Pure and Applied Chemistry

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• Kim Sol, Lee Dong Jin, Kwag Dong Sup, Lee Ung Yeol, Youn Yu Seok, Lee Eun Seong: Acid pH-activated glycol chitosan/fullerene nanogels for efficient tumor therapy. Carbohydrate Polymers 2014, 101, 692. <http://dx.doi.org/10.1016/j.carbpol.2013.09.108>
• Hurtgen Marie, Debuigne Antoine, Hoebeke Maryse, Passirani Catherine, Lautram Nolwenn, Mouithys-Mickalad Ange, Guelluy Pierre-Henri, Jérôme Christine, Detrembleur Christophe: Photochemical Properties and Activity of Water-Soluble Polymer/C60 Nanohybrids for Photodynamic Therapy. Macromol. Biosci. 2013, 13, 106. <http://dx.doi.org/10.1002/mabi.201200251>
• Ikeda Atsushi: Water-soluble fullerenes using solubilizing agents, and their applications. J Incl Phenom Macrocycl Chem 2013, 77, 49. <http://dx.doi.org/10.1007/s10847-013-0319-9>
• Pérez-Manríquez Liliana, Ramos Estrella, Rangel Eduardo, Salcedo Roberto: Interaction between epoxidised estradiol and fullerene (C60): possible anticancer activity. Molecular Simulation 2013, 39, 612. <http://dx.doi.org/10.1080/08927022.2012.758845>
• Lebedev V. T., Kul’velis Yu. V., Orlova D. N., Melenevskaya E. Yu., Nasonova K. V., Vinogradova L. V.: Structure formation of fullerene-containing propylene oxide oligomers in deuterium water. Russ J Appl Chem 2013, 86, 568. <http://dx.doi.org/10.1134/S1070427213040204>
• Ikeda Atsushi, Mori Miyuki, Kiguchi Kazuya, Yasuhara Kazuma, Kikuchi Jun-ichi, Nobusawa Kazuyuki, Akiyama Motofusa, Hashizume Mineo, Ogawa Takuya, Takeya Tatsuo: Advantages and Potential of Lipid-Membrane-Incorporating Fullerenes Prepared by the Fullerene-Exchange Method. Chem —Asian J 2012, 7, 605. <http://dx.doi.org/10.1002/asia.201100792>
• Kwag Dong Sup, Oh Nam Muk, Oh Young Taik, Oh Kyung Taek, Youn Yu Seok, Lee Eun Seong: Photodynamic therapy using glycol chitosan grafted fullerenes. International Journal of Pharmaceutics 2012, 431, 204. <http://dx.doi.org/10.1016/j.ijpharm.2012.04.038>
• Yusa Shin-Ichi, Awa Shigeki, Ito Masanori, Kawase Takeshi, Takada Tadao, Nakashima Kenichi, Liu Dian, Yamago Shigeru, Morishima Yotaro: Solubilization of C60 by micellization with a thermoresponsive block copolymer in water: Characterization, singlet oxygen generation, and DNA photocleavage. J Polym Sci A Polym Chem 2011, 49, 2761. <http://dx.doi.org/10.1002/pola.24709>
• Xu Yingying, Zhu Jiadan, Xiang Kun, Li Yuankai, Sun Ronghua, Ma Jie, Sun Hongfang, Liu Yuanfang: Synthesis and immunomodulatory activity of [60]fullerene–tuftsin conjugates. Biomaterials 2000 2011, 32, 9940. <http://dx.doi.org/10.1016/j.biomaterials.2011.09.022>
• Santos Leandro J., Gonçalves Ana S.P., Krambrock Klaus, Pinheiro Maurício V.B., Eberlin Marcos N., Vaz Boniek G., de Freitas Rossimiriam P., Alves Rosemeire B.: Synthesis of [60]fullerene derivatives bearing five-membered heterocyclic wings and an investigation of their photophysical kinetic properties. J Photochem Photobiol A Chem 2011, 217, 184. <http://dx.doi.org/10.1016/j.jphotochem.2010.10.007>
