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用于通过低密度脂蛋白途径递送抗肿瘤药物的药物 - 低密度脂蛋白复合物的制备。

Preparation of drug-low density lipoprotein complexes for delivery of antitumoral drugs via the low density lipoprotein pathway.

作者信息

Lundberg B

出版信息

Cancer Res. 1987 Aug 1;47(15):4105-8.

PMID:3607752
Abstract

The receptor-mediated assimilation of low density lipoprotein (LDL) by many cancer cells is much higher than that of normal cells. This fact suggests that lipoproteins with incorporated cytotoxic drugs may be used as a carrier for chemotherapeutic agents to neoplastic cells. In this study a lipophilic cytotoxic compound is incorporated into reconstituted LDL by two different methods. Both the structure and cellular uptake were found to be similar to those of native LDL. Tests of the cytotoxic activity on cultured cells demonstrated that the drug delivered to the cells via the LDL pathway was able to kill 100% of the cells. Heparin and a low temperature, which are known to inhibit uptake of LDL by the receptor mechanism, abolished the cytotoxic activity of the drug-lipoprotein conjugates. The results suggest that it may be possible to use reconstituted LDL as a vehicle for lipophilic antineoplastic drugs in order to increase the drug accumulation and selectivity in tumor cell populations with high LDL receptor activity.

摘要

许多癌细胞通过受体介导对低密度脂蛋白(LDL)的摄取比正常细胞高得多。这一事实表明,掺入细胞毒性药物的脂蛋白可作为化疗药物向肿瘤细胞输送的载体。在本研究中,一种亲脂性细胞毒性化合物通过两种不同方法掺入重组LDL中。发现其结构和细胞摄取与天然LDL相似。对培养细胞的细胞毒性活性测试表明,通过LDL途径输送到细胞的药物能够杀死100%的细胞。已知通过受体机制抑制LDL摄取的肝素和低温消除了药物-脂蛋白缀合物的细胞毒性活性。结果表明,有可能将重组LDL用作亲脂性抗肿瘤药物的载体,以增加药物在具有高LDL受体活性的肿瘤细胞群体中的积累和选择性。

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