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Strategic tuning of multi-component NiMoP/TMD-rGO-PANI catalysts for efficient alkaline hydrogen evolution reaction 多组分NiMoP/TMD-rGO-PANI催化剂高效碱性析氢反应的策略调整
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-01-31 DOI: 10.1016/j.matlet.2026.140180
Rijith Sreenivasan , Sarika Sasidharan , Aswathy Retnakaran Sugandhi , Abhilash Sudhakaran , Antony Bruz , Sumi Vijayakumari Sasidharan Nair
We developed a hybrid electrocatalyst of polyaniline (PANI), reduced graphene oxide (rGO), and transition metal dichalcogenides (TMDs) embedded in a NiMoP matrix via electroless plating. This architecture enhances charge carrier mobility, facilitates ion transport, and increases active site exposure, while NiMoP ensures stability. The rGO-PANI-TMD heterostructure lowers kinetic barriers and accelerates charge transfer. The optimized catalyst achieved excellent alkaline HER performance (η10 = 90.1 mV, b = 91 mVdec−1), high exchange current density, and durability, offering a scalable, cost-effective route to robust electrocatalysts for efficient hydrogen production.
我们开发了一种由聚苯胺(PANI)、还原氧化石墨烯(rGO)和过渡金属二硫族化合物(TMDs)通过化学镀嵌入NiMoP基体的杂化电催化剂。这种结构增强了电荷载流子迁移率,促进了离子传输,增加了活性位点暴露,而NiMoP则确保了稳定性。rGO-PANI-TMD异质结构降低了动力学势垒,加速了电荷转移。优化后的催化剂具有优异的碱性HER性能(η10 = 90.1 mV, b = 91 mVdec−1)、高交换电流密度和耐用性,为高效制氢提供了一种可扩展、经济高效的电催化剂途径。
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引用次数: 0
Evaluation of the healing potential of a 3D biomembrane with carrageenan matrix in an excisional wound model 卡拉胶基质三维生物膜在切除伤口模型中的愈合潜力评估
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-05 DOI: 10.1016/j.matlet.2026.140200
Jonathan Elias Rodrigues Martins , David da Silva Braz , Amanda Batista Nascimento , Paulo Elesson Guimarães de Oliveira , Denner Silvino da Silva , José Ednésio da Cruz Freire , Francisco Carlos Carneiro Soares Salomão , Marilia de Albuquerque Oliveira , Carlúcio Roberto Alves , Márjory Lima Holanda Araújo , Felipe Pantoja Mesquita , Jannison Karlly Cavalcante Ribeiro , Pedro Everson Alexandre de Aquino , Luciana Maria de Barros Carlos , Francisca Vânia Barreto Aguiar Ferreira Gomes , Luany Elvira Mesquita Carvalho , Vânia Marilande Ceccatto
Impaired wound healing, particularly under diabetic conditions, demands biomaterials capable of providing structural stability and biological support. In this study, a bioactive iota/kappa-carrageenan hydrogel membrane was fabricated by extrusion-based 3D printing and evaluated in excisional wound models in healthy and diabetic mice. The printed membrane, incorporating proline, hydroxyproline, α-bisabolol, peptides, and zinc sulfate (1% w/v each), exhibited sustained zero-order release kinetics (Y = 0.0163× + 1.336) and reduced water absorption compared with polymeric controls (p < 0.05). Atomic force microscopy revealed increased surface roughness (62.74 nm versus 51.64 nm), indicating polymer reorganization. In vivo, the bioactive membrane significantly accelerated wound contraction, increased collagen deposition, and enhanced fibroblast density in healthy animals (p < 0.05). In diabetic wounds, treatment improved collagen organization and significantly increased VEGF and FGF2 expression, indicating enhanced angiogenesis and fibroplasia. These results demonstrate that the 3D-printed carrageenan membrane provides a stable and biologically active platform for wound repair.
