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Capacitive in-memory vector–matrix multiplication computing with charge-trap memcapacitors 基于电荷阱记忆电容器的电容式内存矢量矩阵乘法计算。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-09-10 DOI: 10.1186/s40580-026-00575-9
Junsu Yu, Hwiho Hwang, Hyungjin Kim, Woo Young Choi

Energy-efficient neural computing is increasingly limited not by computational throughput but by memory access and data movement. In-memory computing architectures offer a promising solution by collocating storage and computation, yet their practical realization remains constrained by static power dissipation, thermal challenges, and limited integration density in existing memory devices. Here, we demonstrate a vertically stackable charge-trap-flash (CTF)-based memcapacitor array that combines the high integration density of 3D NAND technology with the charge-domain computation. A continuous in-situ-doped N+ bottom readout electrode is introduced beneath the lightly doped active layer, decoupling lateral readout resistance from depletion-based capacitance modulation and alleviating the resistance–depletion trade-off of the previous architecture. The fabricated 24 × 48 memcapacitor array operates through transient charge displacement and demonstrates highly uniform array-level characteristics (σ/µ < 0.37%), reliable 16-state closed-loop weight programming, and linear charge-domain VMM with an error below 0.227%. When scaled toward modern 3D NAND dimensions, a verification–inference electrostatic mismatch introduces systematic VMM error, which is reduced by up to 84.6% through an intercell trapped-charge scheme in TCAD simulations. Geometric scaling based on the CV2 relation projects femtojoule-level intrinsic cell read energy at scaled dimensions. A hybrid hardware–software spiking neural network evaluation, in which only the final 24 × 10 layer is mapped to measured arrays, achieves 88.01% CIFAR-10 accuracy compared with 88.17% in software. These results establish vertically stackable memcapacitors as a scalable charge-domain computing platform combining reliable array-level operation with high-density vertical integration.

Graphical abstract

高效能的神经计算越来越受到内存访问和数据移动的限制,而不是计算吞吐量的限制。内存计算架构通过配置存储和计算提供了一个很有前途的解决方案,但它们的实际实现仍然受到静态功耗、热挑战和现有存储设备中有限的集成密度的限制。在这里,我们展示了一个垂直可堆叠的基于电荷阱闪存(CTF)的memcapacitor阵列,它结合了3D NAND技术的高集成度和电荷域计算。在轻掺杂有源层下引入连续的原位掺杂N+底部读出电极,将横向读出电阻从基于耗尽的电容调制中解耦,减轻了先前结构的电阻-耗尽权衡。制备的24 × 48 memcapacitor阵列通过瞬态电荷位移工作,并表现出高度均匀的阵列级特性(σ/µ2关系在缩放尺寸上投射飞焦耳级的固有电池读取能量)。一种混合硬件软件尖峰神经网络评估,其中仅将最后的24 × 10层映射到测量阵列,达到88.01%的CIFAR-10精度,而软件为88.17%。这些结果建立了垂直堆叠memcapacitors作为可扩展的电荷域计算平台,结合了可靠的阵列级操作和高密度的垂直集成。
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引用次数: 0
Dehydration-resistant multi-functional hydrogel-based iontophoretic drug delivery for wound healing 抗脱水多功能水凝胶离子渗透药物在伤口愈合中的应用。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-31 DOI: 10.1186/s40580-026-00572-y
Sang Hun Lee, Tae Hyeon Kim, Jae Wook Song, Na Yeon Kim, Ye-Jin Jo, Tae-Hyung Kim, Bong-Gun Ju, Bong Geun Chung

Wearable wound dressing is a promising approach for treating wound infection and promoting healing process. However, conventional wearable dressing methods have the drawback of poor long-term stability due to water loss. Herein, a novel hydrogel patch is fabricated by incorporating phosphoric acid and glycerol to enhance the water retention capacity. This hydrogel exhibits an excellent water retention rate of 97.7% after 7 days under ambient conditions (25 ℃, 50% relative humidity). Consequently, the stretchability, adhesion, and electrical conductivity required for wearable dressing are stably maintained. The antibiotic loaded into the dressing is effectively delivered via iontophoresis, which is demonstrated through in vitro drug release experiments, ex vivo porcine skin deposition tests, and in vivo mouse models. Therefore, this multi-functional hydrogel patch can be a promising strategy for developing an efficient drug delivery and wound healing platform using anti-drying conductive hydrogels and iontophoresis-based transdermal drug delivery.

