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Scalable manufacturing of layered nanoparticle-polymer composite films through evaporative assembly 通过蒸发装配大规模制造层状纳米粒子-聚合物复合薄膜
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-04-18 DOI: 10.1016/j.colcom.2025.100837
Shaveen Fernando, Surita R. Bhatia
This work explores stratification, a prescribed spatial variation of components in a multi-component film, in particle-polymer films prepared by a single-step evaporative drying technique. Our overall goal is to develop a more efficient and cost-effective way to create vertically structured multi-component polymer and colloid films. Films containing poly(acrylic acid) (PAA) chains and polystyrene (PS) colloidal nanoparticles were analyzed using microbeam small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM) to probe the impact of evaporation rates and colloid sizes on stratification behavior. Under slow drying conditions, particle-on-top stratification was observed, consistent with a diffusive model of stratification behavior. Conversely, moderate evaporation rates resulted in non-stratified configurations for certain mixtures. Fast evaporation, achieved by drying at elevated temperatures, induced polymer-on-top stratification, which aligns with predictions from simulations. Overall, this study proposes a more efficient method for creating vertically structured films, with implications for various industries.
这项工作探讨了分层,多组分薄膜中组分的规定空间变化,在单步蒸发干燥技术制备的颗粒聚合物薄膜中。我们的总体目标是开发一种更有效和更具成本效益的方法来制造垂直结构的多组分聚合物和胶体薄膜。采用微束小角x射线散射(SAXS)和原子力显微镜(AFM)对含有聚丙烯酸(PAA)链和聚苯乙烯(PS)胶体纳米粒子的薄膜进行了分析,探讨了蒸发速率和胶体尺寸对分层行为的影响。在缓慢干燥条件下,观察到颗粒顶部分层,符合分层行为的扩散模型。相反,适度的蒸发速率导致某些混合物的非分层结构。通过高温干燥实现的快速蒸发,导致聚合物在顶部分层,这与模拟的预测一致。总的来说,本研究提出了一种更有效的方法来制作垂直结构的电影,对各个行业都有意义。
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引用次数: 0
Tuning surface assembly of oleyl-capped nanoparticles in AOT microemulsion phase with optimal alkane-to-alkanol ratio 以最佳烷烃-烷醇比调整AOT微乳相中油基包覆纳米颗粒的表面组装
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-04-09 DOI: 10.1016/j.colcom.2025.100836
Rebeca Fortes Martín, Sibylle Rustig, Ilko Bald, Joachim Koetz
A simplified procedure for the surface assembly of oleyl-capped nanoparticles from water-in-oil microemulsions is presented. Changing the heptane-to-pentanol ratio in the oil phase resulted in different surface assemblies. Remarkably, a minor proportion of heptane in pentanol enabled the formation of filament networks, without the assistance of other additives for clustering effects.
提出了一种从油包水微乳液中制备油基包覆纳米颗粒的简化方法。改变油相中庚烷与戊醇的比例会导致不同的表面组合。值得注意的是,在没有其他添加剂的帮助下,戊醇中少量的庚烷可以形成长丝网络。
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引用次数: 0
Horseradish peroxidase-catalyzed crosslinking injectable hydrogel for bone repair and regeneration 辣根过氧化物酶催化交联可注射水凝胶骨修复和再生
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-03-10 DOI: 10.1016/j.colcom.2025.100828
Hongwei Pan , Yue Qu , Feng Wang , Shengbing Zhao , Gaigai Chen
In clinical practice, addressing severe bone defects resulting from trauma, tumors, infections or congenital disorders remains a challenge in the surgical domain. Although bone tissue has a certain capacity for self-repair, artificial substitute materials of bone are still required to facilitate the repair, especially for large-scale bone defects. At present, tissue engineering-related materials that mimic the structure, mechanical properties, and biological characteristics of natural bone have been widely used for addressing bone defects and promoting in situ bone regeneration. Hydrogels that emulate the properties of the extracellular matrix are prevalent materials in bone tissue engineering, with a particular emphasis on those crosslinked through HRP-mediated, which have garnered considerable interest due to their high efficiency of preparation, mild reaction conditions, controllable properties, and excellent biocompatibility. However, the suboptimal osteogenic capability inherent in HRP-mediated crosslinked hydrogels necessitates the integration of additional osteogenic activity materials, such as biological calcium phosphates, biomimetic scaffolds, growth factors, synthetic peptides, and nanomaterials, to bolster the hydrogel scaffolds' osteogenic potential. This manuscript provides a concise overview of the standard methodologies for crafting injectable hydrogels, highlighting the HRP catalytic reaction mechanism, and strategies for modulating hydrogel attributes. Furthermore, this paper delves into the recent advancements in HRP-mediated crosslinked hydrogel scaffolds, highlighting their role in bone defect repair within the realm of bone tissue engineering. These insights establish a robust foundation for the innovation, development, and clinical application of bone tissue substitutes that prioritize biosafety.
