Aggregate (Hoboken, N.J.)最新文献

筛选
英文 中文
A smart lab on a wearable microneedle patch with convolutional neural network-enhanced colorimetry for early warning of syndrome of inappropriate antidiuretic hormone secretion 基于卷积神经网络增强比色法的可穿戴微针贴片智能实验室用于抗利尿激素分泌不当综合征的早期预警
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-08 DOI: 10.1002/agt2.671
Yuanting Xie, Kaidi Li, Jing Liu, Ying Zhou, Chuangjie Zhang, Yan Yu, Jianlong Wang, Lei Su, Xueji Zhang
{"title":"A smart lab on a wearable microneedle patch with convolutional neural network-enhanced colorimetry for early warning of syndrome of inappropriate antidiuretic hormone secretion","authors":"Yuanting Xie,&nbsp;Kaidi Li,&nbsp;Jing Liu,&nbsp;Ying Zhou,&nbsp;Chuangjie Zhang,&nbsp;Yan Yu,&nbsp;Jianlong Wang,&nbsp;Lei Su,&nbsp;Xueji Zhang","doi":"10.1002/agt2.671","DOIUrl":"https://doi.org/10.1002/agt2.671","url":null,"abstract":"<p>Frequent nocturia-induced nighttime visits aggravate falls in seniors, requiring synthetic antidiuretic drugs that risk the dangerous syndrome of inappropriate antidiuretic hormone secretion (SIADH), thus the detection of sodium ion and uric acid alterations during treatment is obligatory for drug-safe management. Herein, we design a convolutional neural network (CNN)-enhanced smart wearable microneedle array-based colorimetric (WMNC) sensor to independently detect in vivo interstitial fluid (ISF) sodium ions and uric acid alterations. The WMNC sensor is composed of a vacuum tube-driven microneedle array patch and a built-in colorimetric sensing paper, enabling an efficient ISF extraction and rapid colorimetric assay. Furthermore, leveraging self-designed CNNs, the WMNC sensor efficiently eliminates the influence of ambient light on colorimetric outcomes, facilitating a rapid and accurate colorimetric result classification. This study provides an ISF-based rapid, intuitionistic, user-friendly, wearable point-of-care technique for the elderly suffering from nocturia in monitoring their health status for early warnings of SIADH.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 2","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.671","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143446681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Constructing benzothiadiazole-based donor‒acceptor covalent organic frameworks for efficient photocatalytic H2 evolution 构建以苯并噻唑为基础的供受体共价有机框架用于高效光催化析氢
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-03 DOI: 10.1002/agt2.669
Yanchang Huang, Bin Gao, Qihang Huang, De-Li Ma, Hongwei Wu, Cheng Qian
{"title":"Constructing benzothiadiazole-based donor‒acceptor covalent organic frameworks for efficient photocatalytic H2 evolution","authors":"Yanchang Huang,&nbsp;Bin Gao,&nbsp;Qihang Huang,&nbsp;De-Li Ma,&nbsp;Hongwei Wu,&nbsp;Cheng Qian","doi":"10.1002/agt2.669","DOIUrl":"https://doi.org/10.1002/agt2.669","url":null,"abstract":"<p>Donor‒acceptor covalent organic frameworks (D‒A COFs) have been regarded as promising materials for photocatalytic water splitting because of their tunable band gaps. However, their efficiency is hindered by fast charge recombination and low photostability. Herein, we proposed a donor structural engineering strategy for improving the photocatalytic activity of D‒A COFs to tackle these problems. Two benzothiadiazole-based D‒A COFs (DHU-COF-BB and DHU-COF-BP) with distinct donors were prepared for photocatalytic H<sub>2</sub> evolution reaction (HER). As a comparison, DHU-COF-TB without benzothiadiazole moieties was also designed and synthesized. Impressively, the photocatalytic H<sub>2</sub> production rate of DHU-COF-BB reaches 12.80 mmol g<sup>−1</sup> h<sup>−1</sup> under visible light irradiation (≥420 nm), which was nearly 2.0 and 3.1 times higher than that of DHU-COF-BP (6.47 mmol g<sup>−1</sup> h<sup>−1</sup>) and DHU-COF-TB (4.06 mmol g<sup>−1</sup> h<sup>−1</sup>), respectively. In addition, the apparent quantum efficiency (AQE) of DHU-COF-BB was up to 5.04% at 420 nm. Photocatalytic and electrochemical measurements indicate that the enhanced hydrogen evolution activity of DHU-COF-BB can be ascribed to the introduction of appropriate benzene moiety into the donors, which increases the charge separation efficiency and thereby suppresses the electron‒hole recombination. Density functional theory (DFT) calculations revealed that both triphenylamine and benzothiadiazole units are the main active sites for HER over the DHU-COF-BB. This work provides new insight into the photocatalytic hydrogen production activity of D‒A COFs by a donor structural engineering strategy.