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Development of a freshness indicator packaging system using cold atmospheric plasma on LLDPE–PVA with Laponite–anthocyanin biohybrid 在含有皂石-花青素生物杂化物的 LLDPE-PVA 上使用冷大气等离子体开发新鲜度指示器包装系统
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-14 DOI: 10.1002/pi.6679
Gabriel Coelho Leandro, Denise Adamoli Laroque, Bruno Augusto Mattar Carciofi, Germán Ayala Valencia

This study developed a freshness indicator based on poly(vinyl alcohol) (PVA) and a biohybrid (BH) of Laponite® and anthocyanins adhered to linear low-density polyethylene (LLDPE) using cold atmospheric plasma (CAP). LLDPE was treated with CAP for 0 to 300 s, which resulted in an increased surface energy, characterized by an important increase in its polar component up to 120 s of treatment, due to the formation of polar groups on the surface of LLDPE. No changes in mechanical properties and water vapor permeability of LLDPE were observed. LLDPE–PVA–BH films were more homogeneous if BH was added before the acidification of the film-forming solution due to more negative zeta potential and lower particle size of BH in basic medium. Indicators made with BH were able to maintain color after 8 weeks of exposure to light, while those made with anthocyanin extract had fully degraded after 3 weeks. The freshness indicator's color changed from purple to blue and finally to green when exposed to ammonia hydroxide (30% NH3) and from purple to blue when exposed to a simulant liquid of spoiled meat (0.03% NH3). Similar color variance was observed when the indicator was applied to monitor shrimp freshness, changing from purple to blue when the shrimp pH reached pH 7.6. Thus, bilayer films of LLDPE–PVA and natural BH produced using CAP have potential food packaging applications. © 2024 Society of Chemical Industry.

本研究利用冷大气等离子体(CAP)开发了一种基于聚乙烯醇(PVA)和生物杂化物(BH)的新鲜度指示剂,生物杂化物包括粘附在线性低密度聚乙烯(LLDPE)上的 Laponite® 和花青素。用 CAP 处理线性低密度聚乙烯的时间为 0 到 300 秒,其结果是增加了表面能,由于在线性低密度聚乙烯表面形成了极性基团,其极性成分在处理 120 秒内显著增加。LLDPE 的机械性能和水蒸气渗透性没有发生变化。如果在成膜溶液酸化之前加入 BH,则 LLDPE-PVA-BH 薄膜会更加均匀,这是因为在碱性介质中,BH 的 Zeta 电位更负,粒径更小。用 BH 制成的指示剂在光照 8 周后仍能保持颜色,而用花青素提取物制成的指示剂在 3 周后已完全降解。当暴露在氢氧化氨(30% NH3)中时,新鲜度指示剂的颜色从紫色变为蓝色,最后变为绿色;当暴露在变质肉类的模拟液(0.03% NH3)中时,新鲜度指示剂的颜色从紫色变为蓝色。当指示剂用于监测虾的新鲜度时,也观察到了类似的颜色变化,当虾的 pH 值达到 pH 7.6 时,指示剂由紫色变为蓝色。因此,使用 CAP 生产的 LLDPE-PVA 和天然 BH 双层薄膜具有潜在的食品包装应用价值。© 2024 化学工业协会。
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引用次数: 0
Uniaxial tensile-induced deformation of spherulite: combining experimental and simulation methods 球状云母的单轴拉伸诱导变形:结合实验和模拟方法
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-14 DOI: 10.1002/pi.6672
Maoqing Yuan, Linjuan Ren, Na Zhao, Yanping Liu, Qian Li

A combination of experimental and simulation methods is adopted to study the relationship between micro-stress and micro-strain of a single spherulite upon uniaxial tensile deformation. To verify the simulation results and establish a suitable spherulite model, large-sized isotactic polypropylene spherulite is first cultured with isothermal crystallization, whose structural deformation upon application of uniaxial tension is recorded using a polarizing optical microscope. A nanoindenter is used to measure the elastic modulus of the spherulite and amorphous region, preparing the property parameters for numerical simulation. Modeling and meshing of the single spherulite are conducted with the finite element software ABAQUS. The entire deformation of the spherulite is analyzed with fixed strain as the boundary condition, and the microscopic stress and strain distribution inside and outside of the spherulite is obtained. The higher micro-stress region mainly locates at two poles in the equatorial direction, where might be the origin of craze. Generally, the simulation result is basically consistent with the experimental deformation process, which provides a new idea for the study of microscale structure and performance. © 2024 Society of Chemical Industry.

