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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/81802
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor羅世強(Shyh-Chyang Luo)
dc.contributor.authorKe-Hsin Wangen
dc.contributor.author王可昕zh_TW
dc.date.accessioned2022-11-25T03:03:56Z-
dc.date.available2023-08-08
dc.date.copyright2021-11-09
dc.date.issued2021
dc.date.submitted2021-08-12
dc.identifier.citation1. M. H. Turabee; T. Thambi; H. T. T. Duong; J. H. Jeong; D. S. Lee, A pH- and temperature-responsive bioresorbable injectable hydrogel based on polypeptide block copolymers for the sustained delivery of proteins in vivo. Biomater Sci 2018, 6 (3), 661-671. 2. J. Deng; N. Gao; Y. Wang; H. Yi; S. Fang; Y. Ma; L. Cai, Self-Assembled Cationic Micelles Based on PEG-PLL-PLLeu Hybrid Polypeptides as Highly Effective Gene Vectors. Biomacromolecules 2012, 13 (11), 3795-3804. 3. J. -Y. Lin; P. -L. Lai; Y. -K. Lin; S. Peng; L. -Y. Lee; C. -N. Chen; I. -M. Chu, A poloxamer-polypeptide thermosensitive hydrogel as a cell scaffold and sustained release depot. Polymer Chemistry 2016, 7 (17), 2976-2985. 4. C.-S. Choa; Y.-I. Jeongb; S.-H. Kimc; J.-W. Nahd; M. Kubotae; T. Komoto, Thermoplastic hydrogel based on hexablock copolymer composed of poly(g-benzyl l-glutamate) and poly(ethylene oxide). Polymer 2000, 41, 9. 5. S. Zhang; D. J. Alvarez; M. V. Sofroniew; T. J. Deming, Design and synthesis of nonionic copolypeptide hydrogels with reversible thermoresponsive and tunable physical properties. Biomacromolecules 2015, 16 (4), 1331-1340. 6. E. H. Kim; M. K. Joo; K. H. Bahk; M. H. Park; B. Chi; Y. M. Lee; B. Jeong, Reverse Thermal Gelation of PAF-PLX-PAF Block Copolymer Aqueous Solution. Biomacromolecules 2009, 10 (9), 2476-2481. 7. H. J. Moon; B. G. Choi; M. H. Park; M. K. Joo; B. Jeong, Enzymatically degradable thermogelling poly(alanine-co-leucine)-poloxamer-poly(alanine-co-leucine). Biomacromolecules 2011, 12 (4), 1234-1242. 8. K. Letchford; H. Burt, A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymersomes. Eur J Pharm Biopharm 2007, 65 (3), 259-269. 9. G. A. Jeffrey; R. K. Mcmullan, The Clathrate Hydrates. In Progress in Inorganic Chemistry, 1967; 43-108. 10. N. Pippa; R. Kalinova; I. Dimitrov; S. Pispas; C. Demetzos, Insulin/poly(ethylene glycol)-block-poly(L-lysine) Complexes: Physicochemical Properties and Protein Encapsulation. J Phys Chem B 2015, 119 (22), 6813-6819. 11. R. Wilder; S. Mobashery, The Use of Triphosgene in Preparation of N-Carboxy-a-amino Acid Anhydrides. J. Org. Chem. 1992, 57, 2. 12. H. Leuchs, Ueber die Glycin-carbonsäure. Berichte der deutschen chemischen Gesellschaft 1906, 39 (1), 857-861. 13. J. R. H. Ndez; H. Klok, Synthesis and Ring-Opening (Co)polymerization of L-Lysine N-Carboxyanhydrides Containing Labile Side-Chain Protective Groups. Journal of Polymer Science: Part A: Polymer Chemistry 2003, 41, 21. 14. B. Li; M. Berliner; R. Buzon; C. K.-F. Chiu; S. T. Colgan; T. Kaneko; N. Keene; W. Kissel; T. Le; K. R. Leeman; B. Marquez; R. Morris; L. Newell; S. Wunderwald; M. Witt; J. Weaver; Z. Zhang; Z. Zhang, Aqueous Phosphoric Acid as a Mild Reagent for Deprotection of tert-Butyl Carbamates, Esters, and Ethers. J. Org. Chem 2006, 71, 6. 