Graphical abstract

可穿戴伤口敷料是治疗伤口感染和促进愈合过程的一种很有前途的方法。然而,传统的可穿戴敷料方法由于水分流失,长期稳定性差。本文通过磷酸和甘油的掺入制备了一种新型的水凝胶贴片,以提高其保水能力。在环境条件(25℃,50%相对湿度)下,该水凝胶在7天后的保水率为97.7%。因此,稳定地保持了可穿戴敷料所需的拉伸性、粘附性和导电性。通过体外药物释放实验、猪离体皮肤沉积实验和小鼠体内模型,证明了敷料中负载的抗生素是通过离子透入的方式有效释放的。因此,这种多功能水凝胶贴片可以作为一种很有前途的策略,用于开发一种利用抗干燥导电水凝胶和基于离子电阻的透皮给药的高效药物传递和伤口愈合平台。
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引用次数: 0
In-line fiber-integrated photon-pair generation from van der Waals crystals 范德华晶体中光纤集成光子对的产生
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-29 DOI: 10.1186/s40580-026-00571-z
Mayank Joshi, Tanumoy Pramanik, Mengting Jiang, Yu Xing, Zhaogang Dong, Yuerui Lu, Jie Zhao, Ping Koy Lam, Syed M. Assad, Xuezhi Ma, In Cheol Seo, Young-Wook Cho

Miniaturized quantum light sources that operate directly in optical fibers are an attractive platform for optical quantum technologies. However, most miniaturized spontaneous parametric down-conversion (SPDC) sources still rely on objective-lens-based free-space pumping and collection, which limits compactness, robustness, and direct compatibility with fiber-based systems. Here we demonstrate a lens-free in-line SPDC photon-pair source by integrating a van der Waals NbOI(_2) flake directly onto the end facet of an optical fiber. In this configuration, the generated photon-pairs are efficiently collected into optical fibers, eliminating the need for bulk free-space collection optics. Despite the limited numerical aperture of the single-mode fiber, efficient photon-pair collection with high coincidence-to-accidental ratio (CAR), characterized by a coincidence-to-accidental ratio of up to (sim )4600, is achieved in an ultracompact configuration. These results establish van der Waals ferroelectric materials as a promising platform for fiber-integrated quantum light sources and provide a pathway toward compact, alignment-free quantum photonic devices.

Graphical abstract

直接在光纤中工作的小型化量子光源是一个具有吸引力的光量子技术平台。然而,大多数小型化的自发参数下转换(SPDC)光源仍然依赖于基于物镜的自由空间抽运和收集,这限制了紧凑性、稳健性以及与基于光纤的系统的直接兼容性。在这里,我们展示了一个无透镜的直线型SPDC光子对源,通过将范德华NbOI (_2)片直接集成到光纤的端面。在这种结构中,产生的光子对被有效地收集到光纤中,从而消除了对大量自由空间收集光学器件的需要。尽管单模光纤的数值孔径有限,但在超紧凑的配置下,实现了具有高巧合比(CAR)的高效光子对收集,其特征是巧合比高达(sim ) 4600。这些结果确立了范德华铁电材料作为光纤集成量子光源的一个有前途的平台,并为紧凑、无对准的量子光子器件提供了一条途径。图形摘要
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引用次数: 0
Damage-free van der Waals metal/NbOx–NbSe2 integration for reliable and flexible memristor in neuromorphic computing 无损伤范德华金属/NbOx-NbSe2集成,用于神经形态计算中可靠和灵活的记忆电阻器。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-08-06 DOI: 10.1186/s40580-026-00569-7
Thanh Luan Phan, Minh Chien Nguyen, Dang Xuan Dang, Van Tu Vu, Thi Thanh Huong Vu, Hong Woon Yun, Huamin Li, Jimin Lee, Max C. Lemme, Pallavi Aggarwal, Woo Jong Yu

