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Artículos de revistas sobre el tema "Polydepsipeptides"

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Publicado: 4 de mayo de 2024

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1

Feng, Yakai y Jintang Guo. "Biodegradable Polydepsipeptides". International Journal of Molecular Sciences 10, n.º 2 (13 de febrero de 2009): 589–615. http://dx.doi.org/10.3390/ijms10020589.

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2

MAMMI, STEFANO y MURRAY GOODMAN. "Polydepsipeptides. 13". International Journal of Peptide and Protein Research 28, n.º 1 (12 de enero de 2009): 29–44. http://dx.doi.org/10.1111/j.1399-3011.1986.tb03227.x.

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3

Dijkstra, Pieter J. y Jan Feijen. "Synthetic pathways to polydepsipeptides". Macromolecular Symposia 153, n.º 1 (marzo de 2000): 67–76. http://dx.doi.org/10.1002/1521-3900(200003)153:1<67::aid-masy67>3.0.co;2-f.

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4

Becktel, W. J., G. Wouters, D. M. Simmons y Murray Goodman. "Polydepsipeptides. 11. Conformational analysis of polydepsipeptides containing methyl, isopropyl, and isobutyl side chains". Macromolecules 18, n.º 4 (julio de 1985): 630–34. http://dx.doi.org/10.1021/ma00146a009.

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5

Dijkstra, Pieter J. y Jan Feijen. "ChemInform Abstract: Synthetic Pathways to Polydepsipeptides". ChemInform 31, n.º 47 (21 de noviembre de 2000): no. http://dx.doi.org/10.1002/chin.200047264.

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6

Mammi, Stefano y Murray Goodman. "Polydepsipeptides. A systematic investigation of guest-host effects". Journal of Peptide Science 11, n.º 5 (2005): 273–77. http://dx.doi.org/10.1002/psc.665.

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7

Ohya, Yuichi, Hidetoshi Yamamoto, Koji Nagahama y Tatsuro Ouchi. "Effects of polydepsipeptide side-chain groups on the temperature sensitivity of triblock copolymers composed of polydepsipeptides and poly(ethylene glycol)". Journal of Polymer Science Part A: Polymer Chemistry 47, n.º 15 (12 de junio de 2009): 3892–903. http://dx.doi.org/10.1002/pola.23456.

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8

Yoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa, Kyoichi Imai y Hidetoshi Yamanaka. "Sequential polydepsipeptides as biodegradable carriers for drug delivery systems". Journal of Biomedical Materials Research 24, n.º 9 (septiembre de 1990): 1173–84. http://dx.doi.org/10.1002/jbm.820240904.

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9

Ouchi, Tasuro, Tatsuya Nozaki, Yoshifumi Okamoto, Masahiro Shiratani y Yuichi Ohya. "Synthesis and enzymatic hydrolysis of polydepsipeptides with functionalized pendant groups". Macromolecular Chemistry and Physics 197, n.º 6 (junio de 1996): 1823–33. http://dx.doi.org/10.1002/macp.1996.021970604.

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10

Yoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa y Hidetoshi Yamanaka. "Sequential polydepsipeptides containing tripeptide sequences and α-hydroxy acids as biodegradable carriers". European Polymer Journal 27, n.º 3 (enero de 1991): 325–29. http://dx.doi.org/10.1016/0014-3057(91)90113-3.

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11

Katakai, Ryoichi, Kyoko Kobayashi, Keiichi Yamada, Hiroyuki Oku y Nobu Emori. "Synthesis of sequential polydepsipeptides utilizing a new approach for the synthesis of depsipeptides". Biopolymers 73, n.º 6 (2004): 641–44. http://dx.doi.org/10.1002/bip.20013.

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12

Franz, Nadja y Harm-Anton Klok. "Synthesis of Functional Polydepsipeptides via Direct Ring-Opening Polymerization and Post-Polymerization Modification". Macromolecular Chemistry and Physics 211, n.º 7 (1 de febrero de 2010): 809–20. http://dx.doi.org/10.1002/macp.200900521.

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13

Makino, Akira, Eri Hara, Isao Hara, Ryo Yamahara, Kensuke Kurihara, Eiichi Ozeki, Fumihiko Yamamoto y Shunsaku Kimura. "Control of in vivo blood clearance time of polymeric micelle by stereochemistry of amphiphilic polydepsipeptides". Journal of Controlled Release 161, n.º 3 (agosto de 2012): 821–25. http://dx.doi.org/10.1016/j.jconrel.2012.05.006.

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14

John, George y Mikio Morita. "Biodegradable cross-linked microspheres from poly- (ε-caprolactone-co-glycolic acid-co-L-serine) based polydepsipeptides". Macromolecular Rapid Communications 20, n.º 5 (1 de mayo de 1999): 265–68. http://dx.doi.org/10.1002/(sici)1521-3927(19990501)20:5<265::aid-marc265>3.0.co;2-j.

