## Abstract Amino semitelechelic poly(__N__‐isopropylacrylamide) (PNIPAAm) was prepared by radical polymerization with aminoethanethiol hydrochloride as a chain‐transfer agent. Semi‐interpenetrating polymer network (semi‐IPN) hydrogels, composed of alginate and amine‐terminated PNIPAAm, were prepar
Temperature- and pH-responsive photosensitization activity of polymeric sensitizers based on poly-N-isopropylacrylamide
✍ Scribed by Yasuhiro Shiraishi; Takeshi Suzuki; Takayuki Hirai
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 916 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0032-3861
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✦ Synopsis
a b s t r a c t
We previously reported that a copolymer consisting of N-isopropylacrylamide (NIPAM) and benzophenone (BP) units, behaves as a photosensitizer showing temperature-controlled oxygenation activity in water (J. Am. Chem. Soc. 2006, 128, 8751). This polymer shows a heat-induced oxygenation enhancement at low temperature region (5-20 C), while showing a heat-induced oxygenation suppression at high temperature region (20-60 C), resulting in an off-on-off activity profile against the temperature window. This is driven by a heat-induced phase transition of the polymer from coil to micelle and then to globule states. In the present work, effects of adding an amine component (N-[3-(dimethylamino)propyl]acrylamide: DMAPAM) to the polymer on the sensitization activity were studied, where the relationship between the phase transition behavior and the activity was clarified by several spectroscopic analyses. The polymers, poly(NIPAM x -co-BP y -co-DMAPAM z ), show activity controlled by temperature and pH. The off-on-off activity profile shifts to higher temperature with a pH decrease. This is because protonation of the DMAPAM units leads to an increase in the polymer polarity and, hence, the polymer aggregates at higher temperature. In addition, increase in the DMAPAM content of the polymer leads to further shift of the activity profile. In contrast, at pH < 8, no activity enhancement is observed because complete protonation of the DMAPAM units suppresses polymer aggregation.
📜 SIMILAR VOLUMES
## Abstract **Summary:** A series of semi‐interpenetrating, polymer network (semi‐IPN), hydrogel beads, composed of calcium alginate (Ca‐alginate) and poly(__N__‐isopropylacrylamide) (PNIPAAM), were prepared for a pH/temperature‐sensitive drug delivery study. The equilibrium swelling showed the ind
Interpenetrating polymer networks (IPNs) of poly(N-isopropylacrylamide)/ polyurethane (PNIPAAm/PU) and poly(N-isopropylacrylamide)/poly(acrylic acid) (PNI-PAAm/PAA) were synthesized to investigate the swelling and drug releasing behavior. The presence of urethane network in PNIPAAm/PU IPNs improved