采用实验和模拟相结合的方法研究了单个球粒在单轴拉伸变形时的微应力和微应变之间的关系。为验证模拟结果并建立合适的球粒模型,首先对大尺寸异策聚丙烯球粒进行等温结晶培养,并使用偏振光学显微镜记录其在施加单轴拉伸时的结构变形。使用纳米压头测量球粒和非晶区的弹性模量,为数值模拟准备属性参数。使用有限元软件 ABAQUS 对单个球晶进行建模和网格划分。以固定应变为边界条件,分析了球晶的整个变形过程,得到了球晶内外的微观应力和应变分布。较高的微应力区域主要位于赤道方向的两极,这里可能是裂纹的起源。总体而言,模拟结果与实验变形过程基本一致,为研究微尺度结构和性能提供了新思路。© 2024 化学工业学会。
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引用次数: 0
Fabrication and characterization of human finger ridge-inspired soft elastomeric pressure sensor with liquid metal-embedded microchannels 带有液态金属嵌入式微通道的人体指脊启发式软弹性压力传感器的制作与特性分析
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-12 DOI: 10.1002/pi.6676
Akshay Saxena, Karali Patra

Soft sensors are flexible and stretchable, and because of this, they can be used on a wide range of surfaces, regardless of their size or shape. Such sensors may have applications such as in human–robot interaction, healthcare, soft robotics and human motion detection, where they can sense their surroundings and provide information. In this work, a soft piezoresistive sensor inspired by human finger ridges has been fabricated with liquid metal (EGaIn) electrode-filled embedded microchannels on elastomeric material (Ecoflex 0030) and characterized for a pressure range of 0 to 280 kPa at different compression rates. The sensitivity of the elastomeric sensor increases and the limit of detection (LOD) decreases with a reduction in compression rate. In this work, microchannels on soft and stretchable elastomers are cast on a metallic mold prepared using the micromilling method. This method reduces the complexity of developing microchannels on the soft material using the metallic mold. The sensor has microchannels with a cross-section of 200 μm × 200 μm, an active sensing area of 10 × 10 mm2 and overall dimensions of 15 × 15 × 2 mm3. At a low compression rate, this sensor exhibits a maximum sensitivity of 0.126 kPa−1 and a high linearity of 0.98, a LOD of 68 Pa, a response time of 30 ms and stability for 10 000 consecutive cycles at 100 kPa load. The developed sensor was shown to successfully differentiate various objects (soft to hard) based on the feedback it received when it was deployed on the gripper of an industrial manipulator. © 2024 The Author(s). Polymer International published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

软传感器具有柔性和可拉伸性,因此可用于各种表面,而不受表面大小或形状的限制。这种传感器可应用于人机交互、医疗保健、软机器人和人体运动检测等领域,它们可以感知周围环境并提供信息。在这项工作中,受人类指脊的启发,在弹性材料(Ecoflex 0030)上制作了液态金属(EGaIn)电极填充嵌入式微通道的软压阻传感器,并在不同压缩率下对 0 至 280 kPa 的压力范围进行了表征。随着压缩率的降低,弹性传感器的灵敏度增加,检测限(LOD)降低。在这项工作中,在使用微钻方法制备的金属模具上浇铸了软质可拉伸弹性体上的微通道。这种方法降低了使用金属模具在软质材料上制作微通道的复杂性。传感器的微通道横截面为 200 μm × 200 μm,有效传感面积为 10 × 10 mm2,总尺寸为 15 × 15 × 2 mm3。在低压缩率条件下,该传感器的最大灵敏度为 0.126 kPa-1,线性度高达 0.98,LOD 为 68 Pa,响应时间为 30 ms,在 100 kPa 负载条件下可连续稳定工作 10 000 次。根据传感器在工业机械手的夹具上安装时收到的反馈,可以证明所开发的传感器能够成功区分各种物体(从软到硬)。© 2024 作者。国际聚合物》由 John Wiley & Sons Ltd 代表化学工业协会出版。
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引用次数: 0
Electrochemical behavior of non-functionalized and sulfonated melanins at different pH values 非官能化和磺化黑色素在不同 pH 值下的电化学行为
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-12 DOI: 10.1002/pi.6678
Nayrim Brizuela Guerra, João Victor Morais Lima, João Vitor Paulin, Natan Luiz Nozella, Miguel Henrique Boratto, Gabriel Leonardo Nogueira, Carlos César Bof Bufon, Carlos Frederico de Oliveira Graeff

