TY - JOUR
T1 - In situ thermal gelation of water-soluble poly(N-isopropylacrylamide-co-vinylphosphonic acid)
AU - Eom, Gyoung Tae
AU - Oh, Seaung Youl
AU - Park, Tae Gwan
PY - 1998
Y1 - 1998
N2 - A copolymer baaed on N-isopropylacrylamide (NIPAAm) and vinylphosphonic acid (VP) was synthesized to investigate its thermal gelation behaviors in the presence of calcium ion. The copolymer showed a variety of temperature-sensitive phase transition properties as a function of temperature. In an aqueous solution, it exhibited 3 distinctive phase transitions with gradually increasing the temperature: a transparent solution state, a cloudy and white solution state (sol), and a white and semisolid (gel) state. Particularly, in situ reversible sol-gel transition behaviors could be observed over a wide range of temperatures in the presence of varying concentrations of calcium ion. This physical gel that initially was formed homogeneously without changing its dimension in the solution container tended to slowly phase-separate out into a polymer-rich phase and a water-rich phase over the following several days, indicating that a synerisis occurred. The in situ thermal gelation behavior was utilized in the controlled release formulation of a model compound.
AB - A copolymer baaed on N-isopropylacrylamide (NIPAAm) and vinylphosphonic acid (VP) was synthesized to investigate its thermal gelation behaviors in the presence of calcium ion. The copolymer showed a variety of temperature-sensitive phase transition properties as a function of temperature. In an aqueous solution, it exhibited 3 distinctive phase transitions with gradually increasing the temperature: a transparent solution state, a cloudy and white solution state (sol), and a white and semisolid (gel) state. Particularly, in situ reversible sol-gel transition behaviors could be observed over a wide range of temperatures in the presence of varying concentrations of calcium ion. This physical gel that initially was formed homogeneously without changing its dimension in the solution container tended to slowly phase-separate out into a polymer-rich phase and a water-rich phase over the following several days, indicating that a synerisis occurred. The in situ thermal gelation behavior was utilized in the controlled release formulation of a model compound.
KW - Drug delivery
KW - Hydrogel
KW - Lower critical solution temperature
KW - Poly(N-isopropylacrylamide)
KW - Thermal gelation
UR - http://www.scopus.com/inward/record.url?scp=0032488168&partnerID=8YFLogxK
U2 - 10.1002/(sici)1097-4628(19981205)70:10<1947::aid-app9>3.0.co;2-i
DO - 10.1002/(sici)1097-4628(19981205)70:10<1947::aid-app9>3.0.co;2-i
M3 - Article
AN - SCOPUS:0032488168
SN - 0021-8995
VL - 70
SP - 1947
EP - 1953
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
IS - 10
ER -