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15

Zavradashvili, Nino, Jordi Puiggali y Ramaz Katsarava. "Artificial Polymers made of α-amino Acids - Poly(Amino Acid)s, Pseudo-Poly(Amino Acid)s, Poly(Depsipeptide)s, and Pseudo-Proteins". Current Pharmaceutical Design 26, n.º 5 (20 de marzo de 2020): 566–93. http://dx.doi.org/10.2174/1381612826666200203122110.

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Degradable polymers (DPs) - “green materials” of the future, have an innumerable use in biomedicine, particularly in the fields of tissue engineering and drug delivery. Among these kind of materials naturally occurring polymers - proteins which constituted one of the most important “bricks of life” - α-amino acids (AAs) are highly suitable. A wide biomedical applicability of proteins is due to special properties such as a high affinity with tissues and releasing AAs upon biodegradation that means a nutritive potential for cells. Along with these positive characteristics proteins as biomedical materials they have some shortcomings, such as batch-to-batch variation, risk of disease transmission, and immune rejection. The last limitation is connected with the molecular architecture of proteins. Furthermore, the content of only peptide bonds in protein molecules significantly restricts their material properties. Artificial polymers with the composition of AAs are by far more promising as degradable biomaterials since they are free from the limitations of proteins retaining at the same time their positive features - a high tissue compatibility and nutritive potential. The present review deals with a brief description of different families of AA-based artificial polymers, such as poly(amino acid)s, pseudo-poly(amino acid)s, polydepsipeptides, and pseudo-proteins - relatively new and broad family of artificial AA-based DPs. Most of these polymers have a different macromolecular architecture than proteins and contain various types of chemical links along with NH-CO bonds that substantially expands properties of materials destined for sophisticated biomedical applications.
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16

Ochkhikidze, Natia, Giorgi Titvinidze, Marekhi Gverdtsiteli, Giuli Otinashvili, David Tugushi y Ramaz Katsarava. "Synthesis of AABB-polydepsipeptides, poly(ester amide)s and functional polymers on the basis of O,O′-diacyl-bis-glycolic acids". Journal of Macromolecular Science, Part A 57, n.º 12 (17 de agosto de 2020): 854–64. http://dx.doi.org/10.1080/10601325.2020.1800411.

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17

Samyn, Celest y Marcel van Beylen. "Polydepsipeptides: Ring-opening polymerization of 3-Methyl-2, 5-Morpholinedione, 3,6-Dimethyl-2,5-morpholinedione and copolymerization thereof with D, L-Lactide". Makromolekulare Chemie. Macromolecular Symposia 19, n.º 1 (junio de 1988): 225–34. http://dx.doi.org/10.1002/masy.19880190119.

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18

Ohya, Yuichi, Megumi Toyohara, Mitsuhiro Sasakawa, Hidetoshi Arimura y Tatsuro Ouchi. "Thermosensitive Biodegradable Polydepsipeptide". Macromolecular Bioscience 5, n.º 4 (19 de abril de 2005): 273–76. http://dx.doi.org/10.1002/mabi.200400221.

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19

Ouchi, Tatsuro, Hidenori Seike, Tatsuya Nozaki y Yuichi Ohya. "Synthesis and characteristics of polydepsipeptide with pendant thiol groups". Journal of Polymer Science Part A: Polymer Chemistry 36, n.º 8 (junio de 1998): 1283–90. http://dx.doi.org/10.1002/(sici)1099-0518(199806)36:8<1283::aid-pola11>3.0.co;2-2.

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20

Wang, Weiwei, Toufik Naolou, Nan Ma, Zijun Deng, Xun Xu, Ulrich Mansfeld, Christian Wischke, Manfred Gossen, Axel T. Neffe y Andreas Lendlein. "Polydepsipeptide Block-Stabilized Polyplexes for Efficient Transfection of Primary Human Cells". Biomacromolecules 18, n.º 11 (20 de octubre de 2017): 3819–33. http://dx.doi.org/10.1021/acs.biomac.7b01034.

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21

Yoshida, M., M. Asano, M. Kumakura, R. Katakai, T. Mashimo, H. Yuasa, K. Imai y H. Yamanaka. "A new biodegradable polydepsipeptide microsphere for application in drug delivery systems". Colloid & Polymer Science 268, n.º 8 (agosto de 1990): 726–30. http://dx.doi.org/10.1007/bf01411103.

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22

MASHIMO, TOORU, HISAKO YUASA, KYOICHI IMAI, HIDETOSHI YAMANAKA, MASAHARU ASANO, MASARU YOSHIDA, ISAO KAETSU, KEIZI SUZUKI y RYOICHI KATAKAI. "NECROSIS OF THE RAT KIDNEY TISSUE CAUSED BY A POLYDEPSIPEPTIDE FORMULATION CONTAINING CIS-PLATINUM". KITAKANTO Medical Journal 38, n.º 3 (1988): 149–55. http://dx.doi.org/10.2974/kmj1951.38.149.

