共查询到19条相似文献,搜索用时 171 毫秒
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智能水凝胶是一类具有三维网络结构、膨胀性好、吸水性强、易保水、超仿生等特点的新型功能高分子材料。由于其合成过程中加入了具有特殊结构、基团的单体或者大分子原料,如聚丙烯酰胺(PNIPA)类大分子、酸/碱基团(如羧基和氨基)、丙烯酸、聚氨类、偶氮苯(As)、聚电解质(高分子链上有可以离子化的基团)等,因此智能水凝胶是能够根据环境的温度、酸度、电场、磁场等变化做出有规律的结构和体积调整,或者导致凝胶组成发生变化的新型智能生物化学水凝胶材料,具有较高的智能性和响应性。本文根据水凝胶对外界环境的刺激不同表现出不同的响应情况,将凝胶分为:温度敏感性水凝胶、pH敏感性水凝胶、光敏感性水凝胶、压力敏感性水凝胶、电场敏感性水凝胶等。近年来,随着人们对医用水凝胶和药物缓释研究的深入,具有环境敏感性和较好生物相容性的智能水凝胶成为临床上药物控释材料的首选。 相似文献
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介绍了伤口愈合的过程以及愈合过程中伤口处微环境的变化,叙述了目前根据伤口处不同环境变化(如pH、温度、活性氧含量和葡萄糖含量等)而设计的智能响应水凝胶,总结了可以应对2种及以上伤口微环境变化的双重或多重刺激响应性水凝胶的制备过程,以及水凝胶如何对伤口实现智能响应和精准治疗的应用,并讨论了今后应用于伤口愈合水凝胶的设计方向。认为目前的水凝胶多数用于浅表创伤的治疗,如何对深度损伤的慢性伤口实现加速愈合的效果是扩展水凝胶应用的关键;从材料角度出发,可以深度研究创面愈合机制,设计开发多重刺激响应水凝胶以满足不同类型的创面的需求,从而使水凝胶在伤口愈合方面有更广阔的应用前景。 相似文献
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刺激响应性水凝胶在药物缓释、物质分离提纯等领域得到了广泛的应用,文章介绍了能响应温度、pH、光、电场和磁场等外界环境因素变化智能凝胶的结构特点和近期研究进展,并展望了智能凝胶的应用前景。 相似文献
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Since the last few decades, the development of smart hydrogels, which can respond to stimuli and adapt their responses based on external cues from their environments, has become a thriving research frontier in the biomedical engineering field. Nowadays, drug delivery systems have received great attention and smart hydrogels can be potentially used in these systems due to their high stability, physicochemical properties, and biocompatibility. Smart hydrogels can change their hydrophilicity, swelling ability, physical properties, and molecules permeability, influenced by external stimuli such as pH, temperature, electrical and magnetic fields, light, and the biomolecules’ concentration, thus resulting in the controlled release of the loaded drugs. Herein, this review encompasses the latest investigations in the field of stimuli-responsive drug-loaded hydrogels and our contribution to this matter. 相似文献
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As emerging artificial biomimetic membranes, smart or intelligent membranes that are able to respond to environmental stimuli are attracting ever-increasing interests from various fields. Their permeation properties including hydraulic permeability and diffusional permeability can be dramatically controlled or adjusted self-regulatively in response to small chemical and/or physical stimuli in their environments. Such environmental stimuli-responsive smart membranes could find myriad applications in numerous fields ranging from controlled release to separations. Here the trans-membrane mass-transfer and membrane separation is introduced as the beginning to initiate the requirement of smart membranes, and then bio-inspired design of environmental stimuli-responsive smart membranes and four essential elements for smart membranes are introduced and discussed. Next, smart membrane types and their applications as smart tools for controllable mass-transfer in controlled release and separations are reviewed. The research topics in the near future are also suggested. 相似文献
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Fast advances in polymer science have provided new hydrogels for applications in drug delivery. Among modern drug formulations, polymeric type stimuli-responsive hydrogels (SRHs), also called smart hydrogels, deserve special attention as they revealed to be a promising tool useful for a variety of pharmaceutical and biomedical applications. In fact, the basic feature of these systems is the ability to change their mechanical properties, swelling ability, hydrophilicity, or bioactive molecules permeability, which are influenced by various stimuli, particularly enzymes. Indeed, among a great number of SHRs, enzyme-responsive hydrogels (ERHs) gain much interest as they possess several potential biomedical applications (e.g., in controlled release, drug delivery, etc.). Such a new type of SHRs directly respond to many different enzymes even under mild conditions. Therefore, they show either reversible or irreversible enzyme-induced changes both in chemical and physical properties. This article reviews the state-of-the art in ERHs designed for controlled drug delivery systems (DDSs). Principal enzymes used for biomedical hydrogel preparation were presented and different ERHs were further characterized focusing mainly on glucose oxidase-, β-galactosidase- and metalloproteinases-based catalyzed reactions. Additionally, strategies employed to produce ERHs were described. The current state of knowledge and the discussion were made on successful applications and prospects for further development of effective methods used to obtain ERH as DDSs. 相似文献