在临床实践中,解决由创伤、肿瘤、感染或先天性疾病引起的严重骨缺损仍然是外科领域的一个挑战。虽然骨组织具有一定的自我修复能力,但仍然需要人工骨替代材料来促进修复,特别是对于大规模的骨缺损。目前,模仿天然骨的结构、力学性能和生物学特性的组织工程相关材料已被广泛用于解决骨缺损和促进原位骨再生。模拟细胞外基质性质的水凝胶是骨组织工程中普遍存在的材料,特别是那些通过酶催化交联的水凝胶,由于其制备效率高、反应条件温和、性能可控和良好的生物相容性而获得了相当大的兴趣。然而,hrp介导的交联水凝胶固有的次优成骨能力需要整合额外的成骨活性材料,如生物磷酸钙、仿生支架、生长因子、合成肽和纳米材料,以增强水凝胶支架的成骨潜力。这份手稿提供了一个简明的概述标准方法的制作可注射的水凝胶,突出HRP催化反应机制,和策略调节水凝胶的属性。此外,本文深入研究了酶解介导的交联水凝胶支架的最新进展,强调了它们在骨组织工程领域骨缺损修复中的作用。这些见解为优先考虑生物安全性的骨组织替代品的创新、开发和临床应用奠定了坚实的基础。
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引用次数: 0
Adjusting morphologies of wound dressing by transferring skin textures through electrospinning technology 通过静电纺丝技术转移皮肤纹理来调整伤口敷料的形态
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-04-09 DOI: 10.1016/j.colcom.2025.100835
Huidan Wei , Jing Wen , Sai Yan , Han Zhang , Yuan Liu , Yuhan Xia , Jidong Li , Ran Cao , Meifang Zhu
Surface topography and mechanical properties of wound dressing significantly influence cell behavior and tissue regeneration process. Skin has unique textures, which are often overlooked in the preparation of wound dressings. Herein, we fabricated biomimetic wound dressings by transferring the surface textures of skin through electrospinning technology. Specifically, the top and bottom surface of pig skin employed as substrates for the collection of electrospinning nanofibers composed of polylactic acid and gelatin (PLLA/GL). Due to the existence of hair on the top surface of pig skin, the transferred nanofiber membrane (skin-top) exhibited scattered small pores (∼50 μm). In contrast, the transferred nanofiber membrane with aluminum foil (Al) as substrate displayed a smooth surface. Benefit from the unique surface properties of skin, the skin-based nanofiber membrane demonstrated improved roughness and enhanced air permeability. Specifically, skin-top based wound dressing showed the best performance in promoting wound healing, including enhanced epithelialization and collagen deposition.
创面敷料的表面形貌和力学性能显著影响细胞行为和组织再生过程。皮肤具有独特的纹理,这在制备伤口敷料时经常被忽视。本研究利用静电纺丝技术转移皮肤表面纹理,制备仿生创面敷料。具体而言,以猪皮的上下表面作为基底,收集聚乳酸和明胶组成的静电纺丝纳米纤维(PLLA/GL)。由于猪皮上表面存在毛发,转移的纳米纤维膜(皮顶)呈现出分散的小孔隙(~ 50 μm)。而以铝箔(Al)为衬底的纳米纤维转移膜表面光滑。得益于皮肤独特的表面特性,基于皮肤的纳米纤维膜表现出改善的粗糙度和增强的透气性。具体而言,基于皮肤的创面敷料在促进伤口愈合方面表现出最好的性能,包括增强上皮化和胶原沉积。
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引用次数: 0
A mitochondrial-targeted nanomedicine based on hollow mesoporous silica nanoparticles for enhanced colorectal cancer therapy 一种基于中空介孔二氧化硅纳米颗粒的线粒体靶向纳米药物,用于增强结直肠癌治疗
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-03-25 DOI: 10.1016/j.colcom.2025.100833
Jin Liu , Tianle Liu , Chi Zhang , Ziyou Wang , Xinyi Zhang , Chuanchuan Hao , Dan Wang , Guohui Cheng
By focusing on mitochondria as a therapeutic target, strategies can be devised to deplete ATP levels, thereby potentially circumventing the emergence of MDR. In this study, we developed a surface-modified hyaluronic acid (HA), mitochondrial targeted hollow mesoporous silicon nanomedicine (PB@HMSN-HA) co-loaded with berberine (BBR) and paclitaxel (PTX) for enhanced colorectal cancer therapy. The modified HA can selectively bind to tumor cells that overexpress the CD44 receptor, leading to the accumulation of PB@HMSN-HA at the tumor site and improving tumor targeting efficiency. After cellular internalization, the liberated positively charged BBR, which is specifically targeted to mitochondria, induces a reduction in ATP levels. Depletion of ATP subsequently results in a reduction of drug efflux, thereby amplifying the antitumor efficacy of PTX. Therefore, this combination therapy strategy targeting mitochondria serves as an important reference for clinical oncological chemotherapy.
