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41.
Jindrich Kopecek 《Journal of polymer science. Part A, Polymer chemistry》2009,47(22):5929-5946
Hydrogels were the first biomaterials designed for clinical use. Their discovery and applications as soft contact lenses and implants are presented. This early hydrogel research served as a foundation for the expansion of biomedical polymers research into new directions: design of stimuli sensitive hydrogels that abruptly change their properties upon application of an external stimulus (pH, temperature, solvent, electrical field, biorecognition) and hydrogels as carriers for the delivery of drugs, peptides, and proteins. Finally, pathways to self‐assembly of block and graft copolymers into hydrogels of precise 3D structures are introduced. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5929–5946, 2009 相似文献
42.
Lixiang Zhang Zhengchao Yuan Muhammad Shafiq Youjun Cai Zewen Wang Piming Nie Xiumei Mo Yuan Xu 《Macromolecular bioscience》2023,23(4):2200500
Growth factors are essential for wound healing owing to their multiple reparative effects. Concentrated growth factor (CGF) is a third-generation platelet extract containing various endogenous growth factors. Herein, a CGF extract solution is combined with gelatin methacrylate (GM) by physical blending to produce GM@CGF hydrogels for wound repair. The GM@CGF hydrogels show no immune rejection during autologous transplantation. Compared to CGF, GM@CGF hydrogels not only exhibit excellent plasticity and adhesivity but also prevent rapid release and degradation of growth factors. The GM@CGF hydrogels display good injectability, self-healing, swelling, and degradability along with outstanding cytocompatibility, angiogenic functions, chemotactic functions, and cell migration-promoting capabilities in vitro. The GM@CGF hydrogel can release various effective molecules to rapidly initiate wound repair, stimulate the expressions of type I collagen, transform growth factor β1, epidermal growth factor, and vascular endothelial growth factor, promote the production of granulation tissues, vascular regeneration and reconstruction, collagen deposition, and epidermal cell migration, as well as prevent excessive scar formation. In conclusion, the injectable GM@CGF hydrogel can release various growth factors and provide a 3D spatial structure to accelerate wound repair, thereby providing a foundation for the clinical application and translation of CGF. 相似文献
43.
Summary: An in‐situ mineralization process in the presence of thermo‐responsive microgels leads to the formation of well‐defined hybrid materials. Experimental data suggest that control of the mineralization process in the presence of the microgels offers the possibility to obtain sub‐micrometer‐sized hybrid particles or macroscopic hybrid hydrogels. The rapid formation of CaCO3 crystals in the microgel structure favors the preparation of the hybrid particles wherein inorganic crystals cover the shell layer of the microgel. The slow formation of CaCO3 crystals leads to the simultaneous self‐assembly of the microgel particles on the bottom of the reaction vessel, and the formation of a physical network. It has been demonstrated that hybrid hydrogel materials with different calcium carbonate contents and temperature‐dependent swelling‐deswelling properties can be prepared.
44.
Dr. Hyewon Lee Rathi L. Srinivas Ankur Gupta Prof. Patrick S. Doyle 《Angewandte Chemie (International ed. in English)》2015,54(8):2477-2481
Although microRNAs (miRNAs) have been shown to be excellent indicators of disease state, current profiling platforms are insufficient for clinical translation. Here, we demonstrate a versatile hydrogel‐based microfluidic approach and novel amplification scheme for entirely on‐chip, sensitive, and highly specific miRNA detection without the risk of sequence bias. A simulation‐driven approach is used to engineer the hydrogel geometry and the gel‐reaction environment is chemically optimized for robust detection performance. The assay provides 22.6 fM sensitivity over a three log range, demonstrates multiplexing across at least four targets, and requires just 10.3 ng of total RNA input in a 2 hour and 15 minutes assay. 相似文献
45.
46.
