Satti SM, Shah AA. Polyester‐based biodegradable plastics: an approach towards sustainable development. Lett Appl Microbiol 2020;70:413–30. https://doi.org/10.1111/lam.13287Article
CAS
PubMed
Google Scholar
Becker G, Wurm FR. Functional biodegradable polymers via ring-opening polymerization of monomers without protective groups. Chem Soc Rev 2018;47:7739–82. https://doi.org/10.1039/c8cs00531aArticle
CAS
PubMed
Google Scholar
Nakamura A, Kobayashi N, Koga N, Iino R. Positive charge introduction on the surface of thermostabilized PET hydrolase facilitates PET binding and degradation. ACS Catal. 2021;11:8550–64. https://doi.org/10.1021/acscatal.1c01204Article
CAS
Google Scholar
Lu H, Diaz DJ, Czarnecki N-J, Zhu C, Kim W, Shroff R, et al. Machine learning-aided engineering of hydrolases for PET depolymerization. Nature. 2022;604:662–7. https://doi.org/10.1038/s41586-022-04599-zArticle
CAS
PubMed
Google Scholar
Yamashita T, Matsumoto T, Yamada R, Ogino H. Display of PETase on the cell surface of Escherichia coli using the anchor protein PgsA. Appl Biochem Biotechnol 2024 https://doi.org/10.1007/s12010-023-04837-8Mecerreyes D, Humes J, Miller R-D, Hedrick J-L, Detrembleur C, Lecomte P, et al. First example of an unsymmetrical difunctional monomer polymerizable by two living/controlled methods. Macromol Rapid Commun 2000;21:779–84.Article
CAS
Google Scholar
Groner MD, Fabreguette FH, Elam JW, George SM. Low-temperature Al2O3 atomic layer deposition. Chem Mater 2004;16:639–45. https://doi.org/10.1021/cm0304546Article
CAS
Google Scholar
Alteheld A, Feng Y, Kelch S, Lendlein A. Biodegradable, amorphous copolyester‐urethane networks having shape‐memory properties. Angew Chem Int Ed 2005;44:1188–92. https://doi.org/10.1002/anie.200461360Article
CAS
Google Scholar
Ebara M, Uto K, Idota N, Hoffman J, Aoyagi T. The taming of the cell: shape-memory nanopatterns direct cell orientation. Int J Nanomed 2014;9:117–26. https://doi.org/10.2147/ijn.s50677Article
CAS
Google Scholar
Uto K, Aoyagi T, DeForest CA, Hoffman AS, Ebara M. A combinational effect of “bulk” and “surface” shape‐memory transitions on the regulation of cell alignment. Adv Healthcare Mater. 2017;6 https://doi.org/10.1002/adhm.201601439Iwamatsu K, Uto K, Takeuchi Y, Hoshi T, Aoyagi T. Preparation of temperature-responsive, cationized, poly(ε-caprolactone)-based, cross-linked materials by a macromonomer design and positive charge control on the surface. Polym J 2018;50:447–54. https://doi.org/10.1038/s41428-018-0030-1Article
CAS
Google Scholar
Makiguchi K, Satoh T, Kakuchi T. Diphenyl phosphate as an efficient cationic organocatalyst for controlled/living ring-opening polymerization of δ-valerolactone and ε-caprolactone. Macromolecules. 2011;44:1999–2005. https://doi.org/10.1021/ma200043xArticle
CAS
Google Scholar
Takao A, Fusae M, Yu N. Preparation of cross-linked aliphatic polyester and application to thermo-responsive material. J Controlled Release 1994;32:87–96. https://doi.org/10.1016/0168-3659(94)90228-3Article
Google Scholar
Uto K, Yamamoto K, Hirase S, Aoyagi T. Temperature-responsive cross-linked poly(ε-caprolactone) membrane that functions near body temperature. J Controlled Release 2006;110:408–13. https://doi.org/10.1016/j.jconrel.2005.10.024Article
CAS
Google Scholar
Zako T, Matsushita S, Hoshi T, Aoyagi T. Direct surface modification of polycaprolactone-based shape memory materials to introduce positive charge aiming to enhance cell affinity. Materials. 2021;14:5797 https://doi.org/10.3390/ma14195797Article