15. P. Heller; B. Weber; A. Birke; M. Barz, Synthesis and sequential deprotection of triblock copolypept(o)ides using orthogonal protective group chemistry. Macromol Rapid Commun 2015, 36 (1), 38-44. 16. J. E. Semple; B. Sullivan; K. N. Sill, Large-scale synthesis of α-amino acid-N-carboxyanhydrides. Synthetic Communications 2016, 47 (1), 53-61. 17. T. Aliferis; H. Iatrou; N. Hadjichristidis, Living Polypeptides. Biomacromolecules 2004, 5, 4. 18. T. J. Deming, Living Polymerization of a-Amino Acid-N-Carboxyanhydrides. Journal of Polymer Science: Part A: Polymer Chemistry 2000, 38, 8. 19. I. Dimitrov; H. Schlaad, Synthesis of nearly monodisperse polystyrene-polypeptide block copolymers via polymerisation of N-carboxyanhydrides. Chem Commun (Camb) 2003, (23), 2944-2945. 20. D. L. Pickel; N. Politakos; A. Avgeropoulos; J. M. Messman, A Mechanistic Study of α-(Amino acid)-N-carboxyanhydride Polymerization: Comparing Initiation and Termination Events in High-Vacuum and Traditional Polymerization Techniques. Macromolecules 2009, 42 (20), 7781-7788. 21. W. Vayaboury; O. Giani; H. Cottet; S. Bonaric; F. Schué, Mechanistic Study ofα-Amino AcidN-Carboxyanhydride (NCA) Polymerization by Capillary Electrophoresis. Macromolecular Chemistry and Physics 2008, 209 (15), 1628-1637. 22. C. D. Vacogne; H. Schlaad, Controlled ring-opening polymerization of α-amino acid N-carboxyanhydrides in the presence of tertiary amines. Polymer 2017, 124, 203-209. 23. D. Thunig; J. Semen; H.-G. Elias, Carbon Dioxide Influence on NCA Polymerizations. Makromol. Chem. 1977, 178, 5. 24. J. Zou; J. Fan; X. He; S. Zhang; H. Wang; K. L. Wooley, A facile glovebox-free strategy to significantly accelerate the syntheses of well-defined polypeptides by N-carboxyanhydride (NCA) ring opening polymerizations. Macromolecules 2013, 46 (10), 4223-4226. 25. T. J. Deming, Facile synthesis of block copolypeptides of defined architecture. Nature 1997, 390, 4. 26. T. J. Deming, Polypeptide hydrogels via a unique assembly mechanism. Soft Matter 2005, 1 (1), 28-35. 27. D. J. Pochan; L. Pakstis; B. O. Andrew; P. Nowak; T. J. Deming, SANS and Cryo-TEM Study of Self-Assembled Diblock Copolypeptide Hydrogels with Rich Nano- through Microscale Morphology. Macromolecules 2002, 35, 3. 28. Zhibo Li; Timothy J. Deming, Tunable hydrogel morphology via self-assembly of amphiphilic pentablock copolypeptides. Soft Matter 2010, 6 (11). 29. C. Y. Yang; B. Song; Y. Ao; A. P. Nowak; R. B. Abelowitz; R. A. Korsak; L. A. Havton; T. J. Deming; M. V. Sofroniew, Biocompatibility of amphiphilic diblock copolypeptide hydrogels in the central nervous system. Biomaterials 2009, 30 (15), 2881-2898. 30. A. P. Nowak; J. Sato; V. Breedveld; T. J. Deming, Hydrogel Formation in Amphiphilic Triblock Copolypeptides. Supramolecular Chemistry 2006, 18 (5), 423-427. 31. B. Chen; L. Yu; Z. Li, Characterization of complexes made of polylysine-polyleucine-polylysine and pDNA. J Mater Chem B 2017, 5 (21), 3842-3851. 32. H. Iatrou; H. Frielinghaus; S. Hanski; N. Ferderigos; J. Ruokolainen; O. Ikkala; D. Richter; J. Mays; N. Hadjichristidis, Architecturally Induced Multiresponsive Vesicles from Well-Defined Polypeptides. Formation of Gene Vehicles. Biomacromolecules 2007, 8, 9. 