Microscopic analysis of arterial microsphere distribution in rabbit liver and hepatic VX2 tumor.

K M Pillai, P E McKeever, C A Knutsen, P A Terrio, D M Prieskorn, W D Ensminger
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引用次数: 40

Abstract

Microspheres conjugated to radioisotopes and chemotherapeutic agents are playing an important investigative and clinical role in the management of metastatic neoplasms. The purpose of our investigation was to histologically assess the basis for regional intra-arterial microsphere therapy, by comparing the spatial distribution of microspheres in the tumor and liver of experimental models of hepatic metastases. Three New Zealand white rabbits with hepatic VX2 tumor implants were arterially injected with hepatic doses of either 15 or 30 million blue-dyed, polystyrene microspheres (27 microns-diameter). Microscopic examination of random liver and tumor samples revealed that 6-12 times as many microspheres were embolized within tumor than in normal liver (p less than 0.002). The majority of microspheres aggregated into clusters of various size within liver and tumor vasculature, though analysis of cluster sizes illustrated an exponentially skewed distribution toward isolated microspheres. Approximately eight times as many clusters were observed in tumor than in liver (p less than 0.008). Finally, a morphometric analysis was used to quantitate the minimal distances separating microsphere clusters, the intercluster distance (ICD). Analysis of over three thousand intercluster measurements revealed a median ICD approximately five times lower in tumor than in liver (p less than 1 x 10(-8)). This microquantitative analysis provides a fundamental description of how regional intra-arterial microsphere therapy allows the targeted delivery of microspheres to neoplastic tissue, to potentially improve the therapeutic index in the treatment of hepatic metastases.

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兔肝脏及肝VX2肿瘤动脉微球分布的显微分析。
结合放射性同位素和化疗药物的微球在转移性肿瘤的治疗中发挥着重要的研究和临床作用。本研究的目的是通过比较肝转移实验模型肿瘤和肝脏中微球的空间分布,从组织学上评估区域动脉内微球治疗的基础。三只新西兰大白兔的肝脏VX2肿瘤植入物被动脉注射了1500万或3000万个蓝染聚苯乙烯微球(直径27微米)。随机肝脏及肿瘤标本镜检显示,肿瘤内微球栓塞数为正常肝脏的6 ~ 12倍(p < 0.002)。大多数微球在肝脏和肿瘤血管中聚集成不同大小的簇,尽管簇大小的分析表明,微球向孤立的微球呈指数倾斜分布。肿瘤中观察到的簇数约为肝脏的8倍(p < 0.008)。最后,使用形态计量学分析来量化微球簇间距离(ICD)。对超过3000个簇间测量的分析显示,肿瘤的中位ICD比肝脏低约5倍(p小于1 × 10(-8))。这种微定量分析提供了一种基本的描述,说明了局部动脉内微球治疗如何允许将微球靶向递送到肿瘤组织,从而潜在地提高肝转移治疗的治疗指数。
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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Expression of the multidrug transporter P-glycoprotein and in vitro chemosensitivity: correlation with in vivo response to chemotherapy in acute myeloid leukemia. A pilot clinical and pharmacokinetic study of intracarotid cisplatin and bleomycin. Detection of P-glycoprotein with JSB-1 monoclonal antibody in B-5 fixed and paraffin-embedded cell lines and tissues. Microscopic analysis of arterial microsphere distribution in rabbit liver and hepatic VX2 tumor. Synthetic polymers conjugated to monoclonal antibodies: vehicles for tumour-targeted drug delivery.
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