Synthesis and investigation of monomodal hydroxy-functionalized PEG methacrylate based copolymers with high polymerization degrees. Modification by “grafting from” |
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| Affiliation: | 1. Department of Physical Chemistry and Technology of Polymers, Faculty of Chemistry, Silesian University of Technology, M. Strzody 9, 44-100 Gliwice, Poland;2. Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 ?ód?, Poland;1. Centro de Investigación en Química Aplicada (CIQA), Departamento de Procesos de Polimerización, # 140, Blvd. Enrique Reyna Hermosillo, Saltillo, 25294, Coahuila, Mexico;2. Department of Chemistry, University of Victoria, 3800, Finnerty Rd, Victoria, BC, Canada;3. CONACYT-CIQA, Departamento de Procesos de Polimerización, # 140, Blvd. Enrique Reyna Hermosillo, Saltillo, 25294, Coahuila, Mexico;1. George & Josephine Butler Polymer Research Laboratory, Center for Macromolecular Science & Engineering, Department of Chemistry, University of Florida, Gainesville, FL 32611, USA;2. Department of Chemistry, International Institute of Nanotechnology, Chemistry of Life Processes Institute, Simpson Querrey Institute, Lurie Cancer Center, Chicago, IL, USA;3. Department of Materials Science & Engineering, Department of Biomedical Engineering, Department of Pharmacology, Northwestern University, Evanston, IL 60208, USA;4. Department of Chemistry & Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA;1. Department of Biotechnology, Institute of Health Sciences, Bezmialem Vak?f University, 34093 Istanbul, Turkey;2. Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Bezmialem Vakif University, 34093 Istanbul, Turkey;3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Bezmialem Vakif University, 34093 Istanbul, Turkey |
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| Abstract: | The synthesis of monomodal copolymers with poly(ethylene glycol) (PEG) side chains from commercial poly(ethylene glycol) methacrylates (PEGMA) by atom transfer radical polymerization (ATRP) is verified. Two hydroxy-functionalized PEGMA macromonomers (520 g/mol and 360 g/mol) were copolymerized with methyl methacrylate (MMA) using various initial feed (1.5/98.5–50/50 mol.%). The copolymers P(MMA-co-PEGMA) with high degree of polymerization, e.g. 100–275 of repeating units in the backbone including 7–56 PEG side chains, were obtained. The relative reactivity ratios of PEGMA and MMA determined by the Jaacks method indicated slightly faster incorporation of macromonomer into polymeric chain than MMA (rMMA = 0.79; rPEGMA = 1.27). The polymers containing at least 17 mol.% of PEGMA units were water-soluble and exhibited clouding point at temperature in a broad range of 39–70 °C. The temperature-sensitive effect makes these polymers as a potential carriers in drug delivery systems. In the case of copolymers insoluble in water, a three-step procedure, including esterification to ATRP multifunctional macroinitiators, ATRP of tert-butyl methacrylate (tBMA) by grafting from, deprotection of carboxylic groups by removing tert-butyl groups, was applied to extend PEG grafts and expand the content of hydrophilic fraction (32–94 mol.%), what efficiently developed polymer solubility in polar solvents giving possibility for the future biomedical applications. |
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| Keywords: | Hydroxy-functionalized PEGMA Graft copolymers Amphiphilicity Temperature-sensitivity |
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