D. Gómez-Vázquez L. R. Cajero-Zul J. A. Torres-Ávalos K. Sandoval-García J. A. Cortés-Ortega F. A. López-Dellamary 《高分子科学杂志,A辑:纯化学与应用化学》2019,56(5):417-428
Carbon nanotubes (CNTs) chemically functionalized were used to synthesize a series of novel nanocomposite hydrogels by in situ polymerization with acrylic acid (AA) and acrylamide (AM). A novel strategy was developed to prepare these hydrogels. CNTs were functionalized following a three-step chemical procedure: (i) purified carbon nanotubes (CNTsp) were partially surface oxidized to obtain CNTs with hydroxyl, carbonyl and carboxyl groups on their sidewalls (CNTsoxi), (ii) CNTsoxi were reacted with oxalyl chloride to obtain CNTs functionalized with acyl chloride groups (CNTsOCl), and (iii) CNTsOCl were reacted with acrylic acid (AA). The product, AA modified CNTsOCl (CNTsOCl-AA) was used to prepare the (CNTsOCl-AA-AM) nanocomposite hydrogels, where anhydride groups were tethered to the surface of the CNTsOCl-AA. The swelling process in water was evaluated as a consequence of the anhydride group hydrolysis, which broke some chemical links between CNTsOCl-AA and crosslinked AA-AM network. Equilibrium-swelling values of all hydrogels increased as the content of AA increased and were larger for AA-AM hydrogels than for CNTsOCl-AA-AM nanocomposite hydrogels. Young’s moduli of CNTsOCl-AA-AM nanocomposite hydrogels prepared with 1 or 2?wt.% AA, reached larger values than those measured for AA-AM hydrogels. This tendency was reversed when the AA content was raised to 3?wt.%. 相似文献
47.
Simple preparation of stimuli-responsive hydrogels with good mechanical properties and mild stimuliresponsiveness is essential for their applications as smart soft robots.Mechanically strong Janus poly(Nisopropylacrylamide)/graphene oxide (PNIPAM/GO) nanocomposite hydrogels with stimuli-responsive bending behaviors are prepared through a simple one-step method by using molds made of a Teflon plate and a glass plate.Residual oxygen in the air bubbles on the Teflon plate surface affects the polymerization and hence the cross-linking density,leading to the different swelling/deswelling rates of the two sides of the gels.Therefore,the hydrogels exhibit bending/unbending behaviors upon heating/cooling in water.The incorporation of GO nanosheets dramatically enhances the mechanical properties of Janus hydrogels.Meanwhile,the photo-responsive property of the GO nanosheets also imparts the hydrogels with remotecontrollable deformation under IR irradiation.The application of the Janus PNIPAM/GO hydrogels as thermo-responsive grippers is demonstrated. 相似文献
48.
环境敏感水凝胶的研究进展 总被引:6,自引:0,他引:6
综述了环境敏感水凝胶在制备、功能性及其应用方面的研究进展 ,尤其是温敏水凝胶、pH敏感水凝胶和盐敏水凝胶的研究状况 ,也对光敏和生物分子敏感水凝胶进行了简单评述 相似文献
49.
M. Iijima T. Hatakeyama M. Takahashi H. Hatakeyama 《Journal of Thermal Analysis and Calorimetry》2001,64(2):617-627
Application of thermomechanometry to the measurement of hydrogels containing a large amount of water was carried out by static
and dynamic methods. A thermomechanical analyzer (TMA) equipped with a quartz compression probe immersed in water was used.
Polysaccharide hydrogels containing ca 98% water were measured. Creep of hydrogels in water was analyzed in a stress range
from 1.04⋅103 to 5.2⋅103 Pa and loading rate from 0.3⋅103 to 3.0⋅103 Pa min−1.Stress relaxation was measured in compressed ratio range from 0.02 to 0.45 m m−1 and in compressing rate was 0.09 to 0.15 m m−1 min−1. Dynamic viscoelasticity was measured by TMA when dynamic Young’s modulus which was larger than 1⋅104 Pa in frequencies ranging from 0.02~0.2 Hz.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
50.
Hai Xin Farshad Oveissi Sina Naficy Geoffrey M. Spinks 《Journal of polymer science. Part A, Polymer chemistry》2018,56(19):1287-1293
Hydrogen bonds are known to play an important role in prescribing the mechanical performance of certain hydrogels such as polyether-based polyurethanes. The quantitative contribution of hydrogen bonds to the toughness of polymer networks, however, has not been elucidated to date. Here, a new physical model is developed to predict the threshold fracture energies of hydrogels physically crosslinked via hydrogen bonds. The model is based on consecutive and sequential dissociation of hydrogen-bonded crosslinks during crack propagation. It is proposed that the scission of hydrogen bonds during crack propagation allows polymer strands in the deformation zone to partially relax and release stored elastic energy. The summation of these partial chain relaxations leads to amplified threshold fracture energies which are 10–45 times larger than those predicted by the classical Lake–Thomas theory. Experiments were performed on a hydrophilic polyurethane hydrogel where urea additions were used to control the density of hydrogen bonds. The measured fracture energies were in good agreement with the calculated values. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 1287–1293 相似文献