Добірка наукової літератури з теми "Hydrogelator"
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Статті в журналах з теми "Hydrogelator"
Li, Jiayang, Yi Kuang, Junfeng Shi, Yuan Gao, Jie Zhou, and Bing Xu. "The conjugation of nonsteroidal anti-inflammatory drugs (NSAID) to small peptides for generating multifunctional supramolecular nanofibers/hydrogels." Beilstein Journal of Organic Chemistry 9 (May 10, 2013): 908–17. http://dx.doi.org/10.3762/bjoc.9.104.
Повний текст джерелаShi, Junfeng, Yuan Gao, Zhimou Yang, and Bing Xu. "Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions." Beilstein Journal of Organic Chemistry 7 (February 7, 2011): 167–72. http://dx.doi.org/10.3762/bjoc.7.23.
Повний текст джерелаOhsedo, Yutaka, Kowichiro Saruhashi, Hisayuki Watanabe, and Nobuyoshi MIyamoto. "Synthesis of an electronically conductive hydrogel from a hydrogelator and a conducting polymer." New Journal of Chemistry 41, no. 18 (2017): 9602–6. http://dx.doi.org/10.1039/c7nj02412f.
Повний текст джерелаYang, Chengbiao, Zhongyan Wang, Caiwen Ou, Minsheng Chen, Ling Wang, and Zhimou Yang. "A supramolecular hydrogelator of curcumin." Chem. Commun. 50, no. 66 (2014): 9413–15. http://dx.doi.org/10.1039/c4cc03139c.
Повний текст джерелаPoolman, Jos M., Chandan Maity, Job Boekhoven, Lars van der Mee, Vincent A. A. le Sage, G. J. Mirjam Groenewold, Sander I. van Kasteren, Frank Versluis, Jan H. van Esch, and Rienk Eelkema. "A toolbox for controlling the properties and functionalisation of hydrazone-based supramolecular hydrogels." Journal of Materials Chemistry B 4, no. 5 (2016): 852–58. http://dx.doi.org/10.1039/c5tb01870f.
Повний текст джерелаGavara, Raquel, João Carlos Lima, and Laura Rodríguez. "Effect of solvent polarity on the spectroscopic properties of an alkynyl gold(i) gelator. The particular case of water." Photochemical & Photobiological Sciences 15, no. 5 (2016): 635–43. http://dx.doi.org/10.1039/c6pp00057f.
Повний текст джерелаOhsedo, Yutaka, Masashi Oono, Kowichiro Saruhashi, Hisayuki Watanabe, and Nobuyoshi Miyamoto. "A new composite thixotropic hydrogel composed of a low-molecular-weight hydrogelator and a nanosheet." RSC Adv. 4, no. 84 (2014): 44837–40. http://dx.doi.org/10.1039/c4ra08542f.
Повний текст джерелаMei, Bin, and Gao-lin Liang. "Paclitaxel Hydrogelator Delays Microtubule Aggregation." Chinese Journal of Chemical Physics 30, no. 2 (April 27, 2017): 239–42. http://dx.doi.org/10.1063/1674-0068/30/cjcp1609179.
Повний текст джерелаvan Herpt, Jochem T., Marc C. A. Stuart, Wesley R. Browne, and Ben L. Feringa. "A Dithienylethene-Based Rewritable Hydrogelator." Chemistry - A European Journal 20, no. 11 (February 13, 2014): 3077–83. http://dx.doi.org/10.1002/chem.201304064.
Повний текст джерелаGuo, Jiaqi, Hongjian He, Beom Jin Kim, Jiaqing Wang, Meihui Yi, Cheng Lin, and Bing Xu. "The ratio of hydrogelator to precursor controls the enzymatic hydrogelation of a branched peptide." Soft Matter 16, no. 44 (2020): 10101–5. http://dx.doi.org/10.1039/d0sm00867b.
