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Biodegradable core/shell fibers by coaxial electrospinning: Processing, fiber characterization, and its application in sustained drug release

机译:通过同轴静电纺丝可生物降解的核/壳纤维:加工,纤维表征及其在持续药物释放中的应用

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Solutions of two biodegradable polymers, that is, poly(dl-lactic acid) (PDLLA) and poly(3-hydroxy butyrate) (PHB), were individually delivered to the inner and outer channel of a coaxial-tube spinneret for electrospinning to prepare core-shell fibers used for drug release applications. By interchanging the inner- and outer-channel solutions, either PDLLA/PHB or PHB/PDLLA core-shell fibers could be conveniently obtained. Their fiber diameters were readily controlled by the flow rate of the core fluid (Q_c). The effects of Q_c on the morphologies of the Taylor cone, the whipping jet, and the electrospun fibers were investigated. Several scaling laws describing the Q _c dependence of the outer fiber diameter (D_f) and the inner fiber diameter (d_f) were derived, that is, D _f~Q_c~(0.02) and d_f~Q _c~(0.18) for the PDLLA/PHB fluids and D_f~ Q_c~(0.3)0 and d_f~Q_c~(0.59) for the PHB/PDLLA fluids. These scaling laws provided the processing guidelines for the manipulation of the final diameters of the core-shell fibers for a given pair of electrospinning solutions. The microstructure revealed by differential scanning calorimetry, Fourier transform infrared spectroscopy, and wide-angle X-ray diffraction showed that the PDLLA component was in the amorphous state. In addition, the crystallizability of the PHB component remained relatively unchanged despite the reduction of its measured melting enthalpy when the PDLLA content was increased through an increase in its flow rate. By controlling Q_c, PDLLA/PHB fibers with a PHB shell of a similar crystallinity but with different thicknesses were readily obtained and used for the sustained release of dimethyloxalylglycine (DMOG) drug, which is a proangiogenic compound acting via the hypoxia-inducible factor system. In contrast with the single-component PDLLA and PHB fibers, which exhibited a burst release behavior, two-stage release kinetics was observed for the present PDLLA/PHB fibers when DMOG was embedded in the core section: an initial fast release before the inflections followed by a constant release. For the first stage, the amount released was 25% within 60 h, irrespective of the PHB thickness. After the burst release, DMOG was linearly released up to an amount of 70%, and the release rate was feasibly controlled by the thickness of the PHB shell.
机译:将两种可生物降解的聚合物,即聚(dl-乳酸)(PDLLA)和聚(3-羟基丁酸)(PHB)的溶液分别输送到同轴管喷丝头的内部和外部通道,以进行静电纺丝,以制备用于药物释放应用的核壳纤维。通过交换内部和外部通道解决方案,可以方便地获得PDLLA / PHB或PHB / PDLLA核-壳纤维。它们的纤维直径很容易通过核心流体的流量(Q_c)控制。研究了Q_c对泰勒锥,搅打射流和电纺纤维形态的影响。推导了描述外纤维直径(D_f)和内纤维直径(d_f)的Q _c依赖性的几个定律,即PDLLA的D _f〜Q_c〜(0.02)和d_f〜Q _c〜(0.18)。 / PHB流体,PHB / PDLLA流体的D_f〜Q_c〜(0.3)0和d_f〜Q_c〜(0.59)。这些缩放定律为给定的一对静电纺丝溶液提供了操纵核-壳纤维最终直径的加工准则。通过差示扫描量热法,傅立叶变换红外光谱法和广角X射线衍射揭示的微观结构表明PDLLA组分处于非晶态。另外,当通过增加其流速增加PDLLA含量时,尽管PHB组分的可结晶性降低,尽管其测量的熔融焓降低了,但其结晶性保持相对不变。通过控制Q_c,可以容易地获得具有类似结晶度但厚度不同的PHB壳的PDLLA / PHB纤维,并将其用于二甲基草酰甘氨酸(DMOG)药物的持续释放,该药物是通过低氧诱导因子系统起作用的促血管生成化合物。与单组分PDLLA和PHB纤维表现出爆发释放行为相反,当将DMOG嵌入芯部时,目前的PDLLA / PHB纤维观察到两阶段释放动力学:在拐点发生之前先快速释放不断释放。对于第一阶段,与PHB厚度无关,在60小时内释放量为25%。爆裂释放后,DMOG线性释放至70%,释放速​​率受PHB壳的厚度控制。

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