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磁性气凝胶的研究进展 总被引:1,自引:0,他引:1
《中国材料进展》2016,(12)
磁性气凝胶以其优异的性能受到越来越多的关注。目前,磁性气凝胶主要采用先将磁功能化材料分散到溶胶中,经凝胶、老化、超临界干燥等工艺制得。磁功能化材料主要是指具有磁性的纳米材料,其中应用最多的是铁酸类,尤其以超顺磁性Fe_3O_4的使用最为广泛。而磁性气凝胶的结构和性能因磁功能化纳米材料、气凝胶基体的不同而变化。无机磁性气凝胶的基体主要是氧化硅、氧化钛等气凝胶,主要研究磁性颗粒与气凝胶基体的相互作用机理,以及对材料的结构、性能的影响。而有机磁性气凝胶基体主要是石墨烯、碳等柔性气凝胶,主要应用在催化、吸附、生物分离等领域,具有磁性分离,以及使用效率、重复性能优异等特点。综述了上述磁性气凝胶的研究进展,介绍了磁性气凝胶材料常用的制备方法、性能以及应用前景。 相似文献
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磁性氧化铁纳米粒是一种多功能材料,在药学、医学、催化化学和磁记录材料等领域具有广泛的应用价值。介绍了目前国内外几种广泛制备磁性氧化铁纳米微粒的方法,包括溶胶-凝胶法、沉淀法、微乳液法、水热法和模板法等,比较了它们各自的优缺点,还介绍了磁性氧化铁纳米微粒近年来的研究与应用情况并展望了其发展方向。 相似文献
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《中国材料进展》2020,(6)
水凝胶是一类物理化学性质接近软组织的先进材料,已有众多聚合物用于水凝胶的制备。丝素蛋白由于具有优异的生物相容性、生物可降解性和易于制备成各种形式的材料等优点,在生物医学领域中具有广泛的应用,其中水凝胶是丝素蛋白在生物医学中应用的重要形式。由于分子的独特结构,丝素蛋白可以通过多种方法形成水凝胶。近年来,光交联水凝胶由于具有制备条件温和、副产物少、反应过程容易控制等优点,逐步成为研究的热点。首先对丝素蛋白的分子结构和特性进行了介绍,总结了丝素蛋白水凝胶的制备方法,重点阐述了光交联丝素蛋白水凝胶的研究现状,并讨论了它们在生物医学领域的应用,最后对光交联丝素蛋白水凝胶未来发展方向进行了展望。 相似文献
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水凝胶在医学领域的热点研究及应用 总被引:2,自引:0,他引:2
水凝胶是一种具有三维网络结构的新型功能高分子材料.它以其含水量高、溶胀快、柔软、具有橡胶般的粘稠性和良好的生物相容性等而得到广泛应用及研究.主要介绍近几年水凝胶在生物医学领域的研究热点及水凝胶在生物医学领域应用的最新进展. 相似文献
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水凝胶作为性能良好的载体,在药物的控释、组织工程等领域有着广泛的应用。壳聚糖是一类天然的带正电荷的碱性多糖,由其形成的水凝胶具有较好的生物相容性、生物降解性、抗菌和低细胞毒性,因此,壳聚糖水凝胶有着良好的生物应用前景。本文综述了壳聚糖水凝胶的制备方法(包括物理交联法和化学交联法),在物理交联法部分着重介绍了离子化合物及聚电解质分子与壳聚糖通过离子交联形成水凝胶,以及利用分子链间的疏水作用形成壳聚糖水凝胶的方法;而在化学交联法部分介绍了合成壳聚糖水凝胶的化学手段,包括交联剂、光照辐射和酶的使用。继而概述了壳聚糖水凝胶在药物缓释应用方面的研究进展,包括温度、pH值和电场响应的药物控释体系。最后展望了壳聚糖水凝胶未来的发展前景。 相似文献
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Yijie Wang Tingjie Lv Keyang Yin Ning Feng Xiaofeng Sun Jin Zhou Hongguang Li 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(17):2370119
Hydrogels have extremely high moisture content, which makes it very soft and excellently biocompatible. They have become an important soft material and have a wide range of applications in various fields such as biomedicine, bionic smart material, and electrochemistry. Carbon dot (CD)-based hydrogels are based on carbon dots (CDs) and auxiliary substances, forming a gel material with comprehensive properties of individual components. CDs embedding in hydrogels could not only solve their aggregation-caused quenching (ACQ) effect, but also manipulate the properties of hydrogels and even bring some novel properties, achieving a win–win situation. In this review, the preparation methods, formation mechanism, and properties of CD-based hydrogels, and their applications in biomedicine, sensing, adsorption, energy storage, and catalysis -are summarized. Finally, a brief discussion on future research directions of CD-based hydrogels will be given. 相似文献
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组织工程技术是有望从根本上解决组织或器官损伤及实现功能重建的前沿技术,其关键之一是制备具有良好生物相容性和生物降解性的支架材料。水凝胶由于具有众多良好的特性,成为组织工程研究中一种优良的支架材料。丝素蛋白水凝胶由于独特的性质、多样化的成胶方式以及优异的可加工性成为了支架材料研究的热点,备受学者的青睐并涌现出了大量的研究成果。本文在阐明丝素蛋白凝胶原理的基础上,回顾了目前较为成熟的凝胶化方法,随后重点综述了丝素蛋白水凝胶在组织工程中的研究进展,最后进行了总结和展望,以期为相关领域的研究者提供参考和借鉴。 相似文献
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Paul Calvert 《Advanced materials (Deerfield Beach, Fla.)》2009,21(7):743-756
Hydrogels have applications in surgery and drug delivery, but are never considered alongside polymers and composites as materials for mechanical design. This is because synthetic hydrogels are in general very weak. In contrast, many biological gel composites, such as cartilage, are quite strong, and function as tough, shock‐absorbing structural solids. The recent development of strong hydrogels suggests that it may be possible to design new families of strong gels that would allow the design of soft biomimetic machines, which have not previously been possible. 相似文献
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Luprano VA Ramires PA Montagna G Milella E 《Journal of materials science. Materials in medicine》1997,8(3):175-178