CAS
PubMed
PubMed Central
Google Scholar
Houk K-N, Jabbari A, Hall H-K, Alemán C. Why δ-valerolactone polymerizes and γ-butyrolactone does not. J Org Chem 2008;73:2674–8. https://doi.org/10.1021/jo702567vArticle
CAS
PubMed
Google Scholar
Moore T, Adhikari R, Gunatillake P. Chemosynthesis of bioresorbable poly(γ-butyrolactone) by ring-opening polymerisation: a review. Biomaterials. 2005;26:3771–82. https://doi.org/10.1016/j.biomaterials.2004.10.002Article
CAS
PubMed
Google Scholar
Lenoir S, Riva R, Lou X, Detrembleur CH, Jérôme R, Lecomte PH. Ring-opening polymerization of α-chloro-ε-caprolactone and chemical modification of poly(α-chloro-ε-caprolactone) by atom transfer radical processes. Macromolecules. 2004;37:4055–61. https://doi.org/10.1021/ma035003lArticle
CAS
Google Scholar
Wang SW, Lin YK, Fang JY, Lee R-S. Photo-responsive polymeric micelles and prodrugs: synthesis and characterization. RSC Adv. 2018;8:29321–37. https://doi.org/10.1039/c8ra04580aArticle
CAS
PubMed
PubMed Central
Google Scholar
Bolley A, Mameri S, Dagorne S. Controlled and highly effective ring‐opening polymerization of α‐chloro‐ε‐caprolactone using Zn‐ and Al‐based catalysts. J Polym Sci 2020;58:1197–206. https://doi.org/10.1002/pol.20190214Article
CAS
Google Scholar
Yin G, Chen G, Zhou Z, Li Q. Modification of PEG-b-PCL block copolymer with high melting temperature by the enhancement of POSS crystal and ordered phase structure. RSC Adv. 2015;5:33356–63. https://doi.org/10.1039/c5ra01971kArticle
CAS
Google Scholar
Bexis P, Thomas AW, Bell CA, Dove A-P. Synthesis of degradable poly(ε-caprolactone)-based graft copolymers via a “grafting-from” approach. Polym Chem 2016;7:7126–34. https://doi.org/10.1039/c6py01674jArticle
CAS
Google Scholar
Liu M, Vladimirov N, Fréchet J-M-J. A new approach to hyperbranched polymers by ring-opening polymerization of an ab monomer: 4-(2-hydroxyethyl)-ε-caprolactone. Macromolecules. 1999;32:6881–4. https://doi.org/10.1021/ma990785xArticle
CAS
Google Scholar
Tian D, Dubois PH, Jérôme R. Macromolecular engineering of polylactones and polylactides. 23. synthesis and characterization of biodegradable and biocompatible homopolymers and block copolymers based on 1,4,8-Trioxa[4.6]Spiro-9-Undecanone. Macromolecules. 1997;30:1947–54. https://doi.org/10.1021/ma961614kArticle
CAS
Google Scholar
Taniguchi I, Lovell N-G. Low-temperature processable degradable polyesters. Macromolecules. 2012;45:7420–8. https://doi.org/10.1021/ma301230yArticle
CAS
PubMed
PubMed Central
Google Scholar
Zhou, Z, Meng, Y, Wei, C, Bai, Y, Wang, X, Quan, D, et al. Linear shape memory polyester with programmable splitting of crystals. Macromol Mater Eng. 2021;306 https://doi.org/10.1002/mame.202100254Van Horn BA, Wooley KL. Toward cross-linked degradable polyester materials: investigations into the compatibility and use of reductive amination chemistry for cross-linking. Macromolecules. 2007;40:1480–8. https://doi.org/10.1021/ma061654gArticle
CAS
Google Scholar
Mecerreyes D, Miller R-D, Hedrick J-L, Detrembleur C, Jérôme R. Ring-opening polymerization of 6-hydroxynon-8-enoic acid lactone: novel biodegradable copolymers containing allyl pendent groups. J Polym Sci Part A: Polym Chem 2000;38:870–5.Article
CAS
Google Scholar
Lou X, Detrembleur C, Lecomte PH, Jérôme R. Living ring-opening (CO)polymerization of 6,7-Dihydro-2(5H)-Oxepinone into unsaturated aliphatic polyesters. Macromolecules. 2001;34:5806–11.Article
