A tacrolimus-eluting nerve guidance conduit enhances regeneration in a critical-sized peripheral nerve injury rat model

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL Biomedical Microdevices Pub Date : 2024-08-05 DOI:10.1007/s10544-024-00717-y
Azur Azapagic, Jayant Agarwal, Bruce Gale, Jill Shea, Susan Wojtalewicz, Himanshu Sant
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Abstract

Critical-sized peripheral nerve injuries pose a significant clinical challenge and lead to functional loss and disability. Current regeneration strategies, including autografts, synthetic nerve conduits, and biologic treatments, encounter challenges such as limited availability, donor site morbidity, suboptimal recovery, potential immune responses, and sustained stability and bioactivity. An obstacle in peripheral nerve regeneration is the immune response that can lead to inflammation and scarring that impede the regenerative process. Addressing both the immunological and regenerative needs is crucial for successful nerve recovery. Here, we introduce a novel biodegradable tacrolimus-eluting nerve guidance conduit engineered from a blend of poly (L-lactide-co-caprolactone) to facilitate peripheral nerve regeneration and report the testing of this conduit in 15-mm critical-sized gaps in the sciatic nerve of rats. The conduit's diffusion holes enable the local release of tacrolimus, a potent immunosuppressant with neuro-regenerative properties, directly into the injury site. A series of in vitro experiments were conducted to assess the ability of the conduit to maintain a controlled tacrolimus release profile that could promote neurite outgrowth. Subsequent in vivo assessments in rat models of sciatic nerve injury revealed significant enhancements in nerve regeneration, as evidenced by improved axonal growth and functional recovery compared to controls using placebo conduits. These findings indicate the synergistic effects of combining a biodegradable conduit with localized, sustained delivery of tacrolimus, suggesting a promising approach for treating peripheral nerve injuries. Further optimization of the design and long-term efficacy studies and clinical trials are needed before the potential for clinical translation in humans can be considered.

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他克莫司洗脱神经引导导管可促进临界大小周围神经损伤大鼠模型的再生。
严重的周围神经损伤是一项重大的临床挑战,会导致功能丧失和残疾。目前的再生策略,包括自体移植、合成神经导管和生物治疗,都遇到了一些挑战,如可用性有限、供体部位发病率高、恢复效果不理想、潜在的免疫反应以及持续稳定性和生物活性。周围神经再生的一个障碍是免疫反应,它可能导致炎症和疤痕,从而阻碍再生过程。同时满足免疫和再生需求对于神经的成功恢复至关重要。在这里,我们介绍了一种新型可生物降解的他克莫司洗脱神经引导导管,这种导管由聚(L-乳酸-共己内酯)混合物制成,可促进外周神经再生。这种导管的扩散孔能将具有神经再生特性的强效免疫抑制剂他克莫司直接释放到损伤部位。我们进行了一系列体外实验,以评估导管能否保持受控的他克莫司释放曲线,从而促进神经元的生长。随后在坐骨神经损伤大鼠模型中进行的体内评估显示,与使用安慰剂导管的对照组相比,神经再生能力显著增强,轴突生长和功能恢复均有所改善。这些研究结果表明,将生物可降解导管与局部持续输送他克莫司相结合具有协同效应,是一种治疗周围神经损伤的可行方法。需要进一步优化设计、开展长期疗效研究和临床试验,才能考虑将其应用于人类临床。
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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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