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Study on the control of the compositions and properties of a biodegradable polyester elastomer

机译:控制可生物降解聚酯弹性体组成和性能的研究

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摘要

Biodegradable polyester elastomers are widely reported to be applied in varied biomedical fields. In this paper, we attempt to investigate how both the thermal-curing time and molar ratio of the monomers affect the final compositions and properties of the novel poly(glycerol-sebacate-citrate) (PGSC) elastomers. First, PGSC elastomers are obtained after the thermal curing of the moldable mixtures consisting of citric acid and poly(glycerol-sebacate) (PGS) prepolymers synthesized in the lab. Then further studies show that, on the one hand, the control of longer thermal-curing time results in elastomers with less sol, lower swelling degree, slower degradation, greater mechanical strength and higher glass transition temperature and, on the other hand, the crosslink with more citric acid is advantageous to greatly improving their mechanical strength and glass transition temperatures, simultaneously decreasing their sol contents, swelling degrees and degradation rates. The PGSC elastomers show thermosetting properties, certain strength, mass losses lower than 20% after 4-week degradation and durative water absorption during degradation. Thus they might be potentially used as degradable bio-coatings, varied soft biomedical membranes and drug delivery matrices.
机译:可生物降解的聚酯弹性体被广泛报道用于各种生物医学领域。在本文中,我们尝试研究热固化时间和单体的摩尔比如何影响新型聚(癸二酸甘油酯)(PGSC)弹性体的最终组成和性能。首先,PGSC弹性体是在实验室合成的柠檬酸和聚癸二酸甘油酯(PGS)预聚物组成的可塑混合物热固化后获得的。然后进一步的研究表明,一方面,控制较长的热固化时间会导致弹性体的溶胶更少,溶胀度更低,降解速度更慢,机械强度更高,玻璃化转变温度更高,另一方面,交联度更高。含有更多柠檬酸的酸有利于大大提高其机械强度和玻璃化转变温度,同时降低其溶胶含量,溶胀度和降解速率。 PGSC弹性体表现出热固性,一定的强度,降解4周后的质量损失低于20%,并且降解期间持续吸水。因此,它们可能被潜在地用作可降解生物涂层,各种生物医学软膜和药物输送基质。

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