Melanins are macromolecular pigments widely spread in many living organisms, with unique physical and chemical properties. Specifically, their conductive properties have drawn attention for applications in different devices; however, the electrochemical response is equally necessary for designing technologies in sustainable bioelectronics. In this sense, we report a comparative study of the redox electrochemical properties of non-functionalized and sulfonated melanins in different pH environments. The electrochemical response was investigated using cyclic voltammetry, electrochemical impedance spectroscopy, dielectric permittivity and AC/DC conductivity at pH 3, 5 and 7. The voltammetric currents were higher at low pH, in agreement with the known proton transport properties of melanins. The effect of pH on electrochemical properties was slightly more significant in non-functionalized pigments. Melanins with a higher 5,6-dihydroxyindole carboxylic acid/5,6-dihydroxyindole ratio showed high DC current and low impedance. No significant difference was observed in the dielectric relaxation process between the different samples. © 2024 Society of Chemical Industry.

黑色素是广泛存在于许多生物体内的大分子色素,具有独特的物理和化学特性。具体来说,它们的导电性能引起了人们对其在不同设备中应用的关注;然而,电化学反应对于设计可持续生物电子学技术也同样必要。因此,我们报告了一项关于非官能化黑色素和磺化黑色素在不同 pH 值环境下的氧化还原电化学性质的比较研究。我们采用循环伏安法、电化学阻抗光谱法、介电常数法和交直流电导法研究了黑色素在 pH 值为 3、5 和 7 时的电化学反应。在 pH 值较低时,伏安电流较高,这与已知的黑色素质子传输特性一致。在非官能化色素中,pH 值对电化学特性的影响略微显著。5,6-二羟基吲哚羧酸/5,6-二羟基吲哚比率较高的黑色素显示出较高的直流电流和较低的阻抗。不同样品的介电弛豫过程没有明显差异。© 2024 化学工业协会。
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引用次数: 0
A highly stretchable and conductive polydimethylsiloxane/nickel-coated graphite composite prepared by a facile sedimentation method by adjusting interface effects 通过调整界面效应,采用简便沉积法制备高拉伸性和导电性聚二甲基硅氧烷/镍涂层石墨复合材料
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-11 DOI: 10.1002/pi.6675
Rong Zhang, Qian Liu, Yifan Xiang, Siqi Li, Wuhou Fan, Chengcheng Xu, Qingting Liu, Xudong Fu, Shengfei Hu

Stretchable electrodes are essential parts for flexible electronics which are widely applied in human health monitoring, wearable electronics, robotics etc. Conductive elastomer composites are good candidates for stretchable electrodes; however, it is a challenge to maintain the resistance of conductive elastomer composites during elongation due to the departure of filler networks. In this work, highly stretchable and conductive polydimethylsiloxane (PDMS)/nickel-coated graphite (NCG) composites were fabricated based on the filler sedimentation method, in which NCG was modified by the coupling agent of the end alkyl group (dodecyltriethoxysilane, DTES) and end vinyl group (vinyltriethoxysilane, VTEO), considering the force between the filler networks and filler–matrix interface. The DTES modified NCG mainly improved the filler–matrix interface, which made the resistance of the composites clearly increase with strain, while the VTEO mainly heightened the NCG networks and made the resistance of the composites insensitive to a strain of 114% when the NCG content was 23.1 wt%. These quite interesting results are closely related to the force between the filler networks and filler–matrix interface during strain and they were proved in detail through the mechanical and electrical hysteresis performance. This work presents a facile method from the concept of stability of filler networks during strain to prepare highly stretchable and conductive composites. © 2024 Society of Chemical Industry.