33. D. Mavrogiorgis; P. Bilalis; A. Karatzas; D. Skoulas; G. Fotinogiannopoulou; H. Iatrou, Controlled polymerization of histidine and synthesis of well-defined stimuli responsive polymers. Elucidation of the structure–aggregation relationship of this highly multifunctional material. Polym. Chem. 2014, 5 (21), 6256-6278. 34. W. Vayaboury; O. Giani; H. Cottet; A. Deratani; F. Schué, Living Polymerization ofα-Amino AcidN-Carboxyanhydrides(NCA) upon Decreasing the Reaction Temperature. Macromolecular Rapid Communications 2004, 25 (13), 1221-1224. 35. G. J. M. Habraken; K. H. R. M. Wilsens; C. E. Koning; A. Heise, Optimization of N-carboxyanhydride (NCA) polymerization by variation of reaction temperature and pressure. Polymer Chemistry 2011, 2 (6). 36. A. Rasines Mazo; S. Allison-Logan; F. Karimi; N. J. Chan; W. Qiu; W. Duan; N. M. O'brien-Simpson; G. G. Qiao, Ring opening polymerization of alpha-amino acids: advances in synthesis, architecture and applications of polypeptides and their hybrids. Chem Soc Rev 2020, 49 (14), 4737-4834. 37. Z. Song; Z. Tan; J. Cheng, Recent Advances and Future Perspectives of Synthetic Polypeptides from N-Carboxyanhydrides. Macromolecules 2019, 52 (22), 8521-8539. 38. I. Conejos-Sánchez; A. Duro-Castano; A. Birke; M. Barz; M. J. Vicent, A controlled and versatile NCA polymerization method for the synthesis of polypeptides. Polymer Chemistry 2013, 4 (11). 39. C. D. Vacogne; H. Schlaad, Primary ammonium/tertiary amine-mediated controlled ring opening polymerisation of amino acid N-carboxyanhydrides. Chem Commun (Camb) 2015, 51 (86), 15645-15648. 40. M. Meyer; H. Schlaad, Poly(2-isopropyl-2-oxazoline)-Poly(L-glutamate) Block Copolymers through Ammonium-Mediated NCA Polymerization. Macromolecules 2006, 39, 4. 41. A. Takao; S. Ken-Ichi; S. Yasuhisa; O. Teruo; K Kazunori, Peptide drug carrier: studies on incorporation of vasopressin into nano-associates comprising poly(ethylene glycol)-poly(L-aspartic acid block copolymer. Colloids and Surfaces B: Biointerfaces 1999, 16, 6. 42. J. Rodríguez-Hernández; S. Lecommandoux, Reversible Inside−Out Micellization of pH-responsive and Water-Soluble Vesicles Based on Polypeptide Diblock Copolymers. Journal of the American Chemical Society 2005, 127 (7), 2026-2027. 43. K. E. Ng; M. C. Amin; H. Katas; M. W. Amjad; A. M. Butt; P. Kesharwani; A. K. Iyer, pH-Responsive Triblock Copolymeric Micelles Decorated with a Cell-Penetrating Peptide Provide Efficient Doxorubicin Delivery. Nanoscale Res Lett 2016, 11 (1), 539. 44. J. Lin; J. Zhu; T. Chen; S. Lin; C. Cai; L. Zhang; Y. Zhuang; X. S. Wang, Drug releasing behavior of hybrid micelles containing polypeptide triblock copolymer. Biomaterials 2009, 30 (1), 108-117. 45. J. Ding; X. Zhuang; C. Xiao; Y. Cheng; L. Zhao; C. He; Z. Tang; X. Chen, Preparation of photo-cross-linked pH-responsive polypeptide nanogels as potential carriers for controlled drug delivery. Journal of Materials Chemistry 2011, 21 (30). 46. C. Dharmayanti; T. A. Gillam; M. Klingler-Hoffmann; H. Albrecht; A. Blencowe, Strategies for the Development of pH-Responsive Synthetic Polypeptides and Polymer-Peptide Hybrids: Recent Advancements. Polymers (Basel) 2021, 13 (4). 