Laboratoire de Chimie Physique Macromoléculaire, UMR 7568 CNRS-Nancy University, Nancy, France.
Colloids Surf B Biointerfaces. 2011 Nov 1;88(1):332-8. doi: 10.1016/j.colsurfb.2011.07.010. Epub 2011 Jul 12.
This study aimed at determining the influence of the mechanism of polymerization on the molar mass and degradation of poly(n-butyl cyanoacrylate) (PBCA) nanoparticles obtained by miniemulsion polymerization. Therefore, nanoparticles of poly(n-butyl cyanoacrylate) were synthesized via radical and/or anionic miniemulsion polymerization stabilized by Brij®78, a POE based surfactant. Polymerization conditions had little influence on the final diameter while it severely affected the final molar masses of PBCA. An increase of the temperature and of the pH of the continuous phase led to higher molar masses. A further increase was observed when a radical initiator was added in the monomer. The evolution of the molar mass of the synthesized poly(n-butyl cyanoacrylate) was followed as a function of time at pH 7.4 by Size Exclusion Chromatography. As expected, the degradation kinetics strongly depended on the polymerization mechanism (anionic or radical).
本研究旨在确定聚合机制对通过细乳液聚合获得的聚(正丁基氰基丙烯酸酯)(PBCA)纳米粒子的摩尔质量和降解的影响。因此,通过自由基和/或阴离子细乳液聚合合成了聚(正丁基氰基丙烯酸酯)纳米粒子,该聚合由 POE 基表面活性剂 Brij®78 稳定。聚合条件对最终直径的影响很小,但对 PBCA 的最终摩尔质量有严重影响。连续相的温度和 pH 值升高会导致摩尔质量升高。当在单体中添加自由基引发剂时,观察到进一步的增加。通过尺寸排阻色谱法在 pH 7.4 下随时间跟踪合成的聚(正丁基氰基丙烯酸酯)的摩尔质量的演变。正如预期的那样,降解动力学强烈取决于聚合机制(阴离子或自由基)。