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Vinyl polymers are widely used in biological, textile and industrial applications and are currently attracting research attention for specialized bio-based applications. Polyvinyl alcohol (PVA) hydrogels show great advantages as a material with high biocompatibility, permeability, hydrophilicity, and low-friction coefficient, allowing applications as smart materials, wound dressings, and flexible sensors. However, the poor mechanical properties of PVA hydrogels and biocompatibility less than natural polymers make them unsuitable in practical applications. Additives are often added to PVA hydrogels to enhance mechanical properties, endow more compatibility, functionality and expand their application range. Among them, bio-additives such as nanocellulose, natural polysaccharides and proteins are biodegradable, biocompatible, and inexpensive, broadening their applications in the biomedical and tissue engineering fields. This work reviews the synthesis of PVA hydrogels, methods to enhance their mechanical properties, types of bio-additives incorporated for biocompatibility, their mechanism of interaction with PVA and future prospects of PVA composite bio-hydrogels for application in various fields. Representative cases are carefully selected and discussed with regard to their composition and pros and cons are discussed. Finally, future requirements, as well as the opportunities and challenges of these bio-additives for improving the multifunctionality of PVA hydrogels are also presented. 相似文献
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《Reactive and Functional Polymers》2007,67(11):1311-1329
We present a review of stimuli-responsive smart PEGylated nanogels and their biomedical applications. We describe the synthesis and characterization of stimuli-responsive PEGylated nanogels composed of a cross-linked poly[2-(N,N-diethylamino)ethyl methacrylate] (PDEAMA) core and PEG tethered chains that bear a carboxylic acid group as a platform moiety for the installation of bio-tags. In addition, PEGylated nanogels show unique properties and functions in synchronizing with the reversible volume phase transition of the PDEAMA core in response to various stimuli, such as pH, ionic strength and temperature. We list some of the biomedical applications of the nanogels, including endosomolytic agents for nonviral gene delivery, drug delivery carriers, nanoreactors, and skin-specific nanocatalysts for reactive oxygen species (ROS). 相似文献
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Lin-Bing Zou Jue-Ying Gong Xiao-Jie Ju Zhuang Liu Wei Wang Rui Xie Liang-Yin Chu 《中国化学工程学报》2022,49(9):34-45
Smart membranes with tunable permeability and selectivity have drawn widespread attention because of their unique biomimetic characteristics. Constructed by incorporating various stimuli-responsive materials into membrane substrates, smart membranes could self-adjust their physical/chemical properties(such as pore size and surface properties) in response to environmental signals such as temperature,pH, light, magnetic field, electric field, redox and specific ions/molecules. Such smart membranes... 相似文献
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Hydrogels capable of stimuli-responsive deformation are widely explored as intelligent actuators for diverse applications. It is still a significant challenge, however, to “program” these hydrogels to undergo highly specific and extensive shape changes with precision, because the mechanical properties and deformation mechanism of the hydrogels are inherently coupled. Herein, two engineering strategies are simultaneously employed to develop thermoresponsive poly(N-isopropyl acrylamide) (PNIPAm)-based hydrogels capable of programmable actuation. First, PNIPAm is copolymerized with poly(ethylene glycol) diacrylate (PEGDA) with varying molecular weights and concentrations. In addition, graphene oxide (GO) or reduced graphene oxide (rGO) is incorporated to generate nanocomposite hydrogels. These strategies combine to allow the refined control of mechanical and diffusional properties of hydrogels over a broad range, which also directly influences variable thermoresponsive actuation. It is expected that this comprehensive design principle can be applied to a wide range of hydrogels for programmable actuation. 相似文献