47. M. Hatip Koc; G. Cinar Ciftci; S. Baday; V. Castelletto; I. W. Hamley; M. O. Guler, Hierarchical Self-Assembly of Histidine-Functionalized Peptide Amphiphiles into Supramolecular Chiral Nanostructures. Langmuir 2017, 33 (32), 7947-7956. 48. S. Khanna; A. K. Singh; S. P. Behera; S. Gupta, Thermoresponsive BSA hydrogels with phase tunability. Mater Sci Eng C Mater Biol Appl 2021, 119, 111590. 49. J. F. Miravet; B. Escuder; M. D. Segarra-Maset; M. Tena-Solsona; I. W. Hamley; A. Dehsorkhi; V. Castelletto, Self-assembly of a peptide amphiphile: transition from nanotape fibrils to micelles. Soft Matter 2013, 9 (13). 50. D. Roy; B. S. Sumerlin, Let there be light: photo-cross-linked block copolymer nanoparticles. Macromol Rapid Commun 2014, 35 (2), 174-179. 51. L. Yu; W. Fu; Z. Li, Tuning the phase transition temperature of thermal-responsive OEGylated poly-L-glutamate via random copolymerization with L-alanine. Soft Matter 2015, 11 (3), 545-550. 52. A. P. Nowak; V. Breedveld; L. Pakstis; B. Ozbas; D. J. Pine; D. J. Pochan; T. J. Deming, Rapidly recovering hydrogel scaffolds from self-assembling diblock copolypeptide amphiphiles. Nature 2002, 417 (6887), 424-428. 53. V. Breedveld; A. P. Nowak; J. Sato; T. J. Deming; D. J. Pine, Rheology of Block Copolypeptide Solutions: Hydrogels with Tunable Properties. Macromolecules 2004, 37 (10), 3943-3953. 54. J. Huang; C. L. Hastings; G. P. Duffy; H. M. Kelly; J. Raeburn; D. J. Adams; A. Heise, Supramolecular hydrogels with reverse thermal gelation properties from (oligo)tyrosine containing block copolymers. Biomacromolecules 2013, 14 (1), 200-206. 55. Y. Cheng; C. He; C. Xiao; J. Ding; X. Zhuang; Y. Huang; X. Chen, Decisive role of hydrophobic side groups of polypeptides in thermosensitive gelation. Biomacromolecules 2012, 13 (7), 2053-2059. 56. Y. Y. Choi; M. K. Joo; Y. S. Sohn; B. Jeong, Significance of secondary structure in nanostructure formation and thermosensitivity of polypeptide block copolymers. Soft Matter 2008, 4 (12). 57. I. W. Hamley; I. A. Ansari; V. Castelletto; H. Nuhn; A. Rösler; H. A. Klok, Solution Self-Assembly of Hybrid Block Copolymers Containing Poly(ethylene glycol) and Amphiphilic β-Strand Peptide Sequences. Biomacromolecules 2005, 6 (3), 1310-1315. 58. H. J. Oh; M. K. Joo; Y. S. Sohn; B. Jeong, Secondary Structure Effect of Polypeptide on Reverse Thermal Gelation and Degradation of l/dl-Poly(alanine)–Poloxamer–l/dl-Poly(alanine) Copolymers. Macromolecules 2008, 41 (21), 8204-8209. 59. P. R. Chiang; T. Y. Lin; H. C. Tsai; H. L. Chen; S. Y. Liu; F. R. Chen; Y. S. Hwang; I. M. Chu, Thermosensitive hydrogel from oligopeptide-containing amphiphilic block copolymer: effect of peptide functional group on self-assembly and gelation behavior. Langmuir 2013, 29 (51), 15981-15991. 60. U. P. Shinde; M. K. Joo; H. J. Moon; B. Jeong, Sol–gel transition of PEG–PAF aqueous solution and its application for hGH sustained release. Journal of Materials Chemistry 2012, 22 (13). 61. U. P. Shinde; H. J. Moon; Y. Ko Du; B. K. Jung; B. Jeong, Control of rhGH Release Profile from PEG-PAF Thermogel. Biomacromolecules 2015, 16 (5), 1461-9. 62. Y. Zhang; H. Song; H. Zhang; P. Huang; J. Liu; L. Chu; J. Liu; W. Wang; Z. Cheng; D. Kong, Fine tuning the assembly and gel behaviors of PEGylated polypeptide conjugates by the copolymerization ofl-alanine and γ-benzyl-l-glutamateN-carboxyanhydrides. Journal of Polymer Science Part A: Polymer Chemistry 2017, 55 (9), 1512-1523. 