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.669","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143111553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metal-coordinated amino acid/peptide/protein-based supramolecular self-assembled nanomaterials for anticancer applications 金属配位氨基酸/肽/蛋白质基超分子自组装纳米材料的抗癌应用
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-03 DOI: 10.1002/agt2.672
Maryam Shabbir, Atia Atiq, Jiahua Wang, Maria Atiq, Nyla Saeed, Ibrahim Yildiz, Xuehai Yan, Ruirui Xing, Manzar Abbas
{"title":"Metal-coordinated amino acid/peptide/protein-based supramolecular self-assembled nanomaterials for anticancer applications","authors":"Maryam Shabbir,&nbsp;Atia Atiq,&nbsp;Jiahua Wang,&nbsp;Maria Atiq,&nbsp;Nyla Saeed,&nbsp;Ibrahim Yildiz,&nbsp;Xuehai Yan,&nbsp;Ruirui Xing,&nbsp;Manzar Abbas","doi":"10.1002/agt2.672","DOIUrl":"https://doi.org/10.1002/agt2.672","url":null,"abstract":"<p>Biomolecules with metals can form supramolecular nanomaterials through coordination assembly, opening new avenues for cancer theranostics and bringing unique insights into personalized nanomedicine. These biomaterials have been considered versatile and innovative nanoagents due to their structure‒function control, biological nature, and simple preparation methods. This review article summarized the recent developments in multicomponent nanomaterials formed from metal coordination interactions with amino acids, peptides, and proteins, together with anticancer drugs, for cancer theranostics. We discussed the role of functional groups anchored in building blocks for coordination interactions, and subsequently, the types of interactions were examined from a structure‒function perspective. Amino acids with different metals and anticancer drugs forming supramolecular nanomaterials and their anticancer mechanisms were highlighted. Peptides with different metals and anticancer drugs, proteins with metals and anticancer drugs used for material formations, and anticancer activity have been discussed. Ultimately, the conclusion and future outlook for multicomponent supramolecular nanomaterials offer fundamental insights into fabrication design and precision medicine.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.672","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143111554","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rational design of aggregation-induced emission-active bisboron complexes (BOQHYs) for high-fidelity lipid droplet imaging 合理设计用于高保真脂滴成像的聚集诱导发射活性双硼配合物(BOQHYs)
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-03 DOI: 10.1002/agt2.670
Sisi Wang, Xian Bi, Hua Zhu, Xiaobo Ji, Hua Lu, Zhen Shen
{"title":"Rational design of aggregation-induced emission-active bisboron complexes (BOQHYs) for high-fidelity lipid droplet imaging","authors":"Sisi Wang,&nbsp;Xian Bi,&nbsp;Hua Zhu,&nbsp;Xiaobo Ji,&nbsp;Hua Lu,&nbsp;Zhen Shen","doi":"10.1002/agt2.670","DOIUrl":"https://doi.org/10.1002/agt2.670","url":null,"abstract":"<p>Lipid droplets (LDs) are dynamic intracellular organelles that participate in a wide range of physiological and pathological processes. Consequently, the development of high-selectivity and high-resolution tools for LD detection and tracking is of paramount importance. In this study, we describe the straightforward synthesis of a series of novel BODIPY analogs, BOQHYs <b>3a</b>–<b>3e</b>, through the condensation of 2,3-dihydrazinylquinoline with acetone or benzophenone, followed by complexation with BF<sub>3</sub>·OEt<sub>2</sub>. Spectroscopic properties indicate that these dyes exhibited significantly larger Stokes shifts (&gt;100 nm) than the commercial LD-Tracker BODIPY 493/503 (≈10 nm). Additionally, the incorporation of phenyl “rotors” endows BOQHYs <b>3b</b>–<b>3e</b> with heightened aggregation-induced emission activity, viscosity responsiveness, and exceptional lipophilicity, enabling their selective staining of LDs in a rapid and wash-free manner, with outstanding signal-to-noise ratios. Time-resolved confocal fluorescence imaging of <b>3d</b> further validates these dyes’ capability to effectively capture LD fusion and fission events, highlighting their potential applications in LD-related cell biology and disease diagnostics.