可拉伸电极是柔性电子产品的重要部件,广泛应用于人体健康监测、可穿戴电子产品、机器人等领域。导电弹性体复合材料是拉伸电极的良好候选材料;然而,由于填料网络的脱离,在拉伸过程中保持导电弹性体复合材料的电阻是一项挑战。考虑到填料网络和填料-基质界面之间的作用力,本研究采用填料沉降法,通过端烷基(十二烷基三乙氧基硅烷,DTES)和端乙烯基(乙烯基三乙氧基硅烷,VTEO)偶联剂对 NCG 进行改性,制备了高拉伸导电性聚二甲基硅氧烷(PDMS)/镍涂层石墨(NCG)复合材料。当 NCG 含量为 23.1 wt% 时,DTES 改性的 NCG 主要改善了填料-基体界面,使复合材料的电阻随应变明显增加;而 VTEO 主要增强了 NCG 网络,使复合材料的电阻对 114% 的应变不敏感。这些有趣的结果与应变过程中填料网络和填料-基体界面之间的作用力密切相关,并通过机械和电滞后性能得到了详细证明。这项工作从填料网络在应变过程中的稳定性概念出发,提出了一种制备高拉伸性和导电性复合材料的简便方法。© 2024 化学工业协会。
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引用次数: 0
Enhanced electromechanical performance of Nafion actuator doped by poly(ethylene glycol)-grafted graphene oxide 掺杂聚乙二醇接枝氧化石墨烯的 Nafion 致动器的机电性能得到增强
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-10 DOI: 10.1002/pi.6674
Li Ma, Xiaowei Guo, Longxiang Mei, Lehui Wang, Yanghai Gui, Dongjie Guo

Current ionic polymer–metal composite (IPMC) actuators have severe actuation drawbacks (i.e. low force output and poor stability), hampering their applications. To address these issues, poly(ethylene glycol)-grafted graphene oxide (PEG-GO) is synthesized and incorporated into a Nafion matrix, thus producing a PEG-GO hybrid Nafion film with better physiochemical properties for fabricating a high-performance, low-cost IPMC actuator. The modification of PEG to GO not only prevents GO agglomeration and sedimentation, but also avoids loss of PEG in water. Driven by a 0.2 Hz, 2.5 V electric field, the hybrid IPMC actuator exhibits superior electromechanical behaviors, i.e. a swing angle of 110.3°, a blocking force of 6.89 mN and a stable working time of 485 s, respectively increasing by 92%, 209% and 294% when compared to a pure Nafion actuator. © 2024 Society of Chemical Industry.

目前的离子聚合物-金属复合材料(IPMC)致动器存在严重的致动缺陷(即力输出低和稳定性差),阻碍了其应用。为了解决这些问题,我们合成了聚乙二醇接枝氧化石墨烯(PEG-GO),并将其加入到 Nafion 基质中,从而产生了具有更好理化特性的 PEG-GO 混合 Nafion 薄膜,用于制造高性能、低成本的 IPMC 激励器。将 PEG 改性为 GO 不仅可以防止 GO 聚结和沉淀,还能避免 PEG 在水中流失。在 0.2 Hz、2.5 V 的电场驱动下,混合 IPMC 执行器表现出卓越的机电性能,与纯 Nafion 执行器相比,摆动角度为 110.3°,阻挡力为 6.89 mN,稳定工作时间为 485 s,分别增加了 92%、209% 和 294%。© 2024 化学工业协会。
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引用次数: 0
A survey of recent publications on polymers employing reactive, halogen-free flame-retardant functionalities 关于采用活性无卤阻燃功能聚合物的最新出版物概览
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-07-09 DOI: 10.1002/pi.6673
Benjamin J Stovall, Timothy E Long

