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间质内药物输注期间大分子在灰质中的对流增强分布。

Convection-enhanced distribution of large molecules in gray matter during interstitial drug infusion.

作者信息

Lieberman D M, Laske D W, Morrison P F, Bankiewicz K S, Oldfield E H

机构信息

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Neurosurg. 1995 Jun;82(6):1021-9. doi: 10.3171/jns.1995.82.6.1021.

Abstract

Many novel experimental therapeutic agents, such as neurotrophic factors, enzymes, biological modifiers, and genetic vectors, do not readily cross the blood-brain barrier. An effective strategy to deliver these compounds to the central nervous system is required for their application in vivo. Under normal physiological conditions, brain interstitial fluid moves by both bulk flow (convection) and diffusion. It has recently been shown that interstitial infusion into the white matter can be used to increase bulk flow, produce interstitial convection, and efficiently and homogeneously deliver drugs to large regions of brain without significant functional or structural damage. In theory, even more uniform distribution is likely in gray matter. In the current study, four experiments were performed to examine if convection-enhanced delivery could be used to achieve regional distribution of large molecules in gray matter. First, the volume and consistency of anatomical distribution of 20 microliters of phaseolus vulgaris-leukoagglutinin (PHA-L; molecular weight (MW) 126 kD) after continuous high-flow microinfusion into the striatum of five rats over 200 minutes were determined using immunocytochemistry and quantified with image analysis. Second, the concentration profile of 14C-albumin (MW 69 kD) infused under identical conditions was determined in four hemispheres using quantitative autoradiography. Third, the volume of distribution after convection-enhanced infusion of 250 or 500 microliters biotinylated dextran (b-dextran, MW 10 kD), delivered over 310 minutes into the caudate and putamen of a rhesus monkey from one (250 microliters) or two (500 microliters) cannulas, was determined using immunocytochemistry and quantified with image analysis. Finally, the ability to target all dopaminergic neurons of the nigrostriatal tract via perfusion of the striatum with subsequent retrograde transport was assessed in three experiments by immunohistochemical analysis of the mesencephalon following a 300-minute infusion of 27 microliters horseradish peroxidase-labeled wheat germ agglutinin (WGA-HRP) into the striatum. Convection-enhanced delivery reproducibly distributed the large-compound PHA-L throughout the rat striatum (the percent volume of the striatum perfused, Vs, was 86% +/- 5%; mean +/- standard deviation) and produced a homogeneous tissue concentration in the perfused region (concentration of 14C-albumin relative to infusate concentration 30% +/- 5%). In the monkey, the infusion widely distributed b-dextran within the striatum using one cannula (caudate and putamen Vs = 76% and 76%) or two cannulas (Vs = 90% and 71%).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

许多新型实验治疗剂,如神经营养因子、酶、生物修饰剂和基因载体,不易穿过血脑屏障。要将这些化合物应用于体内,就需要一种将其递送至中枢神经系统的有效策略。在正常生理条件下,脑间质液通过整体流动(对流)和扩散两种方式移动。最近研究表明,向白质进行间质输注可用于增加整体流动、产生间质对流,并在不对大脑造成明显功能或结构损伤的情况下,将药物有效且均匀地递送至大脑的大片区域。理论上,在灰质中分布可能更均匀。在本研究中,进行了四项实验,以检验对流增强递送是否可用于实现大分子在灰质中的区域分布。首先,通过免疫细胞化学方法确定了在200分钟内对五只大鼠的纹状体进行连续高流量微量输注20微升菜豆白细胞凝集素(PHA-L;分子量(MW)126 kD)后的解剖分布体积和一致性,并通过图像分析进行定量。其次,使用定量放射自显影法在四个半球中确定了在相同条件下输注的14C-白蛋白(MW 69 kD)的浓度分布。第三,通过免疫细胞化学方法确定了在310分钟内从一根(250微升)或两根(500微升)插管向恒河猴的尾状核和壳核输注250或500微升生物素化葡聚糖(b-葡聚糖,MW 10 kD)后通过对流增强输注的分布体积,并通过图像分析进行定量。最后,在三项实验中,通过对中脑进行免疫组织化学分析,评估了在向纹状体灌注27微升辣根过氧化物酶标记的小麦胚芽凝集素(WGA-HRP)300分钟后,通过纹状体灌注随后逆行转运来靶向黑质纹状体束所有多巴胺能神经元的能力。对流增强递送可重复性地将大分子化合物PHA-L分布于整个大鼠纹状体(灌注的纹状体体积百分比,Vs,为86%±5%;平均值±标准差),并在灌注区域产生均匀的组织浓度(14C-白蛋白浓度相对于输注液浓度为30%±5%)。在猴子中,使用一根插管(尾状核和壳核Vs = 76%和76%)或两根插管(Vs = 90%和71%),输注使b-葡聚糖在纹状体内广泛分布。(摘要截断于400字)

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