通过将线粒体作为治疗靶点,可以设计出降低ATP水平的策略,从而潜在地避免耐多药的出现。在这项研究中,我们开发了一种表面修饰透明质酸(HA),线粒体靶向中空介孔硅纳米药物(PB@HMSN-HA),共载小檗碱(BBR)和紫杉醇(PTX),用于增强结直肠癌治疗。修饰后的HA可选择性结合过表达CD44受体的肿瘤细胞,使PB@HMSN-HA在肿瘤部位积累,提高肿瘤靶向效率。在细胞内化后,释放的带正电的BBR,专门针对线粒体,诱导ATP水平的降低。ATP的耗竭随后导致药物外排减少,从而增强PTX的抗肿瘤功效。因此,这种针对线粒体的联合治疗策略可作为临床肿瘤化疗的重要参考。
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引用次数: 0
Synthesis and characterization of enhanced hydrophobic polysilazane coatings with high transparency and durability 高透明耐用增强型疏水性聚硅氮烷涂料的合成与表征
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-03-28 DOI: 10.1016/j.colcom.2025.100832
Yinggang Liu , Zunqing Liu , Guofei Chen , Xingzhong Fang
The development of transparent hydrophobic coatings with durability is crucial required both optical transparency and hydrophobic properties for application. In this study, a series of durable, transparent and hydrophobic coatings were prepared by dispersing hydrophobic fumed silica (SiO2) in the fluorinated polysilazanes (FPSZ) matrix and then spraying the mixture onto microscope slides. The coating FPC-1 achieved excellent comprehensive performances showing a water contact angle of 125°, a transmittance of 88.9 % at 400 nm, a pencil hardness of 6H, and an adhesion class of 5B. In addition, the coating of FPC-1 could withstand chemical corrosion for 7 days and 100 cycles of abrasion without significant degradation. These coatings show has great potential for applications in transparent optical devices.
开发具有耐用性的透明疏水涂层对应用具有光学透明性和疏水性能至关重要。在本研究中,将疏水气相二氧化硅(SiO2)分散在氟化聚硅烷(FPSZ)基体中,然后将混合物喷涂到显微镜载玻片上,制备了一系列耐用、透明和疏水的涂层。涂层FPC-1具有优异的综合性能,水接触角为125°,400 nm透光率为88.9%,铅笔硬度为6H,附着力等级为5B。此外,FPC-1的涂层可以承受7天的化学腐蚀和100次循环的磨损而没有明显的降解。这些涂层在透明光学器件中具有巨大的应用潜力。
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引用次数: 0
A CFD simulation tool for experimental prediction of inflow polymeric microdroplet formation in a T-junction configuration 用于t型结结构中流入聚合物微液滴形成实验预测的CFD模拟工具
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-04-03 DOI: 10.1016/j.colcom.2025.100834
Maria Auriemma , Maria Isabella Maremonti , Edmondo Battista , Filippo Causa
A simulation tool to predict the morphological features and dynamics of polymeric microdroplets in a microfluidic T-junction is presented. A phase-diagram of regimes is created moving from dripping to squeezing within ranges of 10−2–10−4 and 10−1–10−3 for Reynolds and Capillary numbers, respectively. The simulations show the strong influence of the continuous phase over the droplet size, which changes two orders of magnitude -increasing from 101 to 102 μm- as the flowrate becomes higher.
The phase-diagram allows to choose the optimal fluid-flow conditions to have a precise and stable dripping production of spherical drops. Indeed, a successful down-scaling of drop size up to ∼101 μm with a drop rate production of ∼40 drops/s is obtained, with a great accordance between simulative and experimental results (error < 1 %), at high monodispersity (polydispersity index<0.05). Therefore, our tool has proved to be a powerful approach to predict and regulate polymeric microdroplet production in microfluidics.