• Yano Shigenobu, Hirohara Shiho, Obata Makoto, Hagiya Yuichiro, Ogura Shun-ichiro, Ikeda Atsushi, Kataoka Hiromi, Tanaka Mamoru, Joh Takashi: Current states and future views in photodynamic therapy. PHOTOBIO C 2011, 12, 46. <http://dx.doi.org/10.1016/j.jphotochemrev.2011.06.001>
• Kawai Yoshihiko, Kikuchi Jun-ichi, Akiyama Motofusa, Ikeda Atsushi, Nakata Eiji, Uto Yoshihiro, Hori Hitoshi: Formation and regulation of fullerene-incorporation in liposomes under the phase transition temperature. Org Biomol Chem 2011, 9, 2622. <http://dx.doi.org/10.1039/c0ob01030h>
• Vehviläinen T. T., Ganchenkova M. G., Nieminen R. M.: Nanoporous carbon structures based on C_{20}. Phys. Rev. B 2011, 84. <http://dx.doi.org/10.1103/PhysRevB.84.125444>
• Li XiaoHui, Zhang Cheng, Guyader Laurent, Chen ChunYing: “Smart” nanomaterials for cancer therapy. Sci China Chem 2010, 53, 2241. <http://dx.doi.org/10.1007/s11426-010-4122-9>
• Ikeda Atsushi, Kawai Yoshihiko, Kikuchi Jun-ichi, Akiyama Motofusa: Effect of phase transition temperature of liposomes on preparation of fullerene-encapsulated liposomes by the fullerene-exchange reaction. Chem Commun 2010, 46, 2847. <http://dx.doi.org/10.1039/b926949e>
• Kwok Kui S., Chan Yik C., Ng Ka M., Wibowo Christianto: Separation of fullerenes C60 and C70 using a crystallization-based process. AIChE 2009, 56, 1801. <http://dx.doi.org/10.1002/aic.12105>
• Coro Julieta, Rodríguez Hortensia, Rivera Daniel G., Suárez Margarita, Molero Dolores, Herranz María Ángeles, Martínez-Álvarez Roberto, Filippone Salvatore, Martín Nazario: Functional Chimeras: New Bingel–Hirsch-Type Steroid–Fullerene Hybrids. Eur J Org Chem 2009, 2009, 4810. <http://dx.doi.org/10.1002/ejoc.200900583>
• Zhang ZhiYong, Zhao YuLiang, Chai ZhiFang: Applications of radiotracer techniques for the pharmacology and toxicology studies of nanomaterials. Chinese Sci Bull 2009, 54, 173. <http://dx.doi.org/10.1007/s11434-009-0016-7>
• Liu Ying, Jiao Fang, Qiu Yang, Li Wei, Lao Fang, Zhou Guoqiang, Sun Baoyun, Xing Genmei, Dong Jinquan, Zhao Yuliang: The effect of Gd@C82(OH)22 nanoparticles on the release of Th1/Th2 cytokines and induction of TNF-α mediated cellular immunity. Biomater 2009, 30, 3934. <http://dx.doi.org/10.1016/j.biomaterials.2009.04.001>
• Piotrovskii L. B.: Fullerenes in the drug design. Nanotechnol Russia 2009, 4, 541. <http://dx.doi.org/10.1134/S1995078009090018>
• Doi Yuki, Ikeda Atsushi, Akiyama Motofusa, Nagano Mai, Shigematsu Tamami, Ogawa Takuya, Takeya Tatsuo, Nagasaki Takeshi: Intracellular Uptake and Photodynamic Activity of Water-Soluble [60]- and [70]Fullerenes Incorporated in Liposomes. Chem Eur J 2008, 14, 8892. <http://dx.doi.org/10.1002/chem.200801090>
• Zhu Jiadan, Ji Zhiqiang, Wang Jing, Sun Ronghua, Zhang Xiang, Gao Yang, Sun Hongfang, Liu Yuanfang, Wang Zheng, Li Aidong: Tumor-Inhibitory Effect and Immunomodulatory Activity of Fullerol C₆₀(OH)_x. Small 2008, 4, 1168. <http://dx.doi.org/10.1002/smll.200701219>
• Amirshahi Nima, Alyautdin Renad N., Sarkar Saeed, Rezayat Seyed M., Orlova Marina A., Trushkov Igor V., Buchachenko Anatoly L., Kuznetsov Dmitry A.: Fullerene-based Low Toxic Nanocationite Particles (Porphyrin Adducts of Cyclohexyl Fullerene-C60) to Treat Hypoxia-induced Mitochondrial Dysfunction in Mammalian Heart Muscle. Arch Med Res 2008, 39, 549. <http://dx.doi.org/10.1016/j.arcmed.2008.05.007>
