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PEG-雷公藤红素偶联衍生物的水相合成及其自组装纳米粒的抗肿瘤活性研究。

Synthesis and anti-tumor activity study of water-soluble PEG-celastrol coupling derivatives as self-assembled nanoparticles.

机构信息

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, PR China.

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, PR China.

出版信息

Bioorg Med Chem Lett. 2019 Mar 1;29(5):685-687. doi: 10.1016/j.bmcl.2019.01.042. Epub 2019 Feb 1.

Abstract

To improve the drug-ability of celastrol, a series of PEGylation celastrol (PEGC) were designed and synthesized by conjugation with different kinds of polyethylene glycols (PEGs) with celastrol. Most of PEGCs could easily dissolve in water. In particular, one of them (DC1000) could be dispersed in water to form nanoparticles by self-assembly. The cytotoxic evaluation of PEGCs revealed that some of PEGCs showed more potent cytotoxicity than celastrol, and the molecular weight of PEG parts in PEGCs had apparent influence on their cytotoxic activity. Anti-tumor evaluation in vivo showed DC1000 had higher tumor inhibition rate and better safety than celastrol by intravenous administration with equivalent molar weight. These results revealed PEGylation might be an efficient and economical method to improve the water solubility and safety of celastrol and similar natural products.

摘要

为了提高雷公藤红素的成药性,设计并合成了一系列通过与不同种类的聚乙二醇(PEG)与雷公藤红素连接得到的聚乙二醇化雷公藤红素(PEGC)。大多数 PEGC 都可以很容易地溶解在水中。特别是,其中一种(DC1000)可以通过自组装分散在水中形成纳米粒子。对 PEGC 的细胞毒性评估表明,其中一些 PEGC 比雷公藤红素具有更强的细胞毒性,并且 PEGC 中 PEG 部分的分子量对其细胞毒性活性有明显的影响。体内抗肿瘤评估表明,静脉注射等摩尔重量的 DC1000 比雷公藤红素具有更高的肿瘤抑制率和更好的安全性。这些结果表明,聚乙二醇化可能是一种有效且经济的方法,可以提高雷公藤红素和类似天然产物的水溶性和安全性。

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