Ultrathin native oxides formed on two-dimensional (2D) metallic transition metal dichalcogenides (MTMDs), such as NbSe2, have recently emerged as promising active switching layers for memristive devices. However, these oxides are highly susceptible to surface damage during conventional top-electrode deposition processes, which leads to interfacial disorder and degraded switching reliability. Here, we demonstrate a highly reliable and flexible NbOx–NbSe2 memristor utilizing a damage-free van der Waals (vdW) metal transfer technique. By gently laminating a prefabricated gold (Au) electrode onto the NbOx–NbSe2, a pristine and chemically undisturbed metal/oxide interface is achieved. While metallization-induced barrier damage causes a large OFF-state direct tunneling (DT) current in the evaporated-metal memristor (Ev-MEM), preserving the pristine oxide interface in the transferred-metal memristor (T-MEM) effectively suppresses this OFF-state DT current. Consequently, the T-MEM exhibits an ON/OFF ratio of 105—a 1,000 times improvement over the Ev-MEM (102)—along with a stable retention time of > 104 s and an endurance exceeding 103 cycles. Furthermore, the T-MEM exhibits exceptional synaptic linearity (β = 0.6) and a full dynamic range (0–1), in contrast to the Ev-MEM, which suffers from poor linearity (β = 3.1) and a limited dynamic range (0.2–1). As a result, a hardware-aware convolutional neural network (CNN) simulation shows a near-ideal MNIST image recognition accuracy of 98.1% for the T-MEM based system, significantly outperforming the Ev-MEM counterpart (75.8%). In addition, capitalizing on the inherent flexibility of the 2D NbSe2 and the vdW interface, devices fabricated on a polymer substrate demonstrate remarkable mechanical robustness, maintaining stable switching characteristics over 200 bending cycles at a 30° angle. Our findings establish that damage-free vdW metal integration is a crucial prerequisite for developing reliable, highly accurate, and flexible neuromorphic hardware.

Graphical abstract

在二维(2D)金属过渡金属二硫族化合物(mtmd)上形成的超薄天然氧化物,如NbSe2,最近成为忆阻器件中有前途的有源开关层。然而,在传统的顶电极沉积过程中,这些氧化物极易受到表面损伤,从而导致界面紊乱和开关可靠性下降。在这里,我们展示了一种高度可靠和灵活的NbOx-NbSe2忆阻器,利用无损伤范德华(vdW)金属转移技术。通过将预制金(Au)电极轻轻层压到NbOx-NbSe2上,可以实现原始且化学上不受干扰的金属/氧化物界面。虽然金属化引起的势垒损伤会在蒸发金属忆阻器(Ev-MEM)中产生较大的关闭状态直接隧道(DT)电流,但在转移金属忆阻器(T-MEM)中保留原始氧化物界面可以有效抑制这种关闭状态的DT电流。因此,T-MEM的开/关比为105,比Ev-MEM的开/关比(102)提高了1000倍,并且稳定保持时间为10104秒,续航时间超过103次。此外,T-MEM表现出优异的突触线性(β = 0.6)和完整的动态范围(0-1),而Ev-MEM则表现出较差的线性(β = 3.1)和有限的动态范围(0.2-1)。结果,基于硬件感知的卷积神经网络(CNN)仿真显示,基于T-MEM的系统具有接近理想的MNIST图像识别精度,达到98.1%,显著优于Ev-MEM对应的75.8%。此外,利用2D NbSe2和vdW界面固有的灵活性,在聚合物衬底上制造的器件表现出卓越的机械稳稳性,在30°角的200次弯曲循环中保持稳定的开关特性。我们的研究结果表明,无损伤的vdW金属集成是开发可靠、高精度和灵活的神经形态硬件的关键先决条件。
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引用次数: 0
Clinical OCT computation-modeled prognosis of coronary plaque progression with validation by fusogenic macrophage nano-targeting 临床OCT计算模拟冠状动脉斑块进展的预后,并通过巨噬细胞纳米靶向验证
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-30 DOI: 10.1186/s40580-026-00567-9
Sewoom Baek, Hyun-Su Ha, Seyong Chung, Ji Youn Lee, Hyeongyun Choi, Chansik Kim, Seok Joon Lee, Seul-Gee Lee, Yong-Joon Lee, Jung-Sun Kim, Hak-Joon Sung