伤口愈合受损,特别是在糖尿病条件下,需要能够提供结构稳定性和生物支持的生物材料。本研究采用挤压3D打印技术制备了具有生物活性的iota/kappa- carragean水凝胶膜,并在健康小鼠和糖尿病小鼠的切除伤口模型中进行了评价。与聚合物对照相比,含有脯氨酸、羟脯氨酸、α-双abolol、多肽和硫酸锌(各1% w/v)的打印膜表现出持续的零级释放动力学(Y = 0.0163× + 1.336),并且吸水率降低(p < 0.05)。原子力显微镜显示表面粗糙度增加(62.74 nm比51.64 nm),表明聚合物重组。在体内,生物活性膜显著加速了健康动物的伤口收缩,增加了胶原沉积,增强了成纤维细胞密度(p < 0.05)。在糖尿病创面中,治疗改善了胶原组织,显著提高了VEGF和FGF2的表达,表明血管生成和纤维增生增强。这些结果表明,3d打印的卡拉胶膜为伤口修复提供了一个稳定且具有生物活性的平台。
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引用次数: 0
Solvent-dependent Plasmonic response of laser-ablated gold nanoparticles for SERS detection of methylene blue 激光烧蚀金纳米粒子对亚甲基蓝SERS检测的溶剂依赖等离子体响应
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-03 DOI: 10.1016/j.matlet.2026.140214
Omar Gaspar-Ramírez , Jesús Cervantes-Martínez , L.P. Rivera , J.G. Quiñones-Galván
Gold nanoparticles (Au-NPs) were synthesized by pulsed laser ablation in liquids for their application in surface-enhanced Raman spectroscopy (SERS) detection of methylene blue (MB). A Nd:YAG laser was employed to ablate a gold target immersed methanol, ethanol, acetone, or isopropanol. UV–Vis spectroscopy revealed solvent-dependent shifts of the localized surface plasmon resonance (LSPR).
Au-NPs obtained in isopropanol showed the most intense plasmonic response and strongest Raman enhancement, enabling clear identification of MB vibrational modes. The results highlight how solvent polarity and dielectric constant influence nanoparticles aggregation, morphology, and plasmonic coupling, offering a clean and controllable route to design SERS-active nanostructures.
采用脉冲激光烧蚀法在液体中合成了金纳米粒子(Au-NPs),并将其应用于亚甲基蓝(MB)的表面增强拉曼光谱(SERS)检测。采用Nd:YAG激光对浸有甲醇、乙醇、丙酮或异丙醇的金靶进行烧蚀。紫外可见光谱揭示了局部表面等离子体共振(LSPR)的溶剂依赖位移。在异丙醇中获得的Au-NPs表现出最强烈的等离子体响应和最强的拉曼增强,从而能够清楚地识别MB的振动模式。研究结果强调了溶剂极性和介电常数对纳米粒子聚集、形态和等离子体耦合的影响,为设计sers活性纳米结构提供了一条干净、可控的途径。
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引用次数: 0
Design of polycaprolactone/MXene@PDA composite coating on MAO-treated magnesium alloy for enhanced photothermal antimicrobial property 聚己内酯/MXene@PDA复合涂层增强光热抗菌性能的设计
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-08 DOI: 10.1016/j.matlet.2026.140235
Fei Meng, Hongrun Luo, Ruixue Sun
A novel multi-functional composite coating with micro-arc oxidation (MAO) coating as the inner layer, polycaprolactone (PCL) coating doped with polydopamine (PDA) modified MXene (MXene@PDA) as the outer layer was successfully prepared on AZ31B alloy. The few-layer Ti3C2Tx MXene can be uniformly and stably dispersed in PCL layer after modification with PDA. Compared with the AZ31B alloy, the MAO-PCL/MXene@PDA composite coating exhibited an increase of three orders of magnitude in charge-transfer resistance (Rct) and demonstrated self-healing performance driven by near-infrared (NIR) irradiation. The addition of MXene@PDA particles can endow the composite coating with good photothermal antibacterial performance with 92.5% and 95.8% efficacy against E. coli and S. aureus, respectively. Moreover, the cellular experiments confirmed the low cytotoxicity of the composite coating and its great capacity for promoting cell proliferation as well as osteogenic differentiation.