Hydrogels have been prepared by a freezing–thawing procedure and investigations made of the effect of both number of freezing–thawing cycles and different content of hyaluronic acid (HA) on the mechanical properties of the PVA-HA hydrogels using non-destructive testing. The bulk elastic modulus K of hydrogels has been determined by pulse-echo measurements. It is noted that hydrogel elastic properties improve with the number of the cycles in PVA-HA 100/0; on the other hand samples with a high HA (1000000 molecular weight) content, beyond the third cycle, seem to be unaffected by the number of cycles. A bulk elastic modulus fall-off is then observed in samples submitted to an additional overnight freezing between two subsequent cycles. K increases in hydrogels with the highest HA content, when samples undergo pulse-echo measurements soon after their preparation. When hydrogels reach equilibrium, after having been kept in deionized water for 12 h, K values are lower, showing a nearly constant behaviour with different PVA-HA ratios and cycles. Furthermore, by means of scanning laser acoustic microscopy (SLAM) defects have been detected in the hydrogels. In samples which have reached equilibrium, SLAM images show that these defects disappear in PVA-HA hydrogels. 相似文献
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Hydrogels are the most relevant biochemical scaffold due to their tunable properties, inherent biocompatibility, and similarity with tissue and cell environments. Over the past decade, hydrogels have developed from static materials to “smart” responsive materials adapting to various stimuli, such as pH, temperature, chemical, electrical, or light. Light stimulation is particularly interesting for many applications because of the capability of contact‐free remote manipulation of biomaterial properties and inherent spatial and temporal control. Moreover, light can be finely adjusted in its intrinsic properties, such as wavelength and intensity (i.e., the energy of an individual photon as well as the number of photons over time). Water is almost transparent for light in the photochemically relevant range (NIR–UV), thus hydrogels are well‐suited scaffolds for light‐responsive functionality. Hydrogels' chemical and physical variety combined with light responsiveness makes photoresponsive hydrogels ideal candidates for applications in several fields, ranging from biomaterials, medicine to soft robotics. Herein, the progress and new developments in the field of light‐responsive hydrogels are elaborated by first introducing the relevant photochemistries before discussing selected applications in detail. 相似文献
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Moxiao Li Qingzhen Yang Hao Liu Mushu Qiu Tian Jian Lu Feng Xu 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(33):4492-4500
Hydrogels have found broad applications in various engineering and biomedical fields, where the shape and size of hydrogels can profoundly influence their functions. Although numerous methods have been developed to tailor 3D hydrogel structures, it is still challenging to fabricate complex 3D hydrogel constructs. Inspired by the capillary origami phenomenon where surface tension of a droplet on an elastic membrane can induce spontaneous folding of the membrane into 3D structures along with droplet evaporation, a facile strategy is established for the fabrication of complex 3D hydrogel constructs with programmable shapes and sizes by crosslinking hydrogels during the folding process. A mathematical model is further proposed to predict the temporal structure evolution of the folded 3D hydrogel constructs. Using this model, precise control is achieved over the 3D shapes (e.g., pyramid, pentahedron, and cube) and sizes (ranging from hundreds of micrometers to millimeters) through tuning membrane shape, dimensionless parameter of the process (elastocapillary number Ce), and evaporation time. This work would be favorable to multiple areas, such as flexible electronics, tissue regeneration, and drug delivery. 相似文献