Coronary plaque progression often deviates from the diagnostic range of clinical examinations, resulting in the need for emergent follow-ups and increased mortality among outlier patients. This study first analyzes clinical data of fractional flow reserve, optical coherence tomography (OCT), and computed tomography from 180 patients over a 9 years period, with an average follow-up of 2 years. When the plaque progression and healthy control groups were compared in a 1:1 match (n = 10 each), analysis of single artery images failed to detect plaque progression. Therefore, 100–200 image frames were used to reconstruct patient-specific coronary anatomy using computational fluid dynamics, enabling prognostic assessment of plaque progression. The results suggest that steep plaque slopes promote plaque progression by increasing shear stress and hemodynamic disturbance accompanied by greater macrophage recruitment than gentle slopes, which was validated by a microfluidic model. Moreover, increased activation and fusogenic potential of macrophages in steep plagues justified the development of fusogenic macrophage (FM)-vesicles to detect plaque progression. The fusion potential enables FM-vesicles to self-target fusogenic macrophages more efficiently than in vitro compared to macrophages, showing superiority over liposomes and macrophage-vesicles. The membrane fusion mechanism facilitates lysosomal escape, allowing prolonged cytosolic retention without degradation. Rabbit carotid ligation was used to produce steep and gentle plaques by controlling the incision direction. When gold nanoparticles were loaded into FM-vesicles and injected into these arteries ex vivo, OCT accurately imaged the plaque slope and detected changes in signal intensity. This study presents the translational potential of FM-vesicles for clinical application by reducing diagnostic outliers in the detection of plaque progression.

Graphical abstract

冠状动脉斑块的进展往往偏离临床检查的诊断范围,导致需要紧急随访,并增加了异常患者的死亡率。本研究首先分析了180例患者在9年时间里的分数血流储备、光学相干断层扫描(OCT)和计算机断层扫描的临床数据,平均随访时间为2年。当斑块进展与健康对照组按1:1匹配(n = 10)进行比较时,单动脉图像分析未能检测到斑块进展。因此,使用100-200帧图像,利用计算流体动力学重建患者特定的冠状动脉解剖结构,从而对斑块进展进行预后评估。结果表明,与缓坡相比,陡峭的斑块斜坡通过增加剪切应力和血流动力学紊乱来促进斑块的进展,并伴有更大的巨噬细胞募集,这一点得到了微流体模型的验证。此外,巨噬细胞在陡峭斑块中的活化和融合潜能增加,证明了融合性巨噬细胞(FM)囊泡的发展可以检测斑块进展。与体外巨噬细胞相比,与脂质体和巨噬细胞相比,融合电位使fm -囊泡能够更有效地自我靶向融合性巨噬细胞,显示出优越性。膜融合机制促进溶酶体逃逸,允许延长细胞质保留而不降解。采用兔颈动脉结扎术,控制切口方向,形成陡峭、平缓的斑块。当金纳米颗粒被装入泡沫塑料囊泡并在体外注射到这些动脉中时,OCT准确地成像斑块的斜率并检测信号强度的变化。本研究通过减少检测斑块进展的诊断异常值,展示了fm囊泡在临床应用中的转化潜力。图形抽象
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引用次数: 0
Submicron traction-force mapping reveals mitochondrial regulation of nanoscale force coordination during rigidity sensing under oxidative stress 亚微米牵引力映射揭示了氧化应激下刚性感应过程中纳米尺度力协调的线粒体调控
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-29 DOI: 10.1186/s40580-026-00570-0
Muhammad Anwar Ul Hassan, Seok Gi Kim, Dan Bi Im, Jung Seung Lee, Gwang Lee, Sungsu Park