• Akiyama Motofusa, Ikeda Atsushi, Shintani Takashi, Doi Yuki, Kikuchi Jun-ichi, Ogawa Takuya, Yogo Keiichiro, Takeya Tatsuo, Yamamoto Naoyuki: Solubilisation of [60]fullerenes using block copolymers and evaluation of their photodynamic activities. Org Biomol Chem 2008, 6, 1015. <http://dx.doi.org/10.1039/b719671g>
• Ganchenkova M., Vehviläinen T., Nieminen R.: Quasigraphite: Density functional theory based predictions of a structure and its properties. Phys Rev B 2008, 78, 195421. <http://dx.doi.org/10.1103/PhysRevB.78.195421>
• Amirshahi N., Alyautdin R. N., Sarkar S., Rezayat S. M., Orlova M. A., Trushkov I. V., Buchachenko A. L., Kuznetsov D. A.: Porphyrin-fullerene nanoparticles for treatment of hypoxic cardiopathies. Nanotechnol Russia 2008, 3, 611. <http://dx.doi.org/10.1134/S1995078008090115>
• AMIRSHAHI NIMA, ALYAUTDIN RENAD N., SARKAR SAEED, REZAYAT SEYED M., ORLOVA MARINA A., TRUSHKOV IGOR V., BUCHACHENKO ANATOLY L., KUZNETSOV DMITRY A.: NEW PORPHYRIN ADDUCT OF FULLERENE-C60: A PROMISING NANOTOOL FOR MEDICINAL USE IN THE HEART MUSCLE HYPOXIA CASES. Int. J. Nanosci. 2008, 07, 113. <http://dx.doi.org/10.1142/S0219581X08005286>
• Stoilova Olya, Jérôme Christine, Detrembleur Christophe, Mouithys-Mickalad Ange, Manolova Nevena, Rashkov Iliya, Jérôme Robert: C60-containing nanostructured polymeric materials with potential biomedical applications. Polymer 2007, 48, 1835. <http://dx.doi.org/10.1016/j.polymer.2007.02.026>
• Gubskaya Valentina P., Berezhnaya Lucia Sh., Gubaidullin Aidar T., Faingold Irina I., Kotelnikova Raisa A., Konovalova Nina P., Morozov Vladimir I., Litvinov Igor A., Nuretdinov Ildus A.: Synthesis, structure and biological activity of nitroxide malonate methanofullerenes. Org Biomol Chem 2007, 5, 976. <http://dx.doi.org/10.1039/b617892h>
• Ikeda Atsushi, Doi Yuki, Nishiguchi Koji, Kitamura Keiko, Hashizume Mineo, Kikuchi Jun-ichi, Yogo Keiichiro, Ogawa Takuya, Takeya Tatsuo: Induction of cell death by photodynamic therapy with water-soluble lipid-membrane-incorporated [60]fullerene. Org Biomol Chem 2007, 5, 1158. <http://dx.doi.org/10.1039/b701767g>
• Prylutska S. V., Matyshevska O. P., Grynyuk I. I., Prylutskyy Yu. I., Ritter U., Scharff P.: Biological Effects of C₆₀ Fullerenes in vitro and in a Model System. Mol Cryst Liq Cryst 2007, 468, 265/[617]. <http://dx.doi.org/10.1080/15421400701230105>
• Milanesio M. Elisa, Alvarez M. Gabriela, Rivarola Viviana, Silber Juana J., Durantini Edgardo N.: Porphyrin-fullerene C60 Dyads with High Ability to Form Photoinduced Charge-separated State as Novel Sensitizers for Photodynamic Therapy¶. Photchem Photbio 2007, 81, 891. <http://dx.doi.org/10.1111/j.1751-1097.2005.tb01459.x>
• Tabata Hiroshi, Akamatsu Masaaki, Fujii Minoru, Hayashi Shinji: Formation of C₆₀ Colloidal Particles Suspended in Poor Solvent by Pulsed Laser Irradiation . Jpn J Appl Phys 2007, 46, 4338. <http://dx.doi.org/10.1143/JJAP.46.4338>
• Jiang Guichang, Zheng Qixing, Yang Dazhi: Synthesis of a water-soluble fullerene derivative nanoball and its biological activity. J Appl Polym Sci 2006, 99, 2874. <http://dx.doi.org/10.1002/app.22837>
