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Conduction Properties Of Decellularized Nerve Biomaterials

机译:脱细胞神经生物材料的导电特性

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The purpose of this study is to optimize poly(3,4,-ethylenedioxythiophene) (PEDOT) polymerization into decel-lular nerve scaffolding for interfacing to peripheral nerves. Our ultimate aim is to permanently implant highly conductive peripheral nerve interfaces between amputee, stump, nerve fascicles and prosthetic electronics. Decellular nerve (DN) scaffolds are an FDA approved biomaterial (Axogen™) with the flexible tensile properties needed for successful permanent coaptation to peripheral nerves. Biocompatible, electroconduc-tive, PEDOT facilitates electrical conduction through PEDOT coated acellular muscle. New electrochemical methods were used to polymerize various PEDOT concentrations into DN scaffolds without the need for a final dehydration step. DN scaffolds were then tested for electrical impedance and charge density. PEDOT coated DN scaffold materials were also implanted as 15-20mm peripheral nerve grafts. Measurement of in-situ nerve conduction immediately followed grafting. DN showed significant improvements in impedance for dehydrated and hydrated, DN, polymerized with moderate and low PEDOT concentrations when they were compared with DN alone (a < 0.05). These measurements were equivalent to those for DN with maximal PEDOT concentrations. In-situ, nerve conduction measurements demonstrated that DN alone is a poor electro-conductor while the addition of PEDOT allows DN scaffold grafts to compare favorably with the "gold standard", autograft (Table 1). Surgical handling characteristics for conductive hydrated PEDOT DN scaffolds were rated 3 (pliable) while the dehydrated models were rated 1 (very stiff) when compared with autograft ratings of 4 (normal). Low concentrations of PEDOT on DN scaffolds provided significant increases in electro active properties which were comparable to the densest PEDOT coatings. DN pliability was closely maintained by continued hydration during PEDOT electrochemical polymerization without compromising electroconduc-tivity.
机译:这项研究的目的是优化聚(3,4,-乙撑二氧噻吩)(PEDOT)聚合反应到与周围神经接口的小神经支架中。我们的最终目标是永久性地在截肢者,残端,神经束和假体电子设备之间植入高度导电的周围神经接口。脱细胞神经(DN)支架是FDA批准的生物材料(Axogen™),具有成功地永久接合周围神经所需的柔性拉伸特性。具有生物相容性,导电性的PEDOT有助于通过PEDOT涂层的脱细胞肌肉进行导电。使用新的电化学方法将各种浓度的PEDOT聚合到DN支架中,而无需最后的脱水步骤。然后测试DN支架的电阻抗和电荷密度。也将PEDOT涂层的DN支架材料植入15-20mm周围神经移植物中。移植后立即测量原位神经传导。与单独的DN相比,DN表现出以适中和低PEDOT浓度聚合的脱水和水合DN的阻抗显着改善(a <0.05)。这些测量值与具有最大PEDOT浓度的DN的测量值相同。原位神经传导测量结果表明,仅DN的导电性较差,而PEDOT的添加使DN支架移植物可与“金标准”自体移植物相媲美(表1)。与自体移植评分为4(正常)相比,导电的水合PEDOT DN支架的手术处理特性为3(柔韧),而脱水模型的评分为1(非常硬)。 DN支架上的PEDOT浓度低,可提供与最稠密的PEDOT涂层相当的电活性特性。通过在PEDOT电化学聚合过程中持续水合作用,可以保持DN柔韧性,而不会影响导电性。

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