63. M. H. Turabee; T. Thambi; J. S. Lym; D. S. Lee, Bioresorbable polypeptide-based comb-polymers efficiently improves the stability and pharmacokinetics of proteins in vivo. Biomater Sci 2017, 5 (4), 837-848. 64. S. Zhao; H. Zhu; Z. Chen; S. Shuai; N. Zhang; Y. Liu; Z. Rao; Y. Li; C. Zhao; K. Zhou; W. Ge; J. Hao, Preparation and properties of a temperature- and pH- responsive polypeptide hydrogel. Materials Research Express 2019, 6 (8). 65. H. Song; G. Yang; P. Huang; D. Kong; W. Wang, Self-assembled PEG-poly(l-valine) hydrogels as promising 3D cell culture scaffolds. J Mater Chem B 2017, 5 (9), 1724-1733. 66. M. K. Joo; D. Y. Ko; S. J. Jeong; M. H. Park; U. P. Shinde; B. Jeong, Incorporation of d-alanine into poly(ethylene glycol) and l-poly(alanine-co-phenylalanine) block copolymers affects their nanoassemblies and enzymatic degradation. Soft Matter 2013, 9 (33). 67. C. Cai; L. Wang; J. Lin, Self-assembly of polypeptide-based copolymers into diverse aggregates. Chem Commun (Camb) 2011, 47 (40), 11189-11203. 68. J. Qian; X. Yong; W. Xu; X. Jin, Preparation and characterization of bimodal porous poly(γ-benzyl-L-glutamate) scaffolds for bone tissue engineering. Materials Science and Engineering: C 2013, 33 (8), 4587-4593. 69. G. Liu; W. Zhuang; X. Chen; A. Yin; Y. Nie; Y. Wang, Drug carrier system self-assembled from biomimetic polyphosphorycholine and biodegradable polypeptide based diblock copolymers. Polymer 2016, 100, 45-55. 70. Z. -H. Wang; Y. -Y. Chang; J. -G. Wu; C. -Y. Lin; H. -L. An; S. -C. Luo; T. K. Tang; W. -F. Su, Novel 3D Neuron Regeneration Scaffolds Based on Synthetic Polypeptide Containing Neuron Cue. Macromolecular Bioscience 2018, 18 (3), 1700251. 71. T. -C. Chen; P. -Y. She; D. F. Chen; J. -H. Lu; C. -H. Yang; D. -S. Huang; P. -Y. Chen; C. -Y. Lu; K. -S. Cho; H. -F. Chen; W. -F. Su, Polybenzyl Glutamate Biocompatible Scaffold Promotes the Efficiency of Retinal Differentiation toward Retinal Ganglion Cell Lineage from Human-Induced Pluripotent Stem Cells. International Journal of Molecular Sciences 2019, 20 (1). 72. G. J. Brewer, Regeneration and Proliferation of Embryonic and Adult Rat Hippocampal Neurons in Culture. Experimental Neurology 1999, 159 (1), 237-247. 73. C. Y. Brazel; J. L. Nuñez; Z. Yang; S. W. Levison, Glutamate enhances survival and proliferation of neural progenitors derived from the subventricular zone. Neuroscience 2005, 131 (1), 55-65. 74. D. Y. Kwoh; C. C. Coffin; C. P. Lollo; J. Jovenal; M. G. Banaszczyk; P. Mullen; A. Phillips; A. Amini; J. Fabrycki; R. M. Bartholomew; S. W. Brostoff; D. J. Carlo, Stabilization of poly-l-lysine/DNA polyplexes for in vivo gene delivery to the liver. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 1999, 1444 (2), 171-190. 75. L. Zhu; L. Zhao; X. Qu; Z. Yang, pH-sensitive polymeric vesicles from coassembly of amphiphilic cholate grafted poly(L-lysine) and acid-cleavable polymer-drug conjugate. Langmuir 2012, 28 (33), 11988-11996. 76. D. Mazia; G. Schatten; W. Sale, Adhesion of cells to surfaces coated with polylysine. Applications to electron microscopy. Journal of Cell Biology 1975, 66 (1), 198-200. 