Oxidative stress is closely associated with aging, fibrosis, and cancer progression, yet how oxidative stress affects rigidity sensing remains poorly understood. Here, we employed submicron micropillar-based traction-force microscopy to investigate oxidative stress-associated mechanotransduction dysfunction in mouse embryonic fibroblasts (MEFs). Sublethal H2O2 exposure impaired stiffness-dependent cytoskeletal remodeling, focal adhesion maturation, and traction-force generation during cell spreading. Quantitative force mapping further revealed disrupted contraction-unit (CU)-associated nanoscale force coordination at the cell periphery, characterized by increased alignment of neighboring traction-force vectors and reduced opposing contractions. These defects were accompanied by fragmented mitochondrial networks and altered mitochondrial dynamics-associated gene expression. Importantly, mitofusin (MFN)-deficient MEFs phenocopied oxidative stress-induced impairments in stiffness-responsive spreading and traction-force generation, identifying mitochondrial network integrity as a critical regulator of rigidity sensing. Together, these findings establish a mechanistic link between oxidative stress, mitochondrial dynamics, and nanoscale force coordination during rigidity sensing, while highlighting the utility of submicron traction-force mechanophenotyping for quantitative analysis of oxidative stress-associated mechanobiological dysfunction.

Graphical abstract

氧化应激与衰老、纤维化和癌症进展密切相关,但氧化应激如何影响刚性感知仍然知之甚少。在这里,我们采用基于亚微米微柱的牵引力显微镜来研究小鼠胚胎成纤维细胞(mef)中氧化应激相关的机械转导功能障碍。亚致死H2O2暴露损害了细胞扩散过程中依赖刚度的细胞骨架重塑、局灶黏附成熟和牵引力的产生。定量力图进一步揭示了细胞外围与收缩单元(CU)相关的纳米尺度力协调的破坏,其特征是邻近牵引力矢量的对齐增加,而相反收缩减少。这些缺陷伴随着线粒体网络碎片化和线粒体动力学相关基因表达的改变。重要的是,有丝分裂酶(MFN)缺陷的mef在刚性响应性扩散和牵引力产生方面表现出氧化应激诱导的损伤,这表明线粒体网络完整性是刚性感知的关键调节因子。总之,这些发现在刚性感知过程中建立了氧化应激、线粒体动力学和纳米尺度力协调之间的机制联系,同时强调了亚微米牵引力力学表型在氧化应激相关力学生物学功能障碍定量分析中的应用。图形抽象
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引用次数: 0
Programmable nanomedicine via bioorthogonal molecular engineering 基于生物正交分子工程的可编程纳米医学
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-29 DOI: 10.1186/s40580-026-00568-8
Sunwoo Im, Seyoung Koo, Jong Seung Kim

Bioorthogonal chemistry provides a versatile strategy for programming nanomedicines beyond static carrier design. It enables post-synthetic installation of functional modules on nanoparticle surfaces, spatiotemporal control of payload activation and release, and higher-order functions arising from nanoparticle aggregation or nanoparticle–cell conjugation in diseased tissues. These capabilities allow nanomedicines to be activated more selectively in space and time and to generate functions that are difficult to achieve with conventional formulations. This review summarizes recent advances in multiscale bioorthogonal engineering for programmable nanomedicines, focusing on surface functionalization, molecular control of drug release, and interparticle or cell-associated assembly, and discusses challenges and future directions.

Graphical abstract

生物正交化学为编程纳米药物提供了一种超越静态载体设计的通用策略。它可以在纳米颗粒表面安装合成后的功能模块,对有效载荷的激活和释放进行时空控制,以及在患病组织中由纳米颗粒聚集或纳米颗粒-细胞结合产生的高阶功能。这些能力允许纳米药物在空间和时间上更有选择性地被激活,并产生传统配方难以实现的功能。本文综述了可编程纳米药物多尺度生物正交工程的最新进展,重点介绍了表面功能化、药物释放的分子控制、颗粒间或细胞相关组装等方面的研究进展,并讨论了面临的挑战和未来的发展方向。图形抽象
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引用次数: 0
Cavity and waveguide quantum electrodynamics with atoms and optical nanofibers 原子与光学纳米纤维之腔与波导量子电动力学。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-28 DOI: 10.1186/s40580-026-00565-x
Karen E. Webb, Samuel K. Ruddell, Tim Keller, Jameesh Keloth, Ratnesh K. Gupta, Mitsuyoshi Takahata, Takao Aoki

