Peng Hongsen, Zhou Shaobing, Guo Tao, Li Yanshan, Li Xiaohong, Wang Jianxin, Weng Jie
Key Laboratory of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, PR China.
Colloids Surf B Biointerfaces. 2008 Oct 15;66(2):206-12. doi: 10.1016/j.colsurfb.2008.06.021. Epub 2008 Jul 9.
In the paper, the poly(D,L-lactide) (PDLLA) and poly(ethylene glycol)-co-poly(D,L-lactide) (PELA) fibers with and without paracetanol drug loading were prepared with an electrospinning method. The morphology of the fibers was observed by scanning electronic microscope (SEM). Their glass transition temperatures (T(g)) were measured with differential scanning calorimetry (DSC). The water contact angle (CA) measurement was also performed to characterize surface properties of fibers. At 37 degrees C in a PBS buffer solution (pH 7.4), in vitro matrix degradation profiles of these fibers were characterized by measuring their weight loss, the molecular weight decrease, and their morphology change. The result showed that the effects of fiber diameter and porosities on the degradation of the electrospun scaffolds might exceed the effects of the molecular weight and the PEG contents, which was different from the polymeric microspheres degradation. In vitro paracetanol release profiles were also investigated in the same condition. The result showed that the drug burst release behaviour was mainly related with the drug-polymer compatibility and the followed sustained release phase depended on polymer degradation.
在该论文中,采用静电纺丝法制备了载有和未载有对乙酰氨基酚药物的聚(D,L-丙交酯)(PDLLA)和聚(乙二醇)-共-聚(D,L-丙交酯)(PELA)纤维。通过扫描电子显微镜(SEM)观察纤维的形态。用差示扫描量热法(DSC)测量其玻璃化转变温度(T(g))。还进行了水接触角(CA)测量以表征纤维的表面性质。在37℃的PBS缓冲溶液(pH 7.4)中,通过测量这些纤维的重量损失、分子量降低及其形态变化来表征其体外基质降解情况。结果表明,纤维直径和孔隙率对电纺支架降解的影响可能超过分子量和PEG含量的影响,这与聚合物微球的降解情况不同。在相同条件下还研究了体外对乙酰氨基酚的释放情况。结果表明,药物的突释行为主要与药物-聚合物的相容性有关,随后的缓释阶段取决于聚合物的降解。