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 2","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.670","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143446630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integrating self-assembled supramolecular organic frameworks with inorganic semiconductors for infrared photodetection 集成自组装超分子有机框架与无机半导体用于红外光探测
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-03 DOI: 10.1002/agt2.673
Zheng Gao, Shu-Yan Jiang, Peihao Huang, Yao Chen, Qiao-Yan Qi, Hongquan Zhao, Xingzhan Wei, Haofei Shi, Xin Zhao, Zeyun Xiao
{"title":"Integrating self-assembled supramolecular organic frameworks with inorganic semiconductors for infrared photodetection","authors":"Zheng Gao,&nbsp;Shu-Yan Jiang,&nbsp;Peihao Huang,&nbsp;Yao Chen,&nbsp;Qiao-Yan Qi,&nbsp;Hongquan Zhao,&nbsp;Xingzhan Wei,&nbsp;Haofei Shi,&nbsp;Xin Zhao,&nbsp;Zeyun Xiao","doi":"10.1002/agt2.673","DOIUrl":"https://doi.org/10.1002/agt2.673","url":null,"abstract":"<p>The surface coverage of two-dimensional (2D) materials has been a challenge, requiring facile growth of conformal 2D materials as well as considerations for transparency, energy level, and interface contact. Self-assembly holds promise for addressing this challenge by constructing precisely structured 2D assemblies using intentionally designed building blocks, guided by diverse noncovalent interactions. In this study, we utilize a self-assembled 2D supramolecular organic framework (SOF) to cloak inorganic semiconductors and form composite materials for infrared photodetection. The charged SOF backbone regulates the energy levels, facilitating the migration of electrons at the organic-inorganic interface. Additionally, the oxygen (O) of the ethylene glycol chains forms coordination bonds with the Pb(II) in the inorganic semiconductor, establishing ohmic contacts. The composite device shows excellent detectivity under 500 K blackbody and 1550 nm infrared illumination, achieving D*<sub>bb</sub>(500 K) of 6.3 × 10<sup>9</sup> Jones under 500 K blackbody radiation. Moreover, the device exhibits low noise due to the SOF potential barrier impeding the photogenerated and/or thermally excited holes, and high stability as a result of bonding and passivation of vacancy defects. This study showcases the versatile functionality of 2D SOF materials in the field of optoelectronics, opening doors to innovative advancements in composite devices through a self-assembled organic–inorganic approach.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 2","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.673","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143446631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Programmable light-driven soft actuator enabled by structurally anisotropic liquid crystalline network 由结构各向异性液晶网络实现的可编程光驱动软执行器
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-02 DOI: 10.1002/agt2.633
Zhaoping Deng, Xinyu Chen, Xinrui Deng, Jiangmin Yang, Shuai Zhou, Jingyu Chen, Peixiang Wang, Huai Yang, Ruochen Lan
