MIRA Institute for Biomedical Technology and Technical Medicine and Department of Polymer Chemistry and Biomaterials, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE, Enschede, The Netherlands.
J Control Release. 2010 Oct 1;147(1):54-61. doi: 10.1016/j.jconrel.2010.06.031. Epub 2010 Jul 16.
Photo-crosslinkable, fumaric acid monoethyl ester-functionalized poly(trimethylene carbonate) oligomers were synthesized and copolymerized with N-vinyl pyrrolidone (NVP) and vinyl acetate (VAc) to form biodegradable polymer networks. The copolymerization reactions were much faster than homopolymerization of the fumarate end-groups of the macromers. The hydrophilicity of the networks could by varied by mixing NVP and VAc at different ratios. The prepared network extracts were compatible with NIH 3T3 fibroblasts. Release of vitamin B12, used as a model drug, could be tuned by varying network hydrophilicity and macromer molecular weight. A more hydrophilic and less densely crosslinked network resulted in faster release.
合成了可光交联的、富马酸单乙酯功能化的聚三亚甲基碳酸酯低聚物,并将其与 N-乙烯基吡咯烷酮(NVP)和醋酸乙烯酯(VAc)共聚,形成可生物降解的聚合物网络。共聚反应比大分子中富马酸端基的均聚反应快得多。通过混合不同比例的 NVP 和 VAc,可以改变网络的亲水性。所制备的网络提取物与 NIH 3T3 成纤维细胞相容。通过改变网络亲水性和大分子分子量,可以调节维生素 B12 的释放,维生素 B12 被用作模型药物。更亲水和交联密度更低的网络导致更快的释放。