A functional tacrolimus-releasing nerve wrap for enhancing nerve regeneration following surgical nerve repair

Simeon C. Daeschler, Katelyn J.W. So, Konstantin Feinberg, M. Manoraj, Jenny Cheung, Jennifer J. Zhang, Kaveh Mirmoeini, J. P. Santerre, Tessa Gordon, G. Borschel
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Abstract

Axonal regeneration following surgical nerve repair is slow and often incomplete, resulting in poor functional recovery which sometimes contributes to lifelong disability. Currently, there are no FDA-approved therapies available to promote nerve regeneration. Tacrolimus accelerates axonal regeneration, but systemic side effects presently outweigh its potential benefits for peripheral nerve surgery. The authors describe herein a biodegradable polyurethane-based drug delivery system for the sustained local release of tacrolimus at the nerve repair site, with suitable properties for scalable production and clinical application, aiming to promote nerve regeneration and functional recovery with minimal systemic drug exposure. Tacrolimus is encapsulated into co-axially electrospun polycarbonate-urethane nanofibers to generate an implantable nerve wrap that releases therapeutic doses of bioactive tacrolimus over 31 days. Size and drug loading are adjustable for applications in small and large caliber nerves, and the wrap degrades within 120 days into biocompatible byproducts. Tacrolimus released from the nerve wrap promotes axon elongation in vitro and accelerates nerve regeneration and functional recovery in preclinical nerve repair models while off-target systemic drug exposure is reduced by 80% compared with systemic delivery. Given its surgical suitability and preclinical efficacy and safety, this system may provide a readily translatable approach to support axonal regeneration and recovery in patients undergoing nerve surgery.
功能性他克莫司释放神经包膜,用于增强手术神经修复后的神经再生能力
手术神经修复后的轴突再生缓慢且往往不完全,导致功能恢复不佳,有时甚至会造成终身残疾。目前,美国食品和药物管理局尚未批准促进神经再生的疗法。他克莫司可加速轴突再生,但目前其全身副作用超过了其对周围神经手术的潜在益处。作者在本文中描述了一种基于聚氨酯的可生物降解给药系统,该系统可在神经修复部位局部持续释放他克莫司,具有适合规模化生产和临床应用的特性,旨在促进神经再生和功能恢复,同时尽量减少全身性药物暴露。将他克莫司封装在同轴电纺聚碳酸酯-聚氨酯纳米纤维中,生成一种可植入的神经包膜,在 31 天内释放治疗剂量的生物活性他克莫司。这种包膜可在 120 天内降解为生物相容性副产品。从神经包膜中释放的他克莫司可促进体外轴突的伸长,并加速临床前神经修复模型中的神经再生和功能恢复,同时与全身给药相比,脱靶的全身药物暴露减少了 80%。鉴于该系统的手术适用性、临床前疗效和安全性,它可以为接受神经手术的患者提供一种易于转化的支持轴突再生和恢复的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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