Modern society relies heavily on producing commercial and industrial plastics to improve the quality and quantity of our lives. However, increased fire risks threaten commercial operations and the potential impact of high-performance electronic and transportation technologies that utilize polymeric materials. Despite significant monitoring and reduction of commonly used halogenated flame retardants, their worldwide usage still poses environmental hazards. Many non-halogenated flame-retardant compounds are viable additives for synthetic polymers; however, their incorporation often results in reduced composite homogeneity and mechanical strength. This review focuses on reactive flame retardants and the effect of polymer structure on inherent flame retardance in recent studies. The synthesis and characterization of polymeric systems (e.g. polyurethanes, polyamides, polyimides, polyesters and epoxy resins) are discussed in terms of structure–flame-retardant performance using a complement of analytical tools, including thermogravimetric analysis, cone calorimetry, limiting oxygen index and UL 94 testing. These commercially important polymeric systems represent a broad compositional space for future adaptation and the discovery of increasingly modular polymeric materials with, while also contributing to the fundamental understanding of unique combinations of gas- and condensed-phase mechanisms of flame retardance. © 2024 Society of Chemical Industry.

现代社会在很大程度上依赖于商用和工业用塑料的生产,以提高我们生活的质量和数量。然而,火灾风险的增加威胁着商业运营以及使用聚合材料的高性能电子和运输技术的潜在影响。尽管对常用的卤化阻燃剂进行了大量监测并减少了使用量,但它们在全球范围内的使用仍对环境造成危害。许多非卤化阻燃剂化合物是合成聚合物的可行添加剂,但它们的加入往往会降低复合材料的均匀性和机械强度。本综述重点介绍反应型阻燃剂以及近期研究中聚合物结构对固有阻燃性的影响。文章从结构-阻燃性能的角度讨论了聚合物体系(如聚氨酯、聚酰胺、聚酰亚胺、聚酯和环氧树脂)的合成和特性,并使用了一系列分析工具,包括热重分析、锥形量热仪、极限氧指数和 UL 94 测试。这些具有重要商业价值的聚合物系统代表了一个广阔的组成空间,可用于未来的适应性调整,并发现模块化程度越来越高的聚合物材料,同时也有助于从根本上了解气相和凝聚相独特的阻燃机制组合。© 2024 化学工业协会。
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引用次数: 0
Silicone-containing polyurea elastomer possessing main-chain boron–oxygen bonds with delayed stress relaxation and improved adhesive properties 含硅聚脲弹性体具有主链硼氧键,可延迟应力松弛并改善粘合性能
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-06-21 DOI: 10.1002/pi.6671
Shilong Zhang, Youhao Xiong, Yangwei Wang, Yuqi Ma, Jialiang Li, Chaobo Jiang, Ce Wang, Yanling Zhu, Yongsheng Zhao, Guangcheng Zhang

Polyurea (PU) elastomers have attracted considerable attention in the field of protective polymeric coatings. In this work, a dithiol-terminated boronic ester was synthesized and used to incorporate dynamic boron–oxygen (B–O) bonds in the PU main chain based on thiol isocyanate while amino-terminated polydimethylsiloxane (PDMS) was introduced to retain good chain flexibility. The modified PU elastomer was found to have a microphase-separated structure in which the hard blocks served as physical crosslinks. The glass transition temperature (Tg) slightly increases when dynamic B–O bonds exist while further introduction of PDMS soft segment can lower Tg to −55.63 °C. The introduction of dynamic B–O bonds and diminished hydrogen bonding led to a decrease in mechanical strength and elongation at break. Interestingly, the simultaneous incorporation of PDMS and dynamic B–O bonds is favorable for strain rate dependence and suppressing stress relaxation. The potential for bond-exchange interactions between the dynamic B–O bonds and hydroxyl groups on metal surfaces substantially improved the adhesion of the PU elastomer to metal substrates. Therefore, our work can offer valuable insights for the structural design of functional PU coatings tailored for anti-impact applications. © 2024 Society of Chemical Industry.

