pH- and temperature-responsive hydrogels from crosslinked triblock copolymers prepared via consecutive atom transfer radical polymerizations
Well-defined poly((2-dimethyl amino)ethyl methacrylate- co-2-hydroxyethyl methacrylate)- b-poly( N-isopropylacrylamide)- b-poly((2-dimethyl amino)ethyl methacrylate- co-2-hydroxyethyl methacrylate), or P(DMAEMA- co-HEMA)- b-P(NIPAAm)- b-P(DMAEMA- co-HEMA), triblock copolymers were synthesized by con...
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Veröffentlicht in: | Biomaterials 2006-05, Vol.27 (14), p.2787-2797 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Well-defined poly((2-dimethyl amino)ethyl methacrylate-
co-2-hydroxyethyl methacrylate)-
b-poly(
N-isopropylacrylamide)-
b-poly((2-dimethyl amino)ethyl methacrylate-
co-2-hydroxyethyl methacrylate), or P(DMAEMA-
co-HEMA)-
b-P(NIPAAm)-
b-P(DMAEMA-
co-HEMA), triblock copolymers were synthesized by consecutive atom transfer radical polymerizations (ATRPs), using ethylene glycol di-2-bromoisobutyrate (Br–EG–Br) as the starting ATRP initiator. The hydroxyl groups of the incorporated HEMA units were used as crosslinking sites for the preparation of smart hydrogels. The so-prepared hydrogels exhibited both temperature- and pH-sensitive behavior derived, respectively, and independently, from the P(NIPAAm) blocks and P(DMAEMA) units, in the crosslinked matrices. The hydrogels exhibited a lower critical solution temperature (LCST) of 31–32
°C in aqueous media of pH 1–7, not unlike that of the P(NIPAAm) homopolymer. The swelling ratios and swelling/deswelling kinetics of the hydrogels depended strongly on pH and temperature of the medium. The copolymers were characterized by gel-permeation chromatography, X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, and
1H nuclear magnetic resonance (
1H NMR) spectroscopy. The resultant stimuli-responsive hydrogels were characterized by differential scanning calorimetry (DSC). These stimuli-responsive hydrogels will have potential applications in biomedical areas, such as tissue engineering and drug delivery. |
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ISSN: | 0142-9612 1878-5905 |
DOI: | 10.1016/j.biomaterials.2006.01.003 |