首页> 外文期刊>International Journal of Pharmaceutics >Optimizing partition-controlled drug release from electrospun core-shell fibers.
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Optimizing partition-controlled drug release from electrospun core-shell fibers.

机译:优化电纺芯-壳纤维的分区控制药物释放。

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摘要

Controlled release of hydrophilic entities, such as peptides, proteins and even pDNA, is difficult to accomplish with conventional approaches. This work suggests one possible approach for controlled release of such actives using electrospun core-shell fiber structures. In particular, we propose strategies for partition control of the release. The fibers consist of two layers, with the outer polymer sleeve serving containing the inner core, in which the drug is encapsulated. By varying the physical and chemical properties of the core and shell solutions, we have shown that the release rate of a hydrophilic drug, metoclopramide hydrochloride, is controllable. Experimental results show a clear difference in the release pattern between monolithic fibers made of hydrophilic and hydrophobic polymers and various core-shell fibers with PCL, PLLA and PLGA 80/20 as shell polymers. The study yields insight into when partition control of release can be achieved in core-shell fibers, and with that, options for controlled release systems for hydrophilic drugs, peptides and pDNA.
机译:用常规方法很难实现亲水性实体(如肽,蛋白质甚至pDNA)的受控释放。这项工作提出了一种使用电纺核-壳纤维结构控制此类活性成分释放的可能方法。特别是,我们提出了对发布进行分区控制的策略。纤维由两层组成,外部聚合物套筒用于容纳内芯,药物被封装在该内芯中。通过改变核和壳溶液的物理和化学性质,我们已经表明,亲水性药物甲氧氯普胺的释放速率是可控制的。实验结果表明,由亲水性和疏水性聚合物制成的整体式纤维与以PCL,PLLA和PLGA 80/20为壳聚合物的各种核-壳纤维之间的释放方式有明显差异。这项研究深入了解了何时可以在核-壳纤维中实现释放的分配控制,并以此为亲水性药物,肽和pDNA的控释系统提供了选择。

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