosensor. First, electroactive polymer nanospheres were synthesized by infinite coordination polymerization of ferrocenedicarboxylic acid, which could generate strong electrochemical signals due to plentiful ferrocene molecules. Further, the polymer nanospheres were functionalized by Pt NPs and DNAzyme (hemin/G-quadruplex) with the ability of catalyzing H 2 O 2 , which contributes to enhance the electrochemical signals. The prepared conjugations were characterized by transmission electron microscope (TEM) and energy dispersive X-ray spectroscopy (EDX). And the process of preparation was monitored by zeta potential. Based on the sandwich-type immunoassay, the electrochemical immunosensor was constructed employing the conjugations as signal tags. Under optimal conditions, the DPV peak increased with the increasing of alpha fetal protein (AFP) concentration, and the linear range was from 0.1   pg   mL −1 to 100   ng   mL −1 with low detection limit of 0.086   pg   mL −1 . Meanwhile, the designed immunosensor exhibited excellent selectivity and anti-interference property, good reproducibility and stability. More importantly, there were no significant differences in analyzing real clinical samples between designed immunosensor and commercial ELISA .

研究领域: 分析化学 · 生物医学工程 · 癌症研究
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2017 · IF 4.233

Synthesis of ordered mesoporous La2O3-ZrO2 composites with encapsulated Pt NPs and the effect of La-dopping on catalytic activity

Yan Gao,Yiwei Zhang,Yuming Zhou,Chao Zhang,Hongxing Zhang,Shuo Zhao,Jiasheng Fang,Mengqiu Huang,Xiaoli Sheng

In this work, we report a feasible approach to synthesize a ternary nanocomposites , Pt/lanthanum doped mesoporous zirconium oxide (Pt/La 2 O 3 -ZrO 2 ), via an effective two-step method. Ordered mesoporous La 2 O 3 -ZrO 2 composites were firstly fabricated with mesoporous silica KIT-6 as a hard template. Subsequently, uniform Pt nanoparticles encapsulated by 4 hydroxyl-terminated poly (amidoamine) (G4-OH PAMAM) dendrimers were deposited on the La 2 O 3 -ZrO 2 composites. The as-prepared samples were characterized by transmission electron microscope (TEM), N 2 adsorption–desorption isotherm analysis, energy dispersion X-ray analysis (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and temperature programmed reduction (H 2 -TPR). The average size of PtDENs was found to be 1.48   nm in diameter. Furthermore, the introduction of La could improve the structure of the supports which was confirmed by XRD and H 2 -TPR analysis. The reduction of p-nitrophenol to p-aminophenol by NaBH 4 was utilized to evaluate the catalytic performances of catalysts. Results indicated that the Pt/La 2 O 3 -ZrO 2 catalyst calcined in nitrogen at 550   °C exhibited the highest catalytic performance and still kept the high catalytic activity even after six cycles. This phenomenon suggests that synergistic effect among Pt-Zr-La could enhance the catalytic efficiency. Finally, reaction mechanism was proposed for the reduction of p-nitrophenol.

CAS / MDL: 100587-94-8
研究领域: 材料科学 · 催化 · 纳米技术 · 化学工程
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Bioactive Materials · 2021 · IF 14.593

Synergistic enhancement of immunological responses triggered by hyperthermia sensitive Pt NPs via NIR laser to inhibit cancer relapse and metastasis

Jie Yu,Sha Liu,Yupeng Wang,Xidong He,Qingfei Zhang,Yanxin Qi,Dongfang Zhou,Zhigang Xie,Xiaoyuan Li,Yubin Huang

The combination of tumor ablation and immunotherapy is a promising strategy against tumor relapse and metastasis. Photothermal therapy (PTT) triggers the release of tumor-specific antigens and damage associated molecular patterns (DAMPs) in-situ. However, the immunosuppressive tumor microenvironment restrains the activity of the effector immune cells. Therefore, systematic immunomodulation is critical to stimulate the tumor microenvironment and augment the anti-tumor therapeutic effect. To this end, polyethylene glycol (PEG)-stabilized platinum (Pt) nanoparticles (Pt NPs) conjugated with a PD-L1 inhibitor (BMS-1) through a thermo-sensitive linkage were constructed. Upon near-infrared (NIR) exposure, BMS-1 was released and maleimide (Mal) was exposed on the surface of Pt NPs, which captured the antigens released from the ablated tumor cells, resulting in the enhanced antigen internalization and presentation. In addition, the Pt NPs acted as immune adjuvants by stimulating dendritic cells (DCs) maturation. Furthermore, BMS-1 relieved T cell exhaustion and induced the infiltration of effector T cells into the tumor tissues. Thus, Pt NPs can ablate tumors through PTT, and augment the anti-tumor immune response through enhanced antigen presentation and T cells infiltration, thereby preventing tumor relapse and metastasis.

