Synthesis, polymerisation and degradation of poly(lactide-co-propylene glycol) dimethacrylate adhesives

被引:40
作者
Ho, Sze-Man [1 ]
Young, Anne M. [1 ]
机构
[1] UCL, Eastman Dent Inst, London WC1X 8L, England
基金
英国医学研究理事会;
关键词
injectable; biodegradable; adhesive; polymerisation;
D O I
10.1016/j.eurpolymj.2006.03.018
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
Fluid ABA triblock poly(lactide-co-propylene glycol-co-lactide)s with 7, 17 or 34 propylene glycol and 2, 4, or 8 lactic acid units in each B and A block, respectively, end capped with methacrylate groups were prepared and polymerisation rates upon blue light exposure for 60, 120 or 240 s using 0.5, 1 or 2 wt.% initiators determined. The shortest monomer formulation, with 0.5 wt.% initiators, was most promising as an injectable degradable adhesive for biomedical applications, achieving 96% polymerisation by 120 s after the start of 60 s illumination, forming then a semi-rigid polymer that in water released linearly with time poly(methacrylic-co-lactic) acid degradation products. Over 14 weeks, 2 turn thick specimens largely maintained their dimensions as water sorption balanced the 19 wt.% material loss. Raising initiator concentration or monomer length reduced polymerisation rate on the lower surface of samples. Increasing the number of lactic acid units in each A block from 2 to 8 also enhanced photocrosslinked polymer water sorption and increased average total mass loss to 60 wt.% over 14 weeks but acid product release rate decreased with time. Monomers produced with longer polypropylene glycol B blocks required longer periods of light exposure for full cure and the final polymers exhibited slower non-linear hydrolytic degradation. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1775 / 1785
页数:11
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