聚脲(PU)弹性体在聚合物保护涂层领域备受关注。在这项研究中,我们合成了一种二硫醇封端的硼酸酯,并利用它在聚氨酯主链中加入了基于硫醇异氰酸酯的动态硼-氧(B-O)键,同时引入了氨基封端的聚二甲基硅氧烷(PDMS)以保持良好的链柔性。研究发现,改性聚氨酯弹性体具有微相分离结构,其中的硬块起到了物理交联的作用。当存在动态 B-O 键时,玻璃化转变温度(Tg)略有升高,而进一步引入 PDMS 软段可将 Tg 降至 -55.63 °C。动态 B-O 键的引入和氢键的减少导致了机械强度和断裂伸长率的下降。有趣的是,同时加入 PDMS 和动态 B-O 键有利于应变速率依赖性和抑制应力松弛。动态 B-O 键与金属表面羟基之间潜在的键交换相互作用大大提高了聚氨酯弹性体与金属基底的粘附性。因此,我们的工作可为抗冲击应用定制的功能性聚氨酯涂层的结构设计提供有价值的见解。© 2024 化学工业协会。
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引用次数: 0
Quercetin allylation and thiol–ene click photopolymerization to produce biobased polymer thermosets with robust thermomechanical properties 利用槲皮素烯丙基化和硫醇烯点击光聚合技术生产具有强热力学性能的生物基聚合物热固性塑料
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-06-18 DOI: 10.1002/pi.6670
Víctor D Lechuga Islas, Ricardo Acosta Ortiz, Roberto Yañez Macías, Alan I Hernández Jiménez

The development of biobased and functionalized monomers along with eco-friendly photopolymerization processes represent promising methods for the development of renewable and more environmentally friendly thermosets. Thiol–ene ‘click’ photopolymerization is particularly advantageous in this regard; however, the materials derived from this method often exhibit low glass transition temperatures (Tg) and unsuitable thermomechanical properties for applications at room temperature. Herein, we report the synthesis of biobased allyl derivatives from quercetin, a renewable flavonoid compound widely available in fruits, vegetables and plants. We demonstrated the isolation of tetra- and penta-allylated quercetin (Q1 and Q2, respectively) and their subsequent photoactivated thiol–ene polymerization. By introducing a biobased thiol curing agent (PTTMP) derived from glycerol and mercaptopropionic acid, we produced fully biobased crosslinked thermosets with high content of aromatic moieties provided by the framework of the monomers. Real-time infrared spectroscopy showed the effective thiol–ene photopolymerization of Q1 and Q2 and PTTMP with conversions of 60% and 75%, respectively, after 15 min of UV irradiation. Due to the modulated crosslinking degree from the allyl group functionalization in the monomers, the biobased crosslinked networks showed storage moduli from 420 to 739 MPa, thermal stability from 220 to 257 °C and Tg values ranging from 75 to 90 °C. This work outlines straightforward strategies for creating biobased thermosets that overcome the limited thermomechanical properties of thiol–ene networks and offer potential antimicrobial and antioxidant properties. © 2024 Society of Chemical Industry.