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23

Battig, Alexander, Bernhard Hiebl, Yakai Feng, Andreas Lendlein y Marc Behl. "Biological evaluation of degradable, stimuli-sensitive multiblock copolymers having polydepsipeptide- and poly(ε-caprolactone) segments in vitro". Clinical Hemorheology and Microcirculation 48, n.º 1-3 (2011): 161–72. http://dx.doi.org/10.3233/ch-2011-1391.

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24

Makino, Akira, Shinae Kizaka-Kondoh, Ryo Yamahara, Isao Hara, Tatsuya Kanzaki, Eiichi Ozeki, Masahiro Hiraoka y Shunsaku Kimura. "Near-infrared fluorescence tumor imaging using nanocarrier composed of poly(l-lactic acid)-block-poly(sarcosine) amphiphilic polydepsipeptide". Biomaterials 30, n.º 28 (octubre de 2009): 5156–60. http://dx.doi.org/10.1016/j.biomaterials.2009.05.046.

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25

Yamamoto, Fumihiko, Ryo Yamahara, Akira Makino, Kensuke Kurihara, Hideo Tsukada, Eri Hara, Isao Hara et al. "Radiosynthesis and initial evaluation of 18F labeled nanocarrier composed of poly(L-lactic acid)-block-poly(sarcosine) amphiphilic polydepsipeptide". Nuclear Medicine and Biology 40, n.º 3 (abril de 2013): 387–94. http://dx.doi.org/10.1016/j.nucmedbio.2012.12.008.

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26

Zhao, Yanlei, Juan Li, Hua Yu, Guangji Wang y Wen Liu. "Synthesis and characterization of a novel polydepsipeptide contained tri-block copolymer (mPEG–PLLA–PMMD) as self-assembly micelle delivery system for paclitaxel". International Journal of Pharmaceutics 430, n.º 1-2 (julio de 2012): 282–91. http://dx.doi.org/10.1016/j.ijpharm.2012.03.043.

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27

Mammi, Stefano y Murray Goodman. "Polydepsipeptides: A Systematic Investigation of Guest—Host Effects". ChemInform 36, n.º 42 (18 de octubre de 2005). http://dx.doi.org/10.1002/chin.200542271.

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28

Enomoto, Junko, Yukiko Toba, Haruka Yamazaki, Masaki Kanai, Hiroyuki Mizuguchi y Hayato Matsui. "Development of a 3D Cell Culture System Using Amphiphilic Polydepsipeptides and Its Application to Hepatic Differentiation". ACS Applied Bio Materials, 8 de septiembre de 2021. http://dx.doi.org/10.1021/acsabm.1c00816.

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29

Katakai, Ryoichi. "Synthesis of sequential polydepsipeptides involving depsipeptide formation by the 2-nitrophenylsulphenyl N-carboxy α-amino acid anhydride (Nps–NCA) method". J. Chem. Soc., Perkin Trans. 1, 1987, 2249–51. http://dx.doi.org/10.1039/p19870002249.

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30

Feng, Yakai, Doris Klee y Hartwig Höcker. "Biodegradable copolymers based on poly(ethylene oxide), polylactide and polydepsipeptide sequences with functional groups". e-Polymers 1, n.º 1 (1 de diciembre de 2001). http://dx.doi.org/10.1515/epoly.2001.1.1.4.

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AbstractFor the purpose of increasing the hydrophilicity of polylactide, new block copolymers with protected functional groups, poly(lactide-co-(S)-b-benzyl aspartate)-poly(ethylene oxide)-poly(lactide-co-(S)- b-benzyl aspartate), were synthesized via ring-opening polymerization of D,L-lactide and (3S, 6R,S)-3- [(benzyloxycarbonyl)methyl]-6-methylmorpholine-2,5-dione in the presence of hydroxyltelechelic poly(ethylene oxide) (PEO) as an initiator at 140 °C for 24 h. The benzyl protective groups of the block copolymers were completely removed to give poly(lactide-co-(S)-aspartic acid)-PEO-poly(lactide-co-(S)-aspartic acid), (poly(DLLA-co-Asp)-b-PEO-b-poly(DLLA-co-Asp)). This shows lower crystallization and melting temperature compared with the polymers before deprotection. Poly(DLLA-co-Asp)-b-PEO-b-poly(DLLA-co-Asp) with 55.6 wt.-% of PEO is more hydrophilic, shows higher water absorption and is degraded faster than with 39.5 wt.-% of PEO.
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31

Uji, Hirotaka, Naoki Watabe, Tatsuya Komi, Tomoki Sakaguchi, Ryo Akamatsu, Kenta Mihara y Shunsaku Kimura. "Downsizing to 25-nm reverse polymeric micelle composed of AB3-type polydepsipeptide with comprising siRNA". Chemistry Letters, 21 de enero de 2022. http://dx.doi.org/10.1246/cl.210704.

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