{"title":"Programmable light-driven soft actuator enabled by structurally anisotropic liquid crystalline network","authors":"Zhaoping Deng,&nbsp;Xinyu Chen,&nbsp;Xinrui Deng,&nbsp;Jiangmin Yang,&nbsp;Shuai Zhou,&nbsp;Jingyu Chen,&nbsp;Peixiang Wang,&nbsp;Huai Yang,&nbsp;Ruochen Lan","doi":"10.1002/agt2.633","DOIUrl":"https://doi.org/10.1002/agt2.633","url":null,"abstract":"<p>The design and fabrication of advanced soft actuators with programmable actuation are highly desirable in constructing intelligent soft robots. In this work, a programmable light-driven liquid crystalline network (LCN)-based soft actuator was judiciously designed and prepared by constructing structural anisotropy across the thickness of the film. A three-dimensional (3D) deformable LCN actuator was realized by polymerization-induced phase separation of small-molar-weight monomers and polymer networks. The resultant anisotropic LCN displays anisotropic microscale nanoporous architecture across the thickness in addition to uniform alignment at the molecular scale. The actuation behaviors of LCN film are tunable by adjusting the size and distribution of nanopores in LCN bulk via changing polymerization conditions and monomer components. More importantly, the nanoporous LCN film can be harnessed as a promising template to achieve diverse light responsiveness by changing the photothermal dyes via a feasible washing and refilling process, demonstrating a reprogrammable light-driven soft actuator.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.633","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143111016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fluorescence imaging-guided lipid droplets-localized photodynamic therapy 荧光成像引导脂滴定位光动力治疗
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-01 DOI: 10.1002/agt2.665
Shan Wang, Qiang Wang, Yang Lv, Zhe Liu, Kippeum Lee, Dongeun Kim, Miae Won, Jianliang Shen, Jong Seung Kim
{"title":"Fluorescence imaging-guided lipid droplets-localized photodynamic therapy","authors":"Shan Wang,&nbsp;Qiang Wang,&nbsp;Yang Lv,&nbsp;Zhe Liu,&nbsp;Kippeum Lee,&nbsp;Dongeun Kim,&nbsp;Miae Won,&nbsp;Jianliang Shen,&nbsp;Jong Seung Kim","doi":"10.1002/agt2.665","DOIUrl":"https://doi.org/10.1002/agt2.665","url":null,"abstract":"<p>Photodynamic therapy (PDT) has emerged as a promising strategy for cancer treatment due to its non-invasive nature and high specificity toward malignant tissues. In recent years, a variety of protocols have been proposed to improve the PDT efficacy, of which organelle-targeted PDT strategy is supposed to be quite promising. Particularly, lipid droplets (LDs)-localized PDT attracts a lot of interest due to the inherent advantages such as abundant LDs in cancer cells and their close relation with ferroptosis. This review provides a comprehensive summary of the advancements of LDs-localized photosensitizers (PSs) according to their chemical structures and functions. Especially, these PSs are featured with fluorescence emission, thereby facilitating an imaging-guided phototherapy. The review highlights the cytocidal actions of these PSs, such as the cell death pathway and their cytotoxicity. Finally, some unresolved issues and challenges in this domain will be discussed.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.665","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143110326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A new class of organic nanoparticles through hyperbranching and crosslinking 一类通过超支化和交联的新型有机纳米颗粒
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-10-01 DOI: 10.1002/agt2.668
Haoran Wang, Junyi Gong, Ben Zhong Tang
{"title":"A new class of organic nanoparticles through hyperbranching and crosslinking","authors":"Haoran Wang,&nbsp;Junyi Gong,&nbsp;Ben Zhong Tang","doi":"10.1002/agt2.668","DOIUrl":"https://doi.org/10.1002/agt2.668","url":null,"abstract":"&lt;p&gt;Brush-modified nanoparticles, created by grafting functional polymers from nanoparticle surfaces, have demonstrated their versatility in various applications.&lt;sup&gt;[&lt;/sup&gt;&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt;&lt;sup&gt;]&lt;/sup&gt; Traditionally, these nanoparticle brushes are formed by tethering polymer chains onto surface-modified “inorganic” particles. However, customizing the internal molecular structure of these nanoparticles is quite limited. In contrast, “organic” nanoparticles (oNPs) offer significant potential for incorporating small functional molecules, enabling applications in areas such as luminescence, sensing, and drug delivery.