77. Y. Miao; R. Yang; D. Y. B. Deng; L. -M. Zhang, Poly(l-lysine) modified zein nanofibrous membranes as efficient scaffold for adhesion, proliferation, and differentiation of neural stem cells. RSC Advances 2017, 7 (29), 17711-17719. 78. L. Cai; J. Lu; V. Sheen; S. Wang, Promoting Nerve Cell Functions on Hydrogels Grafted with Poly(l-lysine). Biomacromolecules 2012, 13 (2), 342-349. 79. A. Chen; H. He; G. Ma; Y. Li; S. Jiang; X. Xuan; Y. Song; C. Zhang; J. Xiao; Y. Xu; J. Wu; S. Chen, Biodegradable copolypeptide hydrogel prodrug accelerates dermal wound regeneration by enhanced angiogenesis and epithelialization. RSC Advances 2018, 8 (19), 10620-10626. 80. J. Lam; E. C. Clark; E. L. Fong; E. J. Lee; S. Lu; Y. Tabata; A. G. Mikos, Evaluation of cell-laden polyelectrolyte hydrogels incorporating poly(L-Lysine) for applications in cartilage tissue engineering. Biomaterials 2016, 83, 332-346. 81. M. Zheng; M. Pan; W. Zhang; H. Lin; S. Wu; C. Lu; S. Tang; D. Liu; J. Cai, Poly(alpha-l-lysine)-based nanomaterials for versatile biomedical applications: Current advances and perspectives. Bioact Mater 2021, 6 (7), 1878-1909. 82. A. Hall; L. -P. Wu; L. Parhamifar; S. M. Moghimi, Differential Modulation of Cellular Bioenergetics by Poly(L-lysine)s of Different Molecular Weights. Biomacromolecules 2015, 16 (7), 2119-2126. 83. V. Stanić; Y. Arntz; D. Richard; C. Affolter; I. Nguyen; C. Crucifix; P. Schultz; C. Baehr; B. Frisch; J. Ogier, Filamentous Condensation of DNA Induced by Pegylated Poly-l-lysine and Transfection Efficiency. Biomacromolecules 2008, 9 (7), 2048-2055. 84. T. Wu; L. Wang; S. Ding; Y. You, Fluorinated PEG-Polypeptide Polyplex Micelles Have Good Serum-Resistance and Low Cytotoxicity for Gene Delivery. Macromol Biosci 2017, 17 (8). 85. Bruce W. E.; R. B. M., Acid Stability of Several Benzylic Protecting Groups Used in Solid-Phase Peptide Synthesis. Rearrangement of O-Benzyltyrosine to 3-Benzyltyrosine. J. Am. Chem. Soc. 1972, 95 (11), 7. 86. C. Kok; A. Rudin, Relationship between the hydrodynamic radius and the radius of gyration of a polymer in solution. Die Makromolekulare Chemie, Rapid Communications 1981, 2, 655-659. 87. W. L. Mattice; R. W. Mccord; P. M. Shippey, Disorder–order transitions induced in anionic homopolypeptides by cationic detergents. Biopolymers 1979, 18 (3), 723-730. 88. C.-S. Choa; J.-W. Nahb; Y.-I. Jeongc; J.-B. Cheonc; S. Asayamad; H. Ised; T. Akaiked, Conformational transition of nanoparticles composed of poly(g-benzyl l-glutamate) as the core and poly(ethylene oxide) as the shell. Polymer 1999, 40, 6. 89. S. Ziyuan; F. Hailin; W. Ruibo; A. P. Lazaro; W. Xu; L. Yao; C. Jianjun, Secondary structures in synthetic polypeptides from N-carboxyanhydrides: design, modulation, association, and material applications. Chem. Soc. Rev 2018, 47, 25. 90. A. P. Nowak; V. Breedveld; D. J. Pine; T. J. Deming, Unusual Salt Stability in Highly Charged Diblock Co-polypeptide Hydrogels. Journal of the American Chemical Society 2003, 125 (50), 15666-15670. 91. S. H. Park; B. G. Choi; H. J. Moon; S.-H. Cho; B. Jeong, Block sequence affects thermosensitivity and nano-assembly: PEG-l-PA-dl-PA and PEG-dl-PA-l-PA block copolymers. Soft Matter 2011, 7 (14).
