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1.中国科学院成都有机化学研究所 成都 610041
2.中国科学院大学 北京 100049
3.青岛出入境检验检疫局 青岛 266001
陈栋梁, E-mail:1633cdl@cioc.ac.cn Dong-liang Chen, E-mail:1633cdl@cioc.ac.cn
纸质出版日期:2017-4,
收稿日期:2016-6-4,
修回日期:2016-7-24,
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李丽楠, 刘永江, 刘书慧, 杨欢, 熊成东, 陈栋梁. 聚 (对氧环己酮-三亚甲基碳酸酯) 静电纺膜的制备及其生物学与降解性能研究[J]. 高分子学报, 2017,(4):651-660.
Li-nan Li, Yong-jiang Liu, Shu-hui Liu, Huan Yang, Cheng-dong Xiong, Dong-liang Chen. Preparation, Biological Properties and Degradation Studies on the Electrospun Membranes of Poly (
李丽楠, 刘永江, 刘书慧, 杨欢, 熊成东, 陈栋梁. 聚 (对氧环己酮-三亚甲基碳酸酯) 静电纺膜的制备及其生物学与降解性能研究[J]. 高分子学报, 2017,(4):651-660. DOI: 10.11777/j.issn1000-3304.2017.16157.
Li-nan Li, Yong-jiang Liu, Shu-hui Liu, Huan Yang, Cheng-dong Xiong, Dong-liang Chen. Preparation, Biological Properties and Degradation Studies on the Electrospun Membranes of Poly (
通过静电纺丝技术,将二元共聚物聚(对氧环己酮-三亚甲基碳酸酯)(PDT)制成了膜材料,采用扫描电镜(SEM)观察了静电纺膜的形貌,当共聚物中TMC组分含量越高时,纤维丝之间黏结越严重.采用静态接触角仪测定了静电纺膜的接触角,表征了共聚物的亲疏水性,PDT的亲水性介于PPDO与PTMC均聚物静电纺膜之间.对PDT共聚物静电纺膜进行了L929大鼠成纤维细胞培养实验,MTT和荧光染色结果说明PDT膜的细胞相容性良好.通过水解及酶解实验考察了材料的降解过程,PDT静电纺膜在脂肪酶存在下降解速率加快,材料的失重率、分子量损失、材料形貌破坏程度等均高于水解样品,这说明脂肪酶对含有TMC组分的聚合物的降解有促进作用.同时,降解过程中PBS溶液的pH值变化说明TMC组分的加入,减缓了降解过程中酸性物质的产生.
Nano-structured fibers of the synthesized poly (
p
-dioxanone-
co
-trimethylene carbonate) (PDT) were prepared by electrospinning technique. Their physicochemical and biological properties were evaluated with the standards for biomedical materials
and it was found that the content of trimethylene carbonate (TMC) units in PDT copolymer could change these properties. As observed by the scanning electron microscopy (SEM)
more TMC units in the copolymer would lead to severer fiber bonding
which probably is due to the ductility of TMC segments. The results of static water contact angle testing for the electrospun membranes demonstrated that the hydrophilicity of PDT was between that of PPDO and PTMC. The growth status of L929 mouse fibroblasts on the as-spun membranes of PDT and PPDO was evaluated by the fluorescent micrographs and MTT assay. It was shown that the cells grew well
which suggested good biocompatibility of these copolymers and their suitability in biomedical fields. The
in vitro
biodegradability of the electrospun membranes in phosphate buffered saline (PBS) and PBS with lipase was separately investigated
via
measurements of mass loss
M
w
retention
as well as variations in crystallinity
thermal properties
pH value
and morphology. After 35 days of degradation
mass and
M
w
of the polymers significantly reduced while slight differences appeared in pH values before and after. Among the samples
the pH value exhibited the most descent for PBS with PPDO and the least for PBS with PTMC; pH decrement of PBS with PDT was in the middle. These results pointed out that the existence of TMC units in the polymers reduced acidic products in the degradation process
which was good for implanted materials. The changes of SEM images of PTMC at different degradation time indicated that PTMC degraded by surface erosion. And the changes of thermal properties of PDT indicated that PTMC was susceptible to enzymatic degradation by lipase. The lipase enzymatic degradation rate of the polymers containing TMC segments was faster than the hydrolytic degradation rate
which illustrated this point.
对氧环己酮三亚甲基碳酸酯静电纺膜降解
p-DioxanoneTrimethylene carbonateElectrospun membranesDegradation
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