&lt;sup&gt;[&lt;/sup&gt;&lt;span&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/span&gt;&lt;sup&gt;]&lt;/sup&gt; Additionally, materials composed of oNPs are less dense, making them suitable for lightweight equipment, for example, for soft robotics. Despite these advantages, realizing oNPs remains a challenge. Most synthetic approaches rely on “bottom-up” methods such as self-assembly. However, in these systems labile interactions can undermine performance and long-term stability under harsh conditions.&lt;/p&gt;&lt;p&gt;In a recent breakthrough, Matyjaszewski, Bockstaller, and their teams have developed a new class of oNPs by leveraging macromolecular architecture through concurrent hyperbranching and crosslinking, utilizing atom transfer radical polymerization (ATRP) in microemulsion (Figure 1A).&lt;sup&gt;[&lt;/sup&gt;&lt;span&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/span&gt;&lt;sup&gt;]&lt;/sup&gt; Unlike previous work on hyperbranched homopolymers such as poly[2-(2-bromoisobutyryloxy)ethyl methacrylate] (PBiBEM),&lt;sup&gt;[&lt;/sup&gt;&lt;span&gt;&lt;sup&gt;4&lt;/sup&gt;&lt;/span&gt;&lt;sup&gt;]&lt;/sup&gt; the new method introduces copolymerization with ethylene glycol dimethacrylate (EGDMA) to enhance internal rigidity. Within a confined space, these inimer-based oNPs had tunable sizes and mechanical properties through varying crosslinking densities. With BiBEM composition varying from 60 to 90 mol%, the resulting oNPs are spherical macromolecules (&lt;i&gt;M&lt;/i&gt;&lt;sub&gt;n,MALS&lt;/sub&gt; ranged from 2 to 6 million Daltons), with nanometer-scale diameters, uniform distribution, and minimal aggregation after purification. Also, the increasing crosslinker content yielded smaller oNPs (diameters from 17 to 36 nm) with lower dispersity (&lt;i&gt;M&lt;/i&gt;&lt;sub&gt;w&lt;/sub&gt;/&lt;i&gt;M&lt;/i&gt;&lt;sub&gt;n&lt;/sub&gt;), and greater rigidity (Figure 1B). Furthermore, the addition of sodium dodecyl sulfate (SDS) as an anionic cosurfactant improved uniformity, achieving size dispersity below 3% (Figure 1C).&lt;/p&gt;&lt;p&gt;Due to the high concentration of alkyl bromide ATRP functionality from the inimer BiBEM and the retention of polymer chain-end functionality via ATRP, these oNPs are well suited as effective macroinitiators for surface-initiated ATRP (Figure 1D). Surface grafting of poly(methyl methacrylate) brushes from oNPs demonstrated high grafting density (&lt;i&gt;σ&lt;/i&gt; ∼ 0.5 chains nm&lt;sup&gt;−2&lt;/sup&gt;), indicating the potential for direct assembly of brush-modified oNPs or their integration into matrix materials. As crosslinking density increased, each oNP was densely d","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"5 6","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.668","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142859866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancing antibacterial photodynamic therapy with NIR-activated gold nanoclusters: Atomic-precision size effect on reducing bacterial biofilm formation and virulence nir活化金纳米团簇增强抗菌光动力治疗:原子精度尺寸对减少细菌生物膜形成和毒力的影响
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-09-28 DOI: 10.1002/agt2.666
Chengyu Liu, Tenghui Tian, Yujia Shi, Meiqi Li, Le Hong, Jing Zhou, Jia Liu, Yuan Zhong, Xue Wang, Zhenyu Wang, Xue Bai, Lin Wang, Chunyan Li, Zhennan Wu
{"title":"Enhancing antibacterial photodynamic therapy with NIR-activated gold nanoclusters: Atomic-precision size effect on reducing bacterial biofilm formation and virulence","authors":"Chengyu Liu,&nbsp;Tenghui Tian,&nbsp;Yujia Shi,&nbsp;Meiqi Li,&nbsp;Le Hong,&nbsp;Jing Zhou,&nbsp;Jia Liu,&nbsp;Yuan Zhong,&nbsp;Xue Wang,&nbsp;Zhenyu Wang,&nbsp;Xue Bai,&nbsp;Lin Wang,&nbsp;Chunyan Li,&nbsp;Zhennan Wu","doi":"10.1002/agt2.666","DOIUrl":"https://doi.org/10.1002/agt2.666","url":null,"abstract":"<p>Persistent biofilm infections pose a critical health threat with their relentless presence and amplified antibiotic resistance. Traditional antibacterial photodynamic therapy can inhibit bacteria extracellularly but struggles to control biofilm formation and virulence. Thus, there