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采用生物可降解硅纳米胶囊实现天然抗体和 siRNA 的细胞内共递用于联合治疗。

Intracellular Co-delivery of native antibody and siRNA for combination therapy by using biodegradable silica nanocapsules.

机构信息

School of Pharmaceutical Sciences (Shen Zhen), Shenzhen Campus of Sun Yat-sen University, No. 66, Gongchang Road, Guangming District, Shenzhen, Guangdong, 518107, PR China; Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore.

School of Pharmaceutical Sciences (Shen Zhen), Shenzhen Campus of Sun Yat-sen University, No. 66, Gongchang Road, Guangming District, Shenzhen, Guangdong, 518107, PR China.

出版信息

Biomaterials. 2022 Feb;281:121376. doi: 10.1016/j.biomaterials.2022.121376. Epub 2022 Jan 17.

Abstract

Combination therapy is a promising strategy for treating multidrug-resistant (MDR) cancers. Macromolecules such as antibodies and RNAs have been successfully used for targeted therapy owing to their high specificity. However, their application as therapeutics remains limited due to membrane impermeability and poor intracellular stability. Designing drug delivery systems capable of co-administering macromolecules is therefore crucial for advancing them as therapeutics for combination therapy. Herein, by using glutathione (GSH)-responsive biodegradable silica nanocapsules (BS-NPs), we report for the first time a highly versatile nanomaterial-based strategy for co-encapsulation and intracellular co-delivery of different combinations of macromolecules (i.e., siRNA/protein, siRNA/antibody and protein/antibody). This strategy was successfully used in the intracellular co-delivery of siRNA/Cetuximab (also named Erbitux™) for combination therapy in epidermal growth factor receptor (EGFR)-overexpressing cancer cells. These BS-NPs showed good biosafety profiles and antitumor efficacy when administered in vivo, suggesting that the strategy holds potential as a novel delivery platform for combination cancer therapy.

摘要

联合治疗是治疗多药耐药(MDR)癌症的一种有前途的策略。由于具有高特异性,抗体和 RNA 等大分子已被成功用于靶向治疗。然而,由于它们的细胞膜通透性差和细胞内稳定性差,其作为治疗剂的应用仍然受到限制。因此,设计能够同时给药大分子的药物递送系统对于将它们作为联合治疗的治疗剂推进至关重要。在此,通过使用谷胱甘肽(GSH)响应性可生物降解的硅纳米胶囊(BS-NPs),我们首次报道了一种基于高度通用的纳米材料的策略,用于共包封和细胞内共递不同组合的大分子(即,siRNA/蛋白、siRNA/抗体和蛋白/抗体)。该策略成功地用于表皮生长因子受体(EGFR)过表达癌细胞中 siRNA/Cetuximab(也称为 Erbitux™)的细胞内共递,用于联合治疗。这些 BS-NPs 在体内给药时表现出良好的生物安全性和抗肿瘤功效,表明该策略具有作为新型联合癌症治疗递送平台的潜力。

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