研究领域: 癌症研究 · 纳米技术 · 免疫治疗 · 光热疗法
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

A highly sensitive sandwich-type electrochemical sensor for detection glypican-3 based on H-rGO-CMC@Pt NPs and aptamers

Xiaohong Tan,Wenzhan Li,Wei He,Tingting Yu,Bingbing Wan,Yong Huang,Jintao Liang,Guiyin Li

Glypican-3 (GPC3), which is a surface heparan sulfate proteoglycan, has been widely known the ideal biomarker for diagnosis and treatment of hepatocellular carcinoma (HCC). Accurate and sensitive detection of serum GPC3 level is an important and challenging task. In this paper, a sandwich electrochemical aptasensor was designed to specifically detect serum GPC3 level through aptamer-target-aptamer recognition. A GPC3 aptamer (GPC3 Apt ) immobilized on the surface of gold nanoparticles@reduced graphene oxide modified screen-printed electrode (Au NPs@rGO/SPCE) was used as the capture probe. Hemin-reduced graphene oxide-carboxymethyl chitosan@platinum nanoparticles (H-rGO-CMC@Pt NPs), with good mimicking peroxidases activity, were labeled with amination GPC3 aptamer, which was employed as the signal probe. Once the target GPC3 was anchored on the surface of GPC3 Apt /Au NPs@rGO/SPCE, the H-rGO-CMC@Pt NPs-GPC3 Apt was further specifically bound to the GPC3, forming the aptamer-target-aptamer sandwich structure, which can catalyze the oxidation of hydroquinone (HQ) to benzoquinone (BQ) and lead the oxidation current of HQ recorded by DPV to changing. The linear relationship between the current signal of oxidation of HQ and GPC3 concentration range of 0.0001–3.0 µg/mL and 3.0–60.0 µg/mL, with a low detection limit (LOD) of 0.0685 ng/mL. Additionally, the electrochemical aptasensor was successfully applied for the detection of GPC3 in human serum samples with the recovery of 99.95–104.06 % and relative standard deviation (RSD) of 1.31–5.22 %. Thus, the sandwich aptasensor could provide a new strategy for detection of serum GPC3 level and improve the early diagnosis rate of HCC.

研究领域: 生物医学工程 · 肿瘤学 · 分析化学
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Journal of Materials Chemistry A · 2023 ·Vol. 11 ·期 8 ·4319-4333 · IF 11.9

Manipulating the interaction of Pt NPs with N-hollow carbon spheres by F-doping for boosting oxygen reduction/methanol oxidation reactions

Chaojie Lyu,Jiarun Cheng,Yuquan Yang,Jiwen Wu,Kaili Wu,Yunguo Yang,Woon-Ming Lau,Ning Wang,Dawei Pang,Jinlong Zheng

Highly dispersed Pt NPs anchored in hierarchically N,F co-doped hollow carbon spheres (Pt@N,F-HCS) were synthesized through a template-assisted strategy followed by fluorination and wet chemical reduction. Due to the introduction of F heteroatoms into the carbon skeleton, the degree of d–π electron conjugation between Pt NPs and N,F-HCS can be enhanced. This will lead to higher Ptx+ content in Pt species, which is beneficial for the effective adsorption of *OOH intermediates and is conducive to O–O bond breaking and triggers the direct 4-electron transfer mechanism for the ORR. In particular, the onset potential and half-wave potential values for the ORR are more positive than Pt@N-HCS without F doping, even outperforming 20%Pt/C. Besides, the Pt@N,F-HCS catalyst also possesses the smallest onset potential and largest methanol oxidation current for the MOR. In alkaline media, abundant OH− will be adsorbed around the Ptx+ sites due to its higher positive valence, and the reaction intermediate COads generated in Ptx+ sites will be further oxidized to the final product, CO2, thus improving the MOR activity and CO tolerance capacity. This heteroatom-doping strategy is favorable for enhancing the interaction between Pt NPs and the carbon-based support, and also provides insight to promote the activity and selectivity for direct methanol fuel cells.