提出了一种用于预测微流控t型结中聚合物微滴形态特征和动力学的模拟工具。在雷诺数和毛细数分别为10−2-10−4和10−1-10−3的范围内,建立了从滴流到挤压的相图。模拟结果表明,连续相对液滴尺寸的影响较大,随着流量的增大,液滴尺寸变化两个数量级,从101 μm增大到102 μm。相图允许选择最佳流体流动条件,以精确和稳定的滴漏生产球形液滴。事实上,他们成功地将液滴尺寸缩小到~ 101 μm,液滴速率为~ 40滴/秒,模拟结果和实验结果非常吻合(误差<;1%),单分散性高(多分散性指数<;0.05)。因此,我们的工具已被证明是预测和调节微流体中聚合物微滴产生的有力方法。
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引用次数: 0
Smart self-assembled nanomedicine for ferroptotic tumor therapy 用于肿瘤治疗的智能自组装纳米药物
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-05-01 Epub Date: 2025-03-21 DOI: 10.1016/j.colcom.2025.100829
Chen Liang , Tian Zhang , Qingming Zhang , Xiaozhou Mou
Featured by iron-dependent lipid peroxidation, ferroptosis is increasingly recognized as a prominent route for programmed tumor therapy. However, the adaptivity, complexity, and heterogeneity of tumors hamper the performance of ferroptotic tumor therapies. Recent advances in molecularly self-assembled nanomedicine show promise in rejuvenating ferroptotic tumor therapies by leveraging the principles of molecular self-assembly (MSA). This review first sketches the basis of ferroptosis and MSA. Subsequently, representative nanoplatforms are discussed to elucidate how MSA can be devised, either in vitro or in vivo, to improve the precision, efficacy, and biosafety of ferroptotic tumor therapies. Finally, considerations and future perspectives toward clinical translation of molecularly self-assembled ferroptosis nanomedicine are addressed.
铁下垂以铁依赖性脂质过氧化为特征,越来越被认为是程序化肿瘤治疗的重要途径。然而,肿瘤的适应性、复杂性和异质性阻碍了铁系肿瘤治疗的表现。分子自组装纳米药物的最新进展表明,利用分子自组装(MSA)的原理,可以使嗜铁性肿瘤的治疗恢复活力。本文首先概述了铁下垂和MSA的基础。随后,本文讨论了具有代表性的纳米平台,以阐明如何在体外或体内设计MSA,以提高铁致肿瘤治疗的准确性、有效性和生物安全性。最后,讨论了分子自组装铁下垂纳米药物临床翻译的考虑和未来前景。
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引用次数: 0
Effects of grafting architecture of amphiphilic polymer-grafted nanoparticles on stabilization mechanisms of concentrated emulsions 两亲性聚合物接枝纳米颗粒接枝结构对浓乳剂稳定机理的影响
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-03-01 Epub Date: 2025-02-25 DOI: 10.1016/j.colcom.2025.100822
Kojiro Suzuki , Yusei Kobayashi , Takashi Yamazaki , Toshikazu Tsuji , Noriyoshi Arai
This study explores the stabilization mechanisms of concentrated emulsions with tunable morphology using amphiphilic polymer-grafted nanoparticles (PGNPs). We employ coarse-grained molecular simulations to investigate concentrated oil-in-water emulsions stabilized by partially hydrolyzed poly(vinyl alcohol)-grafted poly(methyl methacrylate) (PMMA) particles. Two grafting architectures were examined: hydrophilic-hydrophobic (AB-type) diblock PGNPs and reverse BA-type diblock PGNPs. Our findings reveal that AB-type diblock PGNPs tend to aggregate, leading to droplet-droplet coalescence. In contrast, BA-type diblock PGNPs disperse effectively in the water phase, stabilizing robust emulsion through a space-filling mechanism. The study further demonstrates that the stability and morphology of the emulsions can be tuned by varying the number of PGNPs. Our results suggest that BA-type diblock PGNPs are more effective in stabilizing concentrated emulsions, offering insights for the design of novel emulsifiers in industrial applications.
