离聚物
材料科学
生物材料
离子键合
聚酯纤维
结晶
PLGA公司
化学工程
聚合物
乙醇酸
高分子化学
生物物理学
乳酸
共聚物
纳米技术
化学
有机化学
复合材料
纳米颗粒
离子
细菌
工程类
生物
遗传学
作者
S.-I. Han,Sun‐Woong Kang,Byung‐Soo Kim,Sumin Im
标识
DOI:10.1002/adfm.200400079
摘要
Abstract To evaluate the potential of polyester‐based ionomers as biomaterials, we have characterized them in terms of crystallization behavior, degradation, and in‐vitro cellular interactions. The polymers used are poly(butylene succinate)‐based ionomers (PBSis) with 1 to 5 mol‐% dimethyl 5‐sodium sulfoisophthalate. Even a few incorporated ionic groups significantly decreases the folding surface energy, indicating that folding into crystalline lamellae is more difficult for chains restricted by ionic aggregates. Transmission electron microscopy (TEM) does not reveal any distinct aggregation of ionic clusters following hydrolytic degradation, which suggests that the physical crosslinkage due to ionic interactions is vulnerable to hydrolysis. The in‐vitro cellular interactions of polyester‐based ionomers is assessed by the culture of human dermal fibroblasts with PBSi extracts or in direct contact with the PBSi films. Cells on PBSi films and in their extracts exhibit appropriate specific growth rates and normal metabolic function regardless of the incorporated ionic content compared with poly[( D , L ‐lactic acid)‐ co ‐(glycolic acid)] (75:25, PLGA), which is well known to be biocompatible. The cells growing on PBSi films spread to a sufficient extent, displaying relatively active filopodial growth, as compared to that of parent PBS. These results suggest that the conspicuous topology and hydrophilic nature of the ionomer surface affect cellular interactions, and that this ionomer therefore has potential applications as a biomaterial.
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