is an urgent need to develop photosensitizers, such as ultra-small gold nanoclusters (AuNCs), that can penetrate biofilms and internalize into bacteria. However, AuNCs still face the challenge of insufficient reactive oxygen species (ROS) production and limited near-infrared light absorption. This study develops a model of indocyanine green (ICG)-sensitized AuNCs with atomic-precision size effect. This approach achieved near-infrared light absorption while inhibiting radiation transitions, thereby regulating the generation of ROS. Notably, different-sized AuNCs (Au<sub>10</sub>NCs, Au<sub>15</sub>NCs, Au<sub>25</sub>NCs) yielded varied ROS types, resulting from different energy level distributions and electron transfer rates. ICG-Au<sub>15</sub>NCs achieved a treatment efficacy of 99.94% against <i>Staphylococcus aureus</i> infections in vitro and significantly accelerated wound healing in vivo. Moreover, this study highlights the unique role of ICG-AuNCs in suppressing quorum sensing, virulence, and ABC transporters compared to their larger counterparts. This strategy demonstrates that atomic-precision size effect of AuNCs paves the way for innovative approaches in antibacterial photodynamic therapy for infection control.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.666","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143120430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Aggregation-induced circularly polarized luminescence and delayed fluorescence enabled by activating high-level reverse intersystem crossing 聚集诱导圆偏振发光和延迟荧光激活高水平的反向系统间交叉
IF 13.9
Aggregate (Hoboken, N.J.) Pub Date : 2024-09-25 DOI: 10.1002/agt2.667
Ke Wang, Xinwen Ou, Xiaofei Niu, Zhenghao Wang, Fengyan Song, Xiaobin Dong, Wu-jie Guo, Hui-Qing Peng, Zujin Zhao, Jacky W. Y. Lam, Jianwei Sun, Hongkai Wu, Shu-Yan Yu, Fei Li, Ben Zhong Tang
{"title":"Aggregation-induced circularly polarized luminescence and delayed fluorescence enabled by activating high-level reverse intersystem crossing","authors":"Ke Wang,&nbsp;Xinwen Ou,&nbsp;Xiaofei Niu,&nbsp;Zhenghao Wang,&nbsp;Fengyan Song,&nbsp;Xiaobin Dong,&nbsp;Wu-jie Guo,&nbsp;Hui-Qing Peng,&nbsp;Zujin Zhao,&nbsp;Jacky W. Y. Lam,&nbsp;Jianwei Sun,&nbsp;Hongkai Wu,&nbsp;Shu-Yan Yu,&nbsp;Fei Li,&nbsp;Ben Zhong Tang","doi":"10.1002/agt2.667","DOIUrl":"https://doi.org/10.1002/agt2.667","url":null,"abstract":"<p>Circularly polarized luminescence (CPL) materials with delayed fluorescence have attracted much attention due to their ability to efficiently trap triplet state excitons, thereby improving the photoluminescence quantum yields of CPL materials. However, much effort has been normally focused on the utilization of T<sub>1</sub> excitons but seldom on the utilization of higher excited triplet state T<i><sub>n</sub></i> (<i>n</i> &gt; 1) excitons. Rational manipulation of higher excited triplet state T<i><sub>n</sub></i> (<i>n</i> &gt; 1) excitons and suppression of Kasha's rule of CPL materials remains a major challenge. Herein, two gold complex enantiomers ((<i>R</i>/<i>S</i>)-BPAuBC) based on axially chiral binaphthyls and 3,6-Di-tert-butylcarbazole groups are synthesized and systematically investigated. These materials exhibit aggregation-induced circularly polarized delayed fluorescence. Circularly polarized delayed fluorescence was found to be enabled by activating high-level reverse intersystem crossing (hRISC). The anti-Kasha phosphorescence at 77 K proves that the exciton has a large population in the high-lying triplet state T<sub>2</sub>, which allows the effective hRISC process to cross back to the singlet state S<sub>1</sub> and emit delayed fluorescence. In addition, CPL “on–off” switching is further achieved in nanoparticles by acid–base stimulus, showing its potential as an acid–base responsive material.</p>","PeriodicalId":72127,"journal":{"name":"Aggregate (Hoboken, N.J.)","volume":"6 1","pages":""},"PeriodicalIF":13.9,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/agt2.667","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143119451","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信