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脊髓挫伤损伤后,将包裹在可生物降解纳米颗粒中的神经营养因子持续注入脊髓。

Sustained intraspinal delivery of neurotrophic factor encapsulated in biodegradable nanoparticles following contusive spinal cord injury.

作者信息

Wang Yu-Chao, Wu Yi-Ting, Huang Hsin-Ying, Lin Hsin-I, Lo Leu-Wei, Tzeng Shun-Fen, Yang Chung-Shi

机构信息

Center for Nanomedicine Research, National Health Research Institutes, 35 Keyan Road, Zhunan 350, Taiwan.

出版信息

Biomaterials. 2008 Dec;29(34):4546-53. doi: 10.1016/j.biomaterials.2008.07.050. Epub 2008 Sep 6.

Abstract

Glial cell line derived neurotrophic factor (GDNF) induces neuronal survival and tissue repair after spinal cord injury (SCI). A continuous GDNF supply is believed to gain greater efficacy in the neural restoration of the injured spinal cord. Accordingly, nanovehicle formulation for their efficient delivery and sustained release in injured spinal cord was examined. We first used fluorescence-labeled bovine serum albumin (FBSA) loaded in biodegradable poly(lactic acid-co-glycolic acid) (PLGA) for intraspinal administration after SCI and for in vitro study. Our results showed that the preservation of PLGA-FBSA was observed in the injured spinal cord at 24h, and PLGA-FBSA nanoparticles were well absorbed by neurons and glia, indicating that PLGA as a considerable nanovehicle for the delivery of neuroprotective polypeptide into injured spinal cord. Furthermore, intraspinal injection of GDNF encapsulated in PLGA (PLGA-GDNF) nanoparticles into the injured spinal cord proximal to the lesion center had no effect on gliosis when compared to that observed in SCI rats receiving PLGA injection. However, local administration of PLGA-GDNF effectively preserved neuronal fibers and led to the hindlimb locomotor recovery in rats with SCI, providing a potential strategy for the use of PLGA-GDNF in the treatment of SCI.

摘要

胶质细胞系源性神经营养因子(GDNF)可诱导脊髓损伤(SCI)后神经元存活和组织修复。持续供应GDNF被认为在损伤脊髓的神经修复中能获得更大疗效。因此,研究了用于其在损伤脊髓中高效递送和持续释放的纳米载体制剂。我们首先使用负载于可生物降解聚乳酸-乙醇酸共聚物(PLGA)中的荧光标记牛血清白蛋白(FBSA)进行SCI后的脊髓内给药及体外研究。我们的结果表明,在24小时时损伤脊髓中观察到PLGA-FBSA的留存,并且PLGA-FBSA纳米颗粒被神经元和神经胶质细胞良好吸收,这表明PLGA作为一种将神经保护多肽递送至损伤脊髓的重要纳米载体。此外,与接受PLGA注射的SCI大鼠相比,向损伤中心近端的损伤脊髓内注射包裹在PLGA(PLGA-GDNF)纳米颗粒中的GDNF对胶质增生没有影响。然而,局部给予PLGA-GDNF有效地保留了神经元纤维,并导致SCI大鼠后肢运动功能恢复,为PLGA-GDNF用于SCI治疗提供了一种潜在策略。

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