Повний текст джерелаДисертації з теми "Hydrogelator"
St, Martin Michael J. "Synthesis and Characterization of Sugar Derivatives as Functional Gelators." ScholarWorks@UNO, 2012. http://scholarworks.uno.edu/td/1524.
Повний текст джерелаAwhida, Salmah. "Functionalised dipeptides as hydrogelators for energy transfer and as drug delivery vehicles." Thesis, University of Liverpool, 2015. http://livrepository.liverpool.ac.uk/2014048/.
Повний текст джерелаFleming, Scott. "Aromatic peptide amphiphiles : design rules for hydrogelaion and co-assembly." Thesis, University of Strathclyde, 2014. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=23213.
Повний текст джерелаFoster, Jamie S. "Relating the chemical reactivity of supramolecular hydrogelators and the physical properties of their gels." Thesis, Heriot-Watt University, 2017. http://hdl.handle.net/10399/3400.
Повний текст джерелаYücel, Tuna. "Early-time, beta-hairpin peptide self-assembly and hydrogelation structure, kinetics, and shear-recovery /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 136 p, 2009. http://proquest.umi.com/pqdweb?did=1654493371&sid=4&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Повний текст джерелаBastrop, Martin Verfasser], Karsten [Akademischer Betreuer] [Mäder, Alfred [Akademischer Betreuer] Blume, and Heike [Akademischer Betreuer] Bunjes. "Physico-chemical characterization of a novel class of bolaamphiphilic hydrogelators / Martin Bastrop. Betreuer: Karsten Mäder ; Alfred Blume ; Heike Bunjes." Halle, Saale : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2011. http://d-nb.info/1025135342/34.
Повний текст джерелаBouguéon, Guillaume. "Formulation de nanosystèmes biocompatibles pour l’ingénierie tissulaire par impression 3D (bioprinting)." Thesis, Bordeaux, 2020. http://www.theses.fr/2020BORD0006.
Повний текст джерела3D bioprinting is an emerging field of tissue engineering, that aims at faithfully reproducing the complex microarchitecture of tissues and organs. Despite a wide range of biomaterials used in bioink formulation, it is essential to find an alternative to the natural and synthetic biomaterials conventionally used, mimicking extracellular matrix and presenting printing capabilities jointly.The present work demonstrated for the first time, the ability of the bioinspired nucleolipid molecule diC16dT to formulate an extrusion bioprinting ink. The ink formulated in cell culture medium showed rheological properties allowing its continuous printability. It was also possible to incorporate gingival fibroblasts while maintaining the cell viability within bioconstructions. This ink also offered several adaptation possibilities, especially in terms of diC16dT concentration and cell culture medium to meet other cellular types requirements. Finally, the preliminary work showed the feasibility of the incorporation of liposomes into the ink formulation without affecting its printing capabilities. Thus, it would possible to further consider the delivery of active substances or nutrients within the bioconstructions. This application has to the best of our knowledge not been developed yet for liposomes
Li, Jyun-Ting, and 黎俊廷. "The Reversible pH-Stimulative Hydrogelators Based onGlycolipid without Possessing Conventional pH-ResponsiveMoieties." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/5scdvf.
Повний текст джерела中原大學
化學研究所
103
Two low molecular weight hydrogelators have been developed by us. These two hydrogelators are the glycolipids that consist of glucosamine, tethering the (2S,3S)-2,3-dihydroxydecanoyl acid and (2R,3R)-2,3- dihydroxy tetradecanoyl acid, respectively.(S10 and R14). Among these two compounds, S10 a reversible gelator exhibits the stimulus-responsive ability at pH 3.0-5.0. The asymmetric synthese of these two dihydroxyalkanoyl acids have been accomplished by using chiral-pool method strategy. Herein, D-ribose is used as the starting material to synthesize these two optically active dihydroxyalkanoyl acids that configurations are mirro image each other at the same time.
Nai-ShinFan and 范乃心. "Hydrogelation of Coil-Sheet Poly(L-Lysine)-block-Poly(L-Threonine) Block Copolypeptides." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/94h6wz.