在AZ31B合金上成功制备了一种以微弧氧化(MAO)涂层为内层,掺杂聚多巴胺(PDA)改性MXene (MXene@PDA)的聚己内酯(PCL)涂层为外层的新型多功能复合涂层。经PDA修饰后,可使Ti3C2Tx MXene在PCL层中均匀稳定地分散。与AZ31B合金相比,MAO-PCL/MXene@PDA复合涂层在近红外(NIR)照射下的电荷转移电阻(Rct)提高了3个数量级,并表现出自愈性能。MXene@PDA颗粒的加入使复合涂层具有良好的光热抗菌性能,对大肠杆菌和金黄色葡萄球菌的抗菌效果分别为92.5%和95.8%。细胞实验证实复合涂层具有较低的细胞毒性,具有促进细胞增殖和成骨分化的能力。
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引用次数: 0
Structure and property comparison of bovine cancellous bone, demineralized bone matrix, and hydroxyapatite for localized bone graft applications 牛松质骨、脱矿骨基质和羟基磷灰石局部骨移植的结构和性能比较
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-06 DOI: 10.1016/j.matlet.2026.140230
Octarina , Florencia Livia Kurniawan , Niko Falatehan , Karen Sofiana , Astri Rinanti , Meircurius Dwi Condro Surboyo
Bovine-derived bone graft materials are widely used for localized bone defect treatment, yet direct comparisons of different processing forms remain limited. In this study, bovine cancellous bone (BBC), demineralized bone matrix cancellous (DBMC), and bovine-derived hydroxyapatite (HAp) were prepared from the same source in standardized cube form and comparatively evaluated. BBC retained a natural trabecular architecture with large interconnected pores and exhibited the highest compressive strength (13.27 ± 8.13 MPa). DBMC showed a collagen-rich, amorphous structure with high swelling capacity but markedly reduced mechanical strength (1.49 ± 0.79 MPa). HAp demonstrated high crystallinity, low swelling, and brittle mechanical behavior with low compressive strength (1.22 ± 0.68 MPa). All materials exhibited high cell viability (>90%). These findings reveal clear structure–property relationships among bovine-derived grafts and support informed material selection for localized bone defect applications.
牛源骨移植材料广泛用于局部骨缺损治疗,但不同加工形式的直接比较仍然有限。本研究采用同种材料制备了牛松质骨(BBC)、脱矿骨基质松质骨(DBMC)和牛源羟基磷灰石(HAp),并对其标准化立方体形态进行了比较评价。BBC保留了天然的小梁结构,孔隙连通较大,抗压强度最高(13.27±8.13 MPa)。DBMC表现为富含胶原蛋白的无定形结构,具有较高的溶胀能力,但机械强度明显降低(1.49±0.79 MPa)。HAp具有高结晶度、低溶胀和脆性力学性能,抗压强度低(1.22±0.68 MPa)。所有材料均表现出较高的细胞活力(>90%)。这些发现揭示了牛源性移植物之间清晰的结构-性能关系,并为局部骨缺损应用的材料选择提供了支持。
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引用次数: 0
Synergistic enhancement of ionic transport and interfacial stability in PVA-MgCl2 electrolytes via BaTiO3 nanofiller integration for magnesium-ion batteries 镁离子电池用BaTiO3纳米填料对PVA-MgCl2电解质离子传输和界面稳定性的协同增强
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-01-26 DOI: 10.1016/j.matlet.2026.140167
Rania Gamal , Abdel-Menem Elnemr , Mostafa.A. Moselhy , Reda Khalil , Eslam Sheha
PVA/MgCl2 electrolytes with 5 wt% BTO show enhanced structural and electrochemical properties. FTIR and UV–Vis confirm BTO incorporation, bandgap reduction, and stronger polymer–ceramic interactions. SEM and XRD reveal porous morphologies, lower polymer crystallinity, and preserved BTO structure. EIS indicates increased ionic conductivity (10−4 → 6 × 10−3 S cm−1) and reduced activation energy (0.23 → 0.15 eV). LSV, impedance, and DC polarization analyses show improved oxidative stability, lower interfacial resistance, and higher Mg2+ mobility. Symmetric Mg|PE|Mg cycling demonstrates more uniform Mg deposition/stripping, highlighting the potential of 5 wt% BTO-doped electrolytes for magnesium batteries.
