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一种用于靶向肝癌化疗的分支小分子-药物偶联纳米药物策略。

A branched small molecule-drug conjugate nanomedicine strategy for the targeted HCC chemotherapy.

作者信息

Li Sha-Sha, Zhang Cheng-Mei, Wu Jing-De, Liu Chao, Liu Zhao-Peng

机构信息

Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012, PR China.

Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, 250012, PR China.

出版信息

Eur J Med Chem. 2022 Jan 15;228:114037. doi: 10.1016/j.ejmech.2021.114037. Epub 2021 Dec 2.

Abstract

Off-target toxicity is one of the main challenges faced by anticancer chemotherapeutics. For tumor targeted and precision chemotherapy, we take the advantages of the ligand directed tumor active targeting of small molecule drug conjugates (SMDCs) and the passive tumor targeting of nanoparticles via the enhanced penetration and retention (EPR) effects, put forward a branched small molecule drug conjugate (BSMDC) nanomedicine design concept. In a proof of concept, we used pentaerythritol as the branched moiety, galactosamine (GalN) as the hepatocellular carcinoma (HCC) directing ligands, PTX as a payload, and a stearoyl moiety as the amphiphilic property adjusting group, designed and synthesized BSMDC 1 and prepared its NPs. In cellular level, the BSMDC 1 NPs targeted asialoglycoprotein receptor (ASGPR)-overexpressing HepG2 cells, were effectively taken up in the cells and released in tumor microenvironments, inhibited the HepG2 cell proliferation, arrested HepG2 cell in G2/M phase and induced tumor cell apoptosis. In HepG2 xenograft nude mice, the BSMDC 1 NPs were high specific to target the tumor and demonstrated a higher antitumor efficiency than BSMDC 1, having no apparent influences on mice body weights and major organs, supporting our BSMDC nanomedicine design concept. Therefore, this new strategy may find applications for cancer targeted and precision chemotherapy.

摘要

脱靶毒性是抗癌化疗药物面临的主要挑战之一。对于肿瘤靶向和精准化疗,我们利用小分子药物偶联物(SMDC)的配体导向肿瘤活性靶向以及纳米颗粒通过增强渗透和滞留(EPR)效应的被动肿瘤靶向优势,提出了一种分支小分子药物偶联物(BSMDC)纳米药物设计概念。在概念验证中,我们使用季戊四醇作为分支部分,半乳糖胺(GalN)作为肝细胞癌(HCC)导向配体,紫杉醇(PTX)作为有效载荷,硬脂酰部分作为两亲性调节基团,设计并合成了BSMDC 1并制备了其纳米颗粒。在细胞水平上,靶向过表达去唾液酸糖蛋白受体(ASGPR)的HepG2细胞的BSMDC 1纳米颗粒在细胞中被有效摄取并在肿瘤微环境中释放,抑制HepG2细胞增殖,使HepG2细胞停滞在G2/M期并诱导肿瘤细胞凋亡。在HepG2异种移植裸鼠中,BSMDC 1纳米颗粒对肿瘤具有高特异性,并且显示出比BSMDC 1更高的抗肿瘤效率,对小鼠体重和主要器官没有明显影响,支持了我们的BSMDC纳米药物设计概念。因此,这种新策略可能在癌症靶向和精准化疗中找到应用。

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