• Detrembleur Christophe, Stoilova Olya, Bryaskova Rayna, Debuigne Antoine, Mouithys-Mickalad Ange, Jérôme Robert: Preparation of Well-Defined PVOH/C60 Nanohybrids by Cobalt-Mediated Radical Polymerization of Vinyl Acetate. Macromol Rapid Commun 2006, 27, 498. <http://dx.doi.org/10.1002/marc.200500871>
• Ji Zhi Qiang, Sun Hongfang, Wang Haifang, Xie Qunying, Liu Yuangfang, Wang Zheng: Biodistribution and tumor uptake of C60(OH) x in mice. J Nanopart Res 2006, 8, 53. <http://dx.doi.org/10.1007/s11051-005-9001-5>
• Alvarez M. Gabriela, Prucca César, Milanesio M. Elisa, Durantini Edgardo N., Rivarola Viviana: Photodynamic activity of a new sensitizer derived from porphyrin-C60 dyad and its biological consequences in a human carcinoma cell line. Int J Biochem Cell Biol 2006, 38, 2092. <http://dx.doi.org/10.1016/j.biocel.2006.05.019>
• Rouse Jillian G., Yang Jianzhong, Barron Andrew R., Monteiro-Riviere Nancy A.: Fullerene-based amino acid nanoparticle interactions with human epidermal keratinocytes. toxicol vitro 2006, 20, 1313. <http://dx.doi.org/10.1016/j.tiv.2006.04.004>
• Koeppe R., Sariciftci N. S.: Photoinduced charge and energy transfer involving fullerene derivatives. Photochem Photobiol Sci 2006, 5, 1122. <http://dx.doi.org/10.1039/b612933c>
• Enes Roger F., Tomé Augusto C., Cavaleiro José A.S., El-Agamey Ali, McGarvey David J.: Synthesis and solvent dependence of the photophysical properties of [60]fullerene–sugar conjugates. Tetrahedron 2005, 61, 11873. <http://dx.doi.org/10.1016/j.tet.2005.09.078>
• Ikeda Atsushi, Sato Tomohiko, Kitamura Keiko, Nishiguchi Koji, Sasaki Yoshihiro, Kikuchi Jun-ichi, Ogawa Takuya, Yogo Keiichiro, Takeya Tatsuo: Efficient photocleavage of DNA utilising water-soluble lipid membrane-incorporated [60]fullerenes prepared using a [60]fullerene exchange method. Org Biomol Chem 2005, 3, 2907. <http://dx.doi.org/10.1039/b507954c>
• Ikeda Atsushi, Ejima Akinori, Nishiguchi Koji, Kikuchi Jun-ichi, Matsumoto Takahiro, Hatano Tsukasa, Shinkai Seiji, Goto Masahiro: DNA-photocleaving Activities of Water-soluble Carbohydrate-containing Nonionic Homooxacalix[3]arene·[60]fullerene Complex. Chem Lett 2005, 34, 308. <http://dx.doi.org/10.1246/cl.2005.308>
• Milanesio M. Elisa, Alvarez M. Gabriela, Rivarola Viviana, Silber Juana J., Durantini Edgardo N.: Porphyrin-fullerene C60 Dyads with High Ability to Form Photoinduced Charge-separated State as Novel Sensitizers for Photodynamic Therapy¶. Photchem Photbio 2005, 81, 891. <http://dx.doi.org/10.1562/2005-01-24-RA-426R.1>
• Song T., Goh S.H., Lee S.Y.: Mechanical behavior of double-C60-end-capped poly(ethylene oxide). Polymer 2003, 44, 2563. <http://dx.doi.org/10.1016/S0032-3861(03)00102-2>
• de la Torre Maria D.L, Marcorin Gian L, Pirri Giovanna, Tomé Augusto C, Silva Artur M.S, Cavaleiro José A.S: Synthesis of novel [60]fullerene–flavonoid dyads. Tetrahetron Lett 2002, 43, 1689. <http://dx.doi.org/10.1016/S0040-4039(02)00122-3>
• Wharton Tim, Kini Vinay U, Mortis Rachel A, Wilson Lon J: New non-ionic, highly water-soluble derivatives of C60 designed for biological compatibility. Tetrahetron Lett 2001, 42, 5159. <http://dx.doi.org/10.1016/S0040-4039(01)00956-X>