添加5 wt% BTO的PVA/MgCl2电解质具有增强的结构和电化学性能。FTIR和UV-Vis证实了BTO的掺入,带隙减小和更强的聚合物陶瓷相互作用。SEM和XRD显示多孔形态,较低的聚合物结晶度和保留的BTO结构。EIS表明离子电导率增加(10−4→6 × 10−3 S cm−1),活化能降低(0.23→0.15 eV)。LSV,阻抗和直流极化分析表明,氧化稳定性提高,界面电阻降低,Mg2+迁移率提高。对称Mg|PE|Mg循环显示更均匀的Mg沉积/剥离,突出了5wt % bto掺杂电解质用于镁电池的潜力。
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引用次数: 0
Multifunctional PU@WS2-SiO2@PDMS sponge oil spill remediation and flame retardancy 多功能PU@WS2-SiO2@PDMS海绵溢油修复及阻燃
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-01-27 DOI: 10.1016/j.matlet.2026.140160
Hong Ji , Kexin Hao , Mengye Zhang , Ke Yang , Zhixiang Xing
Through a stepwise impregnation-coating strategy, acetylated lignin (AL), modified porous corn starch (MPCS), hydrophobic silica (SiO2), and titanium disulfide (WS₂) nanoparticles were integrated into a polyurethane (PU) matrix to prepare multifunctional PU@WS2-SiO2@PDMS composites. The resulting sponge exhibits stable high hydrophobicity/oleophobicity with a water contact angle (WCA) of 153°. It demonstrates remarkable adsorption capacity (>24 g/g for both diesel and soybean oil), retaining approximately 18 g/g adsorption capacity after 20 cycles while maintaining stable mechanical properties. This material combines outstanding oil-water separation performance with reusability. Thermogravimetric analysis (TGA) indicates the modified sponge retains 4.8 times the residual mass of the original sponge. Furthermore, the WS₂-induced photothermal enhancement effect reduces crude oil adsorption time under illumination from 636 s to 152 s. these combined properties highlight the application potential of PU@WS2-SiO2@PDMS sponge as a highly efficient, resilient material for oil spill remediation and organic pollutant management
通过逐步浸渍-涂层策略,将乙酰化木质素(AL)、改性多孔玉米淀粉(MPCS)、疏水性二氧化硅(SiO2)和二硫化钛(WS₂)纳米颗粒整合到聚氨酯(PU)基体中,制备了多功能性PU@WS2-SiO2@PDMS复合材料。所得海绵具有稳定的高疏水/疏油性,水接触角(WCA)为153°。它具有显著的吸附能力(对柴油和大豆油均为24 g/g),在循环20次后仍保持约18 g/g的吸附容量,同时保持稳定的力学性能。这种材料结合了出色的油水分离性能和可重复使用性。热重分析(TGA)表明,改性海绵的残余质量是原海绵的4.8倍。此外,WS₂诱导的光热增强效应将原油在照明下的吸附时间从636秒减少到152秒,这些综合性能突出了PU@WS2-SiO2@PDMS海绵作为一种高效、弹性的溢油修复和有机污染物管理材料的应用潜力
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引用次数: 0
Pyrolysis-free cobalt-based conjugated coordination polymer/graphene oxide hybrid for efficient oxygen reduction 无热解钴基共轭配位聚合物/氧化石墨烯杂化物用于高效氧还原
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-05 DOI: 10.1016/j.matlet.2026.140221
Yingmei Zhou , Ran Jin , Huiying Zhang , Zhengnan Wei , Wendan Xue , Xun Cui
The sluggish kinetics of the oxygen reduction reaction (ORR) limits the performance of fuel cells and metal-air batteries, while Pt-based catalysts suffer from high cost and poor durability. Herein, a controllable pyrolysis-free strategy is developed to construct a conjugated coordination polymer with well-defined CoN4 sites on graphene oxide (CCP-CoN4/GO). Strong electronic coupling between the conjugated coordination framework and the GO substrate facilitates electron transfer and optimizes the electronic structure of Co active centers, leading to high ORR activity and durability in alkaline media. The CCP-CoN4/GO delivers an onset potential of 0.96 V and a half-wave potential of 0.85 V. When applied as the cathode in zinc-air batteries, it exhibits high power density and excellent cycling stability, demonstrating strong potential for efficient energy conversion devices.
氧还原反应(ORR)动力学缓慢限制了燃料电池和金属-空气电池的性能,而pt基催化剂成本高,耐用性差。本文提出了一种可控的无热解策略,在氧化石墨烯上构建具有明确定义的CoN4位点的共轭配位聚合物(CCP-CoN4/GO)。共轭配位框架与氧化石墨烯衬底之间的强电子耦合促进了电子转移,优化了Co活性中心的电子结构,从而在碱性介质中具有较高的ORR活性和耐久性。CCP-CoN4/GO的起始电位为0.96 V,半波电位为0.85 V。作为锌空气电池的正极材料,它具有较高的功率密度和良好的循环稳定性,显示出作为高效能量转换器件的强大潜力。
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引用次数: 0
Dual-ion Cu, Ni-doped V₂O₅ as a high-performance cathode material for aqueous zinc-ion batteries 双离子Cu, ni掺杂V₂O₅作为水性锌离子电池的高性能阴极材料
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-02-04 DOI: 10.1016/j.matlet.2026.140217
Song Liu , Zhenhai Yu , Siyu Yang , Zhengfei Zhang
Layered vanadium pentoxide (V₂O₅) is considered a highly promising cathode material for aqueous zinc-ion batteries (AZIBs). However, its practical application is hindered by poor cycling stability and sluggish Zn2+ diffusion kinetics. In this study, a dual-ion Cu, Ni-doped V₂O₅ cathode material, denoted as CNVO 6–1, was successfully synthesized via a convenient one-step hydrothermal method. The incorporation of Cu2+ slightly expands the interlayer spacing, facilitating rapid Zn2+ insertion/extraction. Furthermore, the combined effect of Cu2+ and Ni2+ ions stabilizes the layered structure. The CNVO 6–1 electrode delivers a high specific capacity of 384.49 mAh g−1 at 1 A g−1, superior rate capability (119.47 mAh g−1 at 20 A g−1), and outstanding long-term cycling stability with 85.02% capacity retention after 5000 cycles at 15 A g−1.
