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A novel therapeutic approach encapsulating brain-derived neurotrophic factor in nanoparticles for treating sensorineural hearing loss.

机译:一种将脑源性神经营养因子包裹在纳米颗粒中的新型治疗方法,用于治疗感觉神经性听力损失。

摘要

There are approximately 688,000 adults in the UK with severe to profound sensorineural hearing loss. While many people who suffer from hearing loss benefit from the use of a conventional hearing aid, these devices are not effective in patients with profound sensorineural hearing loss. Spiral ganglion neurons (SGNs) are the target cells of the cochlear implant, a neural prosthesis designed to provide important auditory cues to profoundly deaf patients. The ongoing degeneration of SGNs that occurs following sensorineural hearing loss is therefore considered a limiting factor in cochlear implant efficacy. Exogenous application of neurotrophic factors prevents SGN degeneration and can enhance neurite outgrowth. Both the quantity and the quality of surviving SGNs appear to be important for the success of the cochlear implant. The addition of BDNF to the cochlear fluids can prevent degeneration of SGNs after sensory hair cells are lost in adult rodent cochleae. This neurotrophin has to be continuously delivered to maintain neuronal survival as they are rapidly cleared by the bodyu27s physiological mechanism. Current available methods of neurotrophin application are limited to delivery over a period of less than one month, and carry risks of wound infection and viral inoculation. Alternative methods of delivery are needed. We developed a biodegradable and biocompatible polyglutarnic acid particle which along with glycosaminglycan heparin, successfully sequestered BDNF. This BDNF was shown to be released in a biologically active form over a period of 70 days. Its biological activity was confirmed using the neuroblastoma cell line SHSY5Y. These particles were then successfully inserted into a deafened rat cochlea and improved SGN survival. This work has shown that the PGA-heparin particles are potential carriers for BDNF, for clinical application in an effort to improve patient outcome with profound sensorineural hearing loss.
机译:在英国,大约有688,000名成年人患有严重至严重的感音神经性听力损失。尽管许多患有听力损失的人受益于常规助听器的使用,但这些设备对严重的感音神经性听力损失的患者无效。螺旋神经节神经元(SGNs)是人工耳蜗的目标细胞,这是一种神经假体,旨在为严重耳聋的患者提供重要的听觉提示。因此,在感觉神经性听力丧失后发生的SGN持续退化被认为是人工耳蜗植入效率的限制因素。神经营养因子的外源应用可防止SGN变性,并可增强神经突的长出。存活的SGNs的数量和质量对于人工耳蜗的成功至关重要。在成年啮齿动物耳蜗中失去感觉毛细胞后,向耳蜗液中添加BDNF可以防止SGN变性。这种神经营养蛋白必须不断传递,以维持神经元的存活,因为它们会被人体的生理机制迅速清除。当前可用的神经营养蛋白施用方法限于在不到一个月的时间内递送,并且具有伤口感染和病毒接种的风险。需要替代的递送方法。我们开发了一种可生物降解且具有生物相容性的聚戊二酸颗粒,并将其与糖胺糖加肝素一起成功隔离了BDNF。已显示该BDNF在70天内以生物活性形式释放。使用成神经细胞瘤细胞系SHSY5Y确认了其生物学活性。然后将这些颗粒成功插入耳聋的大鼠耳蜗,并改善SGN的存活率。这项工作表明,PGA-肝素颗粒是BDNF的潜在载体,可用于临床应用,以努力改善具有严重的感音神经性听力损失的患者预后。

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    Glynn Fergal J;

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  • 年度 2010
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