生物基和功能化单体的开发以及环保型光聚合工艺是开发可再生和更环保热固性塑料的有效方法。在这方面,噻吩 "点击 "光聚合尤其具有优势;然而,这种方法制备的材料通常玻璃化温度(Tg)较低,热机械性能不适合在室温下应用。槲皮素是一种广泛存在于水果、蔬菜和植物中的可再生类黄酮化合物,在此,我们报告了从槲皮素合成生物基烯丙基衍生物的过程。我们展示了四烯丙基和五烯丙基槲皮素(分别为 Q1 和 Q2)的分离及其随后的光活化硫醇烯聚合。通过引入源自甘油和巯基丙酸的生物基硫醇固化剂(PTTMP),我们制备出了完全生物基的交联热固性塑料,其单体框架提供了高含量的芳香分子。实时红外光谱显示,在紫外线照射 15 分钟后,Q1 和 Q2 与 PTTMP 的硫醇-烯光聚合效果显著,转化率分别为 60% 和 75%。由于单体中的烯丙基官能化产生了可调节的交联度,生物基交联网络显示出 420 至 739 兆帕的存储模量、220 至 257 °C 的热稳定性和 75 至 90 °C 的 Tg 值。这项工作概述了创建生物基热固塑料的直接策略,这些热固塑料克服了硫醇烯网络有限的热机械性能,并具有潜在的抗菌和抗氧化性能。© 2024 化学工业协会。
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引用次数: 0
Cardiomyocyte differentiation of umbilical cord mesenchymal stem cells on poly(mannitol sebacate)/multi-walled carbon nanotube substrate 聚(甘露醇癸二酸酯)/多壁碳纳米管基底上的脐带间充质干细胞的心肌细胞分化
IF 2.9 4区 化学 Q2 POLYMER SCIENCE Pub Date : 2024-06-14 DOI: 10.1002/pi.6668
Elham Hosseinzadeh, Faraz Sigaroodi, Camellia Ganjoury, Azim Parandakh, Najmeh Najmoddin, Shayan Shahriari, Maryam Mahmoodinia Maymand, Mohammad-Mehdi Khani

Myocardial infarction is one of the main causes of death worldwide. After myocardial infarction, the damaged area is typically occupied with non-contractile scar tissue owing to the limited ability of cardiac cells to proliferate. Cardiac patches can potentially restore heart function by providing sufficient electrochemical properties to the damaged area and supporting the differentiation into and proliferation of cardiac cells. In this study, we developed for the first time a poly(mannitol sebacate) (PMS) based scaffold combined with 1% (w/w)multi-walled carbon nanotubes (MWCNTs) to produce a biocompatible cardiac patch by the solvent casting method. We characterized the resultant PMS-MWCNT scaffold in terms of chemical, physical, mechanical and electrical properties. The PMS/MWCNT patch revealed appropriate hydrophilicity, elasticity close to that of the target tissue, and electrical conductivity suited for a cardiac patch. The cytocompatibility of the composite was confirmed by the successful attachment and proliferation of human umbilical cord mesenchymal stem cells (HUC-MSCs). The PMS/MWCNTs further contributed to the differentiation of HUC-MSCs by significant overexpression of cardiac-specific proteins, i.e. troponin T and connexin 43, in the presence of 5-azacytidine. The findings of this study could be of assistance in the use and development of PMS-based composites as cardiac patches for myocardial tissue engineering applications. © 2024 Society of Chemical Industry.

心肌梗死是导致全球死亡的主要原因之一。心肌梗塞发生后,由于心脏细胞增殖能力有限,受损区域通常被无收缩性的瘢痕组织占据。心脏贴片可为受损区域提供足够的电化学特性,支持心脏细胞的分化和增殖,从而有可能恢复心脏功能。在这项研究中,我们首次开发了一种基于聚(癸二酸甘露醇酯)(PMS)的支架,并将 1%(重量比)多壁碳纳米管(MWCNTs)结合在一起,通过溶剂浇铸法生产出一种生物相容性心脏补片。我们从化学、物理、机械和电学特性等方面对所得到的 PMS-MWCNT 支架进行了表征。PMS/MWCNT 补丁具有适当的亲水性、接近目标组织的弹性以及适合心脏补片的导电性。人脐带间充质干细胞(HUC-MSCs)的成功附着和增殖证实了该复合材料的细胞相容性。在 5-azacytidine 的存在下,PMS/MWCNTs 通过显著过表达心脏特异性蛋白(即肌钙蛋白 T 和连接蛋白 43),进一步促进了 HUC-MSCs 的分化。本研究的发现有助于使用和开发基于 PMS 的复合材料作为心肌组织工程应用的心脏补片。© 2024 化学工业协会。
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引用次数: 0
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Polymer International
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