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通过扫描电子显微镜和透射电子显微镜分析药物释放型可生物降解微球的脑生物相容性。

Analysis of brain biocompatibility of drug-releasing biodegradable microspheres by scanning and transmission electron microscopy.

作者信息

Veziers J, Lesourd M, Jollivet C, Montero-Menei C, Benoit J P, Menei P

机构信息

Service de Neurochirurgie, Centre Hospitalo-Universitaire d'Angers, France.

出版信息

J Neurosurg. 2001 Sep;95(3):489-94. doi: 10.3171/jns.2001.95.3.0489.

Abstract

OBJECT

Stereotactically guided implantation of biodegradable microspheres is a promising strategy for delivery of neurotrophic factors in a precise and spatially defined brain area. The goal in this study was to show the biocompatibility of poly(D,L,lactide-co-glycolide) microspheres with brain tissue at the ultrastructural level and to analyze the three-dimensional (3D) ultrastructure after intrastriatal implantation of these microparticles.

METHODS

Scanning and transmission electron microscopy were used to study the microspheres and their environment after implantation in an inert material (gelatin) and in the rat striatum. Observations were made at different time periods, ranging from 24 hours to 2 months postimplantation.

CONCLUSIONS

The progressive degradation of the microspheres, with vacuolization, deformation, and shrinkage, was well visualized. This degradation was identical in microspheres implanted in the inert material and in the rat brain tissue, independent of the presence of macrophages. The studies preformed in the striatum permitted the authors to demonstrate the structural integrity of axons in contact with microspheres, confirming the biocompatibility of the polymer. Furthermore, scanning electron microscopy showed the preservation of the 3D ultrastructure of the striatum around the microparticles. These microparticles, which can be stereotactically implanted in functional areas of the brain and can release neurotrophic factors, could represent, for some indications, an alternative to gene therapy.

摘要

目的

立体定向引导下植入可生物降解微球是在精确且空间限定的脑区递送神经营养因子的一种有前景的策略。本研究的目的是在超微结构水平上展示聚(D,L-丙交酯-共-乙交酯)微球与脑组织的生物相容性,并分析这些微球纹状体内植入后的三维(3D)超微结构。

方法

使用扫描电子显微镜和透射电子显微镜研究微球及其在植入惰性材料(明胶)和大鼠纹状体后的环境。在植入后24小时至2个月的不同时间段进行观察。

结论

微球的渐进性降解,伴有空泡化、变形和收缩,清晰可见。这种降解在植入惰性材料和大鼠脑组织中的微球中是相同的,与巨噬细胞的存在无关。在纹状体中进行的研究使作者能够证明与微球接触的轴突的结构完整性,证实了聚合物的生物相容性。此外,扫描电子显微镜显示了微粒周围纹状体3D超微结构的保存。这些可以立体定向植入脑功能区并能释放神经营养因子的微粒,对于某些适应症而言,可能是基因治疗的一种替代方法。

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