Optical nanofibers provide a versatile platform for exploring strong light–matter interactions at the single-quantum level, a central goal of quantum optics. Their subwavelength diameter supports tightly confined guided modes with strong evanescent fields, enabling efficient coupling between photons and nearby atoms. By incorporating fiber Bragg gratings, nanofibers can form fully fiber-integrated high-finesse cavities, combining strong atom–photon coupling with efficient and low-loss optical input–output interfacing in the setting of cavity quantum electrodynamics (QED). In parallel, nanofiber systems naturally realize waveguide QED, where atoms interact strongly with propagating photons in a one-dimensional geometry. In this review, we introduce the underlying physical principles, summarize key experimental techniques and representative phenomena, and discuss prospects for applications in quantum information processing, quantum networks, and related quantum technologies.

Graphical abstract

光学纳米纤维为探索单量子水平的强光-物质相互作用提供了一个多功能平台,这是量子光学的中心目标。它们的亚波长直径支持具有强倏逝场的紧密受限引导模式,使光子和附近原子之间的有效耦合成为可能。在腔量子电动力学(QED)的背景下,纳米纤维可以形成完全光纤集成的高精密度腔,将强原子光子耦合与高效、低损耗的光输入输出接口相结合。与此同时,纳米纤维系统自然地实现了波导QED,其中原子在一维几何结构中与传播的光子强烈相互作用。本文介绍了量子量子的基本物理原理,总结了关键实验技术和代表性现象,并讨论了其在量子信息处理、量子网络和相关量子技术中的应用前景。
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引用次数: 0
New approach methodologies for next-generation risk assessment of nanomaterials and nano-enabled products 下一代纳米材料和纳米产品风险评估的新方法。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-22 DOI: 10.1186/s40580-026-00566-w
Eunseo Lee, Aline Chary, Zayakhuu Gerelkhuu, Pamina Weber, Ishita Virmani, Beatrice A. Brugger, Iris Renata Sousa Ribeiro, Emilie Brun, Valentina Lacconi, Hyojoo Bang, Ik Hwan Kwon, Anna Pohl, Juyong Yoon, Shin Woong Kim, Anastasios Tassos Papadiamantis, Riju Roy Chowdhury, Dong-Youn Hwang, Lara Lamon, Melanie-Jasmin Ort, Martin Paparella, Ekaterina A. Sosnina, Angela Serra, Jack Morikka, Lorenzo Campini, Katharina Koch, Antreas Afantitis, Dario Greco, Iseult Lynch, Kristie Sullivan, Seokjoo Yoon, Tae Geol Lee, June-Woo Park, Diego Stéfani Teodoro Martinez, Vivekkumar P. Dadhania, Luisa Campagnolo, Winfried Neuhaus, Steffi Friedrichs, Tina Buerki-Thurnherr, Tae Hyun Yoon, Tommaso Serchi

New Approach Methodologies (NAMs) are increasingly promoted for animal-free nanosafety assessment, yet their regulatory use remains constrained by fragmented regulatory criteria and nanomaterial-specific testing complexities. This review comprehensively analyzes the convergence of advanced cell biology, nanotechnology, and information technology in reshaping safety evaluations, with a focus on regulatory translation across global frameworks. We first summarize enabling technologies, including advanced in vitro and ex vivo systems, organoids, microphysiological systems, high-dimensional single-cell multi-omics and label-free hyperspectral imaging, AutoML, generative AI, physiologically based kinetic modeling, and in vitro-to-in vivo extrapolation. We then analyze the regulatory landscape, emphasizing OECD harmonization efforts, the Mutual Acceptance of Data system, and regional developments across Europe, Africa, the Americas, and Asia–Pacific. A central theme is that regulatory acceptance of NAMs for nanomaterials requires not only biological relevance, reproducibility, and context-of-use definition, but also robust physicochemical characterization, exposure control, dosimetry, and data interoperability. Industrial implementation in pharmaceuticals, cosmetics, agrochemicals, antimicrobials, and environmental protection is discussed as a measure of regulatory readiness and scalability. Finally, we outline future directions involving Smart NAMs, digital twins, and Safe and Sustainable by Design (SSbD) frameworks. By integrating technological, regulatory, and implementation perspectives, this review identifies pathways toward harmonized, mechanistic, and human- or target species-relevant next-generation risk assessment (NGRA) for nanotechnology.