Повний текст джерелаXuan-YouShen and 沈烜右. "Hydrogelation of Star-shaped Poly(L-lysine) Polypeptides Modified with Different Functional Groups." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/53373e.
Повний текст джерелаКниги з теми "Hydrogelator"
Furst, Eric M., and Todd M. Squires. Microrheology applications. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199655205.003.0010.
Повний текст джерелаЧастини книг з теми "Hydrogelator"
Peyrot, Cédric, Pierre Lafite, Loïc Lemiègre, and Richard Daniellou. "Low molecular weight carbohydrate-based hydrogelators." In Carbohydrate Chemistry, 245–65. Cambridge: Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781788010641-00245.
Повний текст джерелаKim, Mi Sook, Yoon Jeong Choi, Gun Woo Kim, In Sup Noh, Yong Doo Park, Kyu Back Lee, In Sook Kim, and Soon Jung Hwang. "Evaluation of Acid-Treated Hyaluronic Acid-Based Hydrogelation." In Advanced Biomaterials VII, 745–48. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-436-7.745.
Повний текст джерелаStuart, M. C. A., A. M. A. Brizard, E. J. Boekema, and J. H. van Esch. "Orthogonal self-assembly of surfactants and hydrogelators: towards new nanostructures." In EMC 2008 14th European Microscopy Congress 1–5 September 2008, Aachen, Germany, 791–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-85226-1_396.
Повний текст джерелаMarin, Luminita, Daniela Ailincai, Manuela Maria Iftime, Anda-Mihaela Craciun, Andrei Bejan, Mariana Pinteala, and Marc Jean M. Abadie. "Hydrogelation of Chitosan with Monoaldehydes Towards Biomaterials with Tuned Properties." In New Trends in Macromolecular and Supramolecular Chemistry for Biological Applications, 345–56. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-57456-7_17.
Повний текст джерелаMishra, Sunita, and M. A. Firdaus. "Formulation of Edible Bigel with Potential to Trans-Fat Replacement in Food Products." In Food Processing [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.110517.
Повний текст джерелаTakahashi, Masato, Takahiro Iseki, Hirotsugu Hattori, Tatsuko Hatakeyama, and Hyoe Hatakeyama. "STRUCTURAL CHANGE IN HYDROGELATION OF HYALURONAN INDUCED BY ANNEALING THE SOLUTION IN SOL STATE." In Hyaluronan, 205–8. Elsevier, 2002. http://dx.doi.org/10.1533/9781845693121.205.
Повний текст джерелаТези доповідей конференцій з теми "Hydrogelator"
Frkanec, Ruža, Karmen Radoševic, Adela Štimac, Lucija Horvat, and Leo Frkanec. "Development of new supramolecular nanostructuredmaterials based on peptide hydrogelator Ac-L-Phe-L-Phe-L-Ala-NH2 with embedded liposomes for potential biomedical application." In 35th European Peptide Symposium. Prompt Scientific Publishing, 2018. http://dx.doi.org/10.17952/35eps.2018.148.
Повний текст джерелаJohn, George, Jose James, Malick Samateh, Siddharth Marwaha, and Vikas Nanda. "Sucralose Hydrogels: Peering into the Reactivity of Sucralose versus Sucrose Using Lipase Catalyzed Trans-Esterification." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/xkza4963.
Повний текст джерелаAbioye, Raliat, Caleb Acquah, Chibuike Udenigwe, Nico Huttmann, and Pei Chun Queenie Hsu. "Self-assembly and hydrogelation properties of egg white-derived peptides." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jzku2300.
Повний текст джерелаYufeng, Tao, Xiong Wei, Wang Fan, Liu Jingwei, and Deng Chunsan. "Resolution Improvement of Two-photon Hydrogelation by Tuning Polarization and Laser Wavelength." In Laser Science and Technology. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/lst.2019.ltu2f.1.
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