Title of article :
pH-Controlled association of PEG-containing terpolymers of N-isopropylacrylamide and 1-vinylimidazole
Author/Authors :
Bisht، نويسنده , , Harender S. and Wan، نويسنده , , Lei and Mao، نويسنده , , Guangzhao and Oupicky، نويسنده , , David، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2005
Pages :
8
From page :
7945
To page :
7952
Abstract :
Temperature- and pH-controlled association of terpolymers of N-isopropylacrylamide (NIPA) with 1-vinylimidazole (VI) and polyethylene glycol (PEG) has been investigated by light scattering and atomic force microscopy (AFM) in situ. The polymers contained 0–15 mol% VI and 0–2 mol% PEG. The phase transition temperatures (Tp) have been in the range of 32–45 °C and exhibited significant dependence on the pH of solution in the pH range between 5 and 8. The Tp of the polymers increased with increasing VI content and with decreasing pH, confirming major effect of VI ionization status on Tp. The presence of PEG grafts in the polymer structure had augmenting effect on the magnitude of pH-responsiveness and on the pH-independent colloidal stability of the polymer particles formed above Tp. Incorporation of VI into the polymer structure had similar, but pH-dependent effect on colloidal stabilization of the polymer particles. The size of the particles formed after the phase transition is driven by the association of the collapsed NIPA segments in the globule conformation and it decreased with decreasing pH. The phase transition temperature of the polymers could be adjusted to increase from temperatures below, to temperatures above body temperature upon decreasing pH from 7 to 6, suggesting that such polymers could provide a material platform for a variety of biomedical applications. AFM analysis in situ showed a fully reversible formation of particles in the solutions of the polymers above their Tp.
Keywords :
N-isopropylacrylamide , Vinylimidazole , PEG
Journal title :
Polymer
Serial Year :
2005
Journal title :
Polymer
Record number :
1723371
Link To Document :
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