Department of Chemistry, The University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599, United States.
Anal Chem. 2013 Nov 5;85(21):10488-94. doi: 10.1021/ac402312b. Epub 2013 Oct 8.
The active release of pharmaceutical agents and the use of porous sensor membranes represent the two most promising strategies for addressing the poor tissue biocompatibility of implantable glucose biosensors. Herein, we describe the combination of these approaches to create nitric oxide (NO)-releasing porous fiber mat-modified sensor membranes. An electrospinning method was used to directly modify needle-type glucose biosensors with the NO donor-loaded fibers. The resulting NO-releasing fiber mat (540 ± 139 nm fiber diameter, 94.1 ± 3.7% porosity) released ~100 nmol of NO per mg of polyurethane over 6 h while maintaining a porous structure without leaching of the NO donor, even in serum. The porous fiber membrane did not influence the analytical performance of the biosensor when ≤50 μm thick.
药物制剂的主动释放和多孔传感器膜的使用是解决可植入葡萄糖生物传感器组织生物相容性差的两个最有前途的策略。在此,我们描述了将这些方法结合起来,创建释放一氧化氮(NO)的多孔纤维垫修饰传感器膜。采用静电纺丝方法,将负载有 NO 供体的纤维直接修饰到针型葡萄糖生物传感器上。所得到的释放一氧化氮的纤维垫(纤维直径 540±139nm,孔隙率 94.1±3.7%)在 6 小时内每毫克聚氨酯可释放约 100nmol 的 NO,同时保持多孔结构,NO 供体没有浸出,即使在血清中也是如此。当厚度≤50μm时,多孔纤维膜不会影响生物传感器的分析性能。