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阿霉素负载于羟基磷灰石植入物中的抗肿瘤作用及其在荷斯旺大鼠软骨肉瘤的癌大鼠模型中的分布

Antitumor effects and distribution of adriamycin incorporated into hydroxyapatite implants in a cancer rat model bearing swarm rat chondrosarcoma.

作者信息

Yamamura K, Iwata H, Osada T, Yotsuyanagi T, Nabeshima T

机构信息

Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University School of Medicine, Japan.

出版信息

Jpn J Pharmacol. 1994 Dec;66(4):433-8. doi: 10.1254/jjp.66.433.

Abstract

We investigated the antitumor effects and tissue distribution of adriamycin (ADR) incorporated into a hydroxyapatite (HAP) bead in a cancer rat model bearing Swarm rat chondrosarcoma. The Porous HAP bead (8.48 mm in diameter, 531 +/- 0.7 mg in weight) was used as a model bone graft. One ADR-HAP bead (ADR 0.4 mg-6.0 mg/bead) was implanted s.c. into a Sprague-Dawley rat at 6 days postinoculation of Swarm rat chondrosarcoma. ADR-HAP beads showed strong antitumor activities in a dose dependent manner. The dose of 6.0 mg/bead showed the highest efficacy with no toxic death: It caused a 98% growth inhibition on Day 31 postinoculation and a survival advantage of a 339% increase in life span. After the implantation of the ADR-HAP bead (0.4 mg/bead/body) and the i.v. administration of an equal dose of free adriamycin, we determined the tissue distribution of ADR for up to 90 days. ADR-HAP bead implanted in the tumors released ADR over a 12-week period in the target area. The diffusion of the drug to other organs such as the heart and liver was very low compared with the tumors. The area under the ADR concentration-time curve (AUC) of the tumors was 181.6 micrograms.day/g and 5.22 micrograms.day/g after the implantation of the ADR-HAP bead and the i.v. administration of free ADR, respectively. The targeting index of the tumors, defined as the ratio of the AUC after the implantation of the ADR-HAP bead to that after administration of free ADR, was 34.8.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们在携带斯沃姆大鼠软骨肉瘤的癌症大鼠模型中,研究了掺入羟基磷灰石(HAP)微珠中的阿霉素(ADR)的抗肿瘤作用和组织分布。多孔HAP微珠(直径8.48毫米,重量531±0.7毫克)用作模型骨移植物。在接种斯沃姆大鼠软骨肉瘤6天后,将一粒ADR-HAP微珠(ADR 0.4毫克 - 6.0毫克/微珠)皮下植入一只Sprague-Dawley大鼠体内。ADR-HAP微珠呈剂量依赖性地显示出强大的抗肿瘤活性。6.0毫克/微珠的剂量显示出最高疗效且无毒性死亡:在接种后第31天引起98%的生长抑制,寿命延长339%。在植入ADR-HAP微珠(0.4毫克/微珠/只)并静脉注射等量游离阿霉素后,我们测定了长达90天的ADR组织分布。植入肿瘤中的ADR-HAP微珠在靶区域12周内持续释放ADR。与肿瘤相比,药物向心脏和肝脏等其他器官的扩散非常低。植入ADR-HAP微珠和静脉注射游离ADR后,肿瘤的ADR浓度 - 时间曲线下面积(AUC)分别为181.6微克·天/克和5.22微克·天/克。肿瘤的靶向指数定义为植入ADR-HAP微珠后的AUC与注射游离ADR后的AUC之比,为34.8。(摘要截断于250字)

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