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/81802-
dc.description.abstract" 含有聚胜肽之雙親性嵌段共聚高分子因其良好的生物相容性與生物降解性,被視為運用在藥物輸送或組織工程學上富有潛力的材料。尤其因為此種高分子在水中有可形成多種穩定的自組裝結構,更有助於開發精準藥物釋放系統或用做組織工程材料上。然而,含有聚胜肽之雙親性嵌段共聚高分子具有結構上的多變性,同時也使其結構難以預測,這是由於多種作用力參與了自組裝結構的形成。因此,我們以釐清主導結構形成的作用力與影響因素,以及理解自組裝造成凝膠化的機制為研究目標,並整理出能使此種高分子凝膠化的配方,以便未來應用於生醫組織工程中。更具體而言,此篇研究以開發用於治療神經相關疾病的生醫材料為目標,利用聚胜肽聚谷氨酸苯酯(PBG)、聚賴氨酸(PLL)與聚乙二醇(PEG)組成新穎嵌段共聚物並探討其特性。透過精準多肽聚合的技術,我們發現當嵌段共聚物的各鏈段以不同方式排列,會展現出明顯不同的組裝結構。 其中,(Bx-r-Ky)-E34-(Bx-r-Ky)因兩端無規排列的鏈段而組成鬆散的聚集;而對於Ky- Bx-E34-Bx-Ky高分子,當PBG鏈段聚集時PLL鏈段僅能構成開環形結構,使得不同微胞之間因高分子鏈糾纏而產生的作用力減弱,疏水作用力因此成為誘發聚集的主導作用力;另一方面,Bx-Ky-E34-Ky-Bx高分子則因為微胞之間較強的作用力,在水溶液中自組裝成網狀結構,故可在低臨界濃度下形成水凝膠。我們也發現以更長鏈段的PLL取代原有結構中的PEG之後,該高分子有更顯著的凝膠化趨勢。考慮聚胜肽之雙親性嵌段共聚高分子的分子量效應與親/疏水平衡,我們構建了Bx-Ky-E34-Ky-Bx高分子的相圖。該圖顯示了在給定聚合物之組成時,能使高分子在水溶液中構成網狀水凝膠結構的最低濃度;若再結合論文中高分子組成對機械性質的圖表,便能夠快速進一步找到具有所需機械性質的水凝膠製備所需之成分。此研究結果整合高分子成分濃度對於自組裝形態與機械性質的影響,希望使該高分子可做為一種方便使用的體內支架, 促進並修復神經元的生長。 藉由系統性的研究,對此聚胜肽之雙親性嵌段共聚高分子在水溶液中的行為獲得全面性的了解,其中有關嵌段序列強烈影響自組裝行為的探討是現有的文獻中鮮少著墨討論的。經由對照相圖,也可快速搜尋所需水凝膠的成分與濃度。希望此凝膠機制能夠在未來,成為設計促進神經元再生的新材料時有力的工具。"zh_TW
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dc.description.tableofcontents"口試委員審定書 i 誌謝 ii 摘要 iii ABSTRACT iv CONTENTS vi LIST OF FIGURES x LIST OF TABLES xv Chapter 1 Introduction 1 1.1 Polypeptides-containing amphiphilic block copolymers and their versatile self-assembly nature 1 1.2 Synthesis of polypeptides-containing block copolymers 5 1.3 Monitoring self-assembly structures 11 1.3.1 Versatile and instantly responding self-assembly structures 11 1.3.2 Susceptive structural transformation 13 1.3.3 Manipulating hydrophobic-interaction-induced gelation 14 1.4 Targeted application and rationale of materials selection 24 1.4.1 Poly(γ-benzyl-L-glutamate) (PBG, abbreviated as Bx in copolymers) 24 1.4.2 Poly(L-lysine) (PLL, abbreviated as Ky in copolymers) 25 1.4.3 Poly(ethylene glycol) (PEG, abbreviated as Ez in copolymers) 26 1.5 Motivation, objective and experimental designs 27 Chapter 2 Chemicals, Instruments and Experimental procedures 30 2.1 Chemicals and Instruments 30 2.2 Nomenclature 35 2.3 Synthesis method of polypeptides-containing block copolymers 36 2.3.1 Synthesis of macro-initiator 36 2.3.2 Synthesis of N-carboxyl anhydrides (NCAs) 37 2.3.3 Polymerization and deprotection 38 2.4 Chemical structure characterizations 41 2.4.1 1H Nuclear Magnetic Resonance (NMR) 41 2.4.2 Fourier Transform Infrared Spectroscopy (FTIR) 41 2.4.3 Gel Permeation Chromatography (GPC) 42 2.4.4 Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectroscopy (MALDI-ToF) 42 2.5 Morphology determination 43 