CAS
Google Scholar
El Jundi A, Buwalda S, Bethry A, Hunger S, Coudane J, Bakkour Y, et al. Double-hydrophilic block copolymers based on functional poly(ε-Caprolactone)s for pH-dependent controlled drug delivery. Biomacromolecules. 2019;21:397–407. https://doi.org/10.1021/acs.biomac.9b01006Article
CAS
PubMed
Google Scholar
Wang G, Shi Y, Fu Z, Yang W, Huang Q, Zhang Y. Controlled synthesis of poly(ε-Caprolactone)-graft-polystyrene by atom transfer radical polymerization with poly(ε-Caprolactone-Co-α-Bromo-ε-Caprolactone) copolymer as macroinitiator. Polymer. 2005;46:10601–6. https://doi.org/10.1016/j.polymer.2005.06.105Article
CAS
Google Scholar
Gao C, Tsou CH, Zeng CY, Yuan L, Peng R, Zhang XM. Organocatalyzed ring-opening copolymerization of α-Bromo-γ-butyrolactone with ε-caprolactone for the synthesis of functional aliphatic polyesters – pre-polymers for graft copolymerization. Des Monomers Polym 2018;21:193–201. https://doi.org/10.1080/15685551.2018.1550288Article
CAS
PubMed
PubMed Central
Google Scholar
Lee R, Huang Y. Synthesis and characterization of amphiphilic block–graft MPEG‐b‐(PαN3CL‐g‐alkyne) degradable copolymers by ring‐opening polymerization and click chemistry. J Polym Sci, Part A Polym Chem 2008;46:4320–31. https://doi.org/10.1002/pola.22741Article
CAS
Google Scholar
Suksiriworapong J, Sripha K, Junyaprasert VB. Synthesis and characterization of bioactive molecules grafted on poly(ɛ-Caprolactone) by “click” chemistry. Polymer. 2010;51:2286–95. https://doi.org/10.1016/j.polymer.2010.03.034Article
CAS
Google Scholar
Conte C, Costabile G, d’Angelo I, Pannico M, Musto P, Grassia G, et al. Skin transport of PEGylated poly(ε-Caprolactone) nanoparticles assisted by (2-Hydroxypropyl)-β-cyclodextrin. J Colloid Interface Sci 2015;454:112–20. https://doi.org/10.1016/j.jcis.2015.05.010Article
CAS
PubMed
Google Scholar
Riva R, Lussis P, Lenoir S, Jérôme C, Jérôme R, Lecomte P. Contribution of “click chemistry” to the synthesis of antimicrobial aliphatic copolyester. Polymer. 2008;49:2023–8. https://doi.org/10.1016/j.polymer.2008.03.008Article
CAS
Google Scholar
Ebara M, Kotsuchibashi Y, Uto K, Aoyagi T, Kim YJ, Narain R, et al. Smart Biomaterials, NIMS Monographs, Springer Tokyo, 2014, p. 321-36.Leroux F, Campagne C, Perwuelz A, Gengembre L. Polypropylene film chemical and physical modifications by dielectric barrier discharge plasma treatment at atmospheric pressure. J Colloid Interface Sci 2008;328:412–20. https://doi.org/10.1016/j.jcis.2008.09.062Article
CAS
PubMed
Google Scholar
Maegawa K, Tanimoto H, Onishi S, Tomohiro T, Morimoto T, Kakiuchi K. Taming the reactivity of alkyl azides by intramolecular hydrogen bonding: site-selective conjugation of unhindered diazides. Org Chem Front. 2021;8:5793–803. https://doi.org/10.1039/D1QO01088CArticle
CAS
Google Scholar
Wang J, Horwitz MA, Dürr AB, Ibba F, Pupo G, Gao Y, et al. Asymmetric azidation under hydrogen bonding phase-transfer catalysis: a combined experimental and computational study. J Am Chem Soc. 2022;144:4572–84. https://doi.org/10.1021/jacs.1c13434Article
CAS
PubMed
PubMed Central
Google Scholar
Uto K, Matsushita Y, Ebara M. Multiphase PCL semi-interpenetrating networks exhibiting the triple- and stress-free two-way shape memory effect. Polym Chem 2023;14:1478–87. https://doi.org/10.1039/d2py01607aArticle
CAS
Google Scholar