Félix Leticia, Hernández Javier, Argüelles-Monal Waldo M, Goycoolea Francisco M
Centro de Investigación en Alimentación y Desarrollo, Laboratory of Biopolymers, P.O. Box 1735, Hermosillo, Sonora, 83000 Mexico.
Biomacromolecules. 2005 Sep-Oct;6(5):2408-15. doi: 10.1021/bm0501297.
N-Acylation of chitosan with carboxylic anhydrides in dilute acetic acid/methanol has been a well documented strategy to selectively modify chitosan. Although this reaction is known to lead to irreversible gel formation, the kinetics and mechanism of this process have not so far been addressed. To this purpose, gel formation during the N-isobutyrylation of chitosan was investigated as a function of the reaction stoichiometry (R), chitosan concentration, and temperature by small deformation oscillatory rheology. Gel formation follows closely the chemical reaction and it proceeds predominantly under second-order kinetics as established from the dependence of critical gel time, t(gel), on R and concentration. The activation energy value derived from t(gel) vs 1/T data (E(a) = 68.29 +/- 1.80 kJ/mol) was almost identical to values reported for the chitosan N-acetylation reaction in previous studies. An excess isobutyric anhydride is suggested to be necessary for nucleation and hydrophobic association. The potential application of N-isobutyrylchitosan (NIBC) hydrogels in the design of thermally sensitive materials is also demonstrated.
在稀醋酸/甲醇中用羧酸酐对壳聚糖进行N-酰化是一种有充分文献记载的选择性修饰壳聚糖的策略。尽管已知该反应会导致不可逆的凝胶形成,但到目前为止,这一过程的动力学和机理尚未得到研究。为此,通过小变形振荡流变学研究了壳聚糖N-异丁酰化过程中凝胶的形成与反应化学计量比(R)、壳聚糖浓度和温度的关系。凝胶形成与化学反应密切相关,并且如从临界凝胶时间t(gel)对R和浓度的依赖性所确定的那样,它主要遵循二级动力学进行。从t(gel)与1/T数据得出的活化能值(E(a) = 68.29 +/- 1.80 kJ/mol)与先前研究中报道的壳聚糖N-乙酰化反应的值几乎相同。有人认为过量的异丁酸酐对于成核和疏水缔合是必要的。还展示了N-异丁酰壳聚糖(NIBC)水凝胶在热敏材料设计中的潜在应用。