Graphical abstract

新方法方法(NAMs)越来越多地被推广用于无动物纳米安全评估,然而它们的监管使用仍然受到分散的监管标准和纳米材料特异性测试复杂性的限制。这篇综述全面分析了先进细胞生物学、纳米技术和信息技术在重塑安全性评估方面的融合,重点是全球框架内的监管翻译。我们首先总结了使能技术,包括先进的体外和离体系统,类器官,微生理系统,高维单细胞多组学和无标签高光谱成像,AutoML,生成式人工智能,基于生理的动力学建模,以及体外到体内的外推。然后,我们分析了监管格局,强调了经合组织的协调努力、数据相互接受系统以及欧洲、非洲、美洲和亚太地区的区域发展。一个中心主题是,纳米材料纳米命名的监管接受不仅需要生物学相关性、可重复性和使用背景定义,还需要强大的物理化学表征、暴露控制、剂量学和数据互操作性。在制药、化妆品、农用化学品、抗菌剂和环境保护方面的工业实施作为监管准备和可扩展性的衡量标准进行了讨论。最后,我们概述了未来的发展方向,包括智能NAMs、数字孪生和安全与可持续设计(SSbD)框架。通过整合技术、监管和实施的观点,本综述确定了纳米技术的协调、机械和与人类或目标物种相关的下一代风险评估(NGRA)的途径。
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引用次数: 0
Bionanotechnology at microplastic and nanoplastic interfaces: detection, adsorption and degradation 微塑料和纳米塑料界面的生物纳米技术:检测、吸附和降解。
IF 13.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-07-20 DOI: 10.1186/s40580-026-00563-z
Angrui Jiang, Wei Mao, Bowen Dai, Jung Heon Lee, Xue Bai, Juewen Liu

Micro-nano plastics (M/NPs) are pervasive environmental pollutants whose small size, persistence, and evolving surface states complicate reliable detection and remediation. As interface-dominated contaminants, their environmental behavior is largely governed by interactions at plastic–bio–nano interfaces. In this article, we review recent advances in three interconnected aspects of M/NPs research: biomolecular recognition, nano-enabled enrichment, and catalytic degradation, with particular emphasis on the central role of interfaces. Biomolecular recognition elements, including antibodies, peptides, aptamers, and molecularly imprinted materials, enable selective identification of plastics through interfacial pattern recognition. Nanomaterials such as magnetic nanoparticles, plasmonic nanostructures, metal–organic frameworks, and carbon-based materials further facilitate selective capture and signal amplification in complex matrices. Emerging degradation strategies, including engineered enzymes, enzyme–nanomaterial hybrids, nanozymes, single-atom nanozymes, and advanced oxidation processes, rely on interface-mediated adsorption, catalytic activation, and polymer transformation. Future research should therefore focus on elucidating plastic–bio–nano interfacial mechanisms and leveraging these insights to integrate molecular recognition, nano-enabled enrichment, and catalytic transformation within multifunctional platforms.

Graphical abstract

微纳米塑料(M/NPs)是普遍存在的环境污染物,其小尺寸,持久性和不断变化的表面状态使可靠的检测和修复复杂化。作为界面主导的污染物,其环境行为在很大程度上受塑料-生物纳米界面相互作用的支配。在本文中,我们回顾了M/NPs研究的三个相互关联的方面的最新进展:生物分子识别、纳米富集和催化降解,特别强调了界面的核心作用。生物分子识别元件,包括抗体、多肽、适体和分子印迹材料,能够通过界面模式识别对塑料进行选择性识别。磁性纳米粒子、等离子体纳米结构、金属有机框架和碳基材料等纳米材料进一步促进了复杂基质中的选择性捕获和信号放大。新兴的降解策略,包括工程酶、酶-纳米材料杂化物、纳米酶、单原子纳米酶和高级氧化工艺,都依赖于界面介导的吸附、催化活化和聚合物转化。因此,未来的研究应侧重于阐明塑料-生物纳米界面机制,并利用这些见解将分子识别、纳米富集和催化转化整合到多功能平台中。
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引用次数: 0
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Nano Convergence
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