本研究探讨了两亲性聚合物接枝纳米颗粒(PGNPs)在可调形态浓乳剂中的稳定机理。我们采用粗粒度的分子模拟来研究由部分水解的聚乙烯醇接枝聚甲基丙烯酸甲酯(PMMA)颗粒稳定的浓缩水包油乳液。研究了两种接枝结构:亲疏水(ab型)双嵌段PGNPs和反向ba型双嵌段PGNPs。我们的研究结果表明,ab型双阻断PGNPs倾向于聚集,导致液滴-液滴聚结。相反,ba型双嵌段PGNPs在水相中有效分散,通过空间填充机制稳定坚固的乳液。研究进一步表明,乳剂的稳定性和形态可以通过改变PGNPs的数量来调节。我们的研究结果表明,ba型双嵌段PGNPs在稳定浓乳剂方面更有效,为工业应用中新型乳化剂的设计提供了见解。
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引用次数: 0
Colistin does not self-assemble at physiologically relevant conditions 粘菌素在生理相关条件下不能自组装
IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-03-01 Epub Date: 2025-02-27 DOI: 10.1016/j.colcom.2025.100824
Vladimir Rosenov Koynarev , Thomas Daniel Vogelaar , Mahmoud Moqadam , Nathalie Reuter , Reidar Lund
Antimicrobial peptides (AMPs) have shown great potential against the ongoing rise of multi-drug resistant bacteria because of their high potency and effectiveness. Their clinical utility has, however, remained limited due to their severe side effects. As an exception, colistin (polymyxin E) is currently utilized as a last-resort option against severe gram-negative infections despite being cyto- and nephrotoxic. The ongoing efforts to reduce these side effects are hampered by the generally poor understanding of its mode of action and behavior in solution. A key question that has been debated is whether colistin self-assembles into micelles or remains as unimers in solution. Herein, we used synchrotron small-angle X-ray scattering (SAXS), small-angle neutron scattering (SANS), and molecular dynamics (MD) to show that colistin does not self-assemble in a wide range of physiologically relevant conditions. These contrasting findings, compared to previously reported results, provide important new insights into the behavior of colistin, aiding the understanding and potential improvement of this relevant AMP-based antibiotic.
抗菌肽(AMPs)由于其高效和高效,在对抗多重耐药细菌方面显示出巨大的潜力。然而,由于其严重的副作用,其临床应用仍然有限。作为例外,粘菌素(多粘菌素E)虽然具有细胞毒性和肾毒性,但目前被用作对抗严重革兰氏阴性感染的最后选择。由于对其在溶液中的作用方式和行为普遍缺乏了解,正在进行的减少这些副作用的努力受到阻碍。一直以来争论的一个关键问题是粘菌素是自组装成胶束还是在溶液中保持为单体。在此,我们使用同步加速器小角x射线散射(SAXS)、小角中子散射(SANS)和分子动力学(MD)来证明粘菌素在广泛的生理相关条件下不会自组装。与先前报道的结果相比,这些对比结果为粘菌素的行为提供了重要的新见解,有助于理解和潜在地改进这种相关的基于amp的抗生素。
{"title":"Colistin does not self-assemble at physiologically relevant conditions","authors":"Vladimir Rosenov Koynarev ,&nbsp;Thomas Daniel Vogelaar ,&nbsp;Mahmoud Moqadam ,&nbsp;Nathalie Reuter ,&nbsp;Reidar Lund","doi":"10.1016/j.colcom.2025.100824","DOIUrl":"10.1016/j.colcom.2025.100824","url":null,"abstract":"<div><div>Antimicrobial peptides (AMPs) have shown great potential against the ongoing rise of multi-drug resistant bacteria because of their high potency and effectiveness. Their clinical utility has, however, remained limited due to their severe side effects. As an exception, colistin (polymyxin E) is currently utilized as a last-resort option against severe gram-negative infections despite being cyto- and nephrotoxic. The ongoing efforts to reduce these side effects are hampered by the generally poor understanding of its mode of action and behavior in solution. A key question that has been debated is whether colistin self-assembles into micelles or remains as unimers in solution. Herein, we used synchrotron small-angle X-ray scattering (SAXS), small-angle neutron scattering (SANS), and molecular dynamics (MD) to show that colistin <em>does not</em> self-assemble in a wide range of physiologically relevant conditions. These contrasting findings, compared to previously reported results, provide important new insights into the behavior of colistin, aiding the understanding and potential improvement of this relevant AMP-based antibiotic.</div></div>","PeriodicalId":10483,"journal":{"name":"Colloid and Interface Science Communications","volume":"65 ","pages":"Article 100824"},"PeriodicalIF":4.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143508644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Colloid and Interface Science Communications
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