层状五氧化二钒(V₂O₅)被认为是水锌离子电池(azib)极有前途的阴极材料。然而,循环稳定性差和Zn2+扩散动力学缓慢阻碍了其实际应用。在本研究中,通过方便的一步水热法成功合成了双离子Cu, ni掺杂V₂O₅阴极材料,记为CNVO 6-1。Cu2+的加入略微扩大了层间间距,有利于快速插入/提取Zn2+。Cu2+和Ni2+离子的共同作用使层状结构更加稳定。CNVO 6-1电极在1 a g- 1时具有384.49 mAh g- 1的高比容量,在20 a g- 1时具有119.47 mAh g- 1的优越倍率能力,并且在15 a g- 1下5000次循环后具有85.02%的长期循环稳定性。
{"title":"Dual-ion Cu, Ni-doped V₂O₅ as a high-performance cathode material for aqueous zinc-ion batteries","authors":"Song Liu ,&nbsp;Zhenhai Yu ,&nbsp;Siyu Yang ,&nbsp;Zhengfei Zhang","doi":"10.1016/j.matlet.2026.140217","DOIUrl":"10.1016/j.matlet.2026.140217","url":null,"abstract":"<div><div>Layered vanadium pentoxide (<em>V</em>₂O₅) is considered a highly promising cathode material for aqueous zinc-ion batteries (AZIBs). However, its practical application is hindered by poor cycling stability and sluggish Zn<sup>2+</sup> diffusion kinetics. In this study, a dual-ion Cu, Ni-doped <em>V</em>₂O₅ cathode material, denoted as CNVO 6–1, was successfully synthesized via a convenient one-step hydrothermal method. The incorporation of Cu<sup>2+</sup> slightly expands the interlayer spacing, facilitating rapid Zn<sup>2+</sup> insertion/extraction. Furthermore, the combined effect of Cu<sup>2+</sup> and Ni<sup>2+</sup> ions stabilizes the layered structure. The CNVO 6–1 electrode delivers a high specific capacity of 384.49 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup>, superior rate capability (119.47 mAh g<sup>−1</sup> at 20 A g<sup>−1</sup>), and outstanding long-term cycling stability with 85.02% capacity retention after 5000 cycles at 15 A g<sup>−1</sup>.</div></div>","PeriodicalId":384,"journal":{"name":"Materials Letters","volume":"409 ","pages":"Article 140217"},"PeriodicalIF":2.7,"publicationDate":"2026-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Aptamer-functionalized Fe3O4@Au nanoparticles for ultrasensitive fluorescence detection of chloramphenicol in food samples 用于食品样品中氯霉素超灵敏荧光检测的适配体功能化Fe3O4@Au纳米颗粒
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-04-15 Epub Date: 2026-01-29 DOI: 10.1016/j.matlet.2026.140163
Chengwei Yang , Yuqin Guo , Xu Jia , Xiao Li
A novel fluorescence sensing platform was developed for the ultrasensitive detection of chloramphenicol (CAP) using aptamer-functionalized Fe3O4@Au nanoparticles. Under optimized conditions, the assay demonstrated a wide linear range from 1 pM to 1 μM with an exceptionally low detection limit of 0.3 pM, high specificity against structural analogs, and remarkable reproducibility. The method was successfully applied to milk, honey, and fish samples, achieving recoveries of 91.4–109.0% with RSDs ≤6.8%, highlighting its strong anti-interference capacity and practicality. This work offers a robust, reliable, and highly sensitive approach for monitoring trace CAP in food safety applications.
利用适体功能化Fe3O4@Au纳米粒子,建立了一种用于氯霉素(CAP)超灵敏检测的新型荧光传感平台。在优化的条件下,该方法在1 pM ~ 1 μM范围内具有较宽的线性范围,检测限极低(0.3 pM),对结构类似物具有较高的特异性,重现性好。该方法成功应用于牛奶、蜂蜜和鱼类样品中,回收率为91.4 ~ 109.0%,rsd≤6.8%,具有较强的抗干扰能力和实用性。这项工作为监测食品安全应用中的痕量CAP提供了一种强大、可靠和高灵敏度的方法。
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引用次数: 0
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