Investigation of Pluronic© F127-Water Solutions Phase Transitions by DSC and Dielectric Spectroscopy

被引:47
作者
Barba, Anna Angela [1 ]
d'Amore, Matteo [1 ]
Grassi, Mario [2 ]
Chirico, Serafina [3 ]
Lamberti, Gaetano [3 ]
Titomanlio, Giuseppe [3 ]
机构
[1] Univ Salerno, Dipartimento Sci Farmaceut, I-84084 Fisciano, SA, Italy
[2] Univ Trieste, Dipartimento Ingn Chim Ambiente & Materie Prime, I-34127 Trieste, Italy
[3] Univ Salerno, Dipartimento Ingn Chim & Alimentare, I-84084 Fisciano, SA, Italy
关键词
biological applications of polymers; block copolymers; dielectric properties; differential scanning calorimetry (DSC); gelation; SOL-GEL TRANSITION; AQUEOUS-SOLUTIONS; TRIBLOCK COPOLYMERS; THERMODYNAMICS; MICELLIZATION; BEHAVIOR; GELATION;
D O I
10.1002/app.30586
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The water solutions of the block copolymers PEO(n)-PPO(m)-PEO(n), known as pluronics, show a complex thermal behavior, since they are liquid at low temperature (5 degrees C), and they can give soft gel when heated at body temperature (37 degrees C). These properties are of great interest in biomedical applications. To properly design these applications, a prerequisite is the knowledge of the thermodynamics-how much-and of the kinetics-how fast-with which these transformations take place. In this work, solutions of F127 (the copolymer for which n = 100 and m = 65) were studied by varying the concentration and the temperature and analyzing their behavior when heated under several heating rates. The studies were performed by differential scanning calorimetry (DCS) and dielectric spectroscopy. The investigations carried out under equilibrium conditions allowed us to determine the thermodynamics of the phase transitions, whereas the investigations carried out wider varying conditions allowed us to quantify the kinetics of the phase transitions. Empirical models were also proposed to describe both the thermodynamics and the kinetics observed. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 114: 688-695, 2009
引用
收藏
页码:688 / 695
页数:8
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