2.5.1 Tube-inverting method 43 2.5.2 Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR) 43 2.5.3 Dynamic Light Scattering (DLS) 43 2.5.4 Circular Dichroism (CD) 44 2.5.5 Scanning Electron Microscopy (SEM) 44 2.5.6 Small Angle X-ray Scattering (SAXS) 44 2.6 Mechanical properties measurements 44 2.6.1 Rheology study 44 2.6.2 Compression modulus study 45 Chapter 3 Results and Discussion 46 3.1 Synthesis and characteristic of block copolymers 46 3.1.1 Macro-initiator and monomers 46 3.1.2 Block copolymers 56 3.2 Study of Copolymer Morphology in Low Concentration Solution 65 3.2.1 Aggregate formation of amphiphiles in DLS 66 3.2.2 Secondary structures in polypeptide segments 70 3.2.3 Summary of study of polymer morphology in low concentration solution 77 3.3 Study of copolymer morphology study in high concentration solution 78 3.3.1 (Bx-r-Ky)-E34-(Bx-r-Ky) 78 3.3.2 Ky-Bx-E34-Bx-Ky 83 3.3.3 Bx-Ky-E34-Ky-Bx 87 3.3.4 Integration of study of polymer morphology in high concentration solution and self—assembly model purposing 95 3.4 Mechanical properties of polypeptides-containing block copolymers hydrogel 100 3.4.1 Shear modulus and compression modulus 100 3.4.2 Temperature effect 114 Chapter 4 Conclusions 117 Chapter 5 Recommendations 120 5.1 Investigating hydrogel stability in the physiological solution 120 5.2 Systematic study of nanostructure with SAXS 121 5.3 Investigating nano-scale assemblies with cryo-TEM 121 REFERENCE 123 APPENDIX 129"
dc.language.isoen
dc.subject形態學zh_TW
dc.subject水凝膠zh_TW
dc.subject嵌段高分子zh_TW
dc.subject雙親性zh_TW
dc.subject機械性質zh_TW
dc.subject自組裝zh_TW
dc.subject聚胜肽zh_TW
dc.subjectmorphologyen
dc.subjectamphiphilicen
dc.subjectself-assemblyen
dc.subjectblock copolymersen
dc.subjectpolypeptideen
dc.subjectmechanical propertyen
dc.subjecthydrogelsen
dc.title含有聚胜肽之新穎雙親性嵌段共聚高分子之設計合成與水溶液中自組裝結構之研究zh_TW
dc.title"Study of Novel Amphiphilic Block Copolymers Containing Polypeptides: Design, Synthesis and Morphology in Aqueous Solution"en
dc.date.schoolyear109-2
dc.description.degree碩士
dc.contributor.coadvisor林唯芳(Wei-Fang Su)
dc.contributor.oralexamcommittee趙基揚(Hsin-Tsai Liu),童世煌(Chih-Yang Tseng)
dc.subject.keyword自組裝,聚胜肽,形態學,機械性質,雙親性,嵌段高分子,水凝膠,zh_TW
dc.subject.keywordself-assembly,polypeptide,morphology,mechanical property,amphiphilic,block copolymers,hydrogels,en
dc.relation.page134
dc.identifier.doi10.6342/NTU202102184
dc.rights.note同意授權(全球公開)
dc.date.accepted2021-08-12
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept材料科學與工程學研究所zh_TW
dc.date.embargo-lift2023-08-08-
顯示於系所單位:材料科學與工程學系

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