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Nano-Patterned Poly-ε-caprolactone with Controlled Release of Retinoic Acid and Nerve Growth Factor for Neuronal Regeneration

机译:纳米图案化多ε-己内酯,具有控制释放的视黄酸和神经生长因子进行神经元再生

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A combination of nanotopography and controlled release could be a potential treatment for damages to the central and peripheral nervous system. Synergistic effects of both physical and chemical guidance were more effective than individual cues in the directional promotion of neurite outgrowth [1]. Hypothesizing that synergistic effect will enhance neuronal differentiation of human mesenchymal stem cells (hMSCs), a fabrication method for neurotrophic factors encapsulation in a nanopatterned (350nm-gratings) poly-E-caprolactone (PCL) film was developed. Nanotopography directs hMSCs into neuronal lineage while controlled release of neurotrophic factors presents biochemical signals with temporal and spatial control. Preliminary results demonstrated synergistic effect on hMSC cultured on substrates with both nanotopographical and biochemical cues. The protein/drug encapsulated PCL films were fabricated by modified solvent casting methods in which the biologies were 'sandwiched' between two layers of PCL on a nanopatterned polydimethylsiloxane mold. Bovine serum albumin (BSA), RA and NGF were encapsulated into the films using this sandwich approach. BSA was first encapsulated to optimize the sustained release. Among different fabrication methods in BSA optimization, encapsulating solid BSA between 2 PCL layers resulted in most sustainable release. Surface topography remained intact after 10 days incubated in PBS with controlled release, verified through SEM. Continuous release of bioactive RA and NGF was observed over the 1 week release period. Human MSCs aligned and elongated along the nano-patterned films. Enhanced upregu-lation of neuronal gene such as microtubule associated protein (MAP2) and neurofilament (NFL) was observed in hMSCs cultured on combination cues, as compared to individual cues. Using quantitative PCR analysis, upregulation of MAP2 in hMSCs on the nanogratings with controlled release NGF was verified, highlighting the synergistic effect of both biochemical and nanotopographical cues in directing hMSC differentiation. This fabrication methodology will allow the delivery of multiple therapeutic cues for potential applications in neural regeneration.
机译:纳米复印术和控制释放的组合可能是对中央和外周神经系统损害的潜在处理。物理和化学指导的协同效应比神经沸肌大多数的定向促进的个体线索更有效[1]。假设该协同效应将增强人间充质干细胞(HMSCs)的神经元分化,开发了一种用于纳米透明构件(350nm光栅)聚 - 己内酮(PCL)膜中的神经营养因子包封的制造方法。 NanoTopography将HMSCs指向神经元谱系,而被控制的神经营养因子的控制释放呈现出具有时间和空间控制的生物化学信号。初步结果证明了对具有纳米波特和生化线索的底物培养的HMSC的协同作用。通过改性溶剂浇铸方法制造蛋白质/药物包封的PCL薄膜,其中将生物学在两层PCL上“夹在纳米透明的聚二甲基硅氧烷模具之间”。使用这种三明治方法将牛血清白蛋白(BSA),Ra和NGF包封在薄膜中。首先封装BSA以优化持续释放。在BSA优化中的不同制造方法中,在2个PCL层之间包封固体BSA导致最可持续的释放。在具有控释的PBS中孵育10天后,表面形貌保持完整,通过SEM验证。在1周释放期间观察到生物活性RA和NGF的连续释放。人体MSCs沿纳米图案薄膜对齐和伸长。与单个提示相比,在组合提示的HMSCs中,在组合提示培养的HMSCs中增强了神经元基因的增强的神经元基因(Map2)和神经嘧膜(NFL)的uchregu。使用定量PCR分析,验证了具有控制释放NGF的HMSC上MAP2在HMSC中的上调,突出了生物化学和纳米检测提示在引导HMSC分化方面的协同效应。该制造方法将允许递送多种治疗提示,用于神经再生中的潜在应用。

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