研究领域: 材料科学 · 电化学 · 能源科学
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SENSORS AND ACTUATORS B-CHEMICAL · 2023 · IF 8.4

Fluorescent biosensor based on MB-APT combined with Pt NPs for the detection of infectious bacteria in mouse and human wounds

Lanmei Gao,Houbing Zheng,Yuanlong Hu,Yi Zhong,Linhai Jiang,Yuanzi Wu,Fen Yan,Da Huang,Jianhua Li,Fang Zhang,Zhenyu Lin,Meishui Wang,Zuquan Weng

Bacterial infection of wounds is one of great concern to patients, and rapid and correct detection of bacterial infection is crucial to ensure accurate diagnosis and early intervention. Based on the principle that glucose can only be consumed by live bacteria, a fluorescent biosensor was constructed to detect four kinds of common infectious bacteria (Acinetobacter baumannii, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus) in skin wounds, taking advantage of magnetic bead-aptamer for recognizing, sorting and enrichment, platinum nanoparticles for signal amplification . The linear detection range of AB, EC, PA and SA were 27– 8 × 10 6 CFU/mL, 10– 2.5 × 10 7 CFU/mL, 34– 2.5 × 10 7 CFU/mL and 10– 1.0 × 10 7 CFU/mL, respectively, and the limits of detection were 27 CFU/mL, 10 CFU/mL, 34 CFU/mL and 2 CFU/mL. Furthermore, all target bacteria in samples containing 8 × 10 8 CFU/mL of other interfering bacteria have been successfully identified and quantified. The proposed method was also successfully applied to the detection of bacterial infection in skin wounds of mouse and human, including the detection of separate bacterial infection as well as a coinfection. The recovery of this method was in the range of 90.161– 109.961%. Thus, this proposed method can be a promising candidate for rapid and convenient evaluation of infectious bacteria in point-of-care settings.

CAS / MDL: 9001-37-0 16940-66-2
研究领域: 医学诊断 · 生物传感技术 · 纳米医学
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2024 · IF 3.1

A Novel MXene@MOF@Pt NPs-Based Enzyme-Free Electrochemical Sensor for highly Sensitive Detection of Hydrogen Peroxide Released from Living Cells

Wenbin Wen,Yuan Dang,Jieli Tang,Changluo Su,Sha Yu,Junping Ma,Yuanzhen Zhou

Rapid and accurate detection of hydrogen peroxide (H2O2), an important reactive oxygen species (ROS) released from living cells, is of great significance for early diagnosis of tumors. Here, a high sensitive enzyme-free electrochemical sensor for the detection of H2O2 released from living cells was constructed based on MXene@ZIF-8@Pt NPs nanocomposites. Through the characterization of physical and chemical properties, it was observed that Pt NPs with excellent catalytic activity were uniformly supported on MXene@ZIF-8, which exhibited excellent conductivity and large specific surface area. Thanks to the significantly enhanced catalytic activity derived from the successful integration of MXene, ZIF-8 and Pt NPs, under the optimal conditions, the sensing platform based on MXene@ZIF-8@Pt NPs exhibited a wide linear range from 355.4 nM to 21.75 mM, with a limit of detection as low as 120.9 nM, while showing satisfactory reproducibility and selectivity. Furthermore, the developed electrochemical sensor enables real-time monitoring of H2O2 released from living Hela cells under N-formylmethionyl-leucyl-phenylalanine stimulation. Overall, the MXene@ZIF-8@Pt NPs developed in this article will become a promising candidate in monitoring physiological processes.

研究领域: 分析化学 · 生物传感器 · 材料科学 · 癌症诊断 · 电化学
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Nanoscale · 2021 ·Vol. 13 ·期 43 ·18273-18280 · IF 7.79

Confinement of Pt NPs by hollow-porous-carbon-spheres via pore regulation with promoted activity and durability in the hydrogen evolution reaction

Zhuofan Gan,Chengyong Shu,Chengwei Deng,Wei Du,Bo Huang,Wei Tang

Electrochemical water splitting is a promising method to generate pollution-free and sustainable hydrogen energy. However, the specific activity and durability of noble metal catalysts is the main hindrance to the hydrogen evolution reaction. Based on the continuous pore regulation of hollow porous carbon spheres (N-HPCSs) by hexadecyl trimethyl ammonium bromide, the 6.21 wt% Pt/N-HPCSs exhibited good dispersibility, according to a low overpotential of 45 mV (10 mA cm−2/1 M KOH). Its mass activity was 4 times that of the commercial 20 wt% Pt/C at −0.07 V (vs. RHE) potential. We analyse that the excellent activity is due to the interaction between Pt nanoparticles and N-HPCSs so that the electron density around the Pt atoms increases, which is beneficial for H2O to obtain electrons and transform into Had. Meanwhile the sea urchin-like structure of N-HPCSs facilitates the desorption of H2. Furthermore, the overpotential showed no obvious decrease in the long-term durability test, which should be attributed to the confinement of Pt nanoparticles by the well-defined pores in N-HPCSs to avoid the aggregation of Pt nanoparticles during long-term testing.

研究领域: 材料科学 · 电化学
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Metal Nanoparticles@Covalent Organic Framework@Enzymes: A Universal Platform for Fabricating a Metal–Enzyme Integrated Nanocatalyst

Hao Zhao,Guanhua Liu,Yunting Liu,Xilin Liu,Hanxi Wang,Huaxun Chen,Jing Gao,Yanjun Jiang

Cascade catalysis that combines chemical catalysis and biocatalysis has received extensive attention in recent years, especially the integration of metal nanoparticles (MNPs) with enzymes. However, the compatibility between MNPs and enzymes, and the stability of the integrated nanocatalyst should be improved to promote the application. Therefore, in this study, we proposed a strategy to space-separately co-immobilize MNPs and enzymes to the pores and surface of a highly stable covalent organic framework (COF), respectively. Typically, Pd NPs that were prepared by in situ reduction with triazinyl as the nucleation site were distributed in COF (Tz-Da), and organophosphorus hydrolase (OPH) was immobilized on the surface of Tz-Da by a covalent method to improve its stability. The obtained integrated nanocatalyst Pd@Tz-Da@OPH showed high catalytic efficiency and reusability in the cascade degradation of organophosphate nerve agents. Furthermore, the versatility of the preparation strategy of COF-based integrated nanocatalyst has been preliminarily expanded: (1) Pd NPs and OPH were immobilized in the triazinyl COF (TTB-DHBD) with different pore sizes for cascade degradation of organophosphate nerve agent and the particle size of MNPs can be regulated. (2) Pt NPs and glucose oxidase were immobilized in COF (Tz-Da) to obtain an integrated nanocatalyst for efficient colorimetric detection of phenol.

研究领域: 催化 · 纳米技术 · 生物化学 · 材料科学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Co-immobilization of LAAO and Pt NPs in HOFs: An enzyme-metal coupled catalysis for enhancing the one-pot synthesis of α-keto acid

Lijun Yang,Tiantian Zhou,Zhiyi Zhang,Wei Qi,Mengfan Wang

The enzymatic oxidation of amino acids using amino acid oxidases (AAOs) as biocatalysts for α-keto acid synthesis has garnered increasing attention due to its environmental friendliness and exceptional reaction efficiency. However, the by-product H 2 O 2 inevitably causes the decarboxylation of α-keto acids and subsequently deactivates the enzyme. Herein, we used a simple in-situ biomineralization method to immobilize Pt NPs with catalase-like activity and L-amino acid oxidase (LAAO) in to a hydrogen-bonded organic framework ( TW HOF) under a mild condition, and the synthesized LAAO-Pt@ TW HOF cascade catalytic system was applied to synthesis of α-keto acid. Compared with free LAAO, the LAAO-Pt@ TW HOF exhibited a 3.3-fold activity, well reusability and complete conversion (100 %) of L-tryptophan to indole-3-pyruvic acid was achieved. This work offers a potential application of HOF materials in constructing high-efficiency enzyme-metal coupled catalyst for cascade reactions.

研究领域: 生物化学 · 材料科学 · 催化反应
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FOOD CHEMISTRY · 2025 · IF 9.8

A resonance energy transfer electrochemiluminescence sensor based on the synergistic effect of luminol@β-cyclodextrin and Ni-MOF@Pt NPs for the oxytetracycline detection

Li Tian,Shuning Yang,Guangping Ma,Pengfei Han,Hanyue Jiang,Wenzhuo Wang,Juan Lu

The electrochemiluminescence (ECL) sensor for detecting oxytetracycline (OTC) was constructed by sequentially modifying luminol@β-cyclodextrin (β-CD) and Ni-MOF@Pt NPs on the electrode surface. In this platform, luminol serves as a luminescent reagent, and Pt NPs serve as co-reaction accelerators of the system. β-CD and Ni-MOF are used as carriers to carry luminol and Pt NPs respectively, and the luminescence intensity was further improved by increasing the carrying capacit. In addition, the OTC quenching strategy is adopted, and the constructed sensor is based on the energy transfer of luminol. Under optimal conditions, this sensor exhibited the linear detection range of OTC was found to be between 2.0 × 10 −12  M to 2.0 × 10 −7  M, with a detection limit of 6.7 × 10 −13  M (S/N = 3). The sensor showed good high selectivity and ultra-sensitivity, and obtained satisfactory results when detecting honey and